Tentative Identification of Phytochemicals from Smilax glabra and Smilax corbularia Extracts by LC-QTOF/MS and Their Bioactive Potential

The Smilacaceae family has been used as a food source and herbal medicine for a long time. This study aims to identify the phytochemicals extracted from Smilax glabra and Smilax corbularia by using LC-QTOF/MS analysis and determine their bioactive potential. Compounds were identified from S. glabra and S. corbularia extracts by LC–QTOF-MS and it was found that longistylin A and CAY10435 have higher degrees of matching compounds (99.66% and 99.87%). Smilax glabra showed antioxidant capacity, i.e., DPPH and ABTS at percentage inhibitions of 71.94 ± 1.46% and 59.84 ± 4.80%, respectively, and FRAP at 730.69 ± 33.62 mg AAE/100 g sample. The total phenolic compound contents of the ethanol, methanol, and water extracts were 0.017 ± 0.001, 0.015 ± 0.001, and 0.016 ± 0.001 mg GAE/g, respectively, while the total flavonoid contents were 0.043 ± 0.002, 0.033 ± 0.002, and 0.006 ± 0.003 mg QE/g, respectively. The anti-inflammatory capacity showed 97.26% protection and 2.74% hemolysis. The antimicrobial activity can inhibit Gram-positive bacteria with a minimum inhibitory concentration (MIC) of 62.5 mg/mL and a minimum bactericidal concentration (MBC) of 500 mg/mL. Smilax corbularia showed antioxidant capacity, i.e., DPPH and ABTS at percentage inhibitions of 72.24 ± 0.64% and 39.87 ± 2.37%, respectively, and FRAP at 208.33 ± 50.80 mg AAE/100 g sample. The total phenolic compound contents of the ethanol, methanol, and water extracts were 0.006 ± 0.000, 0.007 ± 0.002, and 0.002 ± 0.001 mg GAE/g, respectively, while the total flavonoid contents of the ethanol and methanol extracts were 0.012 ± 0.001 and 0.008 ± 0.000 mg QE/g, respectively. The anti-inflammatory capacity showed 96.64% protection and 3.36% hemolysis. The antimicrobial activity of the extracts can inhibit Gram-positive bacteria with a MIC of 31.25 mg/mL and MBC of 125 mg/mL for the ethanol extract and a MIC of 125 mg/mL and MBC of 62.5 mg/mL for the methanol extract. In conclusion, Smilax glabra and Smilax corbularia were found to contain several phytochemicals that can be used for further study. Both Smilax species can also be used as sources of antioxidants and herbal medicines for killing Gram-positive bacteria.


Introduction
Smilax glabra Roxb. and Smilax corbularia Kunth. are herbal species in the Smilacaceae family and are Southeast Asian plants endemic to the area. They have infiltrated nearby species in China, Myanmar, Thailand, and Laos. In Thailand, they are commonly found The experimentally measured mass of each ion was evaluated against the exact mass of the molecular formula and the expected isotope pattern for that formula. These data were used to score the matching of the ions with the database by the MassHunter Qualitative Analysis Software find-by-formula search of the Agilent MassHunter METLIN Metabolomics Database. The top ten compounds in terms of matching scores of the ethanolic crude extract of S. cobularia, which have a higher matching scores (96.96-99.66%), are shown in Table 1, and the mass spectra showing specific peaks and their corresponding compounds are shown in Figure 1.  As a result, all of the compounds were identified as longistylin A, (-)-neolinderatin 2′,4′-dihydroxy-7-methoxy-8-prenylflavan, ent-8-deoxy-J2-IsoP, butoctamide hydrogen succinate, 9Z,12E,15E-octadecatrienoic acid, neolinderatone, geissospermine, (3aS)-1-me  As a result, all of the compounds were identified as longistylin A, (-)-neolinderatin,  2 ,4 -dihydroxy-7-methoxy-8-prenylflavan, ent-8-deoxy-J2-IsoP, butoctamide hydrogen succinate, 9Z,12E,15E-octadecatrienoic acid, neolinderatone, geissospermine, (3aS)-1-methyl-3a-(3-methylbut-2-en-1-yl)-1,2,3,3a,8,8ahexahydropyrrolo [2,3-b] indole, and stigmatellin Y. Longistylin A belongs to the class of organic compounds known as stilbenes, which are organic chemicals. Longistylin A was discovered to have antibacterial qualities and significant antibacterial activity against MRSA in research of its properties [10]. In a previous study, it was found that stilbenes were isolated from S. glabra, but different types showed trans-resveratrol, trans-piceid, and piceatannol. Stigmatellin Y is a chromone [11]. In a previous study, three new stigmatellins were found, namely, stigmatellic acid, isomethoxy-stigmatellin A, and stigmatellin C (3, isolated as isomers), which were isolated from the myxobacterium Vitiosangium cumulatum MCy10943 T [12].
The top nine compounds in terms of matching scores of the ethanolic crude extract of S. glabra, which have higher matching scores (96.29-99.87%), are shown in Table 2, and the mass spectra showing the specific peaks and their corresponding compounds are shown in Figure 2. previous study, it was found that stilbenes were isolated from S. glabra, but different types showed trans-resveratrol, trans-piceid, and piceatannol. Stigmatellin Y is a chromone [11]. In a previous study, three new stigmatellins were found, namely, stigmatellic acid, isomethoxy-stigmatellin A, and stigmatellin C (3, isolated as isomers), which were isolated from the myxobacterium Vitiosangium cumulatum MCy10943 T [12]. The top nine compounds in terms of matching scores of the ethanolic crude extract of S. glabra, which have higher matching scores (96.29-99.87%), are shown in Table 2, and the mass spectra showing the specific peaks and their corresponding compounds are shown in Figure 2.  According to the results, all compounds were identified as CAY10435, methyl cis-pcoumarate 3-(3,7-dimethyl-2,6-octadienyl), hemihydro-guaiaretic acid, 4,4 -dihydroxy-5,5diisopro-pyl-2,2 -dimethyl-3,6-biphenyldione, 8,11,14- indole, stigmatellin Y, and butoctamide hydrogen succinate. From a medicinal chemistry standpoint, CAY10435 (oxazolopyridine) molecules have several benefits, and the antibacterial properties of oxazolopyridines were investigated [13]. In a previous study of the characterization of Smilax glabra by LC-QTOF/MS, six new phenolic compounds named smiglabrone A, smiglabrone B, smilachromanone, smiglastilbene, smiglactone, and smiglabrol were discovered. Smiglabrone A showed antimicrobial activity against Canidia albicans. Smilachromanone and smiglastilbene exhibited inhibitory activity against Staphylococcus aureus [11].

Antioxidant Activity
To evaluate the antioxidant capacity, reducing power determination, as well as DPPH and ABTS radical scavenging activity, experiments were performed. Table 4 demonstrates that S. corbularia and S. glabra exhibited DPPH radical scavenging activity with percent inhibition values of 72.24 ± 0.64 (IC 50 : 583.06 mg/mL) and 71.94 ± 1.46 (IC 50 : 167.96 mg/mL), respectively. S. corbularia and S. glabra extracts had ABTS radical scavenging activity capacities of 59.84 ± 4.80 and 39.87 ± 2.37 percent inhibition, respectively. The percent inhibition values for S. corbularia and S. glabra extracts were significantly different, according to the t-test. The ferric ion reducing antioxidant power showed that S. corbularia had an antioxidant capacity of 208.33 ± 50.80 mg AAE/100 g sample, while S. glabra had an antioxidant capacity of 730.69 ± 33.62 mg AAE/100 g sample. Epicatechin, astilbin, neoastilbin, isoastilbin, and neo-isoastilbin at 50 g/mL displayed  [14]. The percent inhibition values for S. corbularia and S. glabra were significantly different according to the T test. The value for S. corbularia (IC 50 : 583.06 mg/mL) was higher than that of S. glabra, with a percent inhibition value of 71.94 ± 1.46 (IC 50 : 167.96 mg/mL), and a t-test revealed that the percent inhibition values of S. corbularia and S. glabra were significantly different. The DPPH in S. glabra extracted with ethanol was reported in a prior work at 32.3 µg/mL, which is a higher radical scavenging efficiency than the efficiency found in the current studies [15].

Total Phenolic Compound and Total Flavonoid Contents
The total phenolic compound (TPC) and total flavonoid (TFC) contents of S. glabra and S. corbularia are shown in Table 5. The ethanolic extract showed the maximum value for the TFC (0.043 ± 0.002 mg QE/g and 0.012 ± 0.001 mg QE/g, respectively), while the water extract showed the minimum value for the TFC for S. glabra (0.006 ± 0.003 mg QE/g) and was not detected in S. corbularia. In the present study, the total phenolic content of S. glabra was 0.017 ± 0.001 (mg GAE/g sample) in the ethanolic extract, which was higher than those of the methanolic extract and water extract. However, the total phenolic content of S. corbularia was 0.007 ± 0.002 (mg GAE/g sample) in the methanolic extract, which was higher than those in the ethanolic extract and water extract. One-way ANOVA indicated that the ethanol, methanol, and water fraction values were significantly different (p < 0.001) for the total flavonoid content, and p < 0.05 for the total phenolic compounds in the samples. However, for Smilax glabra, the extracts showed nonsignificant differences (p > 0.05). In previous reports, the total flavonoid and total phenolic contents of the ethanol extract of S. glabra were 420.26 ± 125.67 mg RE/g sample and 208.45 ± 3.74 (mg GAE/g sample), respectively [16]. In comparison, the total flavonoid and total phenolic contents of the 60% ethanol extract of S. glabra were 203.4 ± 9.1 mg RE/g sample and 262.6 ± 12.7 mg GAE/g sample, respectively [17]. Each value represents the mean ± SD (n = 3). p < 0.001 corresponded to each extracted total flavonoid content, and p < 0.05 corresponded to each extracted total phenolic compound content. * indicates p > 0.05 compared with each extracted total phenolic compound content, ND = not detected.

Anti-Inflammatory Efficacy
The anti-inflammatory efficacy was measured by the suppression of hypotonicityinduced HRBC membrane lysis, i.e., the stabilization of the HRBC membrane. The percentage of membrane stabilization for ethanol stabilization was calculated at 100, 500, and 1000 µg/mL. Ethanolic extracts of Smilax glabra and Smilax corbularia are effective in inhibiting the heat-induced hemolysis of HRBC at different concentrations (100-1000 µg/mL), as shown in Table 6. It offered maximum protection of 97.26%, and hemolysis was 2.74% at 100 µg/mL in Smilax glabra; meanwhile, in Smilax corbularia, the maximum protection was 96.64%, and hemolysis was 3.36% at 100 µg/mL. Inflammation is an essential contributor to various acute and chronic disease pathologies. A study of the acute oral toxicity of the aqueous crude extract of Smilax glabra in cytotoxicity research revealed that Smilax glabra had no toxicity impact on mice [18]. In another cytotoxic effect study, Gao et al. found that Smilax glabra inhibited the growth of HT-29 cell xenografts in a nude mouse model, and because the effects of Smilax glabra on body weight and lesions in the heart or liver were not observed, it was concluded that there was no toxic effect on mice [19]. Lipopolysaccharide (LPS)-induced inflammation in vitro promoted the release of inflammatory cytokines (IL-1β, IL-6, etc.) and activation of the nuclear factor-kappa B (NF-kB) pathway [2]. The lysosomal membranes that impact the inflammatory process are identical to the human red blood corpuscular membrane. Various illnesses are caused by the lysosomal enzymes generated during inflammation. The extracellular activity of these enzymes is linked to acute or chronic inflammation. Antiinflammatory drugs work by inhibiting the cyclooxygenase enzyme, which is involved in the conversion of arachidonic acid to prostaglandins [20]. The study found that an ethanolic extract of S. glabra and S. corbularia had a membrane-stabilizing effect, suppressing hypotonicity-induced erythrocyte membrane lysis in a concentration-dependent manner. This action might be attributed to active components, such as flavonoids and triterpenoids. The impact of triterpenoids of the additional ethanol of Allium cepa (EEAC), which was shown to be concentration-dependent ligation, was a maximum protection of 95.18% at a concentration of 2000 µg/mL [21]. Additionally, it is known that Smilax contains much higher levels of astilbin.

Minimum Inhibitory Concentration and Minimum Bactericidal Concentration
The MIC and MBC of Smilax corbularia and Smilax glabra (Figure 3) against the two strains ( Figure 4) were measured for antibacterial activity (Table 7) and are shown in Figures 5 and 6. The MIC values of S. corbularia from the ethanol extracted (EE) fraction and methanol extracted (ME) fraction showed activity against bacteria M2 compared with bacteria M1, with MIC values of 31.25 and 250 mg/mL, respectively, in the EE fraction, with MIC values of 125 and 250 mg/mL, respectively, in the ME fraction. The MIC values of S. glabra from the EE fraction and ME fraction showed activity against bacteria M2 compared with bacteria M1, with MIC values of 62.5 and 125 mg/mL, respectively, and the MBC values of S. corbularia from the EE fraction and ME fraction showed activity against bacteria M2 compared with bacteria M1, with MBC values of 125 and 500 mg/mL, respectively. The MBC values of S. corbularia from the ME fraction showed greater activity against bacteria M2 compared with bacteria M1, with MBC values of 62.5 and 500 mg/mL, respectively. The MBC values of S. glabra from the EE fraction and ME fraction showed activity against both bacteria, with MBC values of 500 mg/mL. Both bacteria were unaffected by the water extracted fraction. In a prior investigation, the minimal inhibitory concentration extracted from Smilax macrophylla leaves in 95% methanol demonstrated a substantial inhibitory effect against S. aureus, E. coli, and B. subtilis growth [22]. Smilax China L. polyphenols have antibacterial activity in the range of 195.31 to 781.25 µg/mL. Smilax China L. polyphenols demonstrated greater sensitivity in Escherichia coli and Staphylococcus aureus [23]. In previous studies, they found that seventeen compounds were antimicrobial and had antibacterial activity. (-)-Epicatechin, (+)-catechin, cinchonain Ib, and cinchonain Ia demonstrated antimicrobial properties [11].

Plant Collection
The 10 plants of each Smilax were collected from the BanSaluang Nok community forest, Maerim District, Chiang Mai, Thailand, which is located at 19°01′33.2″ N of the equator and 98°54′39.4″ E of the equator, on the date 2-3 October 2021.

Plant Collection
The 10 plants of each Smilax were collected from the BanSaluang Nok community forest, Maerim District, Chiang Mai, Thailand, which is located at 19 • 01 33.2 N of the equator and 98 • 54 39.4 E of the equator, on the date 2-3 October 2021.

Extraction of Plant Samples
Fresh Smilax glabra and Smilax corbularia were cleaned and dried in an oven at 50 • C for 1 h, which showed 75% and 68% water contents, respectively. Then, the dried samples were crushed into small pieces. One gram of crushed sample was extracted by using 30 mL of distilled water, ethanol (95%, JT Baker, NJ, USA), and methanol (99%, JT Baker, NJ, USA) and then soaked for 3 days at room temperature (25 • C). After that, the soaked sample was shaken at 2500 rpm for 5 min by using a shaker (OHAUS) and then filtered with Whatman No. 1. The filtered sample was evaporated to dryness by using a rotary evaporator (IKA model RV8, Staufen im Breisgau, Germany). The crude extract was weighed and redissolved in dimethyl sulfoxide (RCI Labscan, Bangkok, Thailand). The crude extract was stored in a refrigerator at 4 • C prior to analysis.

Characterization of Extract by LC-QTOF-MS
The qualitative dataset of the extracted sample was qualified by using LC-MS in tandem with a quadrupole time-of-flight mass spectrometer (QTOF-MS), according to the adopted method of Chiwat et al. (2021) [24]. In brief, the extracted samples were dissolved in 0.01% formic acid and ethanol (1:1, v/v) at a concentration of 1 mg/mL and cleaned up using a dispersive SPE kit with fat and pigments (Agilent Technology, Santa Clara, CA, USA). The sample solution was filled through a 0.22 µm filter. The qualitative dataset was determined using an Agilent 1290 Infinity II series coupled to a 6546 LC/Q-TOF instrument (Agilent Tech., Santa Clara, CA, USA), which consisted of a degasser, binary pump, column oven, and thermostat autosampler. The instrument settings were optimized as follows: LC conditions, UV at 330 nm; 0.2 mL/min flow rate; injection volume of 10 µL; and a mobile gradient system starting with 5% ACN and 95% water (1% formic acid), decreasing to 20% ACN in 5 min, 30% ACN in 5 min, 35% ACN in 5 min, 45% ACN in 5 min, 75% ACN in 5 min, and 95% ACN until the run ended. The chromatographic separation was accomplished using a ZORBAX Eclipse Plus C18 column (2.1 × 150 mm, 1.8 µm). The MS conditions involved an electrospray ionization (ESI) probe in the positive mode. The nebulizer was operated at 20 psi with a 7 L/min N 2 flow. The capillary temperature was kept at 300 • C; the flow rate was set at 8 µL/min. The m/z range was 50-1000, the capillary voltage was 4500 V, and the dry heater temperature was 280 • C. The experimentally measured mass of each ion was evaluated against the exact mass of the molecular formula and the expected isotope pattern for that formula. These data were used to score the match of the ions with the database by the MassHunter Qualitative Analysis Software (Agilent MassHunter Workstation Qualitative Analysis version 10.0, California, USA) find-by-formula search of the Agilent MassHunter METLIN Metabolomics Database. The chemical parameters for compounds were determined using the Medlin library.

DPPH Radical Scavenging Activity
The free radical scavenging activity of the plant extract was determined using the method of Siok Peng Kek et al. (2017) [25]. In brief, the sample was analyzed using a 1,1-diphenyl-2-picryhydrazyl (DPPH) assay with minor modifications. The DPPH stock solution was prepared by dissolving 24 mg of DPPH in 100 mL of methanol. The absorbance of a working DPPH solution containing 10 mL of DPPH stock solution was adjusted to 1.1 at 517 nm, by diluting it with 45 mL of methanol. The DPPH working solution (100 µL) was mixed with 100 µL of plant extract solution (0.0156-1.000 mg/mL) in a 96-well plate. After incubation in the dark for 30 min, the absorbance was measured at 517 nm using a microtiter plate reader. The DPPH free radical scavenging activity was calculated as a percentage using the formula DPPH = [(A control − A sample )/A control ] × 100, where A control and A sample are the absorbance readings of the control and sample, respectively. The IC 50 value for DPPH free radical scavenging activity corresponds to the sample concentration necessary to inhibit 50% of DPPH free radicals. The IC 50 was determined graphically from the curve plot between the percentage of DPPH scavenging activity and sample concentration.

ABTS Radical Scavenging Activity
ABTS was used to determine the antioxidative potential based on the method described by Arnao et al. (2001) [26]. The ABTS reagent used 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt as a stable radical in an aqueous solution, and this solution was green. The absorbance measured at a wavelength of 734 nm is the value of the relationship between the percent inhibition of ABTS and sample concentration. ABTS radicals were produced by the reaction between 7 mM ABTS in water and 2.45 mM potassium persulfate and stored in the dark at room temperature for 12-16 h before use. The ABTS solution was then diluted with 80% ethanol to obtain an absorbance of 0.7 ± 0.02 at 734 nm. The ABTS working solution (190 µL) was added to a 96-well plate containing 10 µL of plant extract (0.0156-1.000 mg/mL). After incubation in the dark for 10 min, the absorbance was measured at 734 nm. An appropriate solvent blank was run in each assay. All measurements were carried out at least three times. The percent inhibition of absorbance at 734 nm was calculated using the formula ABTS radical scavenging effect (%) = [(A ab − A a )/A ab ] × 100, where A ab is the absorbance of ABTS radical + methanol and A a is the absorbance of ABTS radical + sample extract/standard. Trolox was used as a standard substance.

Ferric Ion Reducing Antioxidant Power Assay
The FRAP assay was performed using the method of Siok Peng Kek et al. (2017) [25]. In brief, 2.5 mL of 10 mM TPTZ (2,4,6-tripyridyl-s-trizine) solution in 40 mM HCl, 2.5 mL of 20 mM ferric chloride (FeCl 3 ), and 25 mL of 300 mM acetate buffer at a pH of 3.6 were combined to make the FRAP reagent. Each 1 g of plant extract solution was diluted two times with distilled water, and aliquots of 10 µL of plant extract solution were combined with 190 µL of FRAP reagent on a 96-well microtiter plate. After 30 min in the dark, the absorbance of the sample was measured at 593 nm with a microtiter plate reader. Ascorbic acid was used for the standard curve (3.125-200 µg/mL), and FRAP was calculated against the standard curve. The result was expressed as milligrams of ascorbic acid equivalent per 100 g of plant extract (mg AAE/100 g).

Total Phenolic Compound Content
The total phenolic compound content was determined using the Folin-Ciocalteu method, which was modified by Dewanto et al. (2002) [27]. Gallic acid (Fluka, Switzerland) was used as the standard material in this method. As a result, the total phenolic content is given in milligrams of gallic acid per gram of sample weight. Gallic acid was used as the standard ingredient to produce the standard curve. Different concentrations of gallic acid of 0.02, 0.04, 0.08, 0.16, 0.32, and 0.64 mg/mL were obtained in 80% methanol by combining 12.5 µL of the sample and 12.5 µL of the Folin-Ciocalteau solution (MERCK, Germany) diluted 10 times with distilled water. After 6 min, 125 µL of 7% sodium carbonate (Na 2 CO 3 ) and 100 µL of distilled water were added, and the mixture was allowed to react at room temperature for 90 min. After that, the absorbance was measured at 760 nm using a microplate reader (SPECTROstar Nano ). A calibration curve was used to quantify the phenolic concentration. The results were given in milligrams of gallic acid equivalents per gram of sample (mg GAE/g sample).

Total Flavonoid Content
The total flavonoid content was measured by a colorimetric assay described previously by Miliauskas et al. (2004) [28], with slight modifications. A total of 25 µL of sample solution was placed into a 96-well plate, and 7.5 µL of 7% NaNO 2 solution (LOBA CHEMIE PVT. Ltd.) and 12.5 µL of distilled water were added and mixed thoroughly. The solution was allowed to stand at room temperature for 5 min. Next, 15 µL of 10% AlCl 3 solution (QRëC) was added to the flask, mixed well, and kept at room temperature for 5 min. Finally, 50 µL of 1 M NaOH solution (ACI Labscan) and 27.5 µL of distilled water were added, mixed well, and kept at room temperature for 5 min. Absorbance at 510 nm was measured against the water blank using a microplate reader (SPECTROstar Nano ), and the concentration of flavonoids was estimated using calibration curves. The results were expressed as micrograms of quercetin equivalents per gram of sample (µg QE/g sample).

Anti-Inflammatory Activity
The method for stabilizing the membrane of human red blood cells (HRBC) was used [29].
For the plant sample solution, the sample was prepared at concentrations of 1000, 500, and 100 µg/mL in a buffer solution with a pH of 7.4.
For red blood cell preparation, Alsever solution (SIGMA-ALDRICH, Gillingham, UK) was added to the collected volunteers' blood. The samples were centrifuged at 3000 rpm for 20 min at 4 • C with gentle shaking. Only red blood cells were collected, the NaCl solution was added, and the mixture was gently shaken. The samples were centrifuged again at 3000 rpm for 20 min at 4 • C. Only red blood cells were stored for analysis.
For preparation of 10% v/v HRBC, Add 9 mL of NaCl solution to 1 mL of washed red blood cells and then gently shake well.
For sample analysis, one milliliter of a buffer solution with a pH of 7.4 was pipetted into the test tube. Then add 2 mL of NaCl solution, 0.5 mL of 10% v/v HRBC, and 0.5 mL of sample solution in the test tube. Then, the mixture was gently shaken. The samples were incubated for 30 min at 37 • C in a water bath and then centrifuged at 3000 rpm for 10 min. The absorbance of the solution was measured at a wavelength of 560 nm. The control was 10% v/v HRBC solution + distilled water.
The calculation method was as follows: where A 0 = absorbance of control; A 1 = absorbance of the sample.

Antibacterial Activity
The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined using the method of Prashik Parvekar et al. (2022) [30]. In brief, by observing the visible growth of bacteria in the agar broth, the standard broth dilution method (CLSI M07-A8) was employed to investigate the antimicrobial effectiveness of the extracts. Serial twofold dilutions of S. corburalia and S. glabra, with adjusted bacterial concentrations from 500 mg/mL to 15.625 mg/mL (the turbidity was equal to 0.5 McFarland standard turbidity, which was approximately 1 × 10 8 CFU/mL), were used to determine the MIC in LB broth. The control contained only inoculated broth with 1 mg/mL gentamycin and was incubated for 12 h at 37 • C. The extracted concentration at no visible growth in the tubes is known as the MIC endpoint. To confirm the MIC value, the visual turbidity of the tubes was measured both before and after incubation. Following the MIC analysis of the extracts, each tube was seeded on LB agar plates and incubated for 12 h at 37 • C. The MBC endpoint occurs when the bacterial population is eliminated at the lowest antimicrobial agent concentration. This was accomplished by looking for bacteria on pre-and postincubated agar plates.

Conclusions
S. glabra and S. corbularia extracted with ethanol, methanol and water have bioactive potential, can have antioxidant capacity and contain phenolic and flavonoid compounds. The antimicrobial results revealed that both samples inhibited Gram-positive bacteria more than Gram-negative bacteria. The anti-inflammatory results showed the highest protective effect, and LC-QTOF/MS analysis showed that it was due to stilbene longistyline A, CAY10435 (oxazolopyridine) and flavonoids such as (-)-neolinderatin and neolinderatone. S. glabra and S. corbularia might be exploited as possible sources for folk medicine for the discovery of novel products as antibacterial, anti-inflammatory, and antioxidant agents.