Next Article in Journal
Foodborne Helminths in Imported Fish: Molecular Evidence from Fish Products in the Kazakhstan Market
Previous Article in Journal
Advanced Bio-Based Smart Materials for Food Packaging: Applications, Safety, and Sustainability
Previous Article in Special Issue
Prebiotic Effect of Polysaccharides and Flavonoids from Passiflora foetida Fruits on the Human Intestinal Microbiota Associated with Obesity
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

A Systematic Review of Evidence-Based Health Benefits of Oroxylum indicum and Its Functional Food Potential

by
Hai Linh Nguyen
1,
Amporn Sae-Eaw
1,
Dinh Quyen Tran
2,
Witoon Prinyawiwatkul
3 and
Yaowared Chulikhit
4,*
1
Department of Food Technology, Faculty of Technology, Khon Kaen University, Khon Kaen 40002, Thailand
2
Department of Chemistry, Trent School of the Environment, Trent University, Peterborough, ON K9L 0G2, Canada
3
School of Nutrition and Food Sciences, Agricultural Center, Louisiana State University, Baton Rouge, LA 70803, USA
4
Division of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand
*
Author to whom correspondence should be addressed.
Foods 2025, 14(20), 3465; https://doi.org/10.3390/foods14203465
Submission received: 21 September 2025 / Revised: 6 October 2025 / Accepted: 7 October 2025 / Published: 10 October 2025
(This article belongs to the Special Issue Potential Health Benefits of Plant Food-Derived Bioactive Compounds)

Abstract

Oroxylum indicum is a traditional food in Asia rich in flavonoids and health-related effects. However, research into the use of O. indicum as a functional food ingredient is overlooked. This review synthesized literature from 2010 to 2025 using the PRISMA framework, bibliometric mapping, and the Antecedents–Decisions–Outcomes (ADO) model. In total, 185 articles were included, covering in vitro, in vivo, in silico, and limited human investigations. Bibliometric analysis shows a growing global interest, with recent focuses on molecular docking, cancer, and conservation. Phytochemical investigations consistently report key flavonoids, including baicalein, baicalin, oroxylin A, chrysin, oroxin A, and oroxin B. Studies have linked these compounds to different health benefits, including antioxidants, cardiovascular, and neurological protection. Application of the ADO framework organized research into motives, methods, and outcomes, and highlighted scientifically validated ethnomedicinal uses, such as diabetes and liver protection. Meanwhile, gaps, including obesity-related studies, long-term safety, and clinical trials, remain. More importantly, although young fruits are locally consumed as vegetables or beverages, translation into functional foods is limited by bitterness, lack of standardized preparations, and insufficient dose–response data at dietary intakes. This review discusses the bioactive potential of O. indicum and outlines research priorities for its development in functional food.

1. Introduction

Oroxylum indicum (L.) Benth. ex-Kurz (O. indicum) belongs to the family Bignoniaceae and is a culturally important Asian plant. The tree is traditionally consumed as both food and medicine. Young fruits and shoots are eaten as vegetables in Thailand and neighboring countries, whereas the seeds are sometimes used in herbal drinks [1]. Beyond its local dietary use, stems and roots are decocted to treat asthma, diarrhea, bronchitis, and some respiratory problems [2].
Although many ethnomedicinal uses have been reported, some claims are still scientifically unconfirmed. Traditional applications for conditions such as asthma, diarrhea, jaundice, and wound healing are frequently documented in local knowledge systems [3,4,5,6], but mapping between scientific pharmacological effects and conventional uses is lacking. This raises an important question of whether such uses reflect genuine bioactivity or are anecdotal traditions. The identification of validated versus unsubstantiated effects is vital prior to the deployment of O. indicum as a source of bioactive compounds for functional foods.
In recent decades, O. indicum has gained attention for its rich flavonoids associated with health benefits. Nagasaka et al. [7] determined p53 activation and anticancer effects of chrysin isolated from the bark. Meanwhile, Zhang et al. [8] demonstrated antidiabetic activities of baicalein. These findings explain why the plant is valued in both traditional medicine and modern research on functional foods. However, its use in food products is still constrained by bitterness, a lack of standardized formulations, limited safety, and bioavailability at nutritional intake levels.
In the pharmaceutical context, many studies on O. indicum have examined pharmacological effects but rarely cover the full range of methods. Most are limited to in vitro assays, which show cellular activity [9,10,11,12]. Some perform in silico models, which predict compound–target interactions [13,14,15,16]. While valuable, these approaches cannot completely establish efficacy. More biologically relevant evidence comes from in vivo or ex vivo studies, which reflect metabolism, immunity, and absorption [8,17,18,19]. However, these are scarce. This review categorizes the available studies based on their methodological approaches to show which health effects have been biologically validated. It also reveals gaps, especially in linking in vitro/in silico findings with in vivo and clinical validation.
There are several existing reviews on O. indicum, yet many are outdated or too narrow. Some older narrative reviews looked at its traditional and medical uses, while more recent systematic reviews focused only on a specific compound or a medicinal effect [20,21,22]. No comprehensive review has integrated research trends, mapped traditional uses with scientific health benefits, and evaluated the plant’s bioactive chemistry for functional food potential. This paper presents a systematic synthesis of studies on O. indicum from 2010 to 2025. The PRISMA framework and bibliometric mapping were first used to identify trends in publication output, geographic locations, and thematic focus. To move beyond descriptive patterns, the Antecedents–Decisions–Outcomes (ADO) framework was applied to interpret the literature [23]. It helps clarify why studies were conducted (antecedents), how they were designed (decisions), and what results were obtained (outcomes). This integration separates ethnomedicinal and pharmaceutical research, verified from unsubstantiated claims, and highlights gaps, including insufficient safety data, dose–response studies, and clinical validation. The review also identifies the flavonoids most consistently linked to health benefits and discusses barriers, such as bitterness and standardized formulations, that restrict translation into functional food products.
The review answers the three main research questions. (1) What are the research trends and thematic developments of studies on O. indicum between 2010 and 2025? (2) What are scientifically validated and unsubstantiated ethnomedicinal uses? (3) What barriers and opportunities shape the translation of O. indicum into functional food applications, particularly with respect to safety, standardization, and sensory properties?

2. Methodology

The PRISMA framework (2020 guidelines) was used to select relevant papers with research identification, screening, eligibility, and inclusion (Figure 1).

2.1. Identification

The Scopus database was searched on 5 April 2025 for studies on O. indicum between 2010 and April 2025. The search included both the scientific name and common names as keywords in titles, abstracts, and author keywords: “Oroxylum indicum” OR “midnight horror” OR “Indian trumpet flower” OR “broken bones plant” OR “Tree of Damocles” OR “Indian calosanthes” OR “Indian caper” OR “Indian trumpet” [20,24]. A total of 582 records were initially retrieved. Inclusion criteria were peer-reviewed journal articles, reviews, conference papers, and data papers published in English. Exclusion criteria eliminated non-peer-reviewed sources (e.g., book chapters, reports, editorials, working papers) and records from subject areas unrelated to life, health, or agricultural sciences (e.g., mathematics, computer science, economics). After applying these criteria, 517 articles remained, with 65 records removed. Filtering was performed using Scopus’ built-in tools.

2.2. Eligibility and Screening

Articles were assessed using Scimago Journal Rank (SJR) quartiles, and only quartile (Q1 and Q2) studies were considered eligible. After this eligibility, 289 studies remained and 228 were excluded. The shortlisted papers were then screened manually for relevance to O. indicum. Although the initial keyword search included terms such as “Indian trumpet” and “midnight horror,” some results referred to unrelated species, which were removed. Data from each included study was extracted separately by two reviewers using a standardized data extraction sheet. Discrepancies were resolved through discussion. Following this process, 104 additional articles were excluded, resulting in 185 research articles included for analysis.

2.3. Inclusion

The 185 research articles were analyzed using bibliometric methods and interpreted through the ADO framework. For ADO analysis, outcomes were extracted from each study individually, and studies were grouped into predefined categories according to the objectives. Each article could be assigned to one or more categories. Bibliometric analyses were conducted in RStudio (2024.12.0-467) running R version 4.4.2 with the bibliometrix package (version 5.1.1) [25], and a keyword co-occurrence network map was generated with VOSviewer 1.6.20 [26].

2.4. Limitations

This review used only one database (Scopus), but it is widely accepted in bibliometric and systematic reviews for its broad coverage and consistent metadata. Focusing on Q1 and Q2 journals may leave out some relevant studies, yet it helped highlight reliable research trends from higher-quality sources. In addition, the connections between traditional uses and pharmacological effects were based on plausible biological links, not direct scientific proof. In some cases, the absence of traditional context made interpretation limited. In the keyword analysis, six articles (3.24% of the total) did not list author keywords, but this small proportion is unlikely to affect the overall trends.

3. Results

3.1. Bibliometric Landscape

3.1.1. Publication Trends

Figure 2 shows the annual scientific output on O. indicum from 2010 to 2024. Publication numbers remained relatively low, with fewer than 15 papers per year until 2021. A sharp rise occurred in 2022, when annual output reached 24 articles, followed by 24 in 2023 and a peak of 27 in 2024. This upward trajectory indicates the growing research attention to O. indicum in recent years. While the figure captures the scale of publication activity, the specific research directions and thematic developments are examined in the subsequent bibliometric and ADO analyses.

3.1.2. Geographical Distribution

Figure 3a shows the countries where O. indicum samples were collected for investigation. Most collections were reported in India, Thailand, and China, which reflects the species’ native distribution and its cultural importance in South and Southeast Asia. Notably, Cardoso Reis et al. [10] reported a collection from Santana de Pirapama, Brazil. This indicates research interest beyond the species’ natural range. Such findings also point to opportunities for conservation and cultivation in non-native regions [27].
Figure 3b presents the distribution of author affiliations linked to O. indicum publications. India, China, and Thailand dominate, but additional contributions come from the United States, Malaysia, and Japan. These affiliations demonstrate that while research is concentrated in the plant’s native range, international collaboration and global attention are gradually expanding.

3.1.3. Top Journals

Overall, 110 journals have published studies on O. indicum (Table 1). The leading outlets are the Journal of Ethnopharmacology (18 articles), Molecules (11), and Natural Product Research (6). Most of the highly represented journals are pharmacology- or phytochemistry-oriented, which reflects the dominance of biomedical approaches. A smaller number of contributions appeared in food- and nutrition-focused outlets such as Food Chemistry, Nutrients, and the Journal of Functional Foods. Yet, during the full-text screening stage of our review, studies in these journals primarily reported phytochemistry or pharmacological assays rather than food applications. This distribution indicates that although O. indicum is gaining visibility across disciplines, its potential as a functional food ingredient remains underexplored.

3.1.4. Top-Cited Documents

Figure 4 shows the top-cited papers related to O. indicum. The top article was by Dinda et al. [28] (452 citations), which examined the therapeutic potential of baicalin and baicalein against inflammatory disorders [28]. Two highly cited reviews, Sumbul et al. [29] (188 citations) and Dinda et al. [20] (123 citations), provided broad syntheses of phenolic compounds and therapeutic O. indicum potentials, respectively [20,29]. The prominence of these reviews shows that review articles play a key role in bringing together scattered findings and guiding new research directions. Yet, no review has mapped the traditional uses with scientific health effects. In addition, none of the most-cited works addressed sensory evaluation, formulation, or dietary application, underscoring that food-oriented research on O. indicum has not shaped the field to date.

3.1.5. Author Keywords and Thematic Development

Figure 5 is the result of a co-occurrence analysis of author keywords (a minimum threshold of 3), which yielded 39 terms. The two terms with the highest frequency are “Oroxylum indicum” (65 occurrences) and “baicalein” (29 occurrences). This data indicates the central role of this specific flavonoid in the current research domain.
The keyword “Oroxylum indicum” demonstrates extensive connectivity with other terms, including cancer, Ayurveda, COVID-19, baicalein, baicalin, and oroxylin A, which shows a strong emphasis on medicinal benefits. The second most frequent keyword is baicalein, which is clustered with O. indicum, COVID-19, cancer, inflammation, acarbose, and NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells). It is consistent with its reported anticancer, anti-inflammatory, and antidiabetic activities [22]. Figure 5b–d show the three keyword clusters in the most recent studies. The keyword “COVID-19” appeared the most during 2022 (average of publication years). However, since COVID-19 is no longer a concern, research on the herb for treating the virus has declined. Recent clusters highlight molecular docking, cancer, and conservation. It can be observed that researchers increasingly use molecular docking to study O. indicum compounds, especially baicalein, in cancer treatment. In addition, conservation of the plants is also of concern. Kumari et al. [36] reported the tree is endangered because of the destruction of its natural habitat.
The thematic map (Figure 6) further organizes research directions. Research topics are positioned based on their relevance (centrality) and level of development (density). Niche themes are specialized areas that are well developed but not strongly connected to other topics. Some main keywords are nomadic Gujjar (location name), Bhoxa (location name), Manipur (location name), Tharu (location name), traditional knowledge, herbal medicines, and traditional Chinese medicine. These suggest that studies have been well developed on localized ethnobotanical or ethnomedicinal knowledge. Motor themes are highly relevant and actively studied topics. Some main keywords are biodiversity, conservation, Pteropodidae (bat family), and pollination, which are closely related to ecological and environmental context. Emerging or declining themes have low development and low relevance, suggesting they are either new areas just starting to appear or older topics losing importance. Most importantly, basic themes are the foundations of research on O. indicum. They are widely explored, yet less detailed. Some main keywords are cancer, molecular docking, baicalein, baicalin, oroxylin A, and chrysin. Together, keyword and thematic analyses reveal a strong biomedical orientation, with growing attention to conservation, but little evidence of food applications, sensory evaluation, or dietary studies.

3.2. Research Classification Via the ADO Framework

As noted in the top journals section, most studies on O. indicum focus on phytochemistry and pharmacology, with little attention to food applications. Besides descriptive patterns, we applied the Antecedents–Decisions–Outcomes (ADO) framework to classify research motives, methodological choices, and reported outcomes (Figure 7). This approach helps reveal not only what types of studies exist, but also how they were designed and what they achieved.
Manual screening identified eight main antecedent categories: (1) pharmacological studies, (2) traditional and ethnomedicinal uses, (3) phytochemistry, (4) toxicology and safety, (5) clinical trials and human studies, (6) materials, (7) environmental and agricultural studies, and (8) reviews. Three papers were grouped as “Others,” since O. indicum appeared only as part of multi-herb formulations or a reference in substitution without plant-specific methods or outcome relevance.

3.3. Pharmacological Studies, Ethnomedicinal Uses, and Mapping

A total of 106 studies were assigned to the pharmacological category (Table 2). These investigations tested numerous biological effects of O. indicum using extracts from different plant parts, including stem bark, pods, flowers, seeds, leaves, fruits, roots, and root bark. Ethanolic and methanolic extracts by decoction or maceration were the most common preparations, while some studies tested purified flavonoids. Consistent with the keyword analysis (Figure 5), the leading bioactive compounds were baicalein, baicalin, chrysin, oroxylin A, oroxin A, oroxin B, and their derivatives [1,9,37,38,39]. Above all, baicalein was frequently associated with liver protection, bone health, neuroprotection, pain relief, anti-obesity, antidiabetic, anti-infective, anti-inflammatory, antioxidant, and anticancer activities [8,14,40,41,42,43] (Table 2).
The methodologies used covered in vitro assays, in vivo models, in silico studies, and a limited number of ex vivo experiments. In vivo investigations provide the most biologically relevant evidence, as they reflect physiological processes such as immune modulation, metabolism, and absorption. Encouragingly, nearly every pharmacological category had at least one in vivo study with the exception of anti-infective and obesity-related research. The absence of in vivo antimicrobial research may be due to biosafety and ethical complexities in infection models. In contrast, the absence of in vivo obesity models is an indication of research gaps rather than methodological difficulties. This interpretation is supported by the thematic map (Figure 6), which places obesity in the “emerging” category. Given the significant global prevalence of obesity and the promising in vitro data obtained, the development of in vivo animal models and subsequent human clinical trials should be established as a research priority.
Table 3 shows the ethnomedicinal uses of O. indicum, many of which are well scientifically validated with pharmacological activities. The traditional uses are classified into the subgroups of pharmacological activity categories for easy comparison. The degree of alignment between ethnomedicinal applications and experimental data can be described across three levels: strongly supported, moderately supported, and unclear or unsupported.
At the highest level of alignment, there are cancer, diabetes, liver protection, anti-inflammatory activity, antioxidant effects, cardiovascular health, gastrointestinal health, pain relief, and respiratory health (Table 3). For example, Lalou et al. [37] reported that O. indicum had anti-tumor effects, which supports its traditional use in cancer treatment. Similarly, antidiabetic activity was validated by Hengpratom et al. [42], Mei et al. [94], and Mangal et al. [93], aligning with folk remedies for diabetes. Arthritis and rheumatism can be grouped under either bone health or anti-inflammatory. However, both categories are strongly supported by in vivo studies showing NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells), 5-LOX (arachidonate 5-lipoxygenase), and COX-2 (cyclooxygenase-2) inhibition [2,39] and anti-osteoporotic effects [12,14,90,91,92].
Traditional concepts such as “detoxification” or “rejuvenation” also map well to demonstrated antioxidant, cytoprotective, and membrane-stabilizing activities. These traditional terms are not clearly defined, yet their meanings generally match how the plant helps reduce oxidative stress and support cell health. Heart-related problems are supported by Yuvaraj et al. [97] and Pondugula et al. [18]. They found that O. indicum protects the heart, reduces artery buildup, lowers fat levels in the blood, and fights inflammation and harmful oxidation. Respiratory uses, particularly asthma, cough, and allergy, are directly supported [121]. Conditions like laryngitis or tonsillitis lack direct evidence. However, the herbs’ anti-inflammatory properties might be somewhat helpful in non-infectious or chronic cases. Hepatoprotective activity is also consistent with traditional uses for liver ailments [19], though direct validation for jaundice and hepatitis is lacking. Other groups, such as gastrointestinal disorders and pain relief, are similarly well supported, as summarized in Table 3. Taken together, these overlaps provide strong scientific confirmation for most of the plant’s major traditional applications.
In contrast, some traditional uses are moderately supported, including skin health, obesity, neurological protection, anti-infective, and reproductive health. Skin disorders such as leukoderma remain unsupported, whereas wound healing has some backing. Obesity was studied with in vitro and in silico research, but in vivo studies are needed. For neurological protection, no direct experimental models have assessed seizure activity, though neuroprotective studies provide partial support. Anti-infective claims are mixed. Its effectiveness against intestinal worms is strongly supported by lab studies. Pneumonia also has strong support, mainly due to its action against Staphylococcus aureus. Nevertheless, effects on fever, typhoid, and cholera are only indirectly supported. Antiviral studies against DENV-2 (Dengue Virus serotype 2) [112], ZIKV (Zika Virus) [10], and SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) [15] partly match uses for measles and smallpox, but malaria and tuberculosis lack evidence.
Some uses remain unsupported or unmapped, including tonic, hair tonic, dropsy, urinary problems, scrotal swelling, dog bite, enlarged spleen, antipyretic, hemorrhage, and scorpion sting. These indicate the breadth of traditional knowledge but require new research to explore their biological basis. In addition, new activities not described traditionally have emerged, such as anti-gout [124] and anti-sickling [125], showing that modern pharmacology is expanding beyond recorded ethnomedicinal claims.

3.4. Phytochemistry

Phytochemical investigations of O. indicum focus on three objectives, including active compound identification, linking to biological effects, and extraction method improvement (Table S3). Techniques, such as chromatography (high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS)), spectroscopy (nuclear magnetic resonance (NMR)), and multivariate analysis, are commonly used [37,42,66]. In addition, newer eco-friendly approaches like Natural Deep Eutectic Solvent–Ultrasound-Assisted Extraction (NADES–UAE) are also used to enhance flavonoid yield and stability [84]. Throughout studies, flavonoids dominate the chemical profile. Baicalein, baicalin, chrysin, oroxylin A, oroxin A, oroxin B, and their derivatives are the most consistently reported. Some less frequently appearing flavonoids are apigenin, scutellarein, tetuin, luteolin, hispidulin, and their derivatives. These compounds have been linked to different health effects, such as liver protection, skin health, bone health, neurological protection, antioxidant, anti-inflammatory, antidiabetic, and anticancer effects, which explains their central role in the pharmacological activities of the plant.
Some mechanistic studies have discovered how O. indicum flavonoids exert their bioactivities. The antidiabetic effects of baicalein are by modulating gut microbiota and improving metabolic function in diabetic rodent models [8]. Baicalin shows Src kinase (Src tyrosine kinase) and reduces IL-6 (interleukin-6) production, indicating anti-inflammatory effects at the molecular level [89]. Chrysin activates the p53 pathway to induce apoptosis in cancer cells with no genotoxic stress [7]. Oroxylin A gives anti-adipogenic and lipolytic activity Via PPARγ (peroxisome proliferator-activated receptor gamma) suppression [95]. Meanwhile, oroxin A improves porcine embryo development by enhancing blastocyst formation and mitochondrial function while reducing ROS (reactive oxygen species), apoptosis, and autophagy [123]. In contrast, oroxin B has anti-osteoclastogenic and anti-osteoporotic activity in ovariectomized mice by the regulation of the MAPK/NF-κB (mitogen-activated protein kinase/nuclear factor kappa) pathway [91].
In general, the phytochemical profile of O. indicum indicates strong potential for developing functional food ingredients, provided challenges of bitterness and bioavailability can be addressed. Figure 8 shows the chemical structures of the major flavonoids in O. indicum, including baicalein, baicalin, chrysin, oroxylin A, oroxin A, and oroxin B.

3.5. Toxicology, Safety, Clinical Trials, and Human Studies

In general, preclinical studies show that O. indicum is safe at the tested doses (Table S4). Acute, subacute, and in vivo assessments have reported no major adverse effects or organ damage. For example, Singh and Kakkar [70] observed no toxicity in diabetic or normal rats following a 28-day oral administration of stem bark extract at 250 mg/kg/day. Similarly, a single oral dose of 2,000 mg/kg of methanolic bark extract produced no mortality or visible toxicity in Wistar albino rats over two weeks [118]. These findings are consistent with its long-standing traditional use and indicate a broad safety margin. However, most studies were restricted by short-term exposure (≤28 days). There is little information on chronic, reproductive, or developmental toxicity. Addressing these gaps is essential for supporting wider applications.
Human evidence is very limited. Chotchoungchatchai et al. [133] conducted an ethnopharmacological interview and survey documenting its use in Thai traditional medicine for cough, fever, and fatigue. The research indirectly supports its safety profile without clinical endpoints. The only controlled human trial to date was conducted by Lopresti et al. [100]. A standardized extract (Sabroxy®, Sabinsa Corporation, East Windsor, NJ, USA) was used in a placebo-controlled study with people who self-reported having cognitive problems. Participants reported improved mood, thinking, and memory after 12 weeks (doses of 1000 mg daily), with no significant adverse effects. Together, these studies link lab research to human use. Although such findings are encouraging, they remain preliminary. Larger, more well-controlled clinical trials are needed to confirm how well it works, the right dose, and long-term safety.
Within the context of functional food, available data suggests that O. indicum is not acutely toxic. However, its safety at typical dietary consumption levels has not been confirmed. Most pharmacological investigations use extracts or purified compounds at pharmacological dosages and they are far higher than what might be obtained by food intake. To bridge this research gap, the implementation of standardized toxicity protocols, dose–response research at dietary levels, and human clinical validation are required to verify its suitability for functional food applications.

3.6. Food Applications

3.6.1. Traditional and Current Food Uses

O. indicum has been consumed as food in Southeast Asia for a long time. In Malaysia, its young leaves and fruits are sold in local markets and eaten raw as salad (ulam) [22]. In Thailand, Laos, and Northeastern India, immature fruits and shoots are commonly eaten as vegetables [111]. They are often roasted or served with other dishes [9]. Despite this traditional usage, the plant’s nutritional composition, cooking safety, and culinary potential remain poorly described. Only one study by Choonong et al. [9] examined how conventional grilling affected flavonoid concentrations, but this did not address food product development. Meanwhile, severe astringency and bitterness remain the major barriers to wider consumption [135]. Many studies suggest that flavonoid-rich foods have intense bitter tastes and could affect consumer acceptance [136].

3.6.2. Bitterness as a Critical Challenge

Bitterness is one of the least understood basic tastes and can arise from a variety of compounds, including amino acids, peptides, esters, lactones, phenols, polyphenols, flavonoids, terpenes, and alkaloids [135]. In fruits and vegetables, phenolic compounds, especially flavonoids, are commonly the main contributors [135]. Behrens et al. [137] showed that baicalein and baicalin activate human bitter taste receptors TAS2R14. Meanwhile, chrysin is present in other bitter foods such as apricot seeds [138] and bitter melon [139]. This suggests a possible link between the health-promoting flavonoids of O. indicum and its bitterness. If flavonoids are the major drivers, reducing bitterness without losing nutritional and pharmacological value will be difficult.

3.6.3. Approaches to Detect and Manage Bitterness

Bitter compounds can be studied using both sensory and instrumental methods. Analytical techniques, such as HPLC or LC–MS, can be correlated with human sensory taste intensities or electronic tongue, which will indicate the main bitterness contributors. Meanwhile, computational approaches like molecular docking can predict interactions between flavonoids and bitter taste receptors [140]. In general, three methods are used to reduce bitterness, including physicochemical interactions, receptor-level inhibition using bitter blockers, and cognitive mixture suppression [135]. However, processing methods like high temperature or alkalization may reduce bitterness but also degrade bioactive compounds [135]. The traditional Thai roasting method to prepare O. indicum could reduce the bitterness, yet it may also deteriorate its heat-sensitive flavonoids. More promising strategies involve bitterness masking, which improves food flavor and retains bioactive bitter compounds. Sharafi et al. [141] showed that sodium acetate, sodium chloride, and aspartame could partially mask bitterness in vegetables. However, masking vegetable bitterness depends on vegetable type and taste phenotype. Ke et al. [142] used sweeteners and amino acids to suppress bitterness in Zanthoxylum bungeanum, but it was only effective to a certain extent. More recently, people have turned to computer-based techniques such as molecular docking for understanding compound-receptor mechanisms and pharmacophore for discovering inhibitors. Kan et al. [143] found that egg protein-derived peptides can bind TAS2R14 receptors, effectively reducing perceived bitterness. The incorporation of taste-masking agents with receptor inhibitors may therefore be a thorough approach to both reduce bitterness and retain nutritional values of O. indicum products.

3.6.4. Consumer Perception and Acceptability

Not all bitter foods are rejected. Coffee, dark chocolate, and red wine are widely consumed with their bitter taste [135]. Acceptance depends on genetic differences in bitter taste perception (PTC/PROP non-tasters, medium tasters, and supertasters) as well as cultural exposure and repeated dietary contact [135]. In addition, access to health-related information is another significant factor that can increase consumer acceptance [144], particularly within an Asian cultural context where a common belief holds that the more bitter the food, the healthier it is. This suggests that consumer testing is important to determine acceptable levels of O. indicum bitterness in functional food prototypes. Sensory techniques, such as threshold analysis, hedonic scaling, and just-about-right (JAR) scaling, can be taken to identify the balance between bitterness reduction and health perception. Such approaches will help determine whether bitterness should be suppressed, tolerated, or even leveraged as part of a “healthy-bitter” product identity.

3.6.5. Future Directions for Food Applications

The phytochemical, pharmacological, and ethnomedicinal evidence indicates strong potential for O. indicum as a functional food ingredient. However, most efficacy studies were done in vitro or in animal models at pharmacological doses, and only two human studies exist. For functional food development, safety at dietary intake levels must first be established. Then, discovering the compounds responsible for bitterness will guide targeted masking or formulation strategies. Finally, consumer studies should be carried out to determine acceptable bitterness thresholds and preferred product formats, such as snacks, beverages, or extracts. Integrating safety validation, standardization, bitterness management, and consumer insights can support the use of O. indicum in a functional food resource.

3.7. Material, Environmental, and Agricultural Studies

In materials science, the plants have been applied in carbon composites, protein modeling, green nanomaterials, animal feeds, and nanoformulation. Mim et al. [80] used plant extracts to make cerium oxide nanoparticles. Worakitjaroenphon et al. [145] made silver and gold nanoparticles using a microwave-assisted green synthesis method. Beyond nanoparticle synthesis, O. indicum has also been incorporated into biomass-derived carbon materials. For example, Zhang et al. [34] used its biomass to create a 3D micro-nanostructure. This material showed good conductivity and structural properties. Greene et al. [146] studied the use of O. indicum as medicinal feed for elephants.
In the environmental and agricultural domain, research has explored the plant’s role in floral biology, ecological function, taxonomy, commercial value, conservation, alternative resource potential, and growing conditions. Sritongchuay et al. [147] found that O. indicum only reopens after receiving pollen from another plant, not from the same one. Sonia et al. [148] employed leaf anatomy to categorize O. indicum and other Bignoniaceae plants. Saha et al. [35] discovered that O. indicum is a significant non-timber forest product in northeast India. It benefits rural income and indigenous populations. Kumari et al. [36] stressed the critical necessity to protect medicinal plants such as O. indicum because increasing habitat degradation, overexploitation, and lack of systematic cultivation are pushing many valuable species toward vulnerability or extinction.

4. Conclusions

O. indicum is a promising yet underexploited resource for functional food development. Its stem bark, pods, flowers, seeds, leaves, fruits, roots, and root bark are already consumed in many parts of Southeast Asia. This is the first systematic review that integrated the PRISMA framework, bibliometric mapping, and ADO framework for a comprehensive overview of O. indicum. The PRISMA framework was first used for relevant study selection, while bibliometric analysis indicated overall trends. The ADO framework helped to further classify selected studies based on their objectives, methods, and outcomes. It also indicated health effects supported partly or fully by in vitro/in silico/in vivo research. The findings highlight that flavonoids such as baicalein, baicalin, chrysin, oroxylin A, oroxin A, oroxin B, and their derivatives are frequently recognized as the dominant bioactive compounds. These compounds are linked to many validated pharmacological effects, including liver protection and anticancer activities. Mapping traditional knowledge with experimental data shows that many folk uses of the plant, such as for treating cancer, diabetes, liver ailments, and respiratory conditions, are strongly supported by science. However, other uses are only moderately supported or have not been scientifically researched yet.
Despite its rich bioactive profile and cultural history as a food, research on O. indicum is still dominated by phytochemistry and pharmacological assays. Although this review summarizes extensive evidence, most studies differ considerably in sample size, methodological rigor, and dosing strategies. Only a few investigations have used in vivo models, and human clinical trials are still lacking. These limitations highlight the need for more standardized and clinically relevant research designs. Furthermore, nearly all efficacy studies rely on pharmacological doses rather than dietary intake. Bitterness and astringency are also major obstacles for food applications, with little research on sensory evaluation, consumer acceptance, or formulation strategies.
Future work should focus on health benefits that are not yet strongly supported by science, such as conducting in vivo studies for obesity. Since short-term toxicity has been evaluated, studies on long-term safety, reproductive outcomes, and human clinical trials should be considered (1). Standardized toxicity protocols at dietary levels, particularly with human subjects, should be next (2). Determining whether beneficial flavonoids like baicalein and baicalin are major bitterness contributors is essential for developing bitterness removal strategies (3). Following that, testing effective masking and receptor-inhibition strategies will be needed (4). Finally, consumer-focused studies will help establish acceptable sensory thresholds and product formats (5). Integrating these approaches will make the safe and effective transition of O. indicum from a traditional herb into a scientifically validated functional food ingredient.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/foods14203465/s1, Table S1: Studies on pharmacological activities of O. indicum; Table S2: Ethnomedicinal uses of O. indicum; Table S3: Studies on O. indicum phytochemistry; Table S4: Studies on O. indicum safety and toxicology. Additional references cited in the Supplementary Materials are included in the main reference list as [149,150,151,152,153,154,155,156,157,158,159,160,161,162,163,164,165,166,167,168,169].

Author Contributions

Conceptualization, H.L.N., A.S.-E. and Y.C.; methodology, H.L.N.; data curation, H.L.N. and D.Q.T.; formal analysis, H.L.N.; writing—original draft preparation, H.L.N.; project administration, Y.C.; supervision, Y.C., A.S.-E. and W.P.; writing—review and editing, Y.C., A.S.-E. and W.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Fundamental Fund of Khon Kaen University from National Science, Research and Innovation Fund or NSRF, Thailand (FF4776027). Hai Linh Nguyen also gratefully acknowledges the KKU Scholarship for ASEAN and GMS Countries’ Personnel (Grant No. 588/2023).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The original contributions presented in this study are included in the article/Supplementary Materials. Further inquiries can be directed to the corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
ADOAntecedents–Decisions–Outcomes
PRISMAPreferred Reporting Items for Systematic Reviews and Meta-Analyses
PPARγPeroxisome Proliferator-Activated Receptor Gamma
NAFLDNonalcoholic fatty liver disease
DPPH2,2-diphenyl-1-picrylhydrazyl
HPTLCHigh-Performance Thin-Layer Chromatography
ROSReactive Oxygen Species

References

  1. Rojsanga, P.; Schwaiger, S.; Stuppner, H.; Sithisarn, P. Determination of phytochemical contents in extracts from different growth stages of Oroxylum indicum fruits using HPLC-DAD and QAMS methods. Molecules 2023, 28, 6837. [Google Scholar] [CrossRef]
  2. Tran, T.V.A.; Malainer, C.; Schwaiger, S.; Hung, T.; Atanasov, A.G.; Heiss, E.H.; Dirsch, V.M.; Stuppner, H. Screening of Vietnamese medicinal plants for NF-κB signaling inhibitors: Assessing the activity of flavonoids from the stem bark of Oroxylum indicum. J. Ethnopharmacol. 2015, 159, 36–42. [Google Scholar] [CrossRef] [PubMed]
  3. Jha, K.; Smith-Hall, C. Three models to illustrate plant-people relationships in the medicinal plant hotspots of North East India. Ethnobot. Res. Appl. 2023, 26, 1–48. [Google Scholar] [CrossRef]
  4. Bhattarai, K.; Kunwar, R.; Baral, B. Phytochemical analysis and ethnomedicinal uses of Oroxylum indicum in Nepal. Ethnobot. Res. Appl. 2022, 24, 1–12. [Google Scholar] [CrossRef]
  5. Ralte, L.; Sailo, H.; Singh, Y.T. Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India. J. Ethnobiol. Ethnomed. 2024, 20, 2. [Google Scholar] [CrossRef]
  6. Hein, P.P.; Arunachalam, K.; Fu, Y.; Zaw, M.; Yang, Y.; Yang, X. Diversity of medicinal plants and their therapeutic usages of Kachin people (Jinghpaw) in the central part of Kachin State, Myanmar. J. Ethnopharmacol. 2023, 302, 115921. [Google Scholar] [CrossRef]
  7. Nagasaka, M.; Hashimoto, R.; Inoue, Y.; Ishiuchi, K.i.; Matsuno, M.; Itoh, Y.; Tokugawa, M.; Ohoka, N.; Morishita, D.; Mizukami, H. Anti-tumorigenic activity of chrysin from Oroxylum indicum via non-genotoxic p53 activation through the ATM-Chk2 pathway. Molecules 2018, 23, 1394. [Google Scholar] [CrossRef]
  8. Zhang, B.; Sun, W.; Yu, N.; Sun, J.; Yu, X.; Li, X.; Xing, Y.; Yan, D.; Ding, Q.; Xiu, Z. Anti-diabetic effect of baicalein is associated with the modulation of gut microbiota in streptozotocin and high-fat-diet induced diabetic rats. J. Funct. Foods 2018, 46, 256–267. [Google Scholar] [CrossRef]
  9. Choonong, R.; Waewaram, V.; Buraphaka, H.; Krittanai, S.; Boonsnongcheep, P.; Putalun, W. Anti-inflammatory potential of Oroxylum indicum flavonoids: Effects of traditional grilling on aglycone flavonoid content and activity against urban dust-induced inflammation. Food Biosci. 2024, 62, 105523. [Google Scholar] [CrossRef]
  10. Cardoso Reis, A.C.; Valente, G.M.; Silva, B.d.M.; de Brito Magalhães, C.L.; Kohlhoff, M.; Brandão, G.C. Anti-arboviral activity and chemical characterization of hispidulin and ethanolic extracts from Millingtonia hortensis Lf and Oroxylum indicum (L.) Kurz (Bignoniaceae). Nat. Prod. Res. 2023, 37, 613–617. [Google Scholar] [CrossRef]
  11. Panomai, P.; Thapphasaraphong, S.; Nualkaew, N. A Comparative Study of Two Oroxylum indicum (L.) Kurz. Phenotypes Based on Phytochemicals and Antioxidant Effects, and the Anti-Inflammatory Activity of Leaf and Pod Extracts. Plants 2024, 13, 2110. [Google Scholar] [CrossRef] [PubMed]
  12. Prapaipittayakhun, J.; Boonyuen, S.; Zheng, A.L.T.; Apinyauppatham, K.; Arpornmaeklong, P. Biologic effects of biosynthesized Oroxylum indicum/silver nanoparticles on human periodontal ligament stem cells. OpenNano 2023, 9, 100117. [Google Scholar] [CrossRef]
  13. Ahmed, S.S.; Rahman, M.O.; Alqahtani, A.S.; Sultana, N.; Almarfadi, O.M.; Ali, M.A.; Lee, J. Anticancer potential of phytochemicals from Oroxylum indicum targeting Lactate Dehydrogenase A through bioinformatic approach. Toxicol. Rep. 2023, 10, 56–75. [Google Scholar] [CrossRef] [PubMed]
  14. Muniyasamy, R.; Manjubala, I. Elucidating anti-sclerostin mechanism of baicalein using LRP6-Sclersotin complex of canonical Wnt/β-catenin signaling pathway. J. Biomol. Struct. Dyn. 2025, 43, 5009–5019. [Google Scholar] [CrossRef]
  15. Gokhale, M.; Faraz, R.; Deshpande, I.; Garg, A. Isolation of bio-molecule Baicalein (5, 6, 7-Trihydroxy flavone) from root of Oroxylum indicum L. Vent and its prospective interaction with COVID-19 Viral S-Protein Receptor Binding Domain. Res. J. Pharm. Technol. 2022, 15, 5050–5056. [Google Scholar] [CrossRef]
  16. Sala, E.; Guasch, L.; Iwaszkiewicz, J.; Mulero, M.; Salvadó, M.-J.; Bladé, C.; Ceballos, M.; Valls, C.; Zoete, V.; Grosdidier, A. Identification of human IKK-2 inhibitors of natural origin (Part II): In Silico prediction of IKK-2 inhibitors in natural extracts with known anti-inflammatory activity. Eur. J. Med. Chem. 2011, 46, 6098–6103. [Google Scholar] [CrossRef]
  17. Doshi, K.; Ilanchezhian, R.; Acharya, R.; Patel, B.; Ravishankar, B. Anti-inflammatory activity of root bark and stem bark of Shyonaka. J. Ayurveda Integr. Med. 2012, 3, 194. [Google Scholar] [CrossRef]
  18. Pondugula, S.R.; Harshan, A.; Ramesh, S.; Govindarajulu, M.; Almaghrabi, M.; Majrashi, M.; Abbott, K.L.; Nadar, R.; Alturki, M.; Salamat, J.M. Cardioprotective effects of Oroxylum indicum extract against doxorubicin and cyclophosphamide-induced cardiotoxicity. Cardiovasc. Toxicol. 2022, 22, 67–77. [Google Scholar] [CrossRef]
  19. Huang, Y.; Wang, C.; Wang, M.; Xiong, T.; Song, X.; Sun, W.; Li, J. Oroxin B improves metabolic-associated fatty liver disease by alleviating gut microbiota dysbiosis in a high-fat diet-induced rat model. Eur. J. Pharmacol. 2023, 951, 175788. [Google Scholar] [CrossRef]
  20. Dinda, B.; SilSarma, I.; Dinda, M.; Rudrapaul, P. Oroxylum indicum (L.) Kurz, an important Asian traditional medicine: From traditional uses to scientific data for its commercial exploitation. J. Ethnopharmacol. 2015, 161, 255–278. [Google Scholar] [CrossRef]
  21. Deka, D.; Kumar, V.; Prasad, C.; Kumar, K.; Gogoi, B.; Singh, L.; Srivastava, R. Oroxylum indicum–a medicinal plant of North East India: An overview of its nutritional, remedial, and prophylactic properties. J. Appl. Pharm. Sci. 2013, 3, S104–S112. Available online: https://japsonline.com/admin/php/uploads/951_pdf.pdf (accessed on 6 October 2025).
  22. Nik Salleh, N.N.H.; Othman, F.A.; Kamarudin, N.A.; Tan, S.C. The biological activities and therapeutic potentials of baicalein extracted from Oroxylum indicum: A systematic review. Molecules 2020, 25, 5677. [Google Scholar] [CrossRef] [PubMed]
  23. Aggarwal, S.; Dsouza, S.; Joshi, M.; Antoun, R.; Phan, D.H.T. Environmental, social and governance investing: Systematic literature review using ADO model. J. Account. Lit. 2025, in press. [CrossRef]
  24. Singh, V.; Chaudhary, A. A review on the taxonomy, ethnobotany, chemistry and pharmacology of Oroxylum indicum Vent. Indian J. Pharm. Sci. 2011, 73, 483. [Google Scholar] [CrossRef]
  25. Aria, M.; Cuccurullo, C. bibliometrix: An R-tool for comprehensive science mapping analysis. J. Informetr. 2017, 11, 959–975. [Google Scholar] [CrossRef]
  26. Van Eck, N.; Waltman, L. Software survey: VOSviewer, a computer program for bibliometric mapping. Scientometrics 2010, 84, 523–538. [Google Scholar] [CrossRef]
  27. Kumar, D.; Rawat, S.; Joshi, R. Predicting the current and future suitable habitat distribution of the medicinal tree Oroxylum indicum (L.) Kurz in India. J. Appl. Res. Med. Aromat. Plants 2021, 23, 100309. [Google Scholar] [CrossRef]
  28. Dinda, B.; Dinda, S.; DasSharma, S.; Banik, R.; Chakraborty, A.; Dinda, M. Therapeutic potentials of baicalin and its aglycone, baicalein against inflammatory disorders. Eur. J. Med. Chem. 2017, 131, 68–80. [Google Scholar] [CrossRef]
  29. Sumbul, S.; Ahmad, M.A.; Mohd, A.; Mohd, A. Role of phenolic compounds in peptic ulcer: An overview. J. Pharm. Bioallied Sci. 2011, 3, 361–367. [Google Scholar] [CrossRef]
  30. Siriwatanametanon, N.; Fiebich, B.L.; Efferth, T.; Prieto, J.M.; Heinrich, M. Traditionally used Thai medicinal plants: In vitro anti-inflammatory, anticancer and antioxidant activities. J. Ethnopharmacol. 2010, 130, 196–207. [Google Scholar] [CrossRef]
  31. Panda, S.K.; Mohanta, Y.K.; Padhi, L.; Park, Y.-H.; Mohanta, T.K.; Bae, H. Large scale screening of ethnomedicinal plants for identification of potential antibacterial compounds. Molecules 2016, 21, 293. [Google Scholar] [CrossRef] [PubMed]
  32. Sharma, J.; Gairola, S.; Gaur, R.; Painuli, R. The treatment of jaundice with medicinal plants in indigenous communities of the Sub-Himalayan region of Uttarakhand, India. J. Ethnopharmacol. 2012, 143, 262–291. [Google Scholar] [CrossRef] [PubMed]
  33. Sharma, J.; Gairola, S.; Gaur, R.; Painuli, R.; Siddiqi, T. Ethnomedicinal plants used for treating epilepsy by indigenous communities of sub-Himalayan region of Uttarakhand, India. J. Ethnopharmacol. 2013, 150, 353–370. [Google Scholar] [CrossRef] [PubMed]
  34. Zhang, X.; Cheng, J.; Xiang, Z.; Cai, L.; Lu, W. A hierarchical Co@ mesoporous C/macroporous C sheet composite derived from bimetallic MOF and Oroxylum indicum for enhanced microwave absorption. Carbon 2022, 187, 477–487. [Google Scholar] [CrossRef]
  35. Saha, D.; Sundriyal, R. Utilization of non-timber forest products in humid tropics: Implications for management and livelihood. For. Policy Econ. 2012, 14, 28–40. [Google Scholar] [CrossRef]
  36. Kumari, P.; Chandra joshi, G.; Mohan TEWARI, L. Biodiversity status, distribution and use pattern of some ethno-medicinal plants. Int. J. Conserv. Sci. 2012, 3, 309. Available online: https://ijcs.ro/pub/IJCS-12-31-Kumary.pdf (accessed on 6 October 2025).
  37. Lalou, C.; Basak, A.; Mishra, P.; Mohanta, B.; Banik, R.; Dinda, B.; Khatib, A. Inhibition of tumor cells proliferation and migration by the flavonoid furin inhibitor isolated from Oroxylum indicum. Curr. Med. Chem. 2013, 20, 583–591. [Google Scholar] [CrossRef]
  38. Zhang, B.-W.; Sang, Y.-B.; Sun, W.-L.; Yu, H.-S.; Ma, B.-P.; Xiu, Z.-L.; Dong, Y.-S. Combination of flavonoids from Oroxylum indicum seed extracts and acarbose improves the inhibition of postprandial blood glucose: In vivo and in vitro study. Biomed. Pharmacother. 2017, 91, 890–898. [Google Scholar] [CrossRef]
  39. Cheng, X.-J.; Kong, D.-Z.; Li, Y.-H.; Bian, G.-L.; Li, D.-Q. Screening of dual targeted inhibitors of 5-lipoxygenase and cyclooxygenase-2 from Oroxylum indicum by off-line two-dimensional liquid chromatography coupled with mass spectrometry. Ind. Crops Prod. 2022, 186, 115243. [Google Scholar] [CrossRef]
  40. Thrigulla, S.R.; Singh, G.; Soni, H.; Tandon, S.; Koulgi, S.; Uppuladinne, M.V.; Jani, V.; Sonavane, U.; Joshi, R.; Gandhi, Y. In-silico evaluation of Oroxylum indicum vent compounds in the plausible treatment and prevention of nasopharyngeal cancer. J. Ayurveda Integr. Med. 2024, 15, 100986. [Google Scholar] [CrossRef]
  41. Pathak, P.; Novak, J.; Naumovich, V.; Grishina, M.; Balkrishna, A.; Sharma, N.; Sharma, V.; Potemkin, V.; Verma, A. Polyphenolic rich extract of Oroxylum indicum alleviate β-glucuronidase activity via down-regulate oxidative stress: Experimental and computational studies. Biocatal. Agric. Biotechnol. 2020, 29, 101804. [Google Scholar] [CrossRef]
  42. Hengpratom, T.; Lowe, G.M.; Eumkeb, G. An insight into anti-adipogenic properties of an Oroxylum indicum (L.) Kurz extract. Med. Ther. 2020, 20, 319. [Google Scholar] [CrossRef] [PubMed]
  43. Purushothaman, B.; Sumathi, T. 5, 6, 7 trihydroxy flavone armoured neurodegeneration caused by quinolinic acid induced huntington’s like disease in rat striatum-reinstating the level of brain neurotrophins with special reference to cognitive-socio behaviour, biochemical and histopathological aspects. Neurosci. Res. 2022, 174, 25–35. [Google Scholar] [CrossRef] [PubMed]
  44. Kang, I.N.; Nik Salleh, N.N.H.; Chung, W.J.; Lee, C.Y.; Tan, S.C. Baicalein-enriched fraction extracted from Oroxylum indicum (L.) Benth. ex kurz leaves exerts antioxidant and inhibitory effects against glioblastoma multiforme. Processes 2019, 7, 963. [Google Scholar] [CrossRef]
  45. Somsakeesit, L.-o.; Senawong, T.; Senawong, G.; Kumboonma, P.; Samankul, A.; Namwan, N.; Yenjai, C.; Phaosiri, C. Evaluation and molecular docking study of two flavonoids from Oroxylum indicum (L.) Kurz and their semi-synthetic derivatives as histone deacetylase inhibitors. J. Nat. Med. 2024, 78, 236–245. [Google Scholar] [CrossRef]
  46. Yang, P.; Fu, S.; Cao, Z.; Liao, H.; Huo, Z.; Pan, Y.; Zhang, G.; Gao, A.; Zhou, Q. Oroxin B selectively induces tumor-suppressive ER stress and concurrently inhibits tumor-adaptive ER stress in B-lymphoma cells for effective anti-lymphoma therapy. Toxicol. Appl. Pharmacol. 2015, 288, 269–279. [Google Scholar] [CrossRef]
  47. Menon, S.; Albaqami, J.J.; Hamdi, H.; Lawrence, L.; Divya, M.K.; Antony, L.; Padikkala, J.; Mathew, S.E.; Narayanankutty, A. Root bark extract of Oroxylum indicum Vent. inhibits solid and ascites tumors and prevents the development of DMBA-induced skin papilloma formation. Molecules 2022, 27, 8459. [Google Scholar] [CrossRef]
  48. Menon, S.; Albaqami, J.J.; Hamdi, H.; Lawrence, L.; Padikkala, J.; Mathew, S.E.; Narayanankutty, A. Oroxylum indicum vent root bark extract inhibits the proliferation of cancer cells and induce apoptotic cell death. Processes 2023, 11, 188. [Google Scholar] [CrossRef]
  49. Shah, R.K.; Upadhyay, B.; Buragohain, J.; Rai, M. Phytochemical Analysis, Antioxidant, Antimicrobial and Anticancer Activity of Nigella sativa and Oroxylum indicum. Proc. Natl. Acad. Sci. India Sect. B Biol. Sci. 2024, 94, 1059–1065. [Google Scholar] [CrossRef]
  50. Rai, D.; Ram, H.A.; Patel, K.N.; Babu, U.; Kumar, L.S.; Kannan, R. In vitro immuno-stimulatory and anticancer activities of Oroxylum indicum (L.) Kurz.: An evidence for substitution of aerial parts for conservation. J. Ayurveda Integr. Med. 2022, 13, 100523. [Google Scholar] [CrossRef]
  51. Chassagne, F.; Haddad, M.; Amiel, A.; Phakeovilay, C.; Manithip, C.; Bourdy, G.; Deharo, E.; Marti, G. A metabolomic approach to identify anti-hepatocarcinogenic compounds from plants used traditionally in the treatment of liver diseases. Fitoterapia 2018, 127, 226–236. [Google Scholar] [CrossRef]
  52. Pal-Bhadra, M.; Ramaiah, M.J.; Reddy, T.L.; Krishnan, A.; Pushpavalli, S.; Babu, K.S.; Tiwari, A.K.; Rao, J.M.; Yadav, J.S.; Bhadra, U. Plant HDAC inhibitor chrysin arrest cell growth and induce p21 WAF1 by altering chromatin of STAT response element in A375 cells. BMC Cancer 2012, 12, 180. [Google Scholar] [CrossRef]
  53. Sisin, N.N.T.; Kong, A.R.; Edinur, H.A.; Jamil, N.I.N.; Che Mat, N.F. Silencing E6/E7 Oncoproteins in SiHa Cells Treated with siRNAs and Oroxylum indicum Extracts Induced Apoptosis by Upregulating p53/pRb Pathways. Appl. Biochem. Biotechnol. 2024, 196, 4234–4255. [Google Scholar] [CrossRef]
  54. Zhong, W.; Hou, H.; Liu, T.; Su, S.; Xi, X.; Liao, Y.; Xie, R.; Jin, G.; Liu, X.; Zhu, L. Cartilage oligomeric matrix protein promotes epithelial-mesenchymal transition by interacting with transgelin in colorectal cancer. Theranostics 2020, 10, 8790. [Google Scholar] [CrossRef] [PubMed]
  55. Yang, Y.; Liu, K.; Yang, L.; Zhang, G. Bladder cancer cell viability inhibition and apoptosis induction by baicalein through targeting the expression of anti-apoptotic genes. Saudi J. Biol. Sci. 2018, 25, 1478–1482. [Google Scholar] [CrossRef] [PubMed]
  56. Gupta, P.; Singh, S.; Rai, N.; Verma, A.; Tiwari, H.; Kamble, S.C.; Gautam, H.K.; Gautam, V. Unveiling the cytotoxic and anti-proliferative potential of green-synthesized silver nanoparticles mediated by Colletotrichum gloeosporioides. RSC Adv. 2024, 14, 4074–4088. [Google Scholar] [CrossRef] [PubMed]
  57. Rai, N.; Keshri, P.K.; Gupta, P.; Verma, A.; Kamble, S.C.; Singh, S.K.; Gautam, V. Bioprospecting of fungal endophytes from Oroxylum indicum (L.) Kurz with antioxidant and cytotoxic activity. PLoS ONE 2022, 17, e0264673. [Google Scholar] [CrossRef]
  58. Singh, A.R.; Singh, S.A.; Singh, T.D.; Singh, N.T.; Machathoibi, T.C.; Singh, O.M.; Singh, L.S. Bioassay-Guided Isolation of 2-[p-(2-Carboxyhydrazino) phenoxy]-6-(hydroxymethyl) tetrahydro-2H-pyran-3, 4, 5-triol from Oroxylum indicum and the Investigation of Its Molecular Mechanism Action of Apoptosis Induction. Pharmaceuticals 2022, 15, 559. [Google Scholar] [CrossRef]
  59. Kameyanda Poonacha, S.; Harishkumar, M.; Radha, M.; Varadarajan, R.; Nalilu, S.K.; Shetty, S.S.; Shetty, P.K.; Chandrashekharappa, R.B.; Sreenivas, M.G.; Bhandary Bavabeedu, S.K. Insight into oroxylina-7-o-β-d-glucuronide-enriched Oroxylum indicum bark extract in oral cancer hsc-3 cell apoptotic mechanism: Role of mitochondrial microenvironment. Molecules 2021, 26, 7430. [Google Scholar] [CrossRef]
  60. Parvin, M.; Rahaman, A.; Sarkar, A.; Debnath, S.; De, U.C.; Mandal, D.P.; Bhattacharjee, S. Oroxylum indicum stem bark extract reduces tumor progression by inhibiting the EGFR-PI3K-AKT pathway in an in vivo 4NQO-induced oral cancer model. J. Am. Nutr. Assoc. 2023, 42, 573–587. [Google Scholar] [CrossRef]
  61. Buranrat, B.; Noiwetch, S.; Suksar, T.; Ta-Ut, A. Inhibition of cell proliferation and migration by Oroxylum indicum extracts on breast cancer cells via Rac1 modulation. J. Pharm. Anal. 2020, 10, 187–193. [Google Scholar] [CrossRef] [PubMed]
  62. Lalrinzuali, K.; Vabeiryureilai, M.; Jagetia, G.C. Sonapatha (Oroxylum indicum) mediates cytotoxicity in cultured HeLa cells by inducing apoptosis and suppressing NF-κB, COX-2, RASSF7 and NRF2. Bioorg. Chem. 2021, 114, 105126. [Google Scholar] [CrossRef]
  63. Rai, N.; Gupta, P.; Verma, A.; Singh, S.K.; Gautam, V. Isolation and characterization of N-(2-Hydroxyethyl) hexadecanamide from Colletotrichum gloeosporioides with apoptosis-inducing potential in breast cancer cells. Biofactors 2023, 49, 663–683. [Google Scholar] [CrossRef] [PubMed]
  64. Bhaumik, S.; Sarkar, A.; Debnath, S.; Debnath, B.; Ghosh, R.; Zaki, M.E.; Al-Hussain, S.A. α-Glucosidase inhibitory potential of Oroxylum indicum using molecular docking, molecular dynamics, and in vitro evaluation. Saudi Pharm. J. 2024, 32, 102095. [Google Scholar] [CrossRef]
  65. Kumar, G.S.; Tiwari, A.K.; Rao, V.R.S.; Prasad, K.R.; Ali, A.Z.; Babu, K.S. Synthesis and biological evaluation of novel benzyl-substituted flavones as free radical (DPPH) scavengers and α-glucosidase inhibitors. J. Asian Nat. Prod. Res. 2010, 12, 978–984. [Google Scholar] [CrossRef]
  66. Sun, W.; Sang, Y.; Zhang, B.; Yu, X.; Xu, Q.; Xiu, Z.; Dong, Y. Synergistic effects of acarbose and an Oroxylum indicum seed extract in streptozotocin and high-fat-diet induced prediabetic mice. Biomed. Pharmacother. 2017, 87, 160–170. [Google Scholar] [CrossRef]
  67. Sun, W.; Liu, P.; Yang, B.; Wang, M.; Wang, T.; Sun, W.; Wang, X.; Zheng, W.; Song, X.; Li, J. A network pharmacology approach: Inhibition of the NF-κB signaling pathway contributes to the NASH preventative effect of an Oroxylum indicum seed extract in oleic acid-stimulated HepG2 cells and high-fat diet-fed rats. Phytomedicine 2021, 88, 153498. [Google Scholar] [CrossRef]
  68. Sun, W.; Sun, J.; Zhang, B.; Xing, Y.; Yu, X.; Li, X.; Xiu, Z.; Dong, Y. Baicalein improves insulin resistance via regulating SOCS3 and enhances the effect of acarbose on diabetes prevention. J. Funct. Foods 2017, 37, 339–353. [Google Scholar] [CrossRef]
  69. Xing, Y.; Liu, H.; Zhang, D.; Jiang, H.; Xiu, Z.; Dong, Y. Baicalein, a dietary flavonoid, enhances the insulin-sensitizing effect of metformin to prevent type 2 diabetes via the regulation of lipid metabolism and gut microenvironment. Food Front. 2024, 5, 668–690. [Google Scholar] [CrossRef]
  70. Singh, J.; Kakkar, P. Modulation of liver function, antioxidant responses, insulin resistance and glucose transport by Oroxylum indicum stem bark in STZ induced diabetic rats. Food Chem. Toxicol. 2013, 62, 722–731. [Google Scholar] [CrossRef]
  71. Sun, W.; Zhang, B.; Yu, X.; Zhuang, C.; Li, X.; Sun, J.; Xing, Y.; Xiu, Z.; Dong, Y. Oroxin A from Oroxylum indicum prevents the progression from prediabetes to diabetes in streptozotocin and high-fat diet induced mice. Phytomedicine 2018, 38, 24–34. [Google Scholar] [CrossRef]
  72. Cai, T.; Xu, X.; Dong, L.; Liang, S.; Xin, M.; Wang, T.; Li, T.; Wang, X.; Zheng, W.; Wang, C. Oroxin A from Oroxylum indicum improves disordered lipid metabolism by inhibiting SREBPs in oleic acid-induced HepG2 cells and high-fat diet-fed non-insulin-resistant rats. Heliyon 2024, 10, e29168. [Google Scholar] [CrossRef]
  73. Lalrinzuali, K.; Vabeiryureilai, M.; Jagetia, G.C. Topical application of stem bark ethanol extract of Sonapatha, Oroxylum indicum (L.) Kurz accelerates healing of deep dermal excision wound in Swiss albino mice. J. Ethnopharmacol. 2018, 227, 290–299. [Google Scholar] [CrossRef]
  74. Abdulhafiz, F.; Reduan, M.F.H.; Hisam, A.H.; Mohammad, I.; Abdul Wahab, I.R.; Abdul Hamid, F.F.; Mohammed, A.; Nordin, M.L.; Shaari, R.; Bakar, L.A. LC–TOF-MS/MS and GC-MS based phytochemical profiling and evaluation of wound healing activity of Oroxylum indicum (L.) Kurz (Beka). Front. Pharmacol. 2022, 13, 1050453. [Google Scholar] [CrossRef]
  75. Zhao, P.; Alam, M.B.; An, H.; Choi, H.-J.; Cha, Y.H.; Yoo, C.-Y.; Kim, H.-H.; Lee, S.-H. Antimelanogenic effect of an Oroxylum indicum seed extract by suppression of MITF expression through activation of MAPK signaling protein. Int. J. Mol. Sci. 2018, 19, 760. [Google Scholar] [CrossRef]
  76. Kumar, R.A.; Rajkumar, V.; Guha, G.; Mathew, L. Therapeutic potentials of Oroxylum indicum bark extracts. Chin. J. Nat. Med. 2010, 8, 121–126. [Google Scholar] [CrossRef]
  77. Mrazek, N.; Watla-iad, K.; Deachathai, S.; Suteerapataranon, S. Rapid antioxidant capacity screening in herbal extracts using a simple flow injection-spectrophotometric system. Food Chem. 2012, 132, 544–548. [Google Scholar] [CrossRef] [PubMed]
  78. Yan, R.; Cao, Y.; Yang, B. HPLC-DPPH screening method for evaluation of antioxidant compounds extracted from Semen Oroxyli. Molecules 2014, 19, 4409–4417. [Google Scholar] [CrossRef] [PubMed]
  79. Li, D.; Zhao, J.; Li, S. High-performance liquid chromatography coupled with post-column dual-bioactivity assay for simultaneous screening of xanthine oxidase inhibitors and free radical scavengers from complex mixture. J. Chromatogr. A 2014, 1345, 50–56. [Google Scholar] [CrossRef]
  80. Mim, J.; Sultana, M.S.; Dhar, P.K.; Hasan, M.K.; Dutta, S.K. Green mediated synthesis of cerium oxide nanoparticles by using Oroxylum indicum for evaluation of catalytic and biomedical activity. RSC Adv. 2024, 14, 25409–25424. [Google Scholar] [CrossRef]
  81. Ranabhat, K.; Regmi, K.P.; Parajuli, S.; Thapa, R.; Timilsina, A.P.; Katuwal, S.; Fleming, S.; Mishra, A.D.; Sharma, K.R.; Regmi, B.P. Evaluation of Antioxidant, Antimicrobial, and Cytotoxic Activities and Correlation with Phytoconstituents in Some Medicinal Plants of Nepal. J. Chem. 2022, 2022, 4725801. [Google Scholar] [CrossRef]
  82. Chhouk, K.; Kanda, H.; Goto, M. Efficacy of supercritical carbon dioxide integrated hydrothermal extraction of Khmer medicinal plants with potential pharmaceutical activity. J. Environ. Chem. Eng. 2018, 6, 2944–2956. [Google Scholar] [CrossRef]
  83. Masood, N.; Yadav, A.K.; Kumar, N.; Gupta, M.M.; Luqman, S. Density functional theory-based quantum rationalization of flavones from Oroxylum indicum, their correlation with redox effect, molecular interaction studies and osmotic hemolysis. Curr. Sci. 2018, 115, 2085–2094. Available online: https://www.jstor.org/stable/26978555 (accessed on 6 October 2025). [CrossRef]
  84. Srimawong, C.; Putalun, W. Consolidated extraction and conversion of baicalin to baicalein from Oroxylum indicum using a novel NADES-UAE system and bioactivity evaluation in RAW 264.7 cells. Food Biosci. 2025, 65, 106031. [Google Scholar] [CrossRef]
  85. Singh, J.; Chaudhari, B.P.; Kakkar, P. Baicalin and chrysin mixture imparts cyto-protection against methylglyoxal induced cytotoxicity and diabetic tubular injury by modulating RAGE, oxidative stress and inflammation. Environ. Toxicol. Pharmacol. 2017, 50, 67–75. [Google Scholar] [CrossRef] [PubMed]
  86. Yan, R.-Y.; Cao, Y.-Y.; Chen, C.-Y.; Dai, H.-Q.; Yu, S.-X.; Wei, J.-L.; Li, H.; Yang, B. Antioxidant flavonoids from the seed of Oroxylum indicum. Fitoterapia 2011, 82, 841–848. [Google Scholar] [CrossRef]
  87. Tang, Q.; Jia, H.; Qin, X.; Lu, Z.; Huang, W.; Wang, Y.; Cao, Z. Scutellarein ameliorates dextran sulfate sodium-induced ulcerative colitis by inhibiting colonic epithelial cell proinflammation and barrier disruption. Front. Pharmacol. 2024, 15, 1479441. [Google Scholar] [CrossRef] [PubMed]
  88. Huang, J.; Chen, C.; Xie, J.; Zhai, K.; Wei, S.; Cheng, X.; Zhang, R. Oroxin A ameliorates the oleic acid-induced A549 cell injury through the suppression of pyroptosis and degradation of alveolar surfactant. An. Acad. Bras. Cienc. 2022, 94, e20211400. [Google Scholar] [CrossRef]
  89. Jelić, D.; Lower-Nedza, A.D.; Brantner, A.H.; Blažeković, B.; Bian, B.; Yang, J.; Brajša, K.; Vladimir-Knežević, S. Baicalin and Baicalein Inhibit Src Tyrosine Kinase and Production of IL-6. J. Chem. 2016, 2016, 2510621. [Google Scholar] [CrossRef]
  90. Chen, D.-H.; Zheng, G.; Zhong, X.-Y.; Lin, Z.-H.; Yang, S.-W.; Liu, H.-X.; Shang, P. Oroxylin A attenuates osteoarthritis progression by dual inhibition of cell inflammation and hypertrophy. Food Funct. 2021, 12, 328–339. [Google Scholar] [CrossRef]
  91. Huang, J.-M.; Wang, C.-Z.; Lu, S.-Y.; Wang, Z.; Yan, Z.-Q. Oroxin B attenuates ovariectomy-induced bone loss by suppressing osteoclast formation and activity. Drug Des. Devel. Ther. 2021, 15, 4811–4825. [Google Scholar] [CrossRef]
  92. Muniyasamy, R.; Manjubala, I. Identification of potential sclerostin inhibiting flavonoids from Oroxylum indicum: An insilico approach. J. Biomol. Struct. Dyn. 2024, 42, 6588–6599. [Google Scholar] [CrossRef] [PubMed]
  93. Mangal, P.; Khare, P.; Jagtap, S.; Bishnoi, M.; Kondepudi, K.K.; Bhutani, K.K. Screening of six Ayurvedic medicinal plants for anti-obesity potential: An investigation on bioactive constituents from Oroxylum indicum (L.) Kurz bark. J. Ethnopharmacol. 2017, 197, 138–146. [Google Scholar] [CrossRef] [PubMed]
  94. Mei, J.; Yang, R.; Yang, Q.; Wan, W.; Wei, X. Proteomic screening identifies the direct targets of chrysin anti-lipid depot in adipocytes. J. Ethnopharmacol. 2021, 267, 113361. [Google Scholar] [CrossRef] [PubMed]
  95. Singh, J.; Kakkar, P. Oroxylin A, a constituent of Oroxylum indicum inhibits adipogenesis and induces apoptosis in 3T3-L1 cells. Phytomedicine 2014, 21, 1733–1741. [Google Scholar] [CrossRef]
  96. Menon, S.; Lawrence, L.; Sivaram, V.P.; Padikkala, J. Oroxylum indicum root bark extract prevents doxorubicin-induced cardiac damage by restoring redox balance. J. Ayurveda Integr. Med. 2019, 10, 159–165. [Google Scholar] [CrossRef]
  97. Yuvaraj, S.; Sasikumar, S.; Puhari, S.S.M.; Ramprasath, T.; Baskaran, N.; Vasudevan, V.; Selvam, G.S. Chrysin reduces hypercholesterolemia-mediated atherosclerosis through modulating oxidative stress, microflora, and apoptosis in experimental rats. J. Food Biochem. 2022, 46, e14349. [Google Scholar] [CrossRef]
  98. Babu, T.H.; Manjulatha, K.; Kumar, G.S.; Hymavathi, A.; Tiwari, A.K.; Purohit, M.; Rao, J.M.; Babu, K.S. Gastroprotective flavonoid constituents from Oroxylum indicum Vent. Bioorg. Med. Chem. Lett. 2010, 20, 117–120. [Google Scholar] [CrossRef]
  99. Chalermwongkul, C.; Khamphukdee, C.; Maneenet, J.; Daodee, S.; Monthakantirat, O.; Boonyarat, C.; Chotritthirong, Y.; Awale, S.; Kijjoa, A.; Chulikhit, Y. Antidepressant-like effect of Oroxylum indicum seed extract in mice model of unpredictable chronic mild stress. Nutrients 2023, 15, 4742. [Google Scholar] [CrossRef]
  100. Lopresti, A.L.; Smith, S.J.; Majeed, M.; Drummond, P.D. Effects of an Oroxylum indicum Extract (Sabroxy®) on cognitive function in adults with self-reported mild cognitive impairment: A randomized, double-blind, placebo-controlled study. Front. Aging Neurosci. 2021, 13, 728360. [Google Scholar] [CrossRef]
  101. Mairuae, N.; Connor, J.R.; Buranrat, B.; Lee, S.Y. Oroxylum indicum (L.) extract protects human neuroblastoma SH-SY5Y cells against β-amyloid-induced cell injury. Mol. Med. Rep. 2019, 20, 1933–1942. [Google Scholar] [CrossRef]
  102. Pondugula, S.R.; Majrashi, M.; Almaghrabi, M.; Ramesh, S.; Abbott, K.L.; Govindarajulu, M.; Gill, K.; Fahoury, E.; Narayanan, N.; Desai, D. Oroxylum Indicum ameliorates chemotherapy induced cognitive impairment. PLoS ONE 2021, 16, e0252522. [Google Scholar] [CrossRef] [PubMed]
  103. Fuentes, R.G.; Arai, M.A.; Sadhu, S.K.; Ahmed, F.; Ishibashi, M. Phenolic compounds from the bark of Oroxylum indicum activate the Ngn2 promoter. J. Nat. Med. 2015, 69, 589–594. [Google Scholar] [CrossRef] [PubMed]
  104. Thi Vien, L.; Thi Hong Hanh, T.; Quang, T.H.; Cuong, N.T.; Cuong, N.X.; Oh, H.; Sinh, N.V.; Nam, N.H.; Van Minh, C. Phenolic glycosides from Oroxylum indicum. Nat. Prod. Res. 2022, 36, 2336–2340. [Google Scholar] [CrossRef] [PubMed]
  105. Summat, R.; Waiwut, P.; Daodee, S.; Nualkaew, N.; Phemphunananchai, K.; Arsito, P.N.; Chulikhit, Y.; Montakantirat, O.; Khamphukdee, C.; Boonyarat, C. Phytomedicine Potential of Oroxylum indicum Root and Its Constituents: Targeting Alzheimer’s Disease. Plants 2025, 14, 223. [Google Scholar] [CrossRef]
  106. Sohn, S.-H.; Yoon, M.; Kim, J.; Choi, H.-L.; Shin, M.; Hong, M.; Bae, H. Screening herbal medicines for the recovery of alpha-synuclein-induced Parkinson’s disease model of yeast. Mol. Cell. Toxicol. 2012, 8, 343–348. [Google Scholar] [CrossRef]
  107. Kang, I.N.; Lee, C.Y.; Tan, S.C. Selection of best reference genes for qRT-PCR analysis of human neural stem cells preconditioned with hypoxia or baicalein-enriched fraction extracted from Oroxylum indicum medicinal plant. Heliyon 2019, 5, e02156. [Google Scholar] [CrossRef]
  108. Sreedharan, S.; Pande, A.; Pande, A.; Majeed, M.; Cisneros-Zevallos, L. The neuroprotective effects of Oroxylum indicum extract in SHSY-5Y neuronal cells by upregulating BDNF gene expression under LPS induced inflammation. Nutrients 2024, 16, 1887. [Google Scholar] [CrossRef]
  109. Muniyasamy, R.; Manjubala, I. Synergistic combination of baicalein and rifampicin against Staphylococcus aureus biofilms. Front. Microbiol. 2024, 15, 1458267. [Google Scholar] [CrossRef]
  110. Feng, W.-Y.; Cheang, U.-I.; Wong, K.-I.; Cheong, H.-I.; Meng, L.-R.; Fong, P. Synergistic activity of Coptis Chinensis and clotrimazole against Candida Albicans. Pharmacol. Res. Mod. Chin. Med. 2023, 8, 100287. [Google Scholar] [CrossRef]
  111. Sithisarn, P.; Nantateerapong, P.; Rojsanga, P.; Sithisarn, P. Screening for antibacterial and antioxidant activities and phytochemical analysis of Oroxylum indicum fruit extracts. Molecules 2016, 21, 446. [Google Scholar] [CrossRef]
  112. Ratanakomol, T.; Roytrakul, S.; Wikan, N.; Smith, D.R. Oroxylin A shows limited antiviral activity towards dengue virus. BMC Res. Notes 2022, 15, 154. [Google Scholar] [CrossRef]
  113. Fan, Q.-F.; Hu, Z.-Y.; Na, Z.; Tang, H.-S.; Zuo, G.-Y.; Song, Q.-S. One new flavonoid from Oroxylum indicum. Nat. Prod. Res. 2015, 29, 1828–1832. [Google Scholar] [CrossRef] [PubMed]
  114. Kim, G.; Gan, R.-Y.; Zhang, D.; Farha, A.K.; Habimana, O.; Mavumengwana, V.; Li, H.-B.; Wang, X.-H.; Corke, H. Large-scale screening of 239 traditional Chinese medicinal plant extracts for their antibacterial activities against multidrug-resistant Staphylococcus aureus and cytotoxic activities. Pathogens 2020, 9, 185. [Google Scholar] [CrossRef] [PubMed]
  115. Palachum, W.; Chisti, Y.; Choorit, W. In-vitro assessment of probiotic potential of Lactobacillus plantarum WU-P19 isolated from a traditional fermented herb. Ann. Microbiol. 2018, 68, 79–91. [Google Scholar] [CrossRef]
  116. Sithisarn, P.; Rojsanga, P.; Sithisarn, P. Inhibitory effects on clinical isolated bacteria and simultaneous HPLC quantitative analysis of flavone contents in extracts from Oroxylum indicum. Molecules 2019, 24, 1937. [Google Scholar] [CrossRef]
  117. Sithisarn, P.; Rojsanga, P.; Sithisarn, P. Flavone-rich fractions and extracts from Oroxylum indicum and their antibacterial activities against clinically isolated zoonotic bacteria and free radical scavenging effects. Molecules 2021, 26, 1773. [Google Scholar] [CrossRef]
  118. Deori, K.; Yadav, A.K. Anthelmintic effects of Oroxylum indicum stem bark extract on juvenile and adult stages of Hymenolepis diminuta (Cestoda), an in vitro and in vivo study. Parasitol. Res. 2016, 115, 1275–1285. [Google Scholar] [CrossRef]
  119. Singh, K.; Yadav, A.; Khan, S.; Shukla, A.; Alam, M.; Verma, A.K.; Tiwari, N.; Khan, F.; Yadav, P.N.; Dev, K. Baicalein isolated from Oroxylum indicum acts as a potent µ-and κ-opioid receptor antagonist agent via the reversal of agonist-mediated cAMP inhibition. Nat. Prod. Res. 2024, in press. 1–9. [Google Scholar] [CrossRef]
  120. Kiratipaiboon, C.; Wasana, P.W.D.; Sukrong, S.; Ruangrungsri, N.; Towiwat, P. Herbal root extracts in Ben-Cha-Moon-Yai remedy attenuated pain-like behaviors and inflammation through the opioid and prostaglandin systems. J. Ethnopharmacol. 2022, 290, 115088. [Google Scholar] [CrossRef]
  121. Lee, A.-Y.; Kang, S.; Park, S.-J.; Huang, J.; Im, D.-S. Anti-Allergic Effect of Oroxylin A from Oroxylum indicum Using in vivo and in vitro Experiments. Biomol. Ther. 2016, 24, 283. [Google Scholar] [CrossRef] [PubMed]
  122. Das, B.; Mahapatra, M.; Gurung, B.; Dey, A.; Nongalleima, K.; Das, S.; Talukdar, A.D.; Chowdhury, A.; Choudhury, M.D.; Deb, L. Antifertility activity of Oroxylum indicum Vent. stem bark on female Wistar rats. J. Tradit. Knowl. 2024, 23, 189–199. [Google Scholar] [CrossRef]
  123. Liu, R.P.; Wang, X.Q.; Wang, J.; Dan, L.; Li, Y.H.; Jiang, H.; Xu, Y.N.; Kim, N.H. Oroxin A reduces oxidative stress, apoptosis, and autophagy and improves the developmental competence of porcine embryos in vitro. Reprod. Domest. Anim. 2022, 57, 1255–1266. [Google Scholar] [CrossRef] [PubMed]
  124. Li, D.-Q.; Zhao, J.; Li, S.-P.; Zhang, Q.-W. Discovery of xanthine oxidase inhibitors from a complex mixture using an online, restricted-access material coupled with column-switching liquid chromatography with a diode-array detection system. Anal. Bioanal. Chem. 2014, 406, 1975–1984. [Google Scholar] [CrossRef]
  125. Lone, B.A.; Sharma, N.; Kour, D.; Bhushan, A.; Rani, D.; Kumar, A.; Gupta, P.K.; Gupta, P. In-vitro anti-sickling potential of baicalin and naringenin isolated from Oroxylum indicum and Citrus aurantium on human sickle red blood cells. Nat. Prod. Res. 2023, 37, 3902–3908. [Google Scholar] [CrossRef]
  126. Zhang, X.; Zhang, Y.; Wang, N.; Liu, J.; Zhang, L.-T.; Zhang, Z.-Q.; Li, D.-Q. The mysteries of pharmacokinetics and in vivo metabolism of Oroxylum indicum (L.) Kurz: A new perspective from MSOP method. Heliyon 2024, 10, e33234. [Google Scholar] [CrossRef]
  127. Chakraborty, R.; Roy, S.; Mandal, V. Assessment of traditional knowledge of the antidiabetic plants of Darjeeling and Sikkim Himalayas in the context of recent phytochemical and pharmacological advances. J. Integr. Med. 2016, 14, 336–358. [Google Scholar] [CrossRef]
  128. Yaipharembi, N.; Huidrom, E.; Nongalleima, K.; Singh, H.B. An Ethnobotanical study on the dietary use of wild trees as traditional vegetables by three ethnic communities in Manipur, North East India. Econ. Bot. 2023, 77, 324–339. [Google Scholar] [CrossRef]
  129. Panmei, R.; Gajurel, P.; Singh, B. Ethnobotany of medicinal plants used by the Zeliangrong ethnic group of Manipur, northeast India. J. Ethnopharmacol. 2019, 235, 164–182. [Google Scholar] [CrossRef]
  130. Tangjang, S.; Namsa, N.D.; Aran, C.; Litin, A. An ethnobotanical survey of medicinal plants in the Eastern Himalayan zone of Arunachal Pradesh, India. J. Ethnopharmacol. 2011, 134, 18–25. [Google Scholar] [CrossRef]
  131. Deb, L.; Laishram, S.; Khumukcham, N.; Ningthoukhongjam, D.; Nameirakpam, S.S.; Dey, A.; Moirangthem, D.S.; Talukdar, N.C.; Ningthoukhongjam, T.R. Past, present and perspectives of Manipur traditional medicine: A major health care system available for rural population in the North-East India. J. Ethnopharmacol. 2015, 169, 387–400. [Google Scholar] [CrossRef]
  132. Singh, S.S.; Ralte, L.; Sailo, H.; Pinokiyo, A.; Devi, M.R.; Khomdram, S.D.; Singh, Y.T. Ethnobotanical study of medicinal plants used by Lois community of Kakching district, Manipur, India. Trees For. People 2025, 19, 100765. [Google Scholar] [CrossRef]
  133. Chotchoungchatchai, S.; Saralamp, P.; Jenjittikul, T.; Pornsiripongse, S.; Prathanturarug, S. Medicinal plants used with Thai Traditional Medicine in modern healthcare services: A case study in Kabchoeng Hospital, Surin Province, Thailand. J. Ethnopharmacol. 2012, 141, 193–205. [Google Scholar] [CrossRef]
  134. Kadir, M.F.; Sayeed, M.S.B.; Setu, N.I.; Mostafa, A.; Mia, M. Ethnopharmacological survey of medicinal plants used by traditional health practitioners in Thanchi, Bandarban Hill Tracts, Bangladesh. J. Ethnopharmacol. 2014, 155, 495–508. [Google Scholar] [CrossRef]
  135. Aliani, M.; Eskin, M.N. Bitterness: Perception, Chemistry and Food Processing; John Wiley & Sons: Chichester, UK, 2017; ISBN 9781118590232. [Google Scholar]
  136. Cavallo, C.; Cicia, G.; Del Giudice, T.; Sacchi, R.; Vecchio, R. Consumers’ perceptions and preferences for bitterness in vegetable foods: The case of extra-virgin olive oil and brassicaceae—A narrative review. Nutrients 2019, 11, 1164. [Google Scholar] [CrossRef]
  137. Behrens, M.; Gu, M.; Fan, S.; Huang, C.; Meyerhof, W. Bitter substances from plants used in traditional Chinese medicine exert biased activation of human bitter taste receptors. Chem. Biol. Drug Des. 2018, 91, 422–433. [Google Scholar] [CrossRef] [PubMed]
  138. Hamid, Z.; Akbar, A.; Kamran, K.; Achakzai, J.K.; Wong, L.S.; Sadiq, M.B. Unlocking the therapeutic and antimicrobial potential of Prunus armeniaca L. Seed kernel oil. Int. J. Food Sci. 2024, 2024, 5589506. [Google Scholar] [CrossRef]
  139. Lopes, A.P.; Galuch, M.B.; Petenuci, M.E.; Oliveira, J.H.; Canesin, E.A.; Schneider, V.V.A.; Visentainer, J.V. Quantification of phenolic compounds in ripe and unripe bitter melons (Momordica charantia) and evaluation of the distribution of phenolic compounds in different parts of the fruit by UPLC–MS/MS. Chem. Pap. 2020, 74, 2613–2625. [Google Scholar] [CrossRef]
  140. Dai, W.; Xiang, A.; Pan, D.; Xia, Q.; Sun, Y.; Wang, Y.; Wang, W.; Cao, J.; Zhou, C. Insights into the identification of bitter peptides from Jinhua ham and its taste mechanism by molecular docking and transcriptomics analysis. Food Res. Int. 2024, 189, 114534. [Google Scholar] [CrossRef] [PubMed]
  141. Sharafi, M.; Hayes, J.E.; Duffy, V.B. Masking vegetable bitterness to improve palatability depends on vegetable type and taste phenotype. Chemosens. Percept. 2013, 6, 8–19. [Google Scholar] [CrossRef]
  142. Ke, J.; Wang, Y.; Luo, T.; Liang, Y.; Wang, X.; Ma, Y.; Zhao, L.; Zhang, Z. Study on the effect of different bitter masking inhibitors on the bitter masking of Zanthoxylum bungeanum Maxim. Int. J. Gastron. Food Sci. 2024, 35, 100894. [Google Scholar] [CrossRef]
  143. Kan, R.; Yu, Z.; Zhao, W. Identification and molecular action mechanism of novel TAS2R14 blocking peptides from egg white proteins. LWT 2023, 180, 114716. [Google Scholar] [CrossRef]
  144. Cox, D.N.; Melo, L.; Zabaras, D.; Delahunty, C.M. Acceptance of health-promoting Brassica vegetables: The influence of taste perception, information and attitudes. Public Health Nutr. 2012, 15, 1474–1482. [Google Scholar] [CrossRef] [PubMed]
  145. Worakitjaroenphon, S.; Shanmugam, P.; Boonyuen, S.; Smith, S.M.; Chookamnerd, K. Green synthesis of silver and gold nanoparticles using Oroxylum indicum plant extract for catalytic and antimicrobial activity. Biomass Convers. Biorefin. 2023, in press. 1–12. [Google Scholar] [CrossRef]
  146. Greene, A.M.; Panyadee, P.; Inta, A.; Huffman, M.A. Asian elephant self-medication as a source of ethnoveterinary knowledge among Karen mahouts in northern Thailand. J. Ethnopharmacol. 2020, 259, 112823. [Google Scholar] [CrossRef]
  147. Sritongchuay, T.; Bumrung, S.; Meesawat, U.; Mazer, S.J. Stigma closure and re-opening in Oroxylum indicum (Bignoniaceae): Causes and consequences. Am. J. Bot. 2010, 97, 136–143. [Google Scholar] [CrossRef]
  148. Sonia, R.; Shaheen, S.; Waheed, M.; Imran, S.; Haq, S.M.; Muhammad, M.; Hashem, A.; Al Shehri, S.; Abd-Allah, E.F. Anatomical characterization of Semi-arid Bignoniaceae using light and scanning electron microscopy. BMC Plant Biol. 2025, 25, 125. [Google Scholar] [CrossRef]
  149. Yin, X.-s.; Zhong, Z.-f.; Bian, G.-l.; Cheng, X.-j.; Li, D.-q. Ultra-rapid, enhanced and eco-friendly extraction of four main flavonoids from the seeds of Oroxylum indicum by deep eutectic solvents combined with tissue-smashing extraction. Food Chem. 2020, 319, 126555. [Google Scholar] [CrossRef]
  150. Zhao, Y.; Liang, P.; Yu, Q.; Li, P.; Dong, N. Column-free matrix solid-phase dispersion extraction based on cucurbit[8]uril used for the determination of the flavonoid content in Oroxylum indicum (L.) Vent. Ind. Crops Prod. 2022, 175, 114277. [Google Scholar] [CrossRef]
  151. Rojsanga, P.; Bunsupa, S.; Sithisarn, P. Flavones contents in extracts from Oroxylum indicum seeds and plant tissue cultures. Molecules 2020, 25, 1545. [Google Scholar] [CrossRef]
  152. Xie, Z.; Li, G.; Fu, Y.; Sun, M.; Ye, B. Sensitive, simultaneous determination of chrysin and baicalein based on Ta2O5-chitosan composite modified carbon paste electrode. Talanta 2017, 165, 553–562. [Google Scholar] [CrossRef]
  153. Tamta, B.; Kumar, R.; Uniyal, S.; Uniyal, A. Exploration and selection of elite germplasm of Oroxylum indicum (L.) Vent.(Shyonak) in the forest divisions of Punjab, India. Curr. Sci. 2022, 122, 1401–1406. [Google Scholar] [CrossRef]
  154. Othman, F.A.; Mat Zin, A.A.; Zakaria, Y.; Nik Salleh, N.N.H.; Mohd Satar, A.; Tan, S.C. Pre-clinical acute oral toxicity and subacute neurotoxicity risk assessments on sprague dawley rats treated with single dose or repeated doses of flavonoid-enriched fraction extracted from Oroxylum indicum leaves. Drug Chem. Toxicol. 2025, 48, 1104–1120. [Google Scholar] [CrossRef] [PubMed]
  155. Srinivas, K.S.; Aparna, A.S. High Performance Thin Layer Chromatographic determination of chrysin in Oroxylum indicum vent. from different geographical regions of India. J. Chem. 2012, 9, 313–317. [Google Scholar] [CrossRef]
  156. Xie, Z.; Wu, Y.; Kai, S.; Li, G.; Ye, B. A newly competitive electrochemical sensor for sensitive determination of chrysin based on electrochemically activated Ta2O5 particles modified carbon paste electrode. Electroanalysis 2017, 29, 835–842. [Google Scholar] [CrossRef]
  157. Treesuwan, W.; Ichikawa, S.; Wang, Z.; Neves, M.A.; Uemura, K.; Nakajima, M.; Kobayashi, I. Formulation and storage stability of baicalein-loaded oil-in-water emulsions. Eur. J. Lipid Sci. Technol. 2013, 115, 1115–1122. [Google Scholar] [CrossRef]
  158. Zhou, L.; Jing, T.; Zhang, P.; Zhang, L.; Cai, S.; Liu, T.; Fan, H.; Yang, G.; Lin, R.; Zhang, J. Kinetics and modeling for extraction of chrysin from Oroxylum indicum seeds. Food Sci. Biotechnol. 2015, 24, 2045–2050. [Google Scholar] [CrossRef]
  159. Sharma, H.; Narshimhaji, C.V.; Singh, R. Relative estimation of beta-sitosterol in alcoholic extracts of roots and small branches of Oroxylum indicum (L.) Kurz by HPTLC for plant part substitution, medicinal uses and conservation. J. Appl. Res. Med. Aromat. Plants 2023, 35, 100496. [Google Scholar] [CrossRef]
  160. Dong, N.; Yang, L.; Li, X.; Zhao, A. A novel green sample pretreatment method column-free matrix solid-phase dispersion extraction: Application in a high-performance liquid chromatography experiment for undergraduate chemistry. J. Chem. Educ. 2024, 101, 3369–3376. [Google Scholar] [CrossRef]
  161. Feng, R.; Zhang, X.; Yin, J.; Zhang, Y.; Ma, Y.; Zhang, X.; Zhang, L.; Li, D. A comprehensive study of the metabolism of flavonoid oroxin B in vivo and in vitro by UHPLC-Q-TOF-MS/MS. J. Pharm. Biomed. Anal. 2021, 197, 113905. [Google Scholar] [CrossRef]
  162. Krüger, A.; Ganzera, M. Oroxylum indicum seeds–Analysis of flavonoids by HPLC–MS. J. Pharm. Biomed. Anal. 2012, 70, 553–556. [Google Scholar] [CrossRef]
  163. Liu, R.; Xu, L.; Li, A.; Sun, A. Preparative isolation of flavonoid compounds from Oroxylum indicum by high-speed counter-current chromatography by using ionic liquids as the modifier of two-phase solvent system. J. Sep. Sci. 2010, 33, 1058–1063. [Google Scholar] [CrossRef] [PubMed]
  164. Yadav, A.K.; Manika, N.; Bagchi, G.D.; Gupta, M.M. Simultaneous determination of flavonoids in Oroxylum indicum by RP-HPLC. Med. Chem. Res. 2013, 22, 2222–2227. [Google Scholar] [CrossRef]
  165. Chandewar, A.V.; Kochar, N.I.; Shrirao, A.V.; Karpe, S.T. Phytochemical screening, chromatographic and quantitative study of phenols and flavonoids in leaves of Oroxylum indicum and Pongamia pinnata. Res. J. Pharm. Technol. 2023, 16, 2604–2608. [Google Scholar] [CrossRef]
  166. Bhusari, S.; Morey, S.; Nikam, K.; Wakte, P. Comparative evaluation of baicalein from Oroxylum indicum by using conventional and non-conventional extraction methodology. Res. J. Pharm. Technol. 2019, 12, 1817–1822. [Google Scholar] [CrossRef]
  167. Shi, S.; Wei, Y.; Feng, J.; Zhou, C.; Zuo, J.; Yao, L.; Ding, J.; Li, K.; He, Q. Facile and ultrasensitive electrochemical detection of baicalein on bismuth oxide-carboxylated multi-walled carbon nanotube/glassy carbon electrode. J. Food Compos. Anal. 2023, 123, 105557. [Google Scholar] [CrossRef]
  168. Deshmukh, A.B.; Datir, S.S.; Bhonde, Y.; Kelkar, N.; Samdani, P.; Tamhane, V.A. De novo root transcriptome of a medicinally important rare tree Oroxylum indicum for characterization of the flavonoid biosynthesis pathway. Phytochemistry 2018, 156, 201–213. [Google Scholar] [CrossRef]
  169. Gurupasad, K.; Mascarenhas, R.; Gopinath, P.; Satyamoorthy, K. Studies on Brahma rasayana in male Swiss albino mice: Chromosomal aberrations and sperm abnormalities. J. Ayurveda Integr. Med. 2010, 1, 40. Available online: https://pmc.ncbi.nlm.nih.gov/articles/PMC3149391/ (accessed on 6 October 2025). [CrossRef]
Figure 1. PRISMA 2020 flowchart for the selection of studies on O. indicum.
Figure 1. PRISMA 2020 flowchart for the selection of studies on O. indicum.
Foods 14 03465 g001
Figure 2. Growth of annual publications related to O. indicum.
Figure 2. Growth of annual publications related to O. indicum.
Foods 14 03465 g002
Figure 3. (a) Countries where O. indicum samples were collected in the selected papers and (b) the distribution of author affiliations by country across all selected publications related to O. indicum. In (a), countries with similar colors indicate comparable numbers of sample collections, while in (b), darker colors are countries with more author affiliations, and lighter colors indicate fewer records.
Figure 3. (a) Countries where O. indicum samples were collected in the selected papers and (b) the distribution of author affiliations by country across all selected publications related to O. indicum. In (a), countries with similar colors indicate comparable numbers of sample collections, while in (b), darker colors are countries with more author affiliations, and lighter colors indicate fewer records.
Foods 14 03465 g003
Figure 4. Most global cited documents related to O. indicum [8,20,28,29,30,31,32,33,34,35].
Figure 4. Most global cited documents related to O. indicum [8,20,28,29,30,31,32,33,34,35].
Foods 14 03465 g004
Figure 5. Thematic map related to studies on O. indicum. Panel (a) is the overall keyword co-occurrence network, where node color corresponds to the average publication year and node size indicates occurrence frequency. The arrows highlight new topics (yellow clusters). Panels (bd) are zoomed-in views of cropped regions from panel (a) for clearer visualization of individual clusters.
Figure 5. Thematic map related to studies on O. indicum. Panel (a) is the overall keyword co-occurrence network, where node color corresponds to the average publication year and node size indicates occurrence frequency. The arrows highlight new topics (yellow clusters). Panels (bd) are zoomed-in views of cropped regions from panel (a) for clearer visualization of individual clusters.
Foods 14 03465 g005
Figure 6. Thematic map related to studies on O. indicum. Bubble size represents the number of documents associated with each theme, while colors differentiate distinct thematic clusters.
Figure 6. Thematic map related to studies on O. indicum. Bubble size represents the number of documents associated with each theme, while colors differentiate distinct thematic clusters.
Foods 14 03465 g006
Figure 7. ADO framework for research related to O. indicum.
Figure 7. ADO framework for research related to O. indicum.
Foods 14 03465 g007
Figure 8. Chemical structures of the major flavonoids in O. indicum (baicalein, baicalin, chrysin, oroxylin A, oroxin A, and oroxin B).
Figure 8. Chemical structures of the major flavonoids in O. indicum (baicalein, baicalin, chrysin, oroxylin A, oroxin A, and oroxin B).
Foods 14 03465 g008
Table 1. Top 35 journals publishing the selected articles on O. indicum (number of publications in parentheses).
Table 1. Top 35 journals publishing the selected articles on O. indicum (number of publications in parentheses).
Top 35 Journals and Number of Publications
Journal of Ethnopharmacology (18)Cancers (2)Journal of Chemistry (2)
Molecules (11)Current Science (2)Journal of Functional Foods (2)
Natural Product Research (6)Economic Botany (2)Journal of Natural Medicines (2)
Journal of Ayurveda and Integrative Medicine (5)Ethnobotany Research and Applications (2)Journal of Pharmaceutical and Biomedical Analysis (2)
Phytomedicine (4)European Journal of Pharmacology (2)Journal of Pharmacy and Bioallied Sciences (2)
European Journal of Medicinal Chemistry (3)Fitoterapia (2)Medicinal Chemistry Research (2)
Heliyon (3)Food Bioscience (2)Pharmacological Research-Modern Chinese Medicine (2)
Indian Journal of Traditional Knowledge (3)Food Chemistry (2)Plants (2)
Journal of Biomolecular Structure and Dynamics (3)Frontiers in Pharmacology (2)PLoS ONE (2)
Nutrients (3)Industrial Crops and Products (2)Processes (2)
Research Journal of Pharmacy and Technology (3)Journal of Applied Pharmaceutical Science (2)RSC Advances (2)
Biomedicine and Pharmacotherapy (2)Journal of Applied Research on Medicinal and Aromatic Plants (2)
Table 2. Summary of representative pharmacological activities of O. indicum groups.
Table 2. Summary of representative pharmacological activities of O. indicum groups.
GroupRelated ActivitiesExtract/
Compound
Plant PartModelReferences
Canceranticancer, anti-tumor, cytotoxic, anti-metastatic, histone deacetylase (HDAC) inhibition, and anti-lymphoma.Endophytic fungus extract, ethanol extract, ethyl acetate extract, methanol extract, aqueous extract, hydroalcoholic extract, fungal endophyte metabolites, baicalein, chrysin, oroxylin A, oroxylin A glycoside, oroxylin A-7-O-glucuronide, oroxyquinone, methoxy-chrysin, scutellarein-7-rutinoside, oroxin B, chrysin-7-O-glucuronide, oroxindin, oroxin A, and semi-synthetic derivatives.Stem bark, bark, leaves, fruit, young stems, root, and root bark.In vitro, in vivo, in silico.[7,13,30,37,40,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63]
Diabetes Anti-prediabetes, antidiabetic, and anti-NASH (non-alcoholic steatohepatitis).Methanol extract, seed extract, baicalein, chrysin, baicalein-7-O-glucoside, baicalein-7-O-diglucoside, baicalin, oroxylin A, flavone derivatives, and glycosides.Seed, stem bark, root, and bark.In vitro, in vivo, in silico.[8,38,64,65,66,67,68,69,70,71]
Liver ProtectionHepatoprotective and MAFLD (metabolic associated fatty liver disease).Ethanol extract, apigenin, baicalein, chrysin, oroxylin A, scutellarin, tetuin, oroxin B, and oroxin A.Stem bark and seed.In vitro, in vivo, in silico.[19,41,72]
Skin HealthWound healing and
skin-whitening.
Ethanol extract, aqueous extracts, and chrysin.Leaf, seed, and stem bark.In vitro, in vivo.[73,74,75]
AntioxidantAntioxidant.Methanol extract, aqueous extract, ethanol extract, acetone extract, hexane extract, SCeCO2eH extract (supercritical carbon dioxide integrated hydrothermal extract), hydrothermal extract, Soxhlet methanol extract, cerium oxide nanoparticles, baicalin, chrysin, baicalein, oroxylin A, scutellarein, baicalein-7-O-gentiobioside, baicalein-7-O-glucoside, and hispidulin.Bark, fruit, seed, leaf, branch, stem, twig, root, and immature pod.In vitro, in vivo, in silico.[11,76,77,78,79,80,81,82,83,84,85,86]
Anti-inflammatoryAnti-inflammatory.Ethanol extract, dichloromethane extract, ethyl acetate extract, decoction, baicalein, scutellarein, oroxylin A, chrysin, hispidulin, oroxin A, and baicalin.Bark, leaves, seeds, shoots, fruits, grilled fruits, stem bark, and root bark.In vitro, in vivo, in silico.[2,9,16,17,39,87,88,89]
Bone HealthAnti-osteoarthritic, anti-osteoporotic, osteogenic support, and skeletal protective activity.Ethanol extract, oroxin B, oroxylin A, baicalein, and other major flavonoids.Stem bark.In vitro, in vivo, in silico.[12,14,90,91,92]
ObesityAnti-adipogenic and anti-obesity.Ethyl acetate extract, ethanol extract, baicalein, oroxylin A, luteolin, apigenin, and chrysin.Fruit and bark.In vitro, in silico.[42,93,94,95]
Cardiovascular HealthAnti-atherosclerotic and cardioprotective.Sabroxy (O. indicum extract), methanol extract, and chrysin.Stem bark and root bark.In vivo.[18,96,97]
Gastrointestinal HealthAnti-ulcer.Dihydrooroxylin A-7-O-methyl glucuronide and chrysin.Stem bark.In vivo.[98]
Neurological ProtectionNeuroprotective, neuroregenerative,
anti-Alzheimer, antidepressants, and
anti-neuroinflammatory
Sabroxy, water extract, methanol extract, ethanol extract, baicalein, oroxylin A, chrysin, hispidulin, apigenin, baicalin, and isoverbascoside.Leaf, bark, seed, root, root bark, and fruit pod.In vitro, in vivo, in silico.[43,99,100,101,102,103,104,105,106,107,108]
Anti-infectiveAntibacterial, antimicrobial, antiviral, anthelmintic, and antifungal.Aqueous extract, methanol extract, ethanol extract, Lactobacillus plantarum WU-P19, baicalein, baicalin, 5,6,7-trimethoxyflavone-8-O-β-D-glucopyranoside, oroxylin A-7-O-β-D-glucuronide butyl ester, chrysin, 6-methoxybaicalein, oroxylin A-7-O-glucoside, and oroxylin A.Seeds, young fruits, flowers, fermented fruit, leaf, stem, bark, and root.In vitro, in silico.[10,15,31,109,110,111,112,113,114,115,116,117,118]
Pain ReliefAnti-nociceptive.Ethanol extract, water extract, and baicalein.Stem barks and roots.In vitro, in vivo, in silico.[119,120]
Respiratory HealthAnti-allergic and anti-asthmatic.Oroxylin A.Not specified.In vitro, in vivo.[121]
Reproductive HealthAntifertility and embryo supportAqueous extract, methanol extract, and oroxin A.Stem bark.Ex vivo, in vivo,
in vitro.
[122,123]
Miscellaneous Pharmacological ActionsPharmacokinetics, anti-gout, and anti-sicklingEthanol extract, methanol extract, baicalin, oroxylumoside A, oroxylumoside B, darendoside A, and leucosceptoside A.Seeds and stem bark.In vitro, in vivo, ex vivo[124,125,126]
Due to many studies having an extensive number of pharmacological activities tested, only one representative activity in each study is listed here and is used for grouping. A full dataset of all screened studies is provided in Table S1.
Table 3. Summary of ethnomedicinal uses of O. indicum.
Table 3. Summary of ethnomedicinal uses of O. indicum.
GroupEthnomedicinal UsesComparison with Pharmacological ActivitiesReferences
CancerCancer.Strongly supported[3]
DiabetesAntidiabetic.Strongly supported[3,93,127,128]
Liver ProtectionJaundice, liver problems, hepatitis, and hepatoprotective.Strongly supported[3,4,32]
Skin HealthLeukoderma, urticaria, infantile erythema, cuts and wounds, burns, skin disorder, and skin diseases.Moderately supported[3,5,129]
Anti-inflammatoryArthritis, inflammation, and rheumatism.Strongly supported[3,4]
AntioxidantDetoxification and rejuvenation.Strongly supported[2,93]
Bone HealthArthritis and rheumatism.Strongly supported[3,4]
ObesityObesity.Moderately supported[93]
Cardiovascular HealthCardiac disorders, high blood pressure, hypertension, and heart problems.Strongly supported[3,129,130]
Neurological ProtectionHeadache, neuralgia, epilepsy, and paralysis.Moderately supported[3,33,131]
Gastrointestinal HealthStomach problems, diarrhea, carminative, stomachache, dysentery, purgative, astringent, stomachic, dyspepsia, gastropathy, gastralgia, stomach cleaning, colic, indigestion, bloody stool, stomach ulcer, constipation, abdominal pain, gastric ulcer, ulcer, piles, colitis, hemorrhoids, and other digestive ailments.Strongly supported[3,4,5,6,131,132]
Anti-infectiveFever, malaria, tuberculosis, smallpox, cholera, measles, typhoid, gonorrhea, pneumonia, and anthelmintic.Moderately supported[3,5,129]
Pain ReliefMuscle pain, chest pain, body pain, sprains, and analgesic.Strongly supported[3,4,120]
Respiratory HealthCough, bronchitis, pharyngodymia, asthma, sore throat, laryngitis, hoarseness, allergic disease, and tonsillitis.Strongly supported[3]
Reproductive HealthPlacental problem, menstrual disorders, womb ailment, leucorrhea, and a blood tonic.Moderately supported[3,4,129,133]
Miscellaneous and Unmapped Traditional UsesHair tonic, tonic, dropsy, urinary problems, scrotal swelling, and dog bite, enlarged spleen, antipyretic agent, hemorrhage, and scorpion stingUnclear or unsupported[3,4,5,120,134]
A full dataset of all screened studies is provided in Table S2. “Strongly supported” indicates direct and consistent validation through experimental studies, especially in vivo. “Moderately supported” refers to partial or indirect evidence (e.g., in vitro or in silico only, or limited relevance). “Unsupported” includes uses with no scientific evidence or too vague to be pharmacologically assessed.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Nguyen, H.L.; Sae-Eaw, A.; Tran, D.Q.; Prinyawiwatkul, W.; Chulikhit, Y. A Systematic Review of Evidence-Based Health Benefits of Oroxylum indicum and Its Functional Food Potential. Foods 2025, 14, 3465. https://doi.org/10.3390/foods14203465

AMA Style

Nguyen HL, Sae-Eaw A, Tran DQ, Prinyawiwatkul W, Chulikhit Y. A Systematic Review of Evidence-Based Health Benefits of Oroxylum indicum and Its Functional Food Potential. Foods. 2025; 14(20):3465. https://doi.org/10.3390/foods14203465

Chicago/Turabian Style

Nguyen, Hai Linh, Amporn Sae-Eaw, Dinh Quyen Tran, Witoon Prinyawiwatkul, and Yaowared Chulikhit. 2025. "A Systematic Review of Evidence-Based Health Benefits of Oroxylum indicum and Its Functional Food Potential" Foods 14, no. 20: 3465. https://doi.org/10.3390/foods14203465

APA Style

Nguyen, H. L., Sae-Eaw, A., Tran, D. Q., Prinyawiwatkul, W., & Chulikhit, Y. (2025). A Systematic Review of Evidence-Based Health Benefits of Oroxylum indicum and Its Functional Food Potential. Foods, 14(20), 3465. https://doi.org/10.3390/foods14203465

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop