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Genus Parkia: Phytochemical, Medicinal Uses, and Pharmacological Properties

Mohammed S. M. Saleh
Juriyati Jalil
Satirah Zainalabidin
Ahmad Yusof Asmadi
Nor Hidayah Mustafa
2 and
Yusof Kamisah
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Kuala Lumpur 56000, Malaysia
Drug and Herbal Research Centre, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Kuala Lumpur 50300, Malaysia
Program of Biomedical Science, Centre of Toxicology and Health Risk Study, Faculty of Health Sciences, Universiti Kebangsaan Malaysia, Kuala Lumpur 50300, Malaysia
Unit of Pharmacology, Faculty of Medicine and Defence Health, Universiti Pertahanan Nasional Malaysia, Kem Sungai Besi, Kuala Lumpur 57000, Malaysia
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2021, 22(2), 618;
Submission received: 25 December 2020 / Revised: 7 January 2021 / Accepted: 7 January 2021 / Published: 9 January 2021
(This article belongs to the Special Issue Biological Properties of Medicinal Plants)


The genus Parkia (Fabaceae, Subfamily, Mimosoideae) comprises about 34 species of mostly evergreen trees widely distributed across neotropics, Asia, and Africa. This review aims to provide an overview of the current status of the species from the genus Parkia in terms of its relationship between its phytochemistry and medical uses. Comprehensive information on Parkia species was retrieved from electronic databases, which were Web of Science, ScienceDirect, PubMed, and Google Scholar. This review identified nine species from genus Parkia with properties of medicinal use. They are used traditionally to treat several ailments, such as diabetes, diarrhea, wounds, hypertension, cough, chronic piles, conjunctivitis, and measles. The most common species studied are P. biglobosa, P. speciosa, P. javanica, P. bicolor, P. biglandulosa, P. filicoidea, and P. clappertoniana. A considerable number of secondary metabolites, such as terpenoids, phenolic acids, flavonoids (aglycone and glycosides), and numerous volatile compounds have been identified in this genus, which are responsible for their diverse pharmacological activities. Their extracts, pure compounds and seed lectins have been reported for their anticancer, antimicrobial, antihypertensive, antiulcer, antidiabetic, anti-inflammatory, antioxidant, antimalarial, hepatoprotective, and antidiarrheal activities. The information gathered in this review might be of help for future studies in terms of the current knowledge on the link between the phytochemical components and medicinal uses. This could facilitate more discoveries on its potentials particularly in the pharmacological characteristics and potential to be developed into modern medicines.

1. Introduction

Parkia is a genus of flowering plants belonging to the family Fabaceae (subfamily, Mimosoideae) with pan-tropical distribution [1]. The word Parkia was named after the Scottish explorer Mungo Park, who drowned in the Niger River, Nigeria in January 1805 [2]. Thirty-one species from this genus were reported in 1995 [3]. Another four more species were discovered in 2009 [4]. Out of these species, 10 species found in Asia, four in Africa, and 20 in neotropics. Meanwhile, according to a plant list (2018), 80 scientific names are recorded from the genus Parkia containing 41 accepted names and 39 synonym species (The Plant List, 2018). These plants bear fruits called pods. Each pod contains up to 25–30 seeds. Many species from Parkia have been reported to be rich in carbohydrate [5,6,7], protein [8,9,10] and minerals [11,12,13,14].
From our extensive research regarding the biological, pharmacological, and phytochemical constituents of species from the genus Parkia, only 12 species have been scientifically investigated so far. Out of these, nine were studied on phytochemical analysis and determination of biological activities, which include P. bicolor, P. biglobosa, P. biglandulosa, P. filicoidea, P. clappertoniana, P. javanica (synonyms: P. roxburghii, P. timoriana), P. pendula, P. platycephala, and P. speciosa. The most frequently investigated over a wide range of ailments are P. biglobosa and P. speciosa. Studies on the remaining three species (P. velutina, P. nitida, and P. polyads) focused on morphological variations and environmental distribution. This review aims to collate the present state of medicinal uses and phytochemistry of the genus Parkia for future studies. The link between the phytochemical components and medicinal uses of the current knowledge is discussed with the hope it would expedite more discoveries that have potentials to be developed into modern medicines.

2. Methodology

Information of the ethnobotanical use of plants from genus Parkia was retrieved from electronic databases which were ScienceDirect, Web of Science, Google Scholar, and PubMed, using search terms of “Parkia AND ethnobotanical”, Parkia AND pharmacological”, “Parkia AND pharmaceutical”, “Parkia AND toxicological studies”, “Parkia AND bioactivity”, “Parkia AND phytochemistry”, “Parkia AND ethnomedicinal”, and “Parkia AND morphological”. A total of 543 abstracts of research articles books, and conference papers published from 1961 to 2020 were obtained. Duplicates (n = 231) were removed. From the remaining 312 records, one hundred and two titles were excluded due to unavailability of full text or not published in English. Only articles and abstracts published in English were included. Two hundred and ten research articles and book chapters containing relevant and useful information were included in this review (Figure 1). Information gathered on the traditional uses, pharmacology and bioactive compounds identified from Parkia genus were summarized in the form of two tables and four figures. Chemical structures of bioactive compounds reported were drawn using ChemDraw software 16.0 (PerkinElmer Informatics, Waltham, MA, USA).

3. Traditional Medicinal Uses

Parkia species are being used across all tropical countries to cure different ailments. Virtually, all parts of Parkia plants are utilized traditionally for different medicinal purposes. The materials of different parts of Parkia plants are processed as paste, decoction, and juice for the treatment of various ailments (Table 1). Almost all reported Parkia species are used in different forms to cure diarrhea and dysentery [15]. Different parts of P. biglobosa, P. clappertoniana, P. roxburghii, and P. speciosa are reported to be traditionally used for the treatment of diabetes [16,17,18]. Furthermore, skin-related diseases, such as eczema, skin ulcers, measles, leprosy, wound, dermatitis, chickenpox, scabies, and ringworm are treated using leaves, pods, and roots of P. speciosa and P. timoriana [19,20,21]. The stem barks of P. bicolor, P. clappertoniana, P. biglobosa, P. roxburghii as well as roots of P. speciosa are applied in the form of paste and decoction to treat different skin problems [22,23,24,25]. Decoction and paste of stem bark, pod, or root of P. biglobosa and P. speciosa are used to treat hypertension [22,26,27]. Moreover, stem barks of P. bicolor, P. biglobosa and leaves of P. speciosa are used for severe cough and bronchitis [28,29,30]. These aforementioned uses suggested that Parkia plants are likely to contain constituents with broad and diverse biological activities, such as antidiabetic, antimicrobial, antihypertensive, and anti-inflammatory.

4. Phytochemistry of Genus Parkia

Among the numerous species of Parkia plant, the chemistry of only few are known. However, different parts of the reported ones have been validated as good sources of phenolic compounds [11,31,32], saponins [33,34,35], terpenoids [35,36,37], steroids [23,38,39], tannins [38,39,40], fatty acids [23,41], and glycosides [42,43,44].
Various phytochemicals are found in the stem barks, leaves, seeds, and pods of these plants. The stem bark of P. biglobosa is reported to contain phenols, flavonoids, sugars, tannins, terpenoids, steroids, saponins [11,38], alkaloid, and glycosides [35,43,45], while the leaves contain glycosides, tannins, and alkaloids in trace amount [11,23,46], in addition to flavonoids, phenols, and anthraquinones [47]. Phytochemical screening of the seeds shows the presence of saponins, alkaloids, flavonoids, polyphenols, terpenoids, glycosides and tannins [48,49]. Fermentation or roasting of P. biglobosa seeds results in the alteration of the bioactive components.
P. bicolor leaves contain chemical constituents similar to that of P. biglobosa such as glycosides, tannin, and alkaloids in trace amount [23]. The stem bark of P. bicolor contains alkaloids, tannins, saponins, glycosides, flavonoids, and terpenoids [35], while P. biglandulosa contains tannins, saponins, and glycosides, and P. filicoidea possesses flavonoids, sugars, saponins, and tannins [50]. The seed of P. javanica contains flavonoid, saponins, alkaloids, terpenoids, anthraquinones, steroids, and glycosides [44]. The pods are reported to have tannins, flavonoids, and saponins, all of which are significantly diminished when subjected to various processing methods, such as ordinary and pressure cooking methods [51,52]. Alkaloids, glycosides, saponins, and tannins are present in the whole plant of P. clappertoniana [31]. Phytochemical analysis of the leaves of P. platycephala revealed the presence of phenols, terpenoids, flavonoids [53], tannins and saponins [54]. Furthermore, flavonoids, alkaloids, phenols, and terpenoids were reported to be present in all parts of P. speciosa plant [37].
Phytochemicals (primary and secondary metabolites) are well known for their vast medicinal benefits to plants and human [100]. The primary metabolites—such as carbohydrate, proteins, chlorophyll, lipids, nucleic, and amino acids [101,102,103]—are responsible for plants’ biochemical reactions such as respiration and photosynthesis [102]. The secondary metabolites are majorly alkaloids, phenols, terpenoids, flavonoids, saponins, steroids, tannins, and glycosides, which play important roles in protecting the plants against damages and improving plant aroma, coloration and flavor [101,103], The phytochemicals are present in various parts of the plants especially in the three major parts viz. the leaves, stems and roots. Their percentage composition in each plant may vary depending on environmental conditions, variety and processing methods [101]. Previous studies have shown that phenolic compounds are the most abundant and widely distributed phytoconstituents (45%), followed by steroids and terpenoids (27%), and alkaloids (18%) [101,104]. Alkaloids, flavonoids, tannins, and phenolic compounds are the most common constituents that have been studied in phytochemistry [104,105]. Several compounds from these classes have been identified and investigated from Parkia plants for various pharmacological activities. Despite the enormous reports on the phytochemical screening of different species from the genus Parkia, structure identification and purification of compounds from these species are scarcely reported compared to other genera. The compounds were identified using high-performance liquid chromatography with diode-array detector (HPLC-DAD), liquid chromatography mass spectrometry (LCMS), flow analysis-ionization electrospray ion trap tandem mass spectrometry (FIA-ESI-IT-MS), gas chromatography time-of-flight mass spectrometry (GC/ToF-MS), high-performance liquid chromatography-electrospray ion mass spectrometry (HPLC-ESI-MS), and chromatographic purification from the fraction and characterization through nuclear magnetic resonance (NMR).

4.1. Polyphenolic Compounds

Phenolic compounds found in Parkia species are grouped into simple phenol (10 and 31), phenolic acids 2941, flavone 1519 and 24, flavanone 2526, flavonol 1114 and 2022, methoxyflavonol 23, as well as flavanol 110 (Table 2). Phenolic acids are mostly found in the pods and edible parts of Parkia, while polyphenolic compounds are present in the leaves, stem barks, roots, or seeds. The most commonly reported flavonoid in Parkia species are flavanol 1 and its isomer 8, which are obtained from the pod and bark of P. speciosa and P. biglobosa, respectively [106,107,108] and the remaining flavanols 1118 are mainly galloylated catechins. Compound 11 is isolated from ethyl acetate fraction of P. roxburghii pod [18], while compounds 1218 are identified from the ethyl acetate fraction of root/stem of P. biglobosa [18]. One methoxyflavonol 23, two flavanone 2627 and isoflavones 2728 are identified in the edible parts of P. javanica [108]. A new flavanone, naringenin-1-4′-di-O-ß-D-glucopyranoside 26 is isolated from n–butanol fraction of P. biglobosa [109], while a new phenylpropanoid is elucidated as 4-(3-hydroxypropyl)benzyl nonanoate from the leaves of P. javanica [110]. Isolation of compounds 4243 for the first time as a pure compound was reported from the ethanol extract of P. biglobosa bark [111]. The structures of these compounds are illustrated in Figure 2 and Figure 3.

4.2. Terpenoid and Steroid

To date, few terpenoid compounds have been reported in Parkia plants. Most of these compounds were identified from barks, roots, leaves, and seeds of Parkia plants. One is monoterpenoid 50 with two of its glucosides 57 and 58, a diterpene 49, while the rest are triterpenoid 49 and 5156 (Table 2 and Figure 4). Seven out of the triterpenoids 5258 were reported as new compounds. Only 49 is reported in three species (P. biglobosa, P. bicolor, and P. speciosa). Two of the new compounds 57 and 58 are iridoid type of terpenoidal glycoside purified from methanol extract of P. javanica, together with ursolic acid and other steroidal compounds [42]. Compounds 5256 are isolated through different chromatographic techniques from 80% methanol extract of P. bicolor root, with a known diterpene 59 and a benzene glucoside 105. These compounds are reported to exhibit moderate antiproliferative activity with median inhibitory concentration (IC50) ranging from 48.89 ± 0.16 to 81.66 ± 0.17 µM [118].
Steroidal compounds are also reported in the genus of Parkia (Table 2 and Figure 4). β-Sitosterol (60) is one of the major components in P. speciosa [120] and P. biglobosa seeds [121]. The steroid together with stigmasterol are purified from recrystallization of chloroform/methanol fraction of P. speciosa seeds. Its composition in P. biglobosa seeds was reported to be about 377 mg/100 g dry weight [122]. It is also purified from methanol extract of P. javanica leaves [42]. Apart from 60, 61, and 65, which are present in P. javanica and/or P. biglobosa, all other steroids 6264 and 66 reported from different studies are found in P. speciosa seeds. Other than β-sitosterol (60), stigmasterol (61), and campesterol (65) are also among the numerous compounds identified from the seeds of P. speciosa [117,119,120,124]. The percentage composition of 60, 61, 62 and a triterpenoid 49 in the plant was reported as 3.42%, 2.18%, 2.29%, and 0.71% w/w, respectively [37]. In the case of P. biglobosa, the percentage composition of 60, 61 and 62 in the seeds is higher with values of 55.7%, 3.42%, 37.1% for the unfermented, and 56.8%, 3.38%, 35.9% for the fermented, respectively, indicating that fermentation process may lower 61 and 62, but increases 60 contents [129]. Meanwhile, Akintayo (2004) had recorded 60 as the most abundant compound in P. biglobosa seeds, constituting approximately 39.5% w/w. Compound 60 was isolated as a pure compound through column chromatographic separation of benzene fraction of P. bicolor leaves [42].

4.3. Miscellaneous Compounds

In addition to polyphenolic and terpenoids, several other compounds that are mainly volatile including aldehydes, esters, pyrazines, ketones, fatty acids, benzenes, alcohols, amines, sulfides, alkanes, and alkenes have been reported from Parkia species (Table 2). These compounds are identified mainly from the seeds. Compound 81 is identified from the natural product for the first time in pentane/dichloromethane fraction of P. speciosa seed using GC/ToF-MS [125]. A greater number of these compounds is identified through phytochemical quantification using different spectroscopic methods. Seven constituents are detected from the fresh seeds of P. speciosa through GC/ToF/MS and the compounds are dominated by linear polysulfide, alcohol, and 3′-thiobis-didodecyl ester. Other major compounds include palmitic acid, arachidonic acid, linoleic acid, linoleic acid chloride, and myristic acid [124]. However, cyclic polysulfides are the major constituents found in cooked P. speciosa seeds (Figure 5) [125]. In addition, some minor components, such as 8284 are also identified. Meanwhile, 132 content in P. speciosa seed was reported to be 4.15 mg/100 g [37], but that of P. biglobosa in a recent study was found to be much higher (53.47 mg/100 g). Phospholipid content of P. biglobosa seeds was about 451 mg/100 g [122]. The seeds also contain palmitic acid, stearic acid, oleic acid, arachidic acid, and linoleic acid, the most abundant fatty acid [22,121,130]. Similar fatty acids are also reported in the raw seeds of P. roxburghii chloroform/methanol extract, in addition to total free phenol (0.56 g/100 g seed flour) and tannins (0.26 g/100 g seed flour) contents [41].

5. Pharmacological Activities of Parkia Species

Numerous bioactive constituents such as phenolics, flavonoids, terpenoids, and volatile compounds present in Parkia species may account for its various health benefits, and therefore responsible for the vast pharmacological properties (Table 3). However, only few species have been extensively studied.

5.1. Antimicrobial Activity

Various parts of many species of Parkia have good antimicrobial activities. They are most active against S. aureus and E. coli (Table 3). So far, there is still no clinical study conducted on the plants investigating the activity. Enormous reports have been made on antimicrobial activity of different parts of P. biglobosa such as leaves [23,65,131,132,133,134,135], stem barks [31,43,45,65,67,131,134,135,136,137], seeds [138], roots [34,38,139] and pods [133,140]. Furthermore, the stem barks and leaves of P. clappertoniana aqueous and methanol extracts investigated on some Gram-positive and Gram-negative bacteria revealed that both stem barks and leaves were effective in all tested organisms, but methanol extract was more potent [71]. The ethanol extract of both leaves and barks demonstrated growth inhibitory effects on multi-drug resistant Salmonella and Shigella isolates [73]. The ethanol extract of P. platycephala seeds tested against six bacteria strains and three yeasts showed no antimicrobial activity [141]. However, lectin obtained from the seed was reported to significantly enhance antibiotic activity of gentamicin against S. aureus and E. coli multi-resistant strains due to interaction between carbohydrate-binding site of the lectin and the antibiotic [142].
In P. speciosa, the water suspension of the seeds displays some remarkable inhibitory activity against bacteria isolated from the moribund fishes and shrimps—S. aureus, A. hydrophila, S. agalactiae, S. anginosus and V. parahaemolyticus—but no detectable activity against E. coli, V. alginolyticus, E. tarda, C. freundii, and V. vulnificus [143]. The methanol, chloroform, and petroleum ether extracts of the seeds demonstrate growth inhibitory effect against H. pylori [144], while the ethyl acetate extract against E. coli, but no effect on S. typhi, S. sonnei, and S. typhimurium [144]. The antimicrobial activity of P. speciosa is attributable to the presence of cyclic polysulfides 85 and 9294 in the seeds [126]. However, possible mechanism of the polysulfides was not elucidated. Both pod extract and its synthesized silver nanoparticles exhibit antibacterial activity, with the latter shows higher activity against P. aeruginosa [145]. A similar antibacterial activity is also seen with aqueous extract of P. speciosa leaves and its silver nanoparticles against S. aureus, B. subtilis, E. coli, and P. aeruginosa [146]. Its bark methanol extract inhibits the growth of Gloeophyllum trabeum, but not Pycnoporus sanguineus, which effect is not seen with both sapwood and heartwood of the plant [147]. Its ethyl acetate extract of the peel also shows four times higher activity against S. aureus and three times higher against E. coli than streptomycin, but n-hexane extract exhibits lower activity [148].
Various parts of P. timoriana inhibit growth of B. cereus, V. cholerae, E. coli, and S. aureus [149]. Its leaf extract exhibits significant growth inhibitory effect against E. coli, V. cholerae, S. aureus, and B. cereus [150], while its gold and silver nanoparticles from dried leaves inhibit S. aureus growth. The activity is believed to be attributable to the accumulation and absorption of the gold and silver nanoparticles into S. aureus cell wall [151]. The methanol extract and semi-polar fractions (chloroform and ethyl acetate) of the bark demonstrate significant inhibitory effects against Neisseria gonorrhoeae. The chloroform extract shows the best activity [97]. The aqueous extract of the seed, leaf and skin pod also possess antimicrobial activity [152].
Acetone, ethanol and aqueous extracts of P. biglandulosa stem bark were among the plant extracts that show the highest antimicrobial activity against bacteria and fungi [69] as well as plant pathogenic bacteria [153]. The methanol extract of the leaves also shows remarkable growth inhibition against E. coli, P. aeruginosa, and S. aureus [154]. Investigation on P. bicolor indicates that ethyl acetate, ethanol, and aqueous extracts of the leaves demonstrate a concentration-dependent growth inhibitory effect against some Gram-positive of bacteria such as E. coli, S. aureus, P. aeruginosa, A. niger, B. cereus, and a fungus, C. utilis [23]. Methanol, ethyl acetate, and water extracts of the root also exhibit different degrees of inhibition against some common human pathogenic bacteria including C. diphtheriae, K. pneumoniae, P. mirabilis, S. typhi, and S. pyogenes [28]. The possible mechanism of the antimicrobial activity of Parkia plants are yet to be determined. However, terpenoids from the plants could induce lipid flippase activity in the bacterial cellular membrane which then enhances membrane damage for a better cell penetration [155]. Other possible actions could be by damaging bacterial protein, inhibiting DNA gyrase and DNA synthesis, which are yet to be confirmed in further studies.
Collectively, it can be concluded that the antimicrobial properties of Parkia plants depend on the species and parts of Parkia as well as solvent (polar and non-polar). Most of the published report are in in vitro evaluations, which do not assure the same outcomes in animal models and clinical setting. In the rise of resistant pathogenic bacteria to antimicrobial therapy, it is an urgent need to develop new antimicrobial agents, and phytoconstituents from plants like Parkia could be good candidates.

5.2. Antidiabetic Activity

P. speciosa is the most studied among other species for antidiabetic activity. Six studies comprising three in vitro and three in vivo studies have demonstrated hypoglycemic activity of the plant, but no clinical study has been conducted. Most of the studies have studied the activity in the seeds and pods [120,156,157,158].
Pericarps from P. speciosa show significant inhibitory activity (IC50 0.0581 mg/mL; 89.46%) against α-glucosidase [156], an enzyme responsible for breaking down starch and polysaccharide into glucose [159]. The seeds also show inhibitory activity but at lower percentage (45.72%) [156]. In another study, the ethanol extract of the rind had the highest α-glucosidase inhibitory activity followed by the leaf and seed with IC50 of 4596 ppm, 54,341 ppm, and 67,425 ppm, respectively as compared with acarbose having 162,508 ppm [158].
An in vivo study conducted on both seeds and pods of P. speciosa in alloxan-induced diabetic rats, indicated that only chloroform extract of both pods and seeds exhibited strong glucose-lowering activity. The hypoglycemic activity of the seeds was higher than that of the pods (57% and 36%, respectively) [157]. A mixture of 66% β-sitosterol 60 and 34% stigmasterol 61 is believed to be responsible for the hypoglycemic effect of the seeds—demonstrated 83% decrease in blood glucose level (100 mg/kg body weight) compared to glibenclamide (111% at 5 mg/kg bw) [120]. Similarly, stigmast-4-en-3-one 63 was identified as the compound responsible for the 84% reduction in blood glucose level at 100 mg/kg bw of the pod extract of P. speciosa [123]. Both compounds (β-sitosterol and stigmasterol) are believed to reduce blood glucose level by regenerating remnant β-cells and stimulating insulin release [160] via augmentation of GLUT4 glucose transporter expression [161]. Stigmasterol is also reported to inhibit the ß-cells apoptosis [162].
In other Parkia species, methanol crude extracts and fractions of P. timoriana pods showed significant α-glucosidase and α-amylase inhibitory activities in streptozotocin-induced diabetic rats. Ethyl acetate fraction had the highest α-glucosidase inhibitory and moderate α-amylase inhibitory activities, with maximal reduction in blood glucose level back to normal observed on day 14 at the dose of 100 mg/kg body weight [18]. α-Amylase functions to hydrolyze starch into maltose and glucose [163]. Bioassay-guided chemical investigation of the most active ethyl acetate fraction revealed epigallocatechin gallate 4 and apigenin 14 were responsible for the antidiabetic activity [18].
Oral administration of P. biglobosa methanol and aqueous extracts of fermented seeds exhibited different degrees of hypoglycemic effects on fasting plasma glucose when tested on alloxan-induced diabetic rats after four weeks [164,165]. Oral administration of P. biglobosa seeds methanol extract (1 g/kg body weight) lowered blood glucose level by 44.1% at 8 h as compared with glibenclamide (37.9%) in alloxan-induced diabetic rats. Its chloroform fraction exerted maximum glucose-lowering effect (65.7%), while n-hexane fraction had the lowest (4.7%) [39]. As previously mentioned, similar underlying mechanism of the hypoglycemic activity of the plant species is suggested which is via an improvement in pancreatic islet functions to release insulin, while abolishing insulin resistance [166]. For future study directions, investigations on the effects of the plant extracts and pure compounds on insulin release and signaling pathways that might be involved in the glucose-lowering properties could be conducted. The compounds should also be studied clinically.

5.3. Anticancer Activity

Cancer is one of the diseases that cause death of millions worldwide. Dietary intake of raw seeds was also reported to significantly lower the occurrence of esophageal cancer in southern Thailand [167]. The methanol extract of P. speciosa seeds exhibited a moderate antimutagenic activity in the Ames test [168], but weak activity in Epstein–Barr virus inhibitory assay [169]. The methanol extract of the seed coats demonstrated selective cytotoxicity against MCG-7 and T47D (breast cancer), HCT-116 (colon cancer) and HepG2 (hepatocarcinoma) cells, while its ethyl acetate fraction only showed selective cytotoxicity against MCF-7, breast cancer cells [170].
Substances that enhance mitogenesis of lymphocytes may be useful as antitumor or antiproliferative and immunomodulator agents [171]. Lectin obtained from the P. speciosa seeds exerted mitogenic activity in both rat thymocytes and human lymphocytes by stimulating the incorporation of thymidine into DNA cell, which activity was comparable to the known T-cell mitogens like pokeweed mitogen, concanavalin A and phytohemagglutinin [6,172]. Lectins isolated from the seeds of P. biglandulosa and P. roxburghii have demonstrated antiproliferative effect on murine macrophage cancer cell lines—P 388DI and J774. The seed extract P. roxburghii also inhibits the proliferation of B-cell hybridoma cell line, HB98 [173], and HepG2 cells without affecting the normal cells [44]. The monosaccharide saponins 5255 isolated from P. bicolor root also exhibit moderate antiproliferative effect IC50 ranging from 48.49 to 81.66 µM [118]. To our knowledge, the anticancer effects of Parkia extracts were only investigated in cell lines—limited to cell growth inhibition—not yet studied in in vivo models.
An in vitro study on human cancer cell lines has shown that the methanol extracts of P. biglobosa and P. filicoidea exhibit different degrees of antiproliferative activities on T-549 and BT-20 (prostate cancer), PC-3 (acute T cell leukemia Jurka), and SW-480 (colon cancer) at concentrations of 20 and 200 µg/mL. P. biglobosa also exhibits higher cytotoxic activity against all types of cancer cell lines used compared with P. filicoidea [174]. The antitumor property could be attributable to the antiangiogenic activity of some species of Parkia such as P. biglandulosa and P. speciosa extracts [170,175]. Angiogenesis or neovascularization is involved in metastasis of solid tumors. Methanol extract of the P. speciosa fresh pods was reported to exhibit antiangiogenic activity by more than 50% inhibition of microvessel outgrowth in rat aortae and human umbilical vein endothelial cells forming capillary-like structures in Matrigel matrix. The effect may be attributable to the ability of the compounds in the extract to form vacuoles in the cells [170], which is essential in maintaining the viability of the cells, therefore beneficial in the treatment of cancer owing to its capacity to prevent tumor neovascularization [176].
The plant bioactive compounds could also possibly increase apoptotic signaling pathway by elevating caspase activation as similarly shown by the same compounds in other plant species [177], as well as a direct inhibition on DNA synthesis, related to the ability to inhibit the expressions of several tumor- and angiogenesis-associated genes. Future studies should explore on the possible mechanism of action that are responsible for the anticancer activity. Additionally, future research on human studies is needed to confirm the outcomes seen in the laboratories.

5.4. Antihypertensive Activity

Antihypertensive activity of P. biglobosa seeds has been demonstrated in both animals and human. Only a clinical study was conducted which observed lower blood pressure, blood glucose and heart rate, high level of magnesium as well as improved lipid profile in patients with hypertension consuming fermented seeds of P. biglobosa in comparison with the non-consumption group [178]. Administration of 1.9 mg/mL of seed extract of P. biglobosa lowers the arterial blood pressure level in a rat model, possibly due to its ability to slow down the heart rate [179] and to induce vascular relaxation [180]. The latter effect is also seen with roasted seeds of the plant [180]. Other than the seeds, P. biglobosa stem bark aqueous extract also demonstrates good hypotensive effect in adrenaline-induced hypertensive female rabbits, which effect is comparable to antihypertensive drugs, propranolol and nifedipine [181]. The hypotensive properties of P. biglobosa could be owing to its main phytochemicals−phenolics and flavonoids. Catechin and its derivatives are among the most common compounds detected in the plant. These compounds promote vasorelaxation [182] by modulating nitric oxide availability [183] and inhibiting angiotensin-converting enzyme (ACE) [184], in addition to a reduction in oxidative stress [185], leading to blood pressure-lowering effects of the plant extract. The fermented seeds also decrease plasma triglyceride and cholesterol levels in Tyloxapol-induced hyperlipidemic rats [186], and platelet aggregation [187].
P. speciosa empty pod extract has been reported to prevent the development of hypertension in rats given L-NG-nitroarginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, possibly due to its ability to prevent nitric oxide loss [122], which is dependent on the availability of endothelial nitric oxide synthase [188], as well as to inhibit ACE and oxidative stress and inflammation [112]. Both oxidative stress and inflammation are known to play important roles in the pathogenesis of hypertension (Siti et al. 2015). Active peptide obtained from hydrolyzed P. speciosa seeds displays ACE-inhibitory effect, ranging from 50.6% to 80.2%, which effect is not observed in the non-hydrolyzed seeds, possibly due its long and bulky structure [189,190]. However, the study of Khalid and Babji (2018) has demonstrated that the aqueous extract of the seeds also possesses ACE inhibitory activity [191]. These studies suggest that the blood pressure-lowering effect of the P. speciosa is most likely due to its ACE inhibitory property and nitric oxide regulation, attributable to its rich contents of polyphenols and the presence of peptide. Future studies should involve isolation of the active compounds which have a potential to be developed as a specific inhibitor of ACE. Other possible mechanisms—specific receptor antagonism, such as adrenoceptors and calcium channels, or modification of signaling pathways—of blood pressure-lowering effects of the plant extract or compounds should be explored further.

5.5. Antidiarrheal Activity

The antidiarrheal effect of Parkia plants has been investigated using many models such as castor oil- and magnesium-induced diarrhea. The aqueous extract of P. filicoidea stem barks reduces the frequency of stooling in rats with castor oil-induced diarrhea, comparable with loperamide [192]. The aqueous and ethanol extract of P. biglobosa leaves and stem barks also exhibit similar antidiarrheal activity to loperamide, seen as a reduction in stooling frequency and intestinal volume [45,59,193]. These effects could be attributable to its inhibitory capacity on the propulsive movement of gastrointestinal tract smooth muscles [45]. Medicinal plants are believed to exert antidiarrheal activity by enhancing the opening of intestinal potassium channel and stimulating Na+/K+-ATPase activity, as well as decreasing intracellular calcium concentration, which then promotes gastrointestinal smooth muscle relaxation, leading to diminished diarrhea [194,195,196]. The potential of these plants as agents to reduce diarrhea can be explored further in irritable bowel syndrome or chemotherapy-induced diarrhea. Their effects on intestinal mucosal barrier, tight junction proteins and inflammatory cytokines among others can be examined.

5.6. Antiulcer Activity

The gastroprotective effect of Parkia plants was seen in three species which were P. speciosa, P. platycephala and P. biglandulosa (Table 3). The leaves and seeds of P. speciosa protected against ethanol- and indomethacin-induced gastric ulcer in rats, observed by reductions in the gastric ulcer index and acidity of gastric juice [197,198]. Lesser collagen and fibrotic ulcer were significantly diminished in the extract-treated group [197]. The ethanol extract of P. platycephala also showed protective effect in gastric mucosal injury models induced by ethanol, ischemia-reperfusion, and ethanol-HCl. However, the extract could not protect against indomethacin-induced gastric lesion [199]. These plants are rich in flavonoids. The compounds like catechin and quercetin confer antiulcer effects possibly by eradicating the formation of ROS and modulating mucin metabolism in the gastrointestinal tract [200,201,202]. Other possible protective mechanisms could be by reducing gastric acid secretion, thereby decreasing gastric acid pH, as seen with cinnamic caffeic, p-coumaric or ferulic acids—the compounds that are present in the plants [203]. Studies on other possible effects of the extracts or bioactive components such as proton pump inhibition could be of interest. In future, the compounds that are responsible for the protective effects should be identified and the possible protective signaling mechanisms should be elucidated. Moreover, clinical trials can be performed to assess the potential use of Parkia extracts as an antiulcer agent.

5.7. Antianemic Activity

The fermented seeds of P. biglobosa are a rich source of essential minerals such as iron, calcium, thiamine, and phosphorus [57] which are necessary in forestalling either iron or non-iron deficiency anemia. Therefore, the antianemic capacity of P. biglobosa could be owing to its nutritional composition. The fermented seeds of P. biglobosa in combination with other fermented products were reported to be beneficial in the management of anemia as it increased hemoglobin, red blood cells, white blood cells, and packed cell volume [204]. The ethanol extract of P. speciosa seeds were also investigated in NaNO2-induced anemic mice. At doses of 400 and 700 mg/kg, an elevation of hemoglobin levels was noted to 0.92 and 0.82 g/dL, respectively [205]. The exact mechanism of how P. speciosa acts to decrease anemia is still unclear. It could be due to its rich source of the minerals, particularly the iron [171]. Another possible mechanism would be stimulation of erythropoiesis process. Both extracts of P. biglobosa P. biglobosa and P. speciosa can be developed as an alternative iron supplement. However, the effectiveness should be evaluated clinically.

5.8. Anti-Inflammatory Activity

Inflammatory reaction is involved in almost all clinical manifestation. Hence, anti-inflammatory activity of certain plant extracts could be of benefit. Anti-inflammatory activity of P. biglobosa stalk [206], seeds and stem bark [29], P. speciosa pods [187,188] and seeds [84], as well as P. platycephala seeds [207] have been reported using various models of inflammation.
The protective effects of P. biglobosa is believed via its inhibitions on the lipoxygenase and cyclooxygenase pathways [206], leading to inhibition of pro-inflammatory cytokine release and stimulation of anti-inflammatory cytokine [208], as well as increment on membrane stabilization [209]. While the P. speciosa exerts its anti-inflammatory by downregulating nuclear factor kappa B cell (NF-κB) and p38 mitogen-activated protein kinase (MAPK) pathways [187,188]. It is obvious that the plant bioactive components attenuate inflammation by regulating inflammatory and MAPK signaling pathways, which could lead to reduced formation of inflammatory mediators such as cytokines. To date, no study has identified the anti-inflammatory compounds from Parkia, which warrants further studies on this aspect, either in experimental animals or human studies.

5.9. Antioxidant Activity

Polyphenolic compounds present in plant foods have been reported to be responsible for their antioxidant activity due to their ability to serve as a hydrogen donor and reducing agent (Amorati and Valgimigli 2012). Both fermented and unfermented seeds of P. biglobosa have been reported to contain an appreciable amount of phenolic contents [210,211]. P. timoriana pods are also rich in total phenolic and flavonoid contents [212]. The antioxidant capacity of the leaves and seeds of P. speciosa has been reported to be relatively lower than that of the empty pods and seed mixture, suggesting that the pods possess higher antioxidant contents than other parts of the plant [37,176]. The difference in geographical location may affect the composition of the antioxidant compounds in plants. It was reported that P. speciosa seeds collected from central Peninsular Malaysia had higher antioxidant capacity than the southern and southwestern regions [213]. The compounds present in the plants attenuate oxidative stress possibly by activating Nrf2/Keap1 and MAPK signaling pathways, leading to enhanced expressions of Nrf2 and antioxidant enzymes, such as heme oxygenase-1 [214]. P. speciosa extracts of seed coats and pods could also reduce the risk of hemolysis by inhibiting Heinz body production in the erythrocytes incubated with a hemolytic agent [215], indicating the ability of the extracts to inhibit oxidative destruction of erythrocyte. The finding suggests a potential of the plant extract to reduce hemolytic jaundice, which warrants further research.

5.10. Other Pharmacological Activities

Other than previously mentioned activities, the P. biglobosa extract has also been demonstrated to have antimalarial effect [11], whereas P. clappertoniana [75] and P. biglobosa [216] show nephro- and hepatoprotective effects, respectively (Table 3). P. pendula seeds also enhance wound healing in immunosuppressed mice [217]. However, extensive studies regarding these effects were not performed. Further studies need to be conducted to explore the possible mechanisms that are involved in the aforementioned beneficial effects.

6. Toxicity

Daily consumption of cooked pods of P. roxburghii does not impose any significant adverse effect [218]. However, eating raw pods may result in bad breath owing to its rich content in volatile disulfide compounds, which are exhaled in breath and the odor can persist for several hours (Meyer, 1987). Many substances have been identified or isolated from Parkia seed, such as lectins, non-protein amino acids, and alkaloids [219]. However, no acute mortality and observable behavioral change were recorded at doses up to 2000 mg/kg ethyl acetate fraction of P. roxburghii pod in rats [18]. Investigation on acute and sub-acute toxicity profiles of the aqueous and ethanol extracts of the stem bark of P. biglobosa showed that the oral median lethal dose (LD50) was higher than 5000 mg/kg for both extracts in rats [36]. However, in another report, LD50 values of the leaves, stems and roots in an acute toxicity study were within the range of 500–5000 mg/kg body weight of fish, suggesting that they are only slightly toxic and, therefore, not potentially dangerous. The adverse effects included respiratory distress and agitated behavior [220]. Apart from the barks of P. biglobosa, the pods also possess the piscicidal activity that can be used in the management and control of fishponds to eliminate predators [220,221]. Fatty acids and oils identified from the seeds of P. biglobosa and P. bicolor were reported to be non-toxic [22].
The aqueous extract of P. clappertoniana seeds showed no observable maternal and developmental toxicity at 100–500 mg/kg when given orally to Sprague-Dawley rats and mice at different gestational age ([17]. P. platycephala leaves at 1000 mg/kg on the other hand, caused decreases in body mass, food and water consumption in rats. It also shortened the proestrus and prolonged diestrus phases, as well as reduced uterine weight, suggestive of possible alterations on hormonal levels, but no obvious toxicity on other organs [53]. Oral administration of the leaves of P. speciosa for 14 days showed no significant histopathological toxicity or mortality in rats at up to 5000 mg/kg [198]. In vitro, the plant pods (100 μg/mL) showed no significant cytotoxic effect on normal cell lines [170]. Consumption of the seeds up to 30 pieces in a serve does not produce any adverse effects [176].

7. Conclusions

Enormous reports demonstrate that plants from genus Parkia possess medicinal values, attributable to the presence of pharmacological active compounds. Taken together, two most studied species, P. biglobosa and P. speciosa, show potential as antidiabetic, antihypertensive, and antimicrobial, to name a few. Phytochemical investigations indicated terpenoids (monoterpenoids, diterpenoids, and triterpenoids), phenolics acids and flavonoids (flavonols, isoflavone, flavanone, and flavan-3-ols) are the major chemical constituents present in the species of this genus, which are responsible for their diverse pharmacological activities. It seems that certain phytoconstituents in Parkia have their unique pharmacological effects. β-Sitosterol and stigmasterol, for instance, could be investigated further and be developed as hypoglycemic agents; cyclic polysulfides, such as antimicrobials; lectins and monosaccharide saponins for anticancer treatment; and polyphenols, most possibly catechin and its derivatives, and active peptides for blood pressure-lowering effect. The pharmacological properties studied in vitro and in vivo of these compounds should be confirmed in clinical studies. In order to carry out this, there is a need to develop a method, which is effective and cheap to isolate the bioactive constituents in bulks. The potential toxicity and safety of the compounds, as well as their possible protective mechanisms, should also be determined before administration into humans. However, research on other bioactive compounds should continue. It is hoped that discoveries of novel agents from these plants could provide an alternative to the current modern medicine.

Author Contributions

M.S.M.S. drafted and edited the manuscript. J.J., S.Z., A.Y.A., N.H.M. and Y.K. revised the manuscript. All authors have read and agreed to the published version of the manuscript.


The work was supported by the Ministry of Education Malaysia grant (FRGS/1/2019/SKK10/UKM/02/1).

Data Availability Statement

Data is contained within the article.

Conflicts of Interest

All authors declare no conflict of interest.


  1. Heymann, E.W.; Lüttmann, K.; Michalczyk, I.M.; Saboya, P.P.P.; Ziegenhagen, B.; Bialozyt, R. DNA fingerprinting validates seed dispersal curves from observational studies in the neotropical legume Parkia. PLoS ONE 2012, 7, e35480. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Orwa, C.; Mutua, A.; Kindt, R.; Jamnadass, R.; Simons, A. Agroforestree Database: A Tree Reference and Selection Guide, version 4; World Agroforestry Centre: Nairobi, Kenya, 2009. [Google Scholar]
  3. Luckow, M.; Hopkins, H.C.F. A cladistic analysis of Parkia (Leguminosae: Mimosoideae). Am. J. Bot. 1995, 82, 1300–1320. [Google Scholar] [CrossRef]
  4. Neill, D.A. Parkia nana (Leguminosae, Mimosoideae), a new species from the sub-Andean sandstone cordilleras of Peru. Novon A J. Bot. Nomencl. 2009, 19, 204–208. [Google Scholar] [CrossRef]
  5. Ching, L.S.; Mohamed, S. Alpha-tocopherol content in 62 edible tropical plants. J. Agric. Food Chem. 2001, 49, 3101–3105. [Google Scholar] [CrossRef] [PubMed]
  6. Suvachittanont, W.; Peutpaiboon, A. Lectin from Parkia speciosa seeds. Phytochemistry 1992, 31, 4065–4070. [Google Scholar] [CrossRef]
  7. Ogunyinka, B.I.; Oyinloye, B.E.; Osunsanmi, F.O.; Kappo, A.P.; Opoku, A.R. Comparative study on proximate, functional, mineral, and antinutrient composition of fermented, defatted, and protein isolate of Parkia biglobosa seed. Food Sci. Nutr. 2017, 5, 139–147. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Alabi, D.A.; Akinsulire, O.R.; Sanyaolu, M.A. Qualitative determination of chemical and nutritional composition of Parkia biglobosa (Jacq.) Benth. Afr. J. Biotechnol. 2005, 4, 812–815. [Google Scholar] [CrossRef]
  9. Fetuga, B.L.; Babatunde, G.M.; Oyenuga, V.A. Protein quality of some unusual protein foodstuffs. Studies on the African locust-bean seed (Parkia filicoidea Welw.). Br. J. Nutr. 1974, 32, 27–36. [Google Scholar] [CrossRef] [Green Version]
  10. Hassan, L.G.; Umar, K.J. Protein and amino acids composition of African locust bean (Parkia biglobosa). Trop. Subtrop. Agroecosyst. 2005, 5, 45–50. [Google Scholar]
  11. Builders, M.; Alemika, T.; Aguiyi, J. Antimalarial Activity and isolation of phenolic compound from Parkia biglobosa. IOSR J. Pharm. Biol. Sci. 2014, 9, 78–85. [Google Scholar] [CrossRef]
  12. Ifesan, B.O.T.; Akintade, A.O.; Gabriel-Ajobiew, R.A.O. Physicochemical and nutritional properties of Mucuna pruriens and Parkia biglobosa subjected to controlled fermentation. Int. Food Res. J. 2017, 24, 2177–2184. [Google Scholar]
  13. Iheke, E.; Oshodi, A.; Omoboye, A.; Ogunlalu, O. Effect of fermentation on the physicochemical properties and nutritionally valuable minerals of locust bean (Parkia biglobosa). Am. J. Food Technol. 2017, 6, 379–384. [Google Scholar] [CrossRef] [Green Version]
  14. Abdullahi, I.N.; Chuwang, P.Z.; Anjorin, T.S.; Ikemefuna, H. Determination of Mineral Accumulation through Litter Fall of Parkia Biglobosa Jacq Benth and Vitellaria Paradoxa Lahm Trees in Abuja, Nigeria. Int. J. Sci. Res. Agric. Sci. 2015, 2, 0016–0021. [Google Scholar]
  15. Singh, N.P.; Gajurel, P.R.; Rethy, P. Ethnomedicinal value of traditional food plants used by the Zeliang tribe of Nagaland. Indian J. Tradit. Knowl. 2015, 14, 298–305. [Google Scholar]
  16. Mondal, P.; Bhuyan, N.; Das, S.; Kumar, M.; Borah, S.; Mahato, K. Herbal medicines useful for the treatment of diabetes in north-east India: A review. Int. J. Pharm. Biol. Sci. 2013, 3, 575–589. [Google Scholar]
  17. Boye, A.; Boampong, V.A.; Takyi, N.; Martey, O. Assessment of an aqueous seed extract of Parkia clappertoniana on reproductive performance and toxicity in rodents. J. Ethnopharmacol. 2016, 185, 155–161. [Google Scholar] [CrossRef]
  18. Sheikh, Y.; Maibam, B.C.; Talukdar, N.C.; Deka, D.C.; Borah, J.C. In vitro and in vivo anti-diabetic and hepatoprotective effects of edible pods of Parkia roxburghii and quantification of the active constituent by HPLC-PDA. J. Ethnopharmacol. 2016, 191, 21–28. [Google Scholar] [CrossRef]
  19. Singh, M.K. Potential of underutilized legume tree Parkia timoriana (DC.) Merr. In Eco-restoration of Jhum fallows of Manipur. J. Pharmacogn. Phytochem. 2019, 8, 1685–1687. [Google Scholar]
  20. Roosita, K.; Kusharto, C.M.; Sekiyama, M.; Fachrurozi, Y.; Ohtsuka, R. Medicinal plants used by the villagers of a Sundanese community in West Java, Indonesia. J. Ethnopharmacol. 2008, 115, 72–81. [Google Scholar] [CrossRef]
  21. Srisawat, T.; Suvarnasingh, A.; Maneenoon, K. Traditional medicinal plants notably used to treat skin disorders nearby Khao Luang mountain hills region, Nakhon si Thammarat, Southern Thailand. J. HerbsSpices Med. Plants 2016, 22, 35–56. [Google Scholar] [CrossRef]
  22. Aiyelaagbe, O.O.; Ajaiyeoba, E.O.; Ekundayo, O. Studies on the seed oils of Parkia biglobosa and Parkia bicolor. Plant Foods Hum. Nutr. 1996, 49, 229–233. [Google Scholar] [CrossRef] [PubMed]
  23. Ajaiyeoba, E. 0 Phytochemical and antibacterial properties of Parkia biglobosa and Parkia bicolor leaf extracts. Afr. J. Biomed. Res. 2002, 5, 125–129. [Google Scholar] [CrossRef] [Green Version]
  24. Oladunmoye, M.K.; Kehinde, F.Y. Ethnobotanical survey of medicinal plants used in treating viral infections among Yoruba tribe of South Western Nigeria. Afr. J. Microbiol. Res. 2011, 5, 2991–3004. [Google Scholar] [CrossRef] [Green Version]
  25. Rathi, R.S.; Misra, A.K.; Somnath, R.; Verma, S.K.; Singh, S.K. Potential of a lesser known tree species Parkia roxburghii G. Don of North East India. Indian For. 2012, 138, 476–479. [Google Scholar]
  26. Ong, H.C.; Ahmad, N.; Milow, P. Traditional Medicinal Plants Used by the Temuan Villagers in Kampung Tering, Negeri Sembilan, Malaysia. Stud. Ethno-Med. 2011, 5, 169–173. [Google Scholar] [CrossRef]
  27. Ong, H.C.; Chua, S.; Milow, P. Ethno-medicinal plants used by the Temuan villagers in Kampung Jeram Kedah, Negeri Sembilan, Malaysia. Stud. Ethno-Med. 2011, 5, 95–100. [Google Scholar] [CrossRef]
  28. Fotie, J.; Nkengfack, A.E.; Peter, M.G.; Heydenreich, M.; Fomum, Z.T. Chemical constituents of the ethyl acetate extracts of the stem bark and fruits of Dichrostachys cinerea and the roots of Parkia bicolor. Bull. Chem. Soc. Ethiop. 2004, 18, 111–115. [Google Scholar] [CrossRef] [Green Version]
  29. Kouadio, F.; Kanko, C.; Juge, M.; Grimaud, N.; Jean, A.; N’Guessan, Y.T.; Petit, J.Y. Analgesic and antiinflammatory activities of an extract from Parkia biglobosa used in traditional medicine in the ivory coast. Phytother. Res. 2000, 14, 635–637. [Google Scholar] [CrossRef]
  30. Ong, H.C.; Zuki, R.M.; Milow, P. Traditional Knowledge of Medicinal Plants among the Malay Villagers in Kampung Mak Kemas, Terengganu, Malaysia. Stud. Ethno-Med. 2011, 2011, 175–185. [Google Scholar] [CrossRef]
  31. Millogo-Kone, H.; Guissou, I.P.; Nacoulma, O.; Traore, A.S. Antimicrobial effects of the stem bark extracts of Parika biglobosa (Jacq.)Benth. on Shigellae. Afr. J. Tradit. Complementary Altern. Med. 2007, 4, 392–396. [Google Scholar] [CrossRef] [Green Version]
  32. Enujiugha, V.N. The antioxidant and free radical-scavenging capacity of phenolics from African locust bean seeds (Parkia biglobosa). Adv. Food Sci. 2010, 32, 88–93. [Google Scholar]
  33. Gernah, D.I.; Inyang, C.U.; Ezeora, N.L. Incubation and fermentation of African locust beans (Parkia biglobosa) in production of ‘dawadawa’. J. Food Process. Preserv. 2007, 31, 227–239. [Google Scholar] [CrossRef]
  34. El-Mahmood, A.M.; Ameh, J.M. In vitro antibacterial activity of Parkia biglobosa (Jacq.) root bark extract against some microorganisms associated with urinary tract infections. Afr. J. Biotechnol. 2007, 6, 1272–1275. [Google Scholar] [CrossRef]
  35. Adaramola, T.F.; Ariwaodo, J.O.; Adeniji, K.A. Distribution, phytochemistry and antioxidant properties of the genus Parkia (mimosaceae) in Nigeria. Int. J. Pharmacogn. Phytochem. Res. 2012, 4, 172–178. [Google Scholar]
  36. Builders, M. Toxicity studies of the extracts of Parkia biglobosa Stem Bark in Rats. Br. J. Pharm. Res. 2012, 2, 1–16. [Google Scholar] [CrossRef]
  37. Chhikara, N.; Devi, H.R.; Jaglan, S.; Sharma, P.; Gupta, P.; Panghal, A. Bioactive compounds, food applications and health benefits of Parkia speciosa (stinky beans): A review. Agric. Food Secur. 2018, 7, 1–9. [Google Scholar] [CrossRef] [Green Version]
  38. Udobi, C.E.; Onaolapo, J.A. Phytochemical analysis and antibacterial evaluation of the leaf stem bark and root of the African locust bean (Parkia biglobosa). J. Med. Plants Res. 2009, 3, 338–344. [Google Scholar]
  39. Ezema, B.E.; Eze, F.U.; Ezeofor, C.C. Phytochemical and antibacterial studies of eastern nigerian mistletoe (Loranthus micranthus) parasitic on Pentacletra macrophylla and Parkia biglobosa. Int. J. Pharm. Technol. Res. 2016, 9, 360–365. [Google Scholar]
  40. Fred-Jaiyesimi, A.A.; Abo, K.A. Hypoglycaemic effects of Parkia biglobosa (Jacq) Benth seed extract in glucose-loaded and NIDDM rats. Int. J. Biol. Chem. Sci. 2009, 3, 545–550. [Google Scholar] [CrossRef]
  41. Mohan, V.R.; Janardhanan, K. Chemical and nutritional evaluation of raw seeds of the tribal pulses Parkia roxburghii G. Don. and Entada phaseoloides (L.) Merr. Int. J. Food Sci. Nutr. 1993, 44, 47–53. [Google Scholar] [CrossRef]
  42. Dinda, B.; Chandra Mohanta, B.; Debnath, S.; Ghosh, B.; Arima, S.; Sato, N.; Harigaya, Y. Iridoid glucosides from leaves and stem barks of Parkia javanica. J. Asian Nat. Prod. Res. 2009, 11, 229–235. [Google Scholar] [CrossRef] [PubMed]
  43. Abioye, E.O.; Akinpelu, D.A.; Aiyegoro, O.A.; Adegboye, M.F.; Oni, M.O.; Okoh, A.I. Preliminary phytochemical screening and antibacterial properties of crude stem bark extracts and fractions of Parkia biglobosa (Jacq.). Molecules 2013, 18, 8485–8499. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Chanu, K.V.; Geeta Devi, L.; Kumar Srivastava, S.; Telang, A.; Khangembam Victoria Chanu, C.; Thakuria, D.; Kataria, M. Phytochemical analysis and evaluation of anticancer activity of Parkia javanica seeds. Pharma Innov. J. 2018, 7, 305–311. [Google Scholar]
  45. Tijani, A.Y.; Okhale, S.E.; Salawu, T.A.; Onigbanjo, H.O.; Obianodo, L.A.; Akingbasote, J.A.; Salawu, O.A.; Okogun, J.I.; Kunle, F.O.; Emeje, M. Antidiarrhoeal and antibacterial properties of crude aqueous stem bark extract and fractions of Parkia biglobosa (Jacq) R. Br. Ex G. Don. Afr. J. Pharm. Pharmacol. 2009, 3, 347–353. [Google Scholar]
  46. Awotedu, O.L.; Ogunbamowo, P.O.; Emmanuel, I.B.; Lawal, I.O. Phytominerals and Phytochemical Studies of Azadiracthta indica, Leea guineensis and Parkia biglobosa Leaves. Int. Ann. Sci. 2018, 6, 28–34. [Google Scholar] [CrossRef] [Green Version]
  47. Fayinminnu, O.O.; Adeniyi, O.O.; Alabi, O.Y.; Omobusuyi, D.O. Potentials of Aqueous Extract of Pod Husk Parkia biglobosa (Jacq.) Benth as a Biopesticide in Okra (Abelmoschus esculentus (L.) Moench) Production. J. Agric. Ecol. Res. Int. 2017, 1–12. [Google Scholar] [CrossRef] [Green Version]
  48. Sani, U.M. Phytochemical screening and antifeedant activity of the seed extracts of Parkia biglobosa against cowpea vean (Vigna unguiculata) storage pest (Callosobruchus maculatus). Int. J. Innov. Sci. Eng. Technol. 2014, 3, 15991–15995. [Google Scholar] [CrossRef]
  49. Soetan, K.O.; Lasisi, O.T.; Agboluaje, A.K. Comparative assessment of in-vitro anthelmintic effects of the aqueous extracts of the seeds and leaves of the African locust bean (Parkia biglobosa) on bovine nematode eggs. J. Cell Anim. Biol. 2011, 5, 109–112. [Google Scholar]
  50. Iyamu, M.I.; Ekozien, M.I.; Omoigberale, M.N.O. Phytochemical screening and antibacterial activity of the stem back of African Locust bean plant (Parkia Filicoidea Welw.). Glob. J. Biol. Agric. Health Sci. 2014, 3, 36–43. [Google Scholar]
  51. Salam, S.; Jamir, N.S.; Singh, P.K. Traditional uses of medicinal plants by the Tangkhul–Naga tribe in Manipur, India. Pleione 2009, 3, 157–162. [Google Scholar]
  52. Salam, J.S.; Salam, P.; Potshangbam, K.S.; Kumar, D.B. Effect of processing methods on secondary metabolites and enzyme inhibitors in different developmental stages of Parkia roxburghii G. Don pods. Am. J. Food Technol. 2014, 9, 89–96. [Google Scholar]
  53. Costa, B.A.; de Oliveira, J.M.; Sales, P.A.; Lira, S.R.D.S.; Silva, S.M.D.S.; Costa, L.M.; Muratori, M.; Costa, A.P. Systemic and reproductive toxicity induced by Parkia platycephala ethanolic extract in female Wistar rats. Braz. J. Pharmacogn. 2013, 23, 920–926. [Google Scholar] [CrossRef] [Green Version]
  54. SáSantos, M.M.; da Silva, F.M.P.; da Silva, J.F.M.; Pimenta, R.S. Phytochemistry and antibacterial activity of aqueous and hydroalcoholic extracts of three medicinal plants against food pathogens. Acta Sci. Biol. Sci. 2018, 40, 1–6. [Google Scholar] [CrossRef] [Green Version]
  55. Lawal, I.O.; Uzokwe, N.E.; Igboanugo, A.B.I.; Adio, A.F.; Awosan, E.A.; Nwogwugwu, J.O.; Faloye, B.; Olatunji, B.P.; Adesoga, A.A. Ethno medicinal information on collation and identification of some medicinal plants in Research Institutes of South-west Nigeria. Afr. J. Pharm. Pharmacol. 2010, 4, 1–7. [Google Scholar]
  56. Henry, S.G.; Francis, A.; Kofi, A. Ethnobotanical survey of medicinal plants used for the treatment of diarrhoea and skin ulcer in the Brong Ahafo region of Ghana. J. Med. Plants Res. 2013, 7, 3280–3285. [Google Scholar] [CrossRef]
  57. Campbell-Platt, G. African locust bean (Parkia species) and its west african fermented food product, dawadawa. Ecol. Food Nutr. 1980, 9, 123–132. [Google Scholar] [CrossRef]
  58. Igoli, J.O.; Ogaji, O.G.; Tor-Anyiin, T.A.; Igoli, N.P. Traditional medicine practice amongst the Igede people of Nigeria. Part II. Afr. J. Tradit. Complementary Altern. Med. 2005, 2, 134–152. [Google Scholar] [CrossRef]
  59. Agunu, A.; Yusuf, S.; Andrew, G.O.; Zezi, A.U.; Abdurahman, E.M. Evaluation of five medicinal plants used in diarrhoea treatment in Nigeria. J. Ethnopharmacol. 2005, 101, 27–30. [Google Scholar] [CrossRef]
  60. Asuzu, I.U.; Harvey, A.L. The antisnake venom activities of Parkia biglobosa (Mimosaceae) stem bark extract. Toxicon 2003, 42, 763–768. [Google Scholar] [CrossRef]
  61. Karou, S.D.; Tchacondo, T.; Djikpo Tchibozo, M.A.; Abdoul-Rahaman, S.; Anani, K.; Koudouvo, K.; Batawila, K.; Agbonon, A.; Simpore, J.; de Souza, C. Ethnobotanical study of medicinal plants used in the management of diabetes mellitus and hypertension in the Central Region of Togo. Pharm. Biol. 2011, 49, 1286–1297. [Google Scholar] [CrossRef]
  62. Grønhaug, T.E.; Glæserud, S.; Skogsrud, M.; Ballo, N.; Bah, S.; Diallo, D.; Paulsen, B.S. Ethnopharmacological survey of six medicinal plants from Mali, West-Africa. J. Ethnobiol. Ethnomed. 2008, 4, 26. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Abo, K.A.; Fred-Jaiyesimi, A.A.; Jaiyesimi, A.E.A. Ethnobotanical studies of medicinal plants used in the management of diabetes mellitus in South Western Nigeria. J. Ethnopharmacol. 2008, 115, 67–71. [Google Scholar] [CrossRef] [PubMed]
  64. Pare, D.; Hilou, A.; Ouedraogo, N.; Guenne, S. Ethnobotanical study of medicinal plants used as anti-obesity remedies in the nomad and hunter communities of Burkina Faso. Medicines 2016, 3, 9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Millogo-Kone, H.; Guissoe, P.I.; Nacoulma, O.; Traore, A.S. Study of the antibacterial activity of the stem bark and leaf extracts of Parkia biglobosa (Jacq.) Benth. on Satphylococcus aureus. Afr. J. Tradit. Complementary Altern. Med. 2006, 3, 74–78. [Google Scholar] [CrossRef]
  66. Quansah, L.; Mahunu, G.K.; Tahir, H.E.; Mariod, A.A. Parkia biglobosa: Phytochemical Constituents, Bioactive Compounds, Traditional and Medicinal Uses. In Wild Fruits: Composition, Nutritional Value and Products; Springer: Berlin/Heidelberg, Germany, 2019; pp. 271–284. [Google Scholar]
  67. Abreu, P.M.; Martins, E.S.; Kayser, O.; Bindseil, K.U.; Siems, K.; Seemann, A.; Frevert, J. Antimicrobial, antitumor and antileishmania screening of medicinal plants from Guinea-Bissau. Phytomedicine 1999, 6, 187–195. [Google Scholar] [CrossRef]
  68. Rupesh, P.; Pal, S.C.; Pavani, A.; Gadge, M.S. Quantitave estimation of the active constituents of Parkia biglandulosa by using HPTLC and FTIR. Int. J. Pharma Bio Sci. 2010, 1, 315–332. [Google Scholar]
  69. Khond, M.; Bhosale, J.D.; Arif, T.; Mandal, T.K.; Padhi, M.M.; Dabur, R. Screening of some selected medicinal plants extracts for in-vitro antimicrobial activity. Middle-East J. Sci. Res. 2009, 4, 271–278. [Google Scholar]
  70. Pingale, R.; Pokharkar, D.; Phadatare, S.P.; Gorle, A. Pharmacognostic Evaluation of Parkia biglandulosa bark. Int. J. Pharm. Phytochem. Res. 2016, 8, 1160–1163. [Google Scholar]
  71. Banwo, G.O.; Abdullahi, I.; Duguryil, M. The antimicrobial activity of the stem-bark and leaf of Parkia clappertoniana Keay family Leguminosae against selected microorganisms. Niger. J. Pharm. Res. 2004, 3, 16–22. [Google Scholar] [CrossRef]
  72. Nwodo, N.J.; Ibezim, A.; Ntie-Kang, F.; Adikwu, M.U.; Mbah, C.J. Anti-trypanosomal activity of Nigerian plants and their constituents. Molecules 2015, 20, 7750–7771. [Google Scholar] [CrossRef] [Green Version]
  73. Lawal, M.S.; Sani, A.M.; Dangmwan, D.S.; Yahaya, U. Antimicrobial potentials of Parkia clappertoniana Jacq, Boswellia dalzielli hutch and Carica papaya L. ethanolic extract on multi-drug resistant Diarrheal salmonallae and Shigellae Bacteria. Biochem. Mol. Biol. 2016, 1, 27. [Google Scholar]
  74. Muazu, J.; Kaita, M.H. A review of traditional plants used in the treatment of epilepsy amongst the Hausa/Fulani tribes of northern Nigeria. Afr. J. Tradit. Complementary Altern. Med. 2008, 5, 387–390. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Boye, A. Nephroprotective and curative assessment of an aqueous seed extract of Parkia clappertoniana keay in gentamicin-induced renal damage in Sprague-dawley rats. Eur. J. Med. Plants 2014, 4, 234–248. [Google Scholar] [CrossRef]
  76. Patrick-Iwuanyanwu, K.C.; Wegwu, M.O.; Okiyi, J.K. Hepatoprotective effects of African locust bean (Parkia clappertoniana) and negro pepper (Xylopia aethiopica) in CCl4-induced liver damage in wistar albino rats. Int. J. Pharmacol. 2010, 6, 744–749. [Google Scholar] [CrossRef] [Green Version]
  77. Obata, O.O.; Aigbokhan, E.I. Ethnobotanical practices among the people of Okaakoko, Nigeria. Plant Arch. 2012, 12, 627–638. [Google Scholar]
  78. Van Andel, T.; Behari-Ramdas, J.; Havinga, R.; Groenendijk, S. The medicinal plant trade in Suriname. Ethnobot. Res. Appl. 2007, 5, 351–372. [Google Scholar] [CrossRef] [Green Version]
  79. Ferreira, A.B.; Ming, L.C.; Haverroth, M.; Daly, D.C.; Caballero, J.; Ballesté, A.M. Plants used to treat malaria in the regions of Rio Branco-Acre state and southern Amazonas state—Brazil. Int. J. Phytocosmetics Nat. Ingred. 2015, 2, 9. [Google Scholar] [CrossRef]
  80. Mitra, R.; Orbell, J.; Muralitharan, M. Medicinal plants of Malaysia. Asia Pac. Biotech News 2007, 11, 105–110. [Google Scholar] [CrossRef]
  81. Siew, Y.Y.; Zareisedehizadeh, S.; Seetoh, W.G.; Neo, S.Y.; Tan, C.H.; Koh, H.L. Ethnobotanical survey of usage of fresh medicinal plants in Singapore. J. Ethnopharmacol. 2014, 155, 1450–1466. [Google Scholar] [CrossRef]
  82. Ripen, J.E.; Noweg, G.T. Economic valuation of medicinal plants in Jagoi Area, Bau, Malaysia. Procedia Soc. Behav. Sci. 2016, 224, 124–131. [Google Scholar] [CrossRef] [Green Version]
  83. Eswani, N.; Kudus, K.A.; Nazre, M.; Noor, A.G.A.; Ali, M. Medicinal plant diversity and vegetation analysis of logged over hill forest of Tekai Tembeling Forest Reserve, Jerantut, Pahang. J. Agric. Sci. 2010, 2, 189. [Google Scholar] [CrossRef] [Green Version]
  84. Sonia, N.; Dsouza, M.R. Alisha Pharmacological evaluation of Parkia speciosa Hassk for antioxidant, anti-inflammatory, anti-diabetic and anti-microbial activities in vitro. Int. J. Life Sci. Spec. Issue 2018, 11, 49–59. [Google Scholar]
  85. Bahtiar, A.; Vichitphan, K.; Han, J. Leguminous plants in the Indonesian Archipelago: Traditional uses and secondary metabolites. Nat. Prod. Commun. 2017, 12, 461–472. [Google Scholar] [CrossRef] [Green Version]
  86. Batoro, J.; Siswanto, D. Ethnomedicinal survey of plants used by local society in Poncokusumo district, Malang, East Java Province, Indonesia. Asian J. Med Biol. Res. 2017, 3, 158–167. [Google Scholar] [CrossRef]
  87. Samuel, A.J.S.J.; Kalusalingam, A.; Chellappan, D.K.; Gopinath, R.; Radhamani, S.; Husain, H.A.; Muruganandham, V.; Promwichit, P. Ethnomedical survey of plants used by the Orang Asli in Kampung Bawong, Perak, West Malaysia. J. Ethnobiol. Ethnomed. 2010, 6, 5. [Google Scholar] [CrossRef] [Green Version]
  88. Rai, P.K.; Lalramnghinglova, H. Ethnomedicinal plant resources of Mizoram, India: Implication of traditional knowledge in health care system. Ethnobot. Leafl. 2010, 2010, 6. [Google Scholar]
  89. Irvine, F.R. Woody Plants of Ghana; Oxford University Press: England, UK, 1961. [Google Scholar]
  90. Phumthum, M.; Balslev, H. Thai ethnomedicinal plants used for diabetes treatment. OBM ICM 2018, 3, 1–25. [Google Scholar] [CrossRef]
  91. Khumbongmayum, A.; Khan, M.; Tripathi, R. Ethnomedicinal plants in the sacred groves of Manipur. Indian J. Tradit. Knowl. (IJTK) 2005, 4, 21–32. [Google Scholar]
  92. Bhardwaj, S.; Gakhar, S.K. Ethnomedicinal plants used by the tribals of Mizoram to cure cuts & wounds. Indian J. Tradit. Knowl. 2005, 4, 75–80. [Google Scholar]
  93. Jamal, J.A.; Ghafar, Z.A.; Husain, K. Medicinal plants used for postnatal care in Malay traditional medicine in the Peninsular Malaysia. Pharmacogn. J. 2011, 3, 15–24. [Google Scholar] [CrossRef] [Green Version]
  94. Nanda, Y.; Singson, N.; Rao, A.N. Ethnomedicinal plants of Thadou tribe of Manipur (India)-1. Pleione 2013, 7, 138–145. [Google Scholar]
  95. Lalmuanpuii, J.; Rosangkima, G.; Lamin, H. Ethno-medicinal practices among the Mizo ethnic group in Lunglei district, Ethno-medicinal practices among the Mizo ethnic group in Lunglei district, Mizoram. Sci. Vis. 2013, 12, 24–34. [Google Scholar]
  96. Khan, M.H.; Yadava, P.S. Antidiabetic plants used in Thoubal district of Manipur, Northeast India. Indian J. Tradit. Knowl. 2010, 9, 510–514. [Google Scholar]
  97. Mullick, J.B.; Majumdar, T.; Reddy, K.V.R.; Mukherjee, S.; Sil, S.K. Activity of the medicinal plant Parkia Javanica against multidrug-resistant Neisseria gonorrhoeae and other clinical isolates. Asian J. Pharm. Clin. Res. 2019, 12, 83–86. [Google Scholar] [CrossRef]
  98. Quattrocchi, U. CRC World Dictionary of Medicinal and Poisonous Plants: Common Names, Scientific Names, Eponyms, Synonyms, and Etymology (5 Volume Set); CRC Press: Boca Raton, FL, USA, 2012; ISBN 142008044X. [Google Scholar]
  99. Das, A.; Das, M.C.; Sandhu, P.; Das, N.; Tribedi, P.; De, U.C.; Akhter, Y.; Bhattacharjee, S. Antibiofilm activity of Parkia javanica against Pseudomonas aeruginosa: A study with fruit extract. Rsc Adv. 2017, 7, 5497–5513. [Google Scholar] [CrossRef] [Green Version]
  100. Egamberdieva, D.; Ovidi, E.; Tiezzi, A.; Craker, L. Phytochemical and Pharmacological Properties of Medicinal Plants from Uzbekistan: A Review. J. Med. Act. Plants 2016, 5, 59–75. [Google Scholar] [CrossRef]
  101. Saxena, M.; Saxena, J.; Nema, R.; Singh, D.; Gupta, A. Phytochemistry of medicinal plants. J. Pharmacogn. Phytochem. Phytochem. 2013, 1, 168–182. [Google Scholar] [CrossRef]
  102. Tariq, A.L.; Reyaz, A.L. Significances and importance of phytochemical present in Terminalia chebula. Int. J. Drug Dev. Res. 2013, 5, 256–262. [Google Scholar]
  103. Wadood, A.; Ghufran, M.; Jamal, S.B.; Naeem, M.; Khan, A.; Ghaffar, R. Phytochemical analysis of medicinal plants occurring in local area of Mardan. Biochem. Anal. Biochem. 2013, 2. [Google Scholar] [CrossRef]
  104. Ahmad, N.I.; Rahman, S.A.; Leong, Y.H.; Azizul, N.H. A review on the phytochemicals of Parkia speciosa, stinky beans as potential phytomedicine. J. Food Sci. Nutr. Res. 2019, 2, 151–173. [Google Scholar] [CrossRef]
  105. Sikolia, S.F.; Omondi, S. Phytochemical Analysis of Some Selected Plants and Families in the University Botanic Garden of Maseno, Kenya. IOSR J. Pharm. Biol. Sci. 2017, 12, 31–38. [Google Scholar] [CrossRef]
  106. Tala, V.R.S.; Da Silva, V.C.; Rodrigues, C.M.; Nkengfack, A.E.; Dos Santos, L.C.; Vilegas, W. Characterization of proanthocyanidins from Parkia biglobosa (Jacq.) G. Don. (Fabaceae) by flow injection analysis—electrospray ionization ion trap tandem mass spectrometry and liquid chromatography/electrospray ionization mass spectrometry. Molecules 2013, 18, 2803–2820. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  107. Ko, H.J.; Ang, L.H.; Ng, L.T. Antioxidant activities and polyphenolic constituents of bitter bean Parkia speciosa. Int. J. Food Prop. 2014, 17, 1977–1986. [Google Scholar] [CrossRef] [Green Version]
  108. Loukrakpam, B.; Rajendran, A.; Chyne, D.A.L.; Longvah, T. 12th IFDC 2017 Special Issue—Nutrient and phytonutrient profiles of some indigenous vegetables of Manipur, Northeast India. J. Food Compos. Anal. 2019, 79, 12–22. [Google Scholar] [CrossRef]
  109. Mohammad, M.; Garba, M.A.; Haruna, A.; Jimoh, A.A. Characterization of naringenin from the fruit pulp extract of Parkia biglobosa (FABACEAE). Fuw Trends Sci. Technol. J. 2018, 4, 918–920. [Google Scholar]
  110. Dinda, B.; Mohanta, B.C.; Ghosh, P.; Sato, N.; Harigaya, Y. ChemInform Abstract: Chemical Constituents of Parkia javanica, Alocasia indica and Premna latifolia. ChemInform 2011, 42. [Google Scholar] [CrossRef]
  111. Tringali, C.; Spatafora, C.; Longo, O.D. Bioactive constituents of the bark of Parkia biglobosa. Fitoterapia 2000, 71, 118–125. [Google Scholar] [CrossRef]
  112. Kamisah, Y.; Zuhair, J.S.F.; Juliana, A.H.; Jaarin, K. Parkia speciosa empty pod prevents hypertension and cardiac damage in rats given N(G)-nitro-L-arginine methyl ester. Biomed. Pharmacother. 2017, 96, 291–298. [Google Scholar] [CrossRef]
  113. Adewoye, R.O.; Ajayi, O.O. Flavonols, flavones and tannins of Parkia clapperoniana. J. Am. Leather Chem. Assoc. (USA) 1988, 83, 153–156. [Google Scholar]
  114. Adewoye, R.O.; Ajayi, O.O. Anthocyanidins of Parkia clappertoniana. J. Soc. Leather Technol. Chem. 1989, 73, 120–121. [Google Scholar]
  115. Lemmich, E.; Adewunmi, C.O.; Furu, P.; Kristensen, A.; Larsen, L.; Olsen, C.E. 5-Deoxyflavones from Parkia clappertoniana. Phytochemistry 1996, 42, 1011–1013. [Google Scholar] [CrossRef]
  116. Ouoba, L.I.I.; Diawara, B.; Annan, N.T.; Poll, L.; Jakobsen, M. Volatile compounds of Soumbala, a fermented African locust bean (Parkia biglobosa) food condiment. J. Appl. Microbiol. 2005, 99, 1413–1421. [Google Scholar] [CrossRef] [PubMed]
  117. Mohd Azizi, C.Y.; Salman, Z.; Nik Norulain, N.; Mohd Omar, A. Extraction and identification of compounds from Parkia Speciosa seeds by supercritical carbon dioxide. J. Chem. Nat. Resour. Eng. 2008, 2, 153–163. [Google Scholar]
  118. Bitchi, M.B.; Magid, A.A.; Yao-Kouassi, P.A.; Kabran, F.A.; Harakat, D.; Martinez, A.; Morjani, H.; Tonzibo, F.Z.; Voutquenne-Nazabadioko, L. Triterpene saponins from the roots of Parkia bicolor A. Chev. Fitoterapia 2019, 137, 104264. [Google Scholar] [CrossRef] [PubMed]
  119. Rahman, N.N.N.A.; Zhari, S.; Sarker, M.Z.I.; Ferdosh, S.; Yunus, M.A.C.; Kadir, M.O.A. Profile of Parkia speciosa hassk metabolites extracted with SFE using FTIR-PCA method. J. Chin. Chem. Soc. 2012, 59, 507–514. [Google Scholar] [CrossRef]
  120. Jamaluddin, F.; Mohamed, S.; Lajis, M.N. Hypoglycaemic effect of Parkia speciosa seeds due to the synergistic action of β-sitosterol and stigmasterol. Food Chem. 1994, 49, 339–345. [Google Scholar] [CrossRef]
  121. Akintayo, E.T. Characteristics and composition of Parkia biglobbossa and Jatropha curcas oils and cakes. Bioresour. Technol. 2004, 92, 307–310. [Google Scholar] [CrossRef]
  122. Olatunya, A.M.; Omojola, A.; Akinpelu, K.; Akintayo, E.T. Vitamin E, Phospholipid, and Phytosterol Contents of Parkia biglobosa and Citrullus colocynthis Seeds and Their Potential Applications to Human Health. Prev. Nutr. Food Sci. 2019, 24, 338–343. [Google Scholar] [CrossRef]
  123. Jamaluddin, F.; Mohameda, S.; Lajis, M.N. Hypoglycaemic effect of Stigmast-4-en-3-one, from Parkia speciosa empty pods. Food Chem. 1995, 54, 9–13. [Google Scholar] [CrossRef]
  124. Salman, Z.; Mohd Azizi, C.; Nik Norulaini, N.; Mohd Omar, A. Gas chromatography/time-of-flight mass spectrometry for identification of compounds from Parkia speciosa seeds extracted by supercritical carbon dioxide. In Proceedings of the First International Conference on Natural Resources Engineering & Technology, Putrajaya, Malaysia, 24–25 July 2006; pp. 112–120. [Google Scholar]
  125. Frérot, E.; Velluz, A.; Bagnoud, A.; Delort, E. Analysis of the volatile constituents of cooked petai beans (Parkia speciosa) using high-resolution GC/ToF–MS. Flavour Fragr. J. 2008, 23, 434–440. [Google Scholar] [CrossRef]
  126. Gmelin, R.; Susilo, R.; Fenwick, G.R. Cyclic polysulphides from Parkia speciosa. Phytochemistry 1981, 20, 2521–2523. [Google Scholar] [CrossRef]
  127. Miyazawa, M.; Osman, F. Headspace constituents of Parkia speciosa seeds. Nat. Prod. Lett. 2001, 15, 171–176. [Google Scholar] [CrossRef] [PubMed]
  128. Tocmo, R.; Liang, D.; Wang, C.; Poh, J.; Huang, D. Organosulfide profile and hydrogen sulfide-releasing capacity of stinky bean (Parkia speciosa) oil: Effects of pH and extraction methods. Food Chem. 2016, 190, 1123–1129. [Google Scholar] [CrossRef] [PubMed]
  129. Adeyeye, E.I. The effect of fermentation on the dietary quality of lipids from African locust bean (Parkia biglobosa) seeds. Elixir Food Sci. 2013, 58, 14912–14922. [Google Scholar]
  130. Olatunya, A.M.; Akintayo, C.O.; Akintayo, E.T. Determination of qualitative and quantitative fatty acid composition of Parkia biglobbossa seed oil using two different analytical techniques. Int. J. Adv. Res. 2015, 3, 463–473. [Google Scholar]
  131. Millogo-Kone, H.; Guissou, I.; Nacoulma, O.; Traore, A. Comparative study of leaf and stem bark extracts of Parkia biglobosa against enterobacteria. Afr. J. Tradit. Complementary Altern. Med. 2008, 5, 238–243. [Google Scholar] [CrossRef] [Green Version]
  132. Yahaya, U.; Abubakar, S.; Salisu, A. Antifungal activity of Parkia biglobosa extract on pathogenic strain of Candida albicans. J. Appl. Sci. 2019, 19, 235–240. [Google Scholar] [CrossRef]
  133. Bukar, A.; Uba, A.; Oyeyi, T.I. Phytochemical analysis and antimicrobial activity of Parkia biglobosa (Jacq.) Benth. extracts againt some food--borne microrganisms. Adv. Environ. Biol. 2010, 74–80. [Google Scholar]
  134. Joshua, E.; Joshua, E.; Ifeanyichukwu, I.; Chika, E.; Okoro, N.; Carissa, D.; Emmanuel, N.; Chukwuka, A. In vitro evaluation of antibacterial activity of Parkia biglobosa, Hymenocardia acida and Zanthoxylum zanthoxyloides extracts on pathogenic Staphylococcus aureus Isolates. Int. J. Life Sci. 2016, 5, 72–77. [Google Scholar]
  135. Nounagnon, M.; Dah-Nouvlessounon, D.; N’tcha, C.; Nanoukon, C.; Assogba, F.; Lalèyè, F.O.A.; Baba-Moussa, L. Phytochemical composition, antimicrobial and cytotoxicity activities of Parkia biglobosa (Jacq) benth extracts from Benin. J. Pharmacogn. Phytochem. 2017, 6, 35–42. [Google Scholar]
  136. Millogo-Kone, H.; Lompo, M.; Kini, F.; Asimi, S.; Guissou, I.P.; Nacoulma, O. Evaluation of flavonoids and total phenolic contents of stem bark and leaves of Parkia biglobosa (Jacq.) Benth.(Mimosaceae)-free radical scavenging and antimicrobial activities. Res. J. Med Sci. 2009, 3, 70–74. [Google Scholar]
  137. Obajuluwa, A.F.; Onaolapo, J.A.; Oyi, A.R.; Olayinka, B.O. Susceptibility profile of methicillin-resistant Staphylococcus aureus (MRSA) isolates to antibiotics and methanolic extracts of Parkia biglobosa (Jacq.) Benth. Br. J. Pharm. Res. 2013, 3, 587–596. [Google Scholar] [CrossRef]
  138. Dosumu, O.O.; Oluwaniyi, O.O.; Awolola, G.V.; Oyedeji, O.O. Nutritional composition and antimicrobial properties of three Nigerian condiments. Niger. Food J. 2012, 30, 43–52. [Google Scholar] [CrossRef]
  139. Osemwegie, O.O.; Dahunsi, S.O. In-vitro effects of aqueous and ethanolic extracts of Parkia biglobossa (Jacq.) Benth on selected microorganisms. Niger. J. Biotechnol. 2015, 11–20. [Google Scholar] [CrossRef] [Green Version]
  140. Igwo-Ezikpe, M.N.; Ogbunugafor, H.A.; Gureje, A.P.; Ezeonwumelu, I.J. Phytochemical, antioxidant and antimicrobial properties of Parkia biglobosa (African Locust Bean) pods. Bioscientist 2013, 1, 182–191. [Google Scholar]
  141. Farias, D.F.; Souza, T.M.; Viana, M.P.; Soares, B.M.; Cunha, A.P.; Vasconcelos, I.M.; Ricardo, N.M.P.S.; Ferreira, P.M.P.; Melo, V.M.M.; Carvalho, A.F.U. Antibacterial, antioxidant, and anticholinesterase activities of plant seed extracts from Brazilian semiarid region. Biomed Res. Int. 2013, 2013, 510736. [Google Scholar] [CrossRef]
  142. Silva, R.R.S.; Silva, C.R.; Santos, V.F.; Barbosa, C.R.S.; Muniz, D.F.; Santos, A.L.E.; Santos, M.H.C.; Rocha, B.A.M.; Batista, K.L.R.; Costa-Júnior, L.M.; et al. Parkia platycephala lectin enhances the antibiotic activity against multi-resistant bacterial strains and inhibits the development of Haemonchus contortus. Microb. Pathog. 2019, 135, 103629. [Google Scholar] [CrossRef]
  143. Musa, N.; Wei, L.S.; Seng, C.T.; Wee, W.; Leong, L.K. Potential of Edible Plants as Remedies of Systemic Bacterial Disease Infection in Cultured Fish. Glob. J. Pharmacol. 2008, 2, 31–36. [Google Scholar]
  144. Sakunpak, A.; Panichayupakaranant, P. Antibacterial activity of Thai edible plants against gastrointestinal pathogenic bacteria and isolation of a new broad spectrum antibacterial polyisoprenylated benzophenone, chamuangone. Food Chem. 2012, 130, 826–831. [Google Scholar] [CrossRef]
  145. Fatimah, I. Green synthesis of silver nanoparticles using extract of Parkia speciosa Hassk pods assisted by microwave irradiation. J. Adv. Res. 2016, 7, 961–969. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  146. Ravichandran, V.; Vasanthi, S.; Shalini, S.; Shah, S.A.A.; Tripathy, M.; Paliwal, N. Green synthesis, characterization, antibacterial, antioxidant and photocatalytic activity of Parkia speciosa leaves extract mediated silver nanoparticles. Results Phys. 2019, 15, 102565. [Google Scholar] [CrossRef]
  147. Kawamura, F.; Ramle, S.F.M.; Sulaiman, O.; Hashim, R.; Ohara, S. Antioxidant and antifungal activities of extracts from 15 selected hardwood species of Malaysian timber. Eur. J. Wood Wood Prod. 2011, 69, 207–212. [Google Scholar] [CrossRef]
  148. Hasim, H.; Faridah, D.N. Antibacterial activity of Parkia speciosa Hassk. peel to Escherichia coli and Staphylococcus aureus bacteria. J. Chem. Pharm. Res. 2015, 7, 239–243. [Google Scholar]
  149. Thongbam, P.D.; Shakuntala, I.; Fiyaz, A.R.; Moirangthem, S.S.; Pajat, J.J.; Ngachan, S.V. Tree bean (Parkia roxburghii G. Don): A complete food and ethno-medicine for North East India. Res. Bull. 2012, 12–14. [Google Scholar]
  150. Zuhud, E.A.M.; Rahayu, W.P.; Wijaya, C.H.; Sari, P.P. Antimicrobial activity of kedawung extract (Parkia roxburghii G. Don) on food borne pathogens. J. Teknol. Dan Ind. Pangan 2001, 12, 1–5. [Google Scholar]
  151. Paul, B.; Bhuyan, B.; Purkayastha, D.D.; Dhar, S.S. Photocatalytic and antibacterial activities of gold and silver nanoparticles synthesized using biomass of Parkia roxburghii leaf. J. Photochem. Photobiol. B Biol. 2016, 154, 1–7. [Google Scholar] [CrossRef]
  152. Devi, T.P.; Shakuntala, I.; Devi, G.; Nonglait, K.K.L.; Singha, L.B.; Pattanayak, A.; Rahman, H. Antibacterial, nematicidal and nutritional properties of different parts of tree bean, Parkia roxburghii G. Don. Asian J. Microbiol. Biotechnol. Environ. Sci 2007, 9, 621–626. [Google Scholar]
  153. Shrisha, D.L.; Raveesha, K.A. Nagabhushan Bioprospecting of selected medicinal plants for antibacterial activity against some pathogenic bacteria. J. Med. Plants Res. 2011, 5, 4087–4093. [Google Scholar]
  154. Patel, J.R.; Gohil, T.G. Antibacterial efficacy of methanolic leaf extracts of some trees against some common pathogenic bacteria. J. Appl. Sci. Comput. 2018, 5, 404–408. [Google Scholar]
  155. Behuria, H.G.; Sahu, S.K. An Anti-microbial terpenoid fraction from Gymnema sylvestre induces flip-flop of fluorescent-phospholipid analogs in model membrane. Appl. Biochem. Biotechnol. 2020, 192, 1331–1345. [Google Scholar] [CrossRef] [PubMed]
  156. Tunsaringkarn, T.; Rungsiyothin, A.; Ruangrungs, N. α-glucosidase inhibitory activity of Thai mimosaceous plant extracts. J. Health Res. 2008, 22, 29–33. [Google Scholar]
  157. Jamaluddin, F.; Mohameda, S. Hypoglycemic effect of extracts of petai papan (Parkia speciosa, Hassk). Agric. Sci. 1993, 16, 161. [Google Scholar]
  158. Fitria, F.; Annisa, A.; Nikita, S.; Ranna, C. Alpha glukosidase inhibitory test and total phenolic content of ethanol extract of Parkia speciosa plant. Sci. Technol. Indones. 2019, 4, 1. [Google Scholar] [CrossRef]
  159. Saleh, M.S.M.; Siddiqui, M.J.; Mat So’ad, S.Z.; Roheem, F.O.; Saidi-Besbes, S.; Khatib, A. Correlation of FT-IR fingerprint and α-glucosidase inhibitory activity of salak (Salacca zalacca) fruit extracts utilizing orthogonal partial least square. Molecules 2018, 23, 1434. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  160. Ramu, R.; Shirahatti, P.S.; Nayakavadi, S.; Vadivelan, R.; Zameer, F.; Dhananjaya, B.L.; Nagendra Prasad, M.N. The effect of a plant extract enriched in stigmasterol and β-sitosterol on glycaemic status and glucose metabolism in alloxan-induced diabetic rats. Food Funct. 2016, 7, 3999–4011. [Google Scholar] [CrossRef] [PubMed]
  161. Wang, J.; Huang, M.; Yang, J.; Ma, X.; Zheng, S.; Deng, S.; Huang, Y.; Yang, X.; Zhao, P. Anti-diabetic activity of stigmasterol from soybean oil by targeting the GLUT4 glucose transporter. Food Nutr. Res. 2017, 61. [Google Scholar] [CrossRef] [Green Version]
  162. Ward, M.G.; Li, G.; Barbosa-Lorenzi, V.C.; Hao, M. Stigmasterol prevents glucolipotoxicity induced defects in glucose-stimulated insulin secretion. Sci. Rep. 2017, 7, 1–13. [Google Scholar] [CrossRef] [Green Version]
  163. Aiyer, P.V. Amylases and their applications. Afr. J. Biotechnol. 2005, 4, 1525–1529. [Google Scholar]
  164. Odetola, A.A.; Akinloye, O.; Egunjobi, C.; Adekunle, W.A.; Ayoola, A.O. Possible antidiabetic and antihyperlipidaemic effect of fermented Parkia biglobosa (Jacq) ex- tract in alloxan induced diabetic rats. Clin. Exp. Pharmacol. Physiol. 2006, 33, 808–812. [Google Scholar] [CrossRef]
  165. Sule, O.; Godwin, J.; Abdu, A. Preliminary study of hypoglycemic effect of locust bean (Parkia biglobosa) on wistar albino rat. J. Sci. Res. Rep. 2015, 4, 467–472. [Google Scholar] [CrossRef]
  166. Ibrahim, M.A.; Habila, J.D.; Koorbanally, N.A.; Islam, M.S. Butanol fraction of Parkia biglobosa (Jacq.) G. Don leaves enhance pancreatic β-cell functions, stimulates insulin secretion and ameliorates other type 2 diabetes-associated complications in rats. J. Ethnopharmacol. 2016, 183, 103–111. [Google Scholar] [CrossRef] [PubMed]
  167. Chanvitan, A.; Ubolcholket, S.; Chongsuvivatwong, V.; Geater, A. Risk factors for squamous cell carcinoma in southern Thailand. Esophageal Canver Stud. South. Thail. 1990, 81–100. [Google Scholar]
  168. Tangkanakul, P.; Trakoontivakorn, G.; Saengprakai, J.; Auttaviboonkul, P.; Niyomwit, B.; Lowvitoon, N.; Nakahara, K. Antioxidant capacity and antimutagenicity of thermal processed Thai foods. Jpn. Agric. Res. Q. JARQ 2011, 45, 211–218. [Google Scholar] [CrossRef] [Green Version]
  169. Murakami, A.; Ohigashi, H.; Koshimizu, K. Possible anti-tumour promoting properties of traditional Thai food items and some of their active constituents. Asia Pac. J. Clin. Nutr. 1994, 3, 185–191. [Google Scholar]
  170. Aisha, A.F.A.; Abu-Salah, K.M.; Alrokayan, S.A.; Ismail, Z.; Abdul Majid, A.M.S. Evaluation of antiangiogenic and antoxidant properties of Parkia speciosa Hassk extracts. Pak. J. Pharm. Sci. 2012, 25, 7–14. [Google Scholar]
  171. Singh, R.S.; Bhari, R.; Kaur, H.P. Mushroom lectins: Current status and future perspectives. Crit. Rev. Biotechnol. 2010, 30, 99–126. [Google Scholar] [CrossRef]
  172. Suvachittanont, W.; Jaranchavanapet, P. Mitogenic effect of Parkia speciosa seed lectin on human lymphocytes. Planta Med. 2000, 66, 699–704. [Google Scholar] [CrossRef]
  173. Kaur, N.; Singh, J.; Kamboj, S.; Agrewala, J.; Kaur, M. Two Novel Lectins from Parkia biglandulosa and Parkia roxburghii: Isolation, Physicochemical Characterization, Mitogenicity and Anti- Proliferative Activity. Protein Pept. Lett. 2005, 12, 589–595. [Google Scholar] [CrossRef]
  174. Fadeyi, S.A.; Fadeyi, O.O.; Adejumo, A.A.; Okoro, C.; Myles, E.L. In vitro anticancer screening of 24 locally used Nigerian medicinal plants. BMC Complementary Altern. Med. 2013, 13, 79. [Google Scholar] [CrossRef] [Green Version]
  175. Shete, S.V.; Mundada, S.J.; Dhande, S. Comparative effect of crude extract of Parkia biglandulosa and Its isolate on regenerative angiogenesis In adult Zebrafish. Indian Drug 2017, 54, 51–57. [Google Scholar]
  176. Kamisah, Y.; Othman, F.; Qodriyah, H.M.S.; Jaarin, K. Parkia speciosa Hassk.: A potential phytomedicine. Evid. Based Complementary Altern. Med. 2013, 2013, 709028. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  177. Auyeung, K.K.; Han, Q.-B.; Ko, J.K. Astragalus membranaceus: A review of its protection against inflammation and gastrointestinal cancers. Am. J. Chin. Med. 2016, 44, 1–22. [Google Scholar] [CrossRef] [PubMed]
  178. Ognatan, K.; Adi, K.; Lamboni, C.; Damorou, J.M.; Aklikokou, K.A.; Gbeassor, M.; Guilland, J.C. Effect of dietary intake of fermented seeds of Parkia biglobosa (Jacq) Benth (African locust bean) on hypertension in bogou and goumou-kope areas of togo. Trop. J. Pharm. Res. 2011, 10, 603–609. [Google Scholar] [CrossRef] [Green Version]
  179. Kodjo, K.M.; Contesse, V.; Do Rego, J.L.; Aklikokou, K.; Titrikou, S.; Gbeassor, M.; Vaudry, H. In vitro effects of crude extracts of Parkia biglobosa (Mimosaceae), Stereospermum kunthianum (Bignoniaceae) and Biophytum petersianum (Oxalidaceae) on corticosteroid secretion in rat. J. Steroid Biochem. Mol. Biol. 2006, 100, 202–208. [Google Scholar] [CrossRef]
  180. Ouédraogoa, S.; Somé, N.; Ouattara, S.; Kini, F.B.; Traore, A.; Bucher, B.; Guissou, I.P. Acute toxicity and vascular properties of seed of Parkia biglobosa (JACQ) R. Br Gift (Mimosaceae) on rat aorta. Afr. J. Tradit. Complementary Altern. Med. 2012, 9, 260–265. [Google Scholar]
  181. Kassi, Y.; Aka, K.J.; Abo, K.J.C.; Mea, A.; Bi, S.A.N.; Ehile, E.E. Effet antihypertensif d’un extrait aqueux d’écorce de tronc de Parkia biglobosa (mimosaceae) sur la pression artérielle de lapin. Sci. Nat. 2008, 5, 133–143. [Google Scholar]
  182. Yi, Q.Y.; Li, H.B.; Qi, J.; Yu, X.J.; Huo, C.J.; Li, X.; Bai, J.; Gao, H.L.; Kou, B.; Liu, K.L.; et al. Chronic infusion of epigallocatechin-3-O-gallate into the hypothalamic paraventricular nucleus attenuates hypertension and sympathoexcitation by restoring neurotransmitters and cytokines. Toxicol. Lett. 2016, 262, 105–113. [Google Scholar] [CrossRef]
  183. Galleano, M.; Pechanova, O.; G Fraga, C. Hypertension, nitric oxide, oxidants, and dietary plant polyphenols. Curr. Pharm. Biotechnol. 2010, 11, 837–848. [Google Scholar] [CrossRef]
  184. Takagaki, A.; Nanjo, F. Effects of Metabolites Produced from (-)-Epigallocatechin Gallate by Rat Intestinal Bacteria on Angiotensin I-Converting Enzyme Activity and Blood Pressure in Spontaneously Hypertensive Rats. J. Agric. Food Chem. 2015, 63, 8262–8266. [Google Scholar] [CrossRef]
  185. Luo, D.; Xu, J.; Chen, X.; Zhu, X.; Liu, S.; Li, J.; Xu, X.; Ma, X.; Zhao, J.; Ji, X. (−)-Epigallocatechin-3-gallate (EGCG) attenuates salt-induced hypertension and renal injury in Dahl salt-sensitive rats. Sci. Rep. 2020, 10, 1–11. [Google Scholar] [CrossRef] [PubMed]
  186. Ayo-Lawal, R.A.; Osoniyi, O.; Famurewa, A.J.; Lawal, O.A. Evaluation of antioxidant and hypolipidaemic effects of fermented Parkia biglobosa (Jacq) seeds in tyloxapol-induced hyperlipidaemic rats. Afr. J. Food Sci. 2014, 8, 225–232. [Google Scholar] [CrossRef] [Green Version]
  187. Rendu, F.; Saleun, S.; Auger, J. Parkia biglobosa seeds possess anti platelet activity. Thromb. Res. 1993, 71, 505–508. [Google Scholar] [CrossRef]
  188. Appeldoorn, M.M.; Venema, D.P.; Peters, T.H.F.; Koenen, M.E.; Arts, I.C.W.; Vincken, J.P.; Gruppen, H.; Keuer, J.; Hollman, P.C.H. Some phenolic compounds increase the nitric oxide level in endothelial cells in vitro. J. Agric. Food Chem. 2009, 57, 7693–7699. [Google Scholar] [CrossRef]
  189. Siow, H.L.; Gan, C.Y. Extraction of antioxidative and antihypertensive bioactive peptides from Parkia speciosa seeds. Food Chem. 2013, 141, 3435–3442. [Google Scholar] [CrossRef]
  190. Zaini, N.; Mustaffa, F. Review: Parkia speciosa as Valuable, Miracle of Nature. Asian J. Med. Health 2017, 2, 1–9. [Google Scholar] [CrossRef]
  191. Khalid, N.M.; Babji, A.S. Antioxidative and antihypertensive activities of selected Malaysian ulam (salad), vegetables and herbs. J. Food Res. 2018, 7, 27–37. [Google Scholar] [CrossRef]
  192. Owolabi, O.J.; Ukoima, G.S.; Inninh, S.O.; Otokiti, I.O. The anti-diarrhoeal activity of the aqueous stem bark extract of Parkia filicoidea (Fabaceae). J. Med. Biomed. Res. 2016, 15, 12–20. [Google Scholar]
  193. Adebayo, O.L.; Marzuk, S.; Mumuni, S.I. An in vivo assessment of Anti-diarrheal activity of solvent extracts of leaf and stem bark of Ghanian Parkia biglobosa against castor oil induced diarrhea in albino rats. Int. J. Bioassays 2014, 310, 3358–3362. [Google Scholar]
  194. Sahoo, H.B.; Sagar, R.; Kumar, A.; Bhaiji, A.; Bhattamishra, S.K. Antidiarrhoeal investigation of Apium leptophyllum (Pers.) by modulation of Na+K+ATPase, nitrous oxide and intestinal transit in rats. Biomed. J. 2016, 39, 376–381. [Google Scholar] [CrossRef]
  195. Khan, T.; Ali, S.; Qayyum, R.; Hussain, I.; Wahid, F.; Shah, A.J. Intestinal and vascular smooth muscle relaxant effect of Viscum album explains its medicinal use in hyperactive gut disorders and hypertension. BMC Complementary Altern. Med. 2016, 16, 1–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  196. Imtiaz, S.M.; Aleem, A.; Saqib, F.; Ormenisan, A.N.; Neculau, A.E.; Anastasiu, C.V. The potential involvement of an ATP-dependent potassium channel-opening mechanism in the smooth muscle relaxant properties of Tamarix dioica roxb. Biomolecules 2019, 9, 722. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  197. Maria, M.S.; Devarakonda, S.; Kumar, A.T.V.; Balakrishnan, N. Anti-ulcer activity of ethanol extract of Parkia speciosa against indomethacin induced peptic ulcer in albino rats. Int. J. Pharm. Sci. Res. 2015, 6, 895–902. [Google Scholar]
  198. Al Batran, R.; Al-Bayaty, F.; Al-Obaidi, M.M.J.; Abdualkader, A.M.; Hadi, H.A.; Ali, H.M.; Abdulla, M. A In vivo antioxidant and antiulcer activity of Parkia speciosa ethanolic leaf extract against ethanol-induced gastric ulcer in rats. PLoS ONE 2013, 8, e64751. [Google Scholar] [CrossRef] [PubMed]
  199. Fernandes, H.B.; Silva, F.V.; B Passos, F.F.; S Bezerra, R.D.; Chaves, M.H.; Oliveira, F.A.; Meneses Oliveira, R.C. Gastroprotective effect of the ethanolic extract of Parkia platycephala benth. Leaves against acute gastric lesion models in rodents. Biol. Res. 2010, 43, 451–457. [Google Scholar] [CrossRef] [PubMed]
  200. Hamaishi, K.; Kojima, R.; Ito, M. Anti-ulcer effect of tea catechin in rats. Biol. Pharm. Bull. 2006, 29, 2206–2213. [Google Scholar] [CrossRef] [Green Version]
  201. Ito, Y.; Ichikawa, T.; Iwai, T.; Saegusa, Y.; Ikezawa, T.; Goso, Y.; Ishihara, K. Effects of tea catechins on the gastrointestinal mucosa in rats. J. Agric. Food Chem. 2008, 56, 12122–12126. [Google Scholar] [CrossRef]
  202. Suzuki, Y.; Ishihara, M.; Segami, T.; Ito, M. Anti-ulcer effects of antioxidants, quercetin, α-tocopherol, nifedipine and tetracycline in rats. Jpn. J. Pharmacol. 1998, 78, 435–441. [Google Scholar] [CrossRef] [Green Version]
  203. De Barros, M.P.; Lemos, M.; Maistro, E.L.; Leite, M.F.; Sousa, J.P.B.; Bastos, J.K.; de Andrade, S.F. Evaluation of antiulcer activity of the main phenolic acids found in Brazilian Green Propolis. J. Ethnopharmacol. 2008, 120, 372–377. [Google Scholar] [CrossRef]
  204. Ijarotimi, O.S.; Keshinro, O.O. Protein quality, hematological properties and nutritional status of albino rats fed complementary foods with fermented popcorn, African locust bean, and bambara groundnut flour blends. Nutr. Res. Pract. 2012, 6, 381–388. [Google Scholar] [CrossRef] [Green Version]
  205. Nursucihta, S.; Thai’in, H.A.; Putri, D.M.; Utami, D.N.; Ghani, A.P. Antianemia activity of parkia speciosa hassk seed ethanolic extract. Maj. Obat Tradis. 2014, 19, 49–54. [Google Scholar]
  206. Nwaehujor, C.O.; Ezeigbo, I.I.; Udeh, N.E.; Ezeja, M.I.; Asuzu, I.U. Anti-inflammatory anti-oxidant Activities of the methanolic extracts of the stalk of Parkia biglobosa. Hygein J. Med. 2010, 3, 34–40. [Google Scholar]
  207. Bari, A.U.; Santiago, M.Q.; Osterne, V.J.S.; Pinto-Junior, V.R.; Pereira, L.P.; Silva-Filho, J.C.; Debray, H.; Rocha, B.A.M.; Delatorre, P.; Teixeira, C.S.; et al. Lectins from Parkia biglobosa and Parkia platycephala: A comparative study of structure and biological effects. Int. J. Biol. Macromol. 2016, 92, 194–201. [Google Scholar] [CrossRef] [PubMed]
  208. Silva, H.C.; Bari, A.U.; Rocha, B.A.M.; Nascimento, K.S.; Ponte, E.L.; Pires, A.F.; Delatorre, P.; Teixeira, E.H.; Debray, H.; Assreuy, A.M.S. Purification and primary structure of a mannose/glucose-binding lectin from Parkia biglobosa Jacq. seeds with antinociceptive and anti-inflammatory properties. J. Mol. Recognit. 2013, 26, 470–478. [Google Scholar] [CrossRef] [PubMed]
  209. Ukwuani, A.; Ahmad, H. In vitro anti-inflammatory activity of Parkia biglobosa fruit bark extract. Int. J. Life Sci. Sci. Res. 2015, 1, 8–11. [Google Scholar] [CrossRef]
  210. Badu, M.; Mensah, J.K.; Boadi, N.O. Antioxidant activity of methanol and ethanol/water extracts of Tetrapleura tetraptera and Parkia biglobosa. Int. J. Pharma Bio Sci. 2012, 3, 312–321. [Google Scholar]
  211. Oboh, G.; Alabi, K.B.; Akindahunsi, A.A. Fermentation changes the nutritive value, polyphenol distribution, and antioxidant properties of Parkia biglobosa seeds (African locust beans). Food Biotechnol. 2008, 22, 363–376. [Google Scholar] [CrossRef]
  212. Seal, T. Antioxidant activity of some wild edible plants of Meghalaya state of India: A comparison using two solvent extraction systems. Int. J. Nutr. Metab. 2012, 4, 51–56. [Google Scholar]
  213. Ghasemzadeh, A.; Jaafar, H.Z.E.; Bukhori, M.F.M.; Rahmat, M.H.; Rahmat, A. Assessment and comparison of phytochemical constituents and biological activities of bitter bean (Parkia speciosa Hassk.) collected from different locations in Malaysia. Chem. Cent. J. 2018, 12, 1–9. [Google Scholar] [CrossRef] [Green Version]
  214. Bajpai, V.K.; Alam, B.; Ju, M.; Kwon, K.; Suk, Y. Antioxidant mechanism of polyphenol-rich Nymphaea nouchali leaf extract protecting DNA damage and attenuating oxidative stress-induced cell death via Nrf2-mediated heme-oxygenase-1 induction coupled with ERK/p38 signaling pathway. Biomed. Pharmacother. 2018, 103, 1397–1407. [Google Scholar] [CrossRef]
  215. Tunsaringkarn, T.; Soogarun, S.; Rungsiyothin, A.; Palasuwan, A. Inhibitory activity of Heinz body induction in vitro antioxidant model and tannin concentration of Thai mimosaceous plant extracts. J. Med. Plants Res. 2012, 6, 4096–4101. [Google Scholar] [CrossRef] [Green Version]
  216. Ajibola, M.; Olugbemi, O.; Joseph, D.; Denen, A. Hepatoprotective effect of Parkia biglobosa stem bark methanolic extract on paracetamol induced liver damage in wistar rats. Am. J. Biomed. Life Sci 2013, 1, 75–78. [Google Scholar] [CrossRef] [Green Version]
  217. Coriolano, M.C.; de Melo, C.M.L.; de Oliveira Silva, F.; Schirato, G.V.; Porto, C.S.; dos Santos, P.J.P.; dos Santos Correia, M.T.; Porto, A.L.F.; dos Anjos Carneiro-Leão, A.M.; Coelho, L.C.B.B. Parkia pendula seed lectin: Potential use to treat cutaneous wounds in healthy and immunocompromised mice. Appl. Biochem. Biotechnol. 2014, 172, 2682–2693. [Google Scholar] [CrossRef] [PubMed]
  218. Angami, T.; Bhagawati, R.; Touthang, L.; Makdoh, B.; Nirmal; Lungmuana; Bharati, K.A.; Silambarasan, R.; Ayyanar, M. Traditional uses, phytochemistry and biological activities of Parkia timoriana (DC.) Merr., an underutilized multipurpose tree bean: A review. Genet. Resour. Crop Evol. 2018, 65, 679–692. [Google Scholar] [CrossRef]
  219. Hopkins, H.C. Floral biology and pollination ecology of the neotropical species of Parkia. J. Ecol. 1984, 72, 1–23. [Google Scholar] [CrossRef]
  220. Abalaka, S.E.; Fatihu, M.Y.; Ibrahim, N.D.G.; Kazeem, H.M. Histopathologic changes in the gills and skin of adult Clarias gariepinus exposed to ethanolic extract of Parkia biglobosa pods. Basic Appl. Pathol. 2010, 3, 109–114. [Google Scholar] [CrossRef]
  221. Oshimagye, M.I.; Ayuba, V.O.; Annune, P.A. Toxicity of aqueous extracts of Parkia biglobosa pods on Clarias gariepinus (Burchell, 1822) Juveniles. Niger. J. Fish. Aquac. 2014, 2, 24–29. [Google Scholar]
  222. Uyub, A.M.; Nwachukwu, I.N.; Azlan, A.A.; Fariza, S.S. In-vitro antibacterial activity and cytotoxicity of selected medicinal plant extracts from Penang Island Malaysia on some pathogenic bacteria. Ethnobot. Res. Appl. 2010, 8, 95–106. [Google Scholar] [CrossRef] [Green Version]
  223. Sil, S.K.; Saha, S.; Karmakar, P. Reactive oxygen species as possible mediator of antibacterial activity of Parkia javanica, against bacterial species predominantly found in chronic wound. J. Drug Deliv. Ther. 2018, 8, 43–47. [Google Scholar] [CrossRef] [Green Version]
  224. Rupanjali, S.; Basu, J.M.; Syamal, R.; Biswanath, D.; Sil, S.K. In vitro activity of Parkia javanica extract against Leishmania donovani parasite. J. Appl. Biosci. 2010, 36, 85–89. [Google Scholar]
  225. Favacho, A.R.M.; Cintra, E.A.; Coelho, L.C.B.B.; Linhares, M.I.S. In vitro activity evaluation of Parkia pendula seed lectin against human cytomegalovirus and herpes virus 6. Biologicals 2007, 35, 189–194. [Google Scholar] [CrossRef] [PubMed]
  226. Ogunyinka, B.I.; Oyinloye, B.E.; Osunsanmi, F.O.; Opoku, A.R.; Kappo, A.P. Modulatory influence of Parkia biglobosa protein isolate on testosterone and biomarkers of oxidative stress in brain and testes of streptozotocin-induced diabetic male rats Bolajoko. Int. J. Physiol. Pathophysiol. Pharm. 2016, 8, 78–86. [Google Scholar] [CrossRef] [Green Version]
  227. Patra, K.; Jana, S.; Sarkar, A.; Karmakar, S.; Jana, J.; Gupta, M.; Mukherjee, G.; De, U.C.; Mandal, D.P.; Bhattacharjee, S. Parkia javanica extract induces apoptosis in S-180 cells via the intrinsic pathway of apoptosis. Nutr. Cancer 2016, 68, 689–707. [Google Scholar] [CrossRef] [PubMed]
  228. Aisha, A.F.A.; Abu-Salah, K.M.; Darwis, Y.; Majid, A.M.S.A. Screening of antiangiogenic activity of some tropical plants by rat aorta ring assay. Int. J. Pharmacol. 2009, 5, 370–376. [Google Scholar] [CrossRef] [Green Version]
  229. Gui, J.S.; Jalil, J.; Jubri, Z.; Kamisah, Y. Parkia speciosa empty pod extract exerts anti-inflammatory properties by modulating NFκB and MAPK pathways in cardiomyocytes exposed to tumor necrosis factor-α. Cytotechnology 2019, 71, 79–89. [Google Scholar] [CrossRef]
  230. Mustafa, N.H.; Ugusman, A.; Jalil, J.; Kamisah, Y. Anti-inflammatory property of Parkia speciosa empty pod extract in human umbilical vein endothelial cells. J. Appl. Pharm. Sci. 2018, 8, 152–158. [Google Scholar] [CrossRef] [Green Version]
  231. Ruthiran, P.; Selvaraj, C.I. Phytochemical screening and in vitro antioxidant activity of Parkia timoriana (DC.) Merr. Res. J. Biotechnol. 2017, 12, 12. [Google Scholar]
  232. Chanu, K.V.; Ali, M.A.; Kataria, M. Antioxidant activities of two medicinal vegetables: Parkia javanica and Phlogacanthus thyrsiflorus. Int. J. Pharm. Pharm. Sci. 2012, 4, 102–106. [Google Scholar]
  233. Balaji, K.; Nedumaran, S.A.; Devi, T.; Sikarwar, M.S.; Fuloria, S. Phytochemical analysis and in vitro antioxidant activity of Parkia speciosa. Int. J. Green Pharm. 2015, 9, S50–S54. [Google Scholar] [CrossRef]
  234. Ramli, S.; Bunrathep, S.; Tansaringkarn, T.; Ruangrungsi, N. Screening for free radical scavenging activity from ethanolic extract of Mimosaceous plants Endemic to Thailand. J. Health Res. 2008, 22, 55–59. [Google Scholar]
  235. Komolafe, K.; Olaleye, T.M.; Omotuyi, O.I.; Boligon, A.A.; Athayde, M.L.; Akindahunsi, A.A.; da Rocha, J.B.T. In vitro antioxidant activity and effect of Parkia biglobosa bark extract on mitochondrial redox status. Jams J. Acupunct. Meridian Stud. 2014, 7, 202–210. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The preferred reporting items for systematic review and meta-analysis flowchart indicating the numbers of identified, screened, included and excluded articles in the review.
Figure 1. The preferred reporting items for systematic review and meta-analysis flowchart indicating the numbers of identified, screened, included and excluded articles in the review.
Ijms 22 00618 g001
Figure 2. Structural formulas of polyphenolics 128, as previously listed in Table 2.
Figure 2. Structural formulas of polyphenolics 128, as previously listed in Table 2.
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Figure 3. Structural formulas of polyphenolics 2946, as previously listed in Table 2.
Figure 3. Structural formulas of polyphenolics 2946, as previously listed in Table 2.
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Figure 4. Structural formulas of terpenoids 4959 and steroids 6066, as previously listed in Table 2.
Figure 4. Structural formulas of terpenoids 4959 and steroids 6066, as previously listed in Table 2.
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Figure 5. Structural formulas of cyclic polysulfides 8193, as previously listed in Table 2.
Figure 5. Structural formulas of cyclic polysulfides 8193, as previously listed in Table 2.
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Table 1. The medicinal uses of plants from genus Parkia.
Table 1. The medicinal uses of plants from genus Parkia.
SpeciesPart UsedMethod of PreparationMedicinal UsesRegion/CountryReference
P. bicolorStem barkPulverized powderWound healingWest coast of Africa and Nigeria[23]
Tree Diarrhea, dysenterySouthwest Nigeria[55]
Stem barksDecoctionBad cough, measles, and
woman infertility
Stem barksDecoctionDiarrhea and skin ulcersGhana[56]
P. biglobosaRoots & barkPasteDental disorderIvory Coast[29]
Seed and stem barkFresh seedsFish poisonWest Africa[57,58]
RootDecoction combined with other plantsInfertilityNigeria[58]
Bark infusion with lemonDiarrheaNigeria[59]
Stem bark Anti-snake venomNigeria[60]
BarkPaste, decoctionWound healing leprosy, hypertension, mouth wash, toothpasteNigeria[22,23]
Leaves and rootsEyesoreLotionGambia[23]
BarkHot decoctionFeverGambia[23]
BarkDecoctionMalaria, diabetes, amenorrhea, and hypertensionSenegal, Mali, Ghana Togo, and South Africa[11,40,61,62,63]
Roots and barkDecoction of the roots with Ximenia americanaWeight lossBurkina Faso[64]
Stem barkBoiled barkDiarrhea, conjunctivitis, severe cough, and leprosyWest Coast Africa[23,65,66]
LeavesDecoctionViolent colic chest and muscular painNorthern Nigeria[38]
barkInfusionDental caries and astringentGuinea Bissau[67]
P. biglandulosaSeed barkSaponinsAstringentIndia[68]
Stem bark Hemagglutination, ulcerIndia[69]
Tree Inflammation and ulcerIndia[70]
P. clappertonianaTree HypertensionSouthwest Nigeria[55]
Root Dental caries and conjunctivitisAfrican[71,72]
SeedCrudely poundedLabor inductionGhana[17]
Tree DiarrheaKaduna and Nigeria[73]
Leaves and barkMacerationEpilepsyNorthern Nigeria[74]
Stem bark Chickenpox and measlesSouthwest Nigeria[24]
Tree Diabetes, leprosy, and ulcersGhana[75]
Tree Mouthwash and toothacheNigeria[76]
Tree Eczema and skin diseasesNigeria[77]
P. pendulaLeaves bark Genital bathNetherland[78]
P. speciosaSeedEaten raw or cooked oral decoctionDiabetesMalaysia[80]
LeavesPounded with rice and applied on the neckCoughMalaysia[30]
RootDecoctionSkin problemsSouthern Thailand[21]
RootDecoction taken orallyHypertension and diabetesMalaysia[26]
FruitEaten rawDiabetesMalaysia[30]
SeedEaten rawDetoxification and hypertensionSingapore[81]
Ringworm Malaysia[82]
RootOral decoctionToothacheMalaysia[27]
Tree Heart problem, constipation and edemaIndia[83,84]
Leaves DermatitisIndonesia[85]
Seed Loss of appetiteIndonesia[86]
SeedCooked Kidney disorderWest Malaysia[87]
P. timorianaBark and twig Decoction of bark and twig pasteDiarrhea, dysentery, and woundIndia[88]
BarkDecoction used to bathFeverGambia[89]
Pulp barkMixed with lemonUlcer and woundGambia[89]
Fruit DiabetesThailand[90]
PodPounded in waterHair washing, skin diseases, and ulcersIndia[19]
Bark and leaves Head washing, skin diseases, and ulcersIndia[19]
BarkDecoction with Centella. asiatica and Ficus glomerataDiabetesIndia[16]
P. roxburghiiTreeTender pod and bark taken orallyDiarrhea, dysentery, intestinal disorder, and bleeding pilesIndia[91]
The fruit or young shootGreen portion of the fruit mixed with water to be taken orallyDysentery, diarrhea, food poisoning, wound, and scabiesIndia[92]
SeedGrounded and mixed with hot waterPostnatal care, diarrhea, edema and tonsillitisMalaysia[93]
Pod Diabetes, hypertension, and urinary tract infectionsIndia[18]
Leaves, pod, peals, and bark Diarrhea and dysenteryIndia[94]
Stem barkHot water extractionDiarrhea and dysenteryIndia[95]
BarkTurn into pasteUsed as plaster for eczemaIndia[25]
P. javanicaBark, pod, and seedTaking orally as vegetableDysentery and diarrheaIndia[15]
Tree InflammationIndia[96]
Bark fruit Dysentery and pilesIndia[51]
Stomachache and choleraIndia[97]
Bark and leavesLotionSores and skin diseases [98]
Tree Diarrhea, cholera dysentery, and food poisoningIndia[99]
Table 2. Phytochemical compounds from Parkia.
Table 2. Phytochemical compounds from Parkia.
Structure NumberTypeCompoundSpeciesPartReference
1FlavanolCatechinP. speciosaPod[107]
P. biglobosaRoot/bark[106]
P. javanicaEdible part[108]
2FlavanolEpicatechinP. speciosaPod[107]
P. javanicaEdible part[108]
3FlavanolEpigallocatechinP. biglobosaRoot/bark[111]
P. javanicaEdible part[108]
4FlavanolEpigallocatechin gallateP. roxburghiiPod[18]
P. biglobosaRoot/bark[106,111]
5FlavanolEpicatechin-3-O-gallateP. biglobosaBark[111]
6Flavanol4-O-methyl-epigallocate-chinP. biglobosaBark[111]
7FlavanolEpigallocatechin-O-glucuronideP. biglobosaRoot/bark[106]
8FlavanolEpicatechin-O-gallate-O-glucuronideP. biglobosaRoot/bark[106]
9FlavanolEpigallocatechin-O-gallate-O-glucuronideP. biglobosaRoot/bark[106]
10FlavanolTheaflavin gallateP. speciosaPod[112]
11FlavonolKaempferolP. speciosaPod[107]
P. javanicaEdible part[108]
12FlavonolQuercetinP. speciosaPod[107]
13FlavonolHyperinP. roxburghiiPod[18]
14FlavonolApigeninP. speciosaPod[112]
15Flavone3,7,3′,4′-TetrahydroxyflavoneP. clappertonianaSeeds[113,114]
16Flavone7-Hydroxy-3, 8, 4′-trimethoxyflavoneP. clappertonianaLeaves[115]
17Flavone2′-Hydroxy-3,7,8,4′,5′′pentamethoxyflavoneP. clappertonianaLeaves[115]
18FlavoneNobiletinP. speciosaPod[112]
19FlavoneTangeritinP. speciosaPod[112]
20FlavonolMyricetinP. javanicaEdible part[108]
P. speciosaPod[112]
21Flavonol glycosideRutinP. javanicaEdible part[108]
P. speciosaPod[112]
22Flavonol glycosideDidyminP. speciosaPod[112]
23Methoxy flavonolIsorhamnetinP. javanicaEdible part[108]
24FlavoneLuteolinP. javanicaEdible part[108]
25FlavanoneNaringeninP. javanicaEdible part[108]
26FlavanoneNaringenin-1-4′-di-O-ß-d-glucopyranosideP. biglobosaFruit pulp[109]
27IsoflavoneGenisteinP. javanicaEdible part[108]
28IsoflavoneDaidzeinP. javanicaEdible part[108]
29Phenolic acidGallic acidP. speciosaPod[107]
P. bicolorRoot[28]
30Phenolic acidMethyl gallateP. bicolorRoot[28]
31Phenolic acidHydroxybenzoic acidP. speciosaPod[107]
32Phenolic acidVanillic acidP. speciosaPod[107]
33Phenolic acidChlorogenic acidP. speciosaPod[107]
P. javanicaEdible part[108]
34Phenolic acidEllagic acidP. speciosaPod[107]
35Phenolic acidPunicalinP. speciosaPod[112]
36Phenolic acidCaffeic acidP. speciosaPod[107]
P. javanicaEdible part[108]
37Phenolic acidCinnamic acidP. speciosaPod[107]
38Phenolic acidP-Coumaric acidP. speciosaPod[107]
P. javanicaEdible part[108]
39Phenolic acidFerulic acidP. speciosaPod[107]
P. javanicaEdible part[108]
40Phenolic acidCoutaric acidP. speciosaPod[112]
41Phenolic acidCaftaric acidP. speciosaPod[112]
42Phenolic1-(w-Feruloyllignoceryl) -glycerolP. biglobosaBark[111]
43Phenolic1-(w-Isoferuloylalkanoyl) -glycerolP. biglobosaBark[111]
44PhenolicMalvidinP. speciosaPod[112]
45PhenolicPrimulinP. speciosaPod[112]
46Pheny propanoidParkinolP. javanicaLeaves[110]
47Phenol2-Methoxy phenolP. biglobosaSeed[116]
48Phenol2,4-Disiopropyl-phenolP. biglobosaSeed[116]
Terpenoid and steroid
49TriterpenoidLupeolP. biglobosaBark[111]
P. bicolorRoot[28]
P. speciosaSeeds[117]
50MonoterpenoidLimoneneP. biglobosaSeed[116]
51TriterpenoidUrsolic acidP. javanicaLeaf/stem[42]
52TriterpenoidParkibicoloroside AP. bicolorRoot[118]
53TriterpenoidParkibicoloroside BP. bicolorRoot[118]
54TriterpenoidParkibicoloroside CP. bicolorRoot[118]
55TriterpenoidParkibicoloroside DP. bicolorRoot[118]
56TriterpenoidParkibicoloroside EP. bicolorRoot[118]
57Monoterpenoidal glucoside8-O-p-Hydroxl-6′-O-p-coumaryl-missaeno-sidic acidP. javanicaLeaf[42]
58Monoterpenoidal glucoside7-O-E-3,4-Dimethoxycinnamoyl-6′-O-ß-d-glucopyranosylloganic acidP. javanicaLeaf[42]
59Diterpene16-O-Methyl-cass-13(15) ene-16,18-dionic acidP. bicolorRoot[118]
60Steroidβ-SitosterolP. speciosaSeed[117,119,120]
P. javanicaLeaf/stem[42]
P. biglobosaSeed oil[121,122]
61SteroidStigmasterolP. speciosaSeed[117,119,120]
P. biglobosaSeed oil[121,122]
62SteroidStigmasterol methyl esterP. speciosaSeed[117,119]
63SteroidStigmast-4-en-3-oneP. speciosaSeed[123]
64SteroidStigmasta-5,24(28)-diene-3-olP. speciosaSeed[117]
65SteroidCampesterolP. speciosaSeed[117,119]
P. biglobosaSeed oil[121,122]
66SteroidStigmastan-6,22-diien,3,6-dedihydo-P. speciosaSeed[119]
Miscellaneous Compounds
67Fatty acidArachidonic acidP. speciosaSeed[117,119]
P. bicolorSeed[22]
P. biglobosaSeed[22]
68Fatty acidLinoleic acid chlorideP. speciosaSeed[117,119]
69Fatty acidLinoleic acidP. speciosaSeed[117,119]
P. biglobosaSeed[22]
P. bicolorSeed[22]
70Fatty acidSqualeneP. speciosaSeed[117,119]
71Fatty acidLauric acidP. speciosaSeed[117,124]
72Fatty acidStearic acidP. speciosaSeed[117,119,124]
P. biglobosaSeed[22]
P. bicolorSeed[22]
73Fatty acidStearoic acidP. speciosaSeed[124]
74Fatty acidEicosanic acidP. speciosaSeed[124]
75Fatty acidOleic acidP. speciosaSeed[117,119,124]
76Fatty acidPalmitic acidP. speciosaSeed[117,119,124]
P. biglobosaSeed[22]
P. bicolorSeed[22]
77Fatty acidMyristic acidP. speciosaSeed[117,119,124]
78Fatty acidUndecanoic acidP. speciosaSeed[119,124]
79Fatty acidStearolic acidP. speciosaSeed[119]
80Fatty acidHydnocarpic acidP. speciosaSeed[124]
81Cyclic polysulfide1,3-dithiabutane P. speciosaSeed[125]
82Cyclic polysulfide2,4- DithiapentaneP. speciosaSeed[125]
83Cyclic polysulfide2,3,5-TrithiahexaneP. speciosaSeed[125]
84Cyclic polysulfide2,4,6-TrithiaheptaneP. speciosaSeed[125]
85Cyclic polysulfide1,2,4-TrithiolaneP. biglobosaSeed[116,126]
P. speciosaSeed[126,127,128]
86Cyclic polysulfide1,3,5-TrithianeP. speciosaSeed[128]
87Cyclic polysulfide3,5-Dimethyl-1,2,4-trithiolaneP. speciosaSeed[128]
88Cyclic polysulfideDimethyl tetrasulfidP. speciosaSeed[128]
89Cyclic polysulfide1,2,5,6-Tetrathio-caneP. speciosaSeed[128]
90Cyclic polysulfide1,2,3,5-TetrathianeP. speciosaSeed[128]
91Cyclic polysulfide1,2,4,5-TetrathianeP. speciosaSeed[128]
92Cyclic polysulfide1,2,4,6-Tetrathie-paneP. speciosaSeed[126,128]
93Cyclic polysulfide1,2,4,5,7,8-
P. speciosaSeed[126]
94Cyclic poly-sulfideLenthionineP. speciosaSeed[117,124,126,128]
95Estersn-Tetradecyl acetateP. speciosaSeed[124]
96EstersMethyl linoleateP. speciosaSeed[124]
97EstersEthyl linoleateP. speciosaSeed[117,124]
P. biglobosaSeed[116]
98EsterButyl palmitateP. speciosaSeed[117]
99EstersEthyl palmitateP. speciosaSeed[124]
100EstersMethyl palmitateP. speciosaSeed[124]
101EstersMethyl laurateP. speciosaSeed[124]
102EstersDodecyl acrylateP. speciosaSeed[124]
103EstersMethyl hexadecanoateP. biglobosaSeed[116]
104EsterEthyl stearateP. speciosaSeed[117,124]
105EsterMethyl octadecanoateP. biglobosaSeed[116]
106EsterButyl stearateP. speciosaSeed[124]
107EsterPropanoic acid, 3,3′-thiobis-didodecyl esterP. speciosaSeed[124]
108EsterLinoleaidic acid methyl esterP. speciosaSeed[119]
109Alcohol2,6,10,14-Hexadecatetraen-1-olP. speciosaSeed[117]
110Alcohol1-Octen-3-olP. biglobosaSeed[116]
111Alcohol3-Ethyl-4-nonanolP. speciosaSeed[117]
112Alcohol1-TridecanolP. speciosaSeed[117,124]
113AcidEicosanoic acidP. speciosaSeed[117]
114Acid16-O-Methyl-cass-13(15)ene-16,18-dionic acidP. bicolorRoot[118]
115AcidElaidic acidP. speciosaSeed[117,124]
116Pyrazine2,5-Dimethyl pyrazineP. biglobosaSeed[116]
117PyrazineTrimethyl pyrazineP. biglobosaSeed[116]
118Pyrazine2-Ethyl-3,5-dimethyl pyrazineP. biglobosaSeed[116]
119Ketone2-Nonade-canoneP. speciosaSeed[117,124]
120Ketone2-Pyrrolidi-noneP. speciosaSeed[117]
121KetoneCyclodecanoneP. speciosaSeed[124]
122AlkaneCyclododecaneP. biglobosaSeed[116]
123AlkaneTetradecaneP. speciosaSeed[119]
124Benzene glucoside3,4,5-Trimethoxyphenyl-1-O-ß-d-glucopy-ranosideP. bicolorRoot[118]
125Aldehyde2-DecenalP. speciosaSeed[117]
126AldehydeCyclo-decanone-2,4-decadienalP. speciosaSeed[117]
127AldehydePentanalP. biglobosaSeed[116]
P. speciosaSeed[125]
128Aldehyde3-Methylthio-propanalP. biglobosaSeed[116]
129AldehydeTetradecanalP. speciosaSeed[119,124]
130AldehydePentadecanalP. speciosaSeed[117,124]
131AldehydeHexadecanalP. speciosaSeed[117,124]
132AmineHexanamideP. speciosaSeed[117]
133OilVitamin EP. speciosaSeed[117,124]
Table 3. Pharmacological activities of Parkia species extracts and fractions.
Table 3. Pharmacological activities of Parkia species extracts and fractions.
ActivitySpeciesPartType of Extract/CompoundKey FindingsReferences
AntimicrobialP. biglobosaLeaf, stem bark, and rootMethanolic and aqueousActive against S. aureus, B. subtilis, E. coli, P. aeruginosa.[38]
P. biglobosaRoot barkAqueous and methanolActive against E. coli, S. aureus, K. pneumoniae, P. aeruginosa.
Activity: Aqueous > methanol
P. biglobosaLeaves and podAqueous and ethanolActive against S. aureus, E. aerogenes, S. typi, S. typhimurium, Shigella spp., E. coli, and P. aeruginosa (bacteria), Mucor spp., and Rhizopus spp. (fungi)[133]
P. biglobosaBark and leavesHydro-alcohol and aqueousActive against E. coli, S. enterica, and S. dysenteriae. Activity: hydroalcoholic > aqueous[65]
P. speciosaSeedsWater suspensionActive against S. aureus, A. hydrophila, S. agalactiae, S. anginosus, and V. parahaemolyticus isolated from moribund fishes and shrimps[143]
P. speciosaSeed peelEthyl acetate (EA) Hexane
EA: Four times higher than streptomycin against S. aureus and three times higher for E. coli. Hexane: 50% inhibitory ability of streptomycin for both bacteria. Ethanol: no inhibition[148]
P. speciosaPod extract and its silverAqueousPod: active against P. aeruginosa Silver particles: active against P. aeruginosa[145]
P. speciosaSapwood, heartwood, and barkMethanolBark: Active against G. trabeum. Sapwood and heartwood: No effect[147]
P. speciosaSeedsChloroform, petroleum ether, Aqueous and methanolActive against H. pylori except aqueous extract. Activity: chloroform > methanol > petroleum ether[222]
P. speciosaSeedMethanol
Ethyl acetate
Methanol: active against H. pylori. Ethyl acetate: active against E. coli
Both: no effect on S. typhimurium, S. typhi, and S sonnei
P. javanicaStem barkMethanolGood inhibitory activity against E. coli, S. aureus S. pyogenes found in chronic wound[223]
P. javanicaStem barkMethanolActive against four Vibrio cholerae strains[224]
P. javanicaLeavesGold and silver nanoparticlesGood inhibitory activity against S. aureus[151]
P. javanicaBarkMethanol extract and semi-polar fractions (chloroform and ethyl acetate)Active against Neisseria gonorrhoeae. Chloroform showed the best activity[97]
P. javanicaSeeds, leaves and skin podsAqueousActive against S. aureus, A. hydrophila, and S. typhimurium Not active against E. coli[152]
P. clappertonianaLeaves and barksEthanolActive against Salmonellae and Shigella[73]
P. clappertonianaStem bark and leavesAqueous and methanolActive against S. aureus and P. aeruginosa.
Methanol extract was more potent
P. biglandulosaLeafMethanolActive against E. coli, P. aeruginosa, and S. aureus[154]
P. filicoideaStem barksAqueous, acetone and ethanolActive against S. aureus, K. pneumoniae, P. aeruginosa, S. viridans and B. subtilis. Not active against E. coli[50]
P. bicolorLeavesEthyl acetate, ethanol and aqueousActive against E. coli, S. aureus, P. aeruginosa, A. niger, B. cereus and a fungus, C. utilis[23]
P. bicolorRootsMethanol, ethyl acetate and AqueousActive against C. diphtheria, K. pneumoniae, P. mirabilis, S. typhi, and S. pyogenes[28]
P. pendulaSeedsLectinReduced cellular infectivity of human cytomegalovirus in human embryo lung (HEL) cells.[225]
HypoglycemicP. speciosaSeeds and podsChloroformStrong glucose-lowering activity in alloxan-induced diabetic rats
Activity: seeds > pod
P. speciosaRind, leaves and seedsEthanolInhibited α-glucosidase activity in rat
Activity: rind > leaf > seed
P. speciosaSeedChloroformReduced plasma glucose levels in alloxan-induced diabetic rats[120]
P. biglobosaFermented seedsMethanol and aqueousReduced fasting plasma glucose in alloxan-induced diabetic rats[160,161]
P. biglobosaSeedsProteinSignificantly increased lipid peroxidation product levels in brain and testes of diabetic rats[226]
P. biglobosaSeedsMethanol and fractions (chloroform and n-hexane)Showed glucose-lowering effect
Activity: chloroform > methanol > n-hexane
P. javanicaFruitsEthyl acetate fractionReduced blood glucose inhibited α-glucosidase and α-amylase in streptozotocin-induced diabetic rats[18]
P javanicaFruitsAqueous methanolIncreased apoptosis in sarcoma-180 cancer cell lines[227]
P javanicaSeedsMethanolCaused 50% death in HepG2 (liver cancer cell) but not cytotoxic to normal cells[44]
P javanicaSeedsLectinInhibited proliferation in cancerous cell lines; P388DI and J774, B-cell hybridoma and HB98 cell line[173]
P. speciosaSeed coatsMethanol extractDemonstrated selective cytotoxicity to MCG-7 and T47D (breast cancer), HCT-116 (colon cancer)[228]
P. speciosaPodsMethanolic ethyl acetate fractionShowed selective cytotoxicity on breast cancer cells MCF-7[170]
P. biglobosaLeaves and stemMethanolAntiproliferative effect in human cancer cells T-549, BT-20, and PC-3[174]
P. filicoideaLeavesMethanolAntiproliferative effect in in human cancer cells T-549, BT-20, and PC-3[174]
Antiproliferative and anti-mutagenicP. biglandulosaSeedsLectinT cell mitogen and antiproliferative against P388DI and J774 cancer cell lines[173]
AntihypertensiveP. speciosaSeedsAqueousShowed moderate ACE-inhibitory activity in in vitro[191]
P. speciosaSeedsPeptideInhibited angiotensin-converting enzyme (ACE) in rats. No effect observed in non-hydrolyzed samples[189,190]
P. speciosaPodsMethanolPrevented the increases in blood pressure and angiotensin-converting enzyme (ACE) and restored nitric oxide in hypertensive rat model[112]
P. biglobosaStem barkAqueousInduced hypotension in adrenaline-induced hypertensive rabbits[181]
P. biglobosaRoasted and fermented seedsAqueousInduced relaxation in rat aorta precontracted with phenylephrine in the presence or absence of endothelium.[180]
P. biglobosafermented seedsAqueousLower blood pressure, blood glucose, and heart rate, high level of magnesium as well as improved lipid profile in patients with hypertension[178]
AntidiarrhealP. biglobosaStem barkAqueous and fractionsThe extract of stem bark exhibit dose-dependent antidiarrheal activity at different concentrations in albino rats with castor oil-induced diarrhea[45]
P. biglobosaLeaves and stem barkAqueous and ethanolReduced frequency of stooling in castor-oil induced diarrhea in rats[193]
P. biglobosaStem-bark70% MethanolThe extract exhibited 100% protections at 100 and 200 mg/kg bw in the diarrheal rats[59]
P. filicoideaStem barkAqueousReduced frequency of stooling and improved transit time at 100 and 200 mg/kg bw[192]
AntiulcerP. speciosaLeavesEthanolReduced mucosal injury and increased in periodic acid-Schiff (PAS) staining induced by ethanol[198]
P. speciosaSeedEthanolDecreased gastric juice acidity, lesion length, collagen content and fibrosis in indomethacin-induced peptic ulcer in rats[197]
P. platycephalaLeavesEthanolReduced gastric mucosal lesion induced by ethanol, ischemia-reperfusion and ethanol-HCl[199]
P. biglobosaCombination of fermented seed with other fermented productsAqueousIncreased hemoglobin, red blood cell, white blood cell levels and packed cell volume in albino rats[204]
P. biglobosaSeedsEthanolIncreased hemoglobin levels in NaNO2-induced anemic mice[205]
P. speciosaSeedsEthanolIncreased hemoglobin levels in NaNO2-induced anemic mice[205]
P.biglandulosaFruit and β-sitosterolEthanolThe extract and the isolated compound showed antiangiogenic activity on the caudal fin of adult zebrafish[175]
P. speciosaPodsMethanol and water sub-extractInhibited more than 50% micro vessel outgrowth in rat aortae and HUVECs[170]
AntimalarialP. biglobosaStem barkMethanol and fractionsShowed antiplasmodial activity caused by P. berghei and P. falciparum[11]
NephroprotectiveP. clappertonianaSeedAqueousReduced serum creatinine, Na, urine proteins and leukocytes and kidney weight in gentamicin-induced renal damage in rats[75]
HepatoprotectiveP. biglobosaStem barksMethanolReduced serum alanine and aspartate transaminases, and alkaline phosphatase in paracetamol-induced hepatotoxicity rat model[216]
Wound healingP. pendulaSeedsLectinIncreased skin wound repair in immunosuppressed mice[217]
Anti-inflammatoryP. speciosaPodsEthyl acetate fractionReduced iNOS activity, COX-2, VCAM-1 and NF-κB expressions in cardiomyocytes exposed to tumor necrosis factor-α[229]
P. speciosaPodsEthyl acetate fractionReduced iNOS activity, COX-2, VCAM-1 and NF-κB expressions in HUVECs exposed to tumor necrosis factor-α[230]
P. biglobosaStalkMethanolInhibited croton pellet granuloma formation and carrageenin-induced rat paw edema[206]
P. biglobosaSeedsLectinLectin showed anti-inflammatory effect by inhibition of pro-inflammatory cytokine release and stimulation of anti-inflammatory cytokine release on peritonitis induced model mice[208]
P. biglobosaStem barkHexaneReduced carrageenan- and PMA-induced edema in mice[29]
P. biglobosaFruit70% MethanolIncreased percentage protection of the human red blood cell membrane[209]
P. platycephalaSeedsLectinLectin showed antinociceptive effect in the mouse model of acetic acid-induced[207]
AntioxidantP. javanicaLeavesHexane, ethyl acetate, and methanolMethanol extract showed the highest antioxidant potential activities (DPPH test) of about 85% and (FRAP test) of about 0.9 mM Fe (II)/g dry[231]
P. javanicaLeavesAqueous, ethanol and methanolAll the extracts exhibited good antioxidant activity. The aqueous extract showed the highest values of 47.42 and 26.6 mg of ascorbic acid equivalent/g in DPPH and FRAP tests, respectively[232]
P. javanicaPodsMethanol and acetoneHigh content of total phenolic and flavonoid. Showed high reducing power and strong radical scavenging activity.[212]
P. javanicaFruitMethanolShowed increased DPPH and ferric-reducing power activities concentration-dependently[210]
P. speciosaPodMethanolIncreased DPPH scavenging activity[233]
P. speciosaPodEthyl acetate fractionReduced NOX4, SOD1, p38 MAPK protein expressions and ROS level[230]
P. speciosaPodAqueous and ethanolicIncreased DPPH and ABTS scavenging activities, reduced lipid peroxidation Activity: ethanol > aqueous[107]
P. speciosaSeedsEthanolExtract exhibited significant activity (DPPH and FRAP tests)[213]
P. speciosaSeed coats and podsEthanolReduced Heinz body formation in erythrocytes incubated with acetyl phenylhydrazine.
Activity: seed coat > pods >
P. speciosaPodsEthanolIncreased DPPH scavenging activity[234]
P. biglobosaFermented and unfermented seedAqueousFermented seed increased reduction of Fe3+ to Fe2+.[211]
P. biglobosaStem barkAqueous-methanolicMitigated ferric-induced lipid peroxidation in rat tissues and increased scavenging activities against DPPH and ABTS, ferric-reducing ability[235]
P. biglobosaFruitMethanol and hydro-ethanolIncreased DPPH scavenging activity and reducing power.[210]
P. biglobosaFruitHydroethanolic and methanolIncreased scavenging activity against DPPH free radical
Activity: methanol > hydroethanolic
Abbreviations: HUVECs, human umbilical vein endothelial cells; DPPH, 2,2-Diphenyl-1-picrylhydrazy; ABTS, 2,20-Azinobis (3-ethylbenzothiazoline-6-sulphonic acid) diammonium salt; FRAP, ferric reducing antioxidant power; iNOS, inducible nitric oxide synthase; PMA, phorbol myristate acetate; COX-2, cyclooxygenase-2; VCAM-1, vascular cell adhesion moelcule-1; NF-κB, nuclear factor kappa-B; ACE, angiotensin converting enzyme; HEL, human embryo lung; PAS, periodic acid-Schiff; bw, body weight.
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Saleh, M.S.M.; Jalil, J.; Zainalabidin, S.; Asmadi, A.Y.; Mustafa, N.H.; Kamisah, Y. Genus Parkia: Phytochemical, Medicinal Uses, and Pharmacological Properties. Int. J. Mol. Sci. 2021, 22, 618.

AMA Style

Saleh MSM, Jalil J, Zainalabidin S, Asmadi AY, Mustafa NH, Kamisah Y. Genus Parkia: Phytochemical, Medicinal Uses, and Pharmacological Properties. International Journal of Molecular Sciences. 2021; 22(2):618.

Chicago/Turabian Style

Saleh, Mohammed S. M., Juriyati Jalil, Satirah Zainalabidin, Ahmad Yusof Asmadi, Nor Hidayah Mustafa, and Yusof Kamisah. 2021. "Genus Parkia: Phytochemical, Medicinal Uses, and Pharmacological Properties" International Journal of Molecular Sciences 22, no. 2: 618.

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