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2000
Volume 24, Issue 2
  • ISSN: 2211-3525
  • E-ISSN: 2211-3533

Abstract

Introduction

The bioactive constituents found in herbal medicines play a crucial role in their therapeutic effects. is a well-known medicinal plant, traditionally used for the treatment of kidney and bladder-related ailments. In Ayurveda, its bark has been employed for over 3,000 years as a natural remedy for various kidney disorders.

Objective

In this research article, the ethanolic bark extract of was characterized through physical evaluation, preliminary phytochemical screening, LC-MS, FT-IR, and HPTLC analyses, along with assessments of its antioxidant and antimicrobial activities.

Methods

The extraction process was performed using petroleum ether, and 150 g of weighed powdered bark was carried out in a Soxhlet apparatus for 36 hours. The extraction was completed by putting one drop from a thimble onto a filter paper that exhibited no oil spots. The bark marcs were removed and allowed to dry before being individually exposed to a 24-hour hot extraction process using 90% ethanol in a soxhlet apparatus. The solvent was vaporized and concentrated to produce a dry residue after the extraction.

Results and Discussion

LC-MS analysis identified several major phytoconstituents in the ethanolic extract, including scoulerin, formononetin, L-carnosine, resveratrol, flavanone, quercetin, kaempferide, rhamnetin, daidzein, and isorhamnetin. FT-IR spectroscopy revealed characteristic peaks corresponding to various functional groups present in the extract. HPTLC studies confirmed the presence of active compounds, such as lupeol and gallic acid. Phytochemical screening of bark extract further detected saponins, glycosides, alkaloids, anthraquinones, flavonoids, and tannins. This study also demonstrated notable antioxidant and antimicrobial activities associated with the plant extract.

Conclusion

It can be concluded that bark contains numerous bioactive compounds, making it a valuable plant for phytopharmaceutical applications. The ethanolic extracts of bark demonstrated significant antioxidant and antimicrobial activities. For the first time, LC-MS and HPTLC analyses revealed high contents of L-anserine nitrate, resveratrol, flavanone, chlorogenic acid hemihydrate, quercetin, kaempferide, isorhamnetin, rhamnetin, gallic acid, and lupeol, which likely contribute to these biological effects. Additionally, the study suggests that the ethanolic extract may possess antibiotic, anti-inflammatory, antibacterial, antioxidant, antidiabetic, anticancer, and anti-obesity properties due to the presence of 16 phytochemical compounds identified by LC-MS. Fluorescent analysis of the bark powder showed characteristic coloration upon exposure to various chemical reagents, supporting the presence of diverse phytochemicals. Preliminary phytochemical screening further confirmed the presence of saponins, alkaloids, flavonoids, anthraquinones, glycosides, and tannins in the ethanolic bark extract.

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References

  1. KendreN. SalunkeM. WakureB. WakteP. HR-LCMS based phytochemical analysis and anticancer activity of Triumfetta rhomboidea with molecular docking approach.J. Appl. Pharm. Sci.2024140320921910.7324/JAPS.2024.148412
    [Google Scholar]
  2. GomathiD. RavikumarG. KalaiselviM. VidyaB. UmaC. HPTLC fingerprinting analysis of Evolvulus alsinoides (L.) L.J. Acute Med.201223778210.1016/j.jacme.2012.08.004
    [Google Scholar]
  3. BhattacharjeeA. ShashidharaS.C. Phytochemical and ethno-pharmacological profile of Crataeva nurvala Buch-Hum (Varuna): A review.Asian Pac. J. Trop. Biomed.201222S1162S116810.1016/S2221‑1691(12)60379‑7
    [Google Scholar]
  4. KumarD. SharmaS. KumarS. Botanical description, phytochemistry, traditional uses, and pharmacology of Crataeva nurvala Buch. Ham.: An updated review.Future J. Pharm. Sci.20206111310.1186/s43094‑020‑00106‑1
    [Google Scholar]
  5. HajjiM. JarrayaR. LassouedI. MasmoudiO. DamakM. NasriM. GC/MS and LC/MS analysis, and antioxidant and antimicrobial activities of various solvent extracts from Mirabilis jalapa tubers.Process Biochem.20104591486149310.1016/j.procbio.2010.05.027
    [Google Scholar]
  6. SmithB.C. Fundamentals of fourier transform infrared spectroscopy2nd ed120710.1201/b10777
    [Google Scholar]
  7. MohamedM.A. JaafarJ. IsmailA.F. OthmanM.H.D. RahmanM.A. Fourier transform infrared (FTIR) spectroscopy.Membrane Characterization.Elsevier201732910.1016/B978‑0‑444‑63776‑5.00001‑2
    [Google Scholar]
  8. SoniaK. BeddiB.S. LakshmiK.S. HPTLC method development and validation: An overview.J. Pharm. Sci.201795652657
    [Google Scholar]
  9. ShuklaR. SinghP.K. UpadhyayS. A comprehensive review of high-performance thin layer chromatography (HPTLC).IJPPR2023271398410
    [Google Scholar]
  10. PratimaN.A. GadikarR. Liquid chromatography-mass spectrometry and its applications: A brief review.Arch. Org. Inorg. Chem. Sci.201811263410.32474/AOICS.2018.01.000103
    [Google Scholar]
  11. TeohW.Y. YongY.S. RazaliF.N. StephenieS. Dawood ShahM. TanJ.K. GnanarajC. Mohd EsaN. LC-MS/MS and GC-MS analysis for the identification of bioactive metabolites responsible for the antioxidant and antibacterial activities of Lygodium microphyllum (Cav.).R. Br. Separations202310321510.3390/separations10030215
    [Google Scholar]
  12. DwivediM.K. SonterS. MishraS. SinghP. SinghP.K. Secondary metabolite profiling and characterization of diterpenes and flavones from the methanolic extract of Andrographis paniculata using HPLC-LC-MS/MS.Future J. Pharm. Sci.20217118410.1186/s43094‑021‑00292‑6
    [Google Scholar]
  13. NursantyR. Phytochemical analysis of ethanolic Psidium guajava leaves extract using GC-MS and LC-MS.Biodiversitas20232452723273210.13057/biodiv/d240526
    [Google Scholar]
  14. EvansW.C. Trease and evans pharmacognosy.15th edLondonSaunders Ltd2003545547
    [Google Scholar]
  15. Quality control methods for medicinal plants materialWorld Health Organization1998
    [Google Scholar]
  16. HoughtonP. RamanA. Laboratory hand book for the fractionation of natural extracts.New York, NYSpringer201210.1007/978‑1‑4615‑5809‑5
    [Google Scholar]
  17. KhandelwalK.R. Practical pharmacognosy techniques and experiments.ScienceOpen, Inc.2016
    [Google Scholar]
  18. GuptaM.K. SharmaP.K. AnsariS.H. LagarkhaR. Pharmacognostical evaluation of Grewia asiatica fruits.Int. J. Plant Sci.200612249251
    [Google Scholar]
  19. AnsariS.H. Essential of pharmacognosy.Birla publications Pvt, Ltd2006
    [Google Scholar]
  20. OniszczukA. OlechM. OniszczukT. Wojtunik-KuleszaK. WójtowiczA. Extraction methods, LC-ESI-MS/MS analysis of phenolic compounds and antiradical properties of functional food enriched with elderberry flowers or fruits.Arab. J. Chem.20191284719473010.1016/j.arabjc.2016.09.003
    [Google Scholar]
  21. FowlerP.W. WrightC. SpiersH. ZhuT. BaetenE.M.L. HoosdallyS.W. Gibertoni CruzA.L. RoohiA. KouchakiS. WalkerT.M. PetoT.E.A. MillerG. LintottC. CliftonD. CrookD.W. WalkerA.S. A crowd of BashTheBug volunteers reproducibly and accurately measure the minimum inhibitory concentrations of 13 antitubercular drugs from photographs of 96-well broth microdilution plates.eLife202211e7504610.7554/eLife.75046 35588296
    [Google Scholar]
  22. AdelekeA.R. TawakaltuM.B. Busari. Comparative in vitro antioxidant activities of aqueous extract of Garcinia kola and Buchholzia coriacea seeds.Tanzan. J. Sci.20204649850710.4314/tjs.v46i2.18
    [Google Scholar]
  23. ImamM.Z. AkterS. MazumderM.E.H. RanamM.D. Antioxidant activities of different parts of Musa sapientum L. ssp. sylvestris fruit.J. Appl. Pharm. Sci.20111106872
    [Google Scholar]
  24. HabartovaK. HavelekR. SeifrtovaM. KralovecK. CahlikovaL. ChlebekJ. CermakovaE. MazankovaN. MarikovaJ. KunesJ. NovakovaL. RezacovaM. Scoulerine affects microtubule structure, inhibits proliferation, arrests cell cycle and thus culminates in the apoptotic death of cancer cells.Sci. Rep.201881482910.1038/s41598‑018‑22862‑0 29555944
    [Google Scholar]
  25. TianJ. WangX.Q. TianZ. Focusing on formononetin: Recent perspectives for its neuroprotective potentials.Front. Pharmacol.20221390589810.3389/fphar.2022.905898 35712702
    [Google Scholar]
  26. LiewS.C. Folic acid and diseases - supplement it or not?Rev. Assoc. Med. Bras.20166219010010.1590/1806‑9282.62.01.90 27008500
    [Google Scholar]
  27. AliS.A. AliL. FaddaM. ElebiaryH. SolimanM. Evaluation of the radioprotective action of anserine along with zinc in albino rats exposed to gamma-radiation.J. Appl. Pharm. Sci.201220411512210.7324/JAPS.2012.2419
    [Google Scholar]
  28. SureshkumarK. DurairajM. SrinivasanK. GohK.W. UndelaK. MahalingamV.T. Effect of L-carnosine in patients with age-related diseases: A systematic review and meta-analysis.Front. Biosci.20232811810.31083/j.fbl2801018 36722274
    [Google Scholar]
  29. SalehiB. MishraA.P. NigamM. SenerB. KilicM. Sharifi-RadM. FokouP.V.T. MartinsN. Sharifi-RadJ. Resveratrol: A double-edged sword in health benefits.Biomedicines2018639110.3390/biomedicines6030091 30205595
    [Google Scholar]
  30. BrahmachariG. Naturally occurring flavanones: An overview.Nat. Prod. Commun.2008381934578X080030082010.1177/1934578X0800300820
    [Google Scholar]
  31. Al-MashhadaneF.A. Al-MashhadaneA.A. Rhman TaqaA.A. Folic acid supplementation: A review of the known advantages and risks.Public Health Prev. Med.2018435159
    [Google Scholar]
  32. MichelP. DobrowolskaA. KicelA. OwczarekA. BazylkoA. GranicaS. PiwowarskiJ. OlszewskaM. Polyphenolic profile, antioxidant and anti-inflammatory activity of eastern teaberry (Gaultheria procumbens L.) leaf extracts.Molecules20141912204982052010.3390/molecules191220498 25493634
    [Google Scholar]
  33. ScottI.M. HorganR. McGawB.A. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue.Planta1980149547247510.1007/BF00385750 24306475
    [Google Scholar]
  34. MaalikA. KhanF.A. MumtazA. MehmoodA. AzharS. AtifM. KarimS. AltafY. TariqI. Pharmacological applications of quercetin and its derivatives: A short review.Trop. J. Pharm. Res.20141391561156610.4314/tjpr.v13i9.26
    [Google Scholar]
  35. ShahbazM. ImranM. AlsagabyS.A. NaeemH. Al AbdulmonemW. HussainM. AbdelgawadM.A. El-GhorabA.H. GhoneimM.M. El-SherbinyM. AtokiA.V. AwuchiC.G. Anticancer, antioxidant, ameliorative and therapeutic properties of kaempferol.Int. J. Food Prop.20232611140116610.1080/10942912.2023.2205040
    [Google Scholar]
  36. GongG. GuanY.Y. ZhangZ.L. RahmanK. WangS.J. ZhouS. LuanX. ZhangH. Isorhamnetin: A review of pharmacological effects.Biomed. Pharmacother.202012811030110.1016/j.biopha.2020.110301 32502837
    [Google Scholar]
  37. MedeirosD.L. LimaE.T.G. SilvaJ.C. MedeirosM.A. PinheiroE.B.F. Rhamnetin: A review of its pharmacology and toxicity.J. Pharm. Pharmacol.202274679379910.1093/jpp/rgab163 34931654
    [Google Scholar]
  38. SunM-Y. YeY. XiaoL. RahmanK. XiadW. ZhangH. Daidzein: A review of pharmacological effects.Afr. J. Tradit. Complement. Altern. Med.201613311713210.21010/ajtcam.v13i3.15
    [Google Scholar]
  39. KapoorR. HuangY.S. Gamma linolenic acid: An antiinflammatory omega-6 fatty acid.Curr. Pharm. Biotechnol.20067653153410.2174/138920106779116874 17168669
    [Google Scholar]
  40. Mendham DenneyJ.R.C. BarnesJ.D. ThomasM. SivasankarB. Vogel`s Text book of quantitative chemical analysis6th ed678
    [Google Scholar]
  41. SharmaY.R. Elementary organic spectroscopy Principles and chemical applications.5th edS Chand Publishing2023
    [Google Scholar]
  42. LiuQ.L. ChenA.H. TangJ.Y. MaY.L. JiangZ.H. LiuY.P. ChenG.Y. FuY.H. XuW. A new indole alkaloid with anti-inflammatory activity from Nauclea officinalis.Nat. Prod. Res.201731182107211210.1080/14786419.2016.1277351 28067066
    [Google Scholar]
  43. BenelliG. MaggiF. PetrelliR. CanaleA. NicolettiM. RakotosaonaR. RasoanaivoP. Not ordinary antimalarial drugs: Madagascar plant decoctions potentiating the chloroquine action against Plasmodium parasites.Ind. Crops Prod.2017103193810.1016/j.indcrop.2017.03.032
    [Google Scholar]
  44. SunN. HanY. Cytotoxic isoquinoline alkaloids from the roots of Thalictrum foliolosum.J. Asian Nat. Prod. Res.20212311810.1080/10286020.2019.1694515 31773979
    [Google Scholar]
  45. El HazzamK. HafsaJ. SobehM. MhadaM. TaourirteM. EL KacimiK. YasriA. An insight into saponins from quinoa (Chenopodium quinoa Willd): A review.Molecules2020255105910.3390/molecules25051059 32120971
    [Google Scholar]
  46. HussainG. HuangJ. RasulA. AnwarH. ImranA. MaqboolJ. RazzaqA. AzizN. MakhdoomE.H. KonukM. SunT. Putative roles of plant-derived tannins in neurodegenerative and neuropsychiatry disorders: An updated review.Molecules20192412221310.3390/molecules24122213 31200495
    [Google Scholar]
  47. JucáM.M. Cysne FilhoF.M.S. de AlmeidaJ.C. MesquitaD.S. BarrigaJ.R.M. DiasK.C.F. BarbosaT.M. VasconcelosL.C. LealL.K.A.M. RibeiroJ.E. VasconcelosS.M.M. Flavonoids: Biological activities and therapeutic potential.Nat. Prod. Res.202034569270510.1080/14786419.2018.1493588 30445839
    [Google Scholar]
  48. TianJ. MoJ. XuL. ZhangR. QiaoY. LiuB. JiangL. MaS. ShiG. Scoulerine promotes cell viability reduction and apoptosis by activating ROS-dependent endoplasmic reticulum stress in colorectal cancer cells.Chem. Biol. Interact.202032710918410.1016/j.cbi.2020.109184 32590070
    [Google Scholar]
  49. Tay, Kai-Ching; Tan, Loh Teng-Hern; Chan, Chin Kei; Hong, Sok Lai Formononetin: A review of its anticancer potentials and mechanisms.Front. Pharmacol.20191010.3389/fphar.2019.00820
    [Google Scholar]
  50. Machado DutraJ. EspitiaP.J.P. Andrade BatistaR. Formononetin: Biological effects and uses - A review.Food Chem.202135912997510.1016/j.foodchem.2021.129975 33962193
    [Google Scholar]
  51. JainP.G. NayseP.G. PatilD.J. ShindeS.D. SuranaS.J. The possible antioxidant capabilities of formononetin in guarding against streptozotocin-induced diabetic nephropathy in rats.Future J. Pharm. Sci.2020615310.1186/s43094‑020‑00071‑9
    [Google Scholar]
  52. SinghL. KaurH. Chandra AryaG. BhattiR. Neuroprotective potential of formononetin, a naturally occurring isoflavone phytoestrogen.Chem. Biol. Drug Des.20241031e1435310.1111/cbdd.14353 37722967
    [Google Scholar]
  53. MahmoudvandH. Khudair KhalafA. KarbasianN. MasooriL. Zareh RajabiP. SakiM. Ghasemian YadegariJ. Promising effects of formononetin, a natural isoflavone derived from herbs, against Toxoplasma gondii.J. Herbmed. Pharmacol.202312336236610.34172/jhp.2023.39
    [Google Scholar]
  54. CarusoG. Di PietroL. CardaciV. MaugeriS. CaraciF. The therapeutic potential of carnosine: Focus on cellular and molecular mechanisms.Curr. Res. Pharmacol. Drug Discov.2023410015310.1016/j.crphar.2023.100153 37441273
    [Google Scholar]
  55. AlvarezM.A.R.V. MoreiraM.A.R.R. PonceA. Antiquorum sensing and antimicrobial activity of natural agents with potential use in food.J. Food Saf.201232337938710.1111/j.1745‑4565.2012.00390.x
    [Google Scholar]
  56. MakwanaS.M. Study of antibacterial property of plant based phenolic compounds and food contact materials coated with functionalized nanoparticles.Southern Illinois University at Carbondale2013
    [Google Scholar]
  57. Abu-AmeroK. KondkarA. ChalamK. Resveratrol and ophthalmic diseases.Nutrients20168420021010.3390/nu8040200 27058553
    [Google Scholar]
  58. OliveiraAR DominguesFC FerreiraS The influence of resveratrol adaptation on resistance to antibiotics, benzalkonium chloride, heat and acid stresses of Staphylococcus aureus and Listeria monocytogenes. Food. Control.201773Part B1420142510.1016/j.foodcont.2016.11.011
    [Google Scholar]
  59. SeukepJ.A. SandjoL.P. NgadjuiB.T. KueteV. Antibacterial and antibiotic-resistance modifying activity of the extracts and compounds from Nauclea pobeguinii against Gram-negative multi-drug resistant phenotypes.BMC Complement. Altern. Med.201616119310.1186/s12906‑016‑1173‑2 27386848
    [Google Scholar]
  60. ZhangL.X. LiC.X. KakarM.U. KhanM.S. WuP.F. AmirR.M. DaiD.F. NaveedM. LiQ.Y. SaeedM. ShenJ.Q. RajputS.A. LiJ.H. Resveratrol (RV): A pharmacological review and call for further research.Biomed. Pharmacother.202114311216410.1016/j.biopha.2021.112164 34649335
    [Google Scholar]
  61. HădărugăD.I. HădărugăN.G. Flavanones in Plants and Humans. In: Jafari, S.M., Rashidinejad, A., Simal-Gandara, J. (eds) Handbook of Food Bioactive Ingredients. Springer, Cham.2023, pp. 1-53.10.1007/978‑3‑030‑81404‑5_6‑1
    [Google Scholar]
  62. DawidowiczA.L. TypekR. HołowińskiP. Olszowy-TomczykM. The hydrates of chlorogenic acid in its aqueous solution and in stored food products.Eur. Food Res. Technol.2024250102669268010.1007/s00217‑024‑04567‑z
    [Google Scholar]
  63. ParasuramanS. Anand DavidA.V. ArulmoliR. Overviews of biological importance of quercetin: A bioactive flavonoid.Pharmacogn. Rev.20161020848910.4103/0973‑7847.194044 28082789
    [Google Scholar]
  64. AghababaeiF. HadidiM. Recent advances in potential health benefits of quercetin.Pharmaceuticals2023167102010.3390/ph16071020 37513932
    [Google Scholar]
  65. WangG. WangY. YaoL. GuW. ZhaoS. ShenZ. LinZ. LiuW. YanT. Pharmacological activity of quercetin: An updated review.Evid. Based Complement. Alternat. Med.2022202211210.1155/2022/3997190 36506811
    [Google Scholar]
  66. BahareS. MachinL. MonzoteL. Sharifi-RadJ. ShahiraM. SalemM.A. RanaM.M. NihalM.E.M. CeydaS.K. Therapeutic potential of quercetin: New insights and perspectivesfor human health.ACS Omega2020520118491187210.1021/acsomega.0c01818 32478277
    [Google Scholar]
  67. SongB. NiuW. ZhangS. HaoM. LiY. ChenQ. LiS. TongC. A mechanistic review of the pharmacological aspects of Kaempferide as a natural compound.Heliyon20241019e3824310.1016/j.heliyon.2024.e38243 39397988
    [Google Scholar]
  68. SartoriA.A. SonN.T. Silva, MD Effects of Caatinga propolis from Mimosa tenuiflora and its constituents (santin, sakuranetin and kaempferide) on human immune cells.J. Ethnopharmacol.2024319Pt 211729710.1016/j.jep.2023.117297 37813289
    [Google Scholar]
  69. LiH.L. LiS.M. LuoY.H. XuW-T. ZhangY. ZhangT. ZhangD-J. JinC-H. Kaempferide induces G0/G1 phase arrest and apoptosis via ROS-mediated signaling pathways in A549 human lung cancer cells.Nat. Prod Commun20201571934578X2093522610.1177/1934578X20935226
    [Google Scholar]
  70. WangY. MaJ. TongY. LiN. LiJ. QiZ. Antidiabetic effects and mechanisms of Cyclocarya paliurus leaf flavonoids via PIK3CA.J. Funct. Foods202411310603110.1016/j.jff.2024.106031
    [Google Scholar]
  71. KalaiF.Z. BoulaabaM. FerdousiF. IsodaH. Effects of isorhamnetin on diabetes and its associated complications: A review of in vitro and in vivo studies and a post hoc transcriptome analysis of involved molecular pathways.Int. J. Mol. Sci.202223270410.3390/ijms23020704 35054888
    [Google Scholar]
  72. SeoK. YangJ.H. KimS.C. KuS.K. KiS.H. ShinS.M. The antioxidant effects of isorhamnetin contribute to inhibit COX-2 expression in response to inflammation: A potential role of HO-1.Inflammation201437371272210.1007/s10753‑013‑9789‑6 24337631
    [Google Scholar]
  73. LiC. YangX. HuJ.B. LiaoJ.Z. Isorhamnetin suppresses the growth of gefitinib resistant human lung cancer PC9 cells.Herbal Med.201231831834
    [Google Scholar]
  74. ChauhanA.K. KimJ. LeeY. BalasubramanianP.K. KimY. Isorhamnetin has potential for the treatment of Escherichia coli-induced sepsis.Molecules20192421398410.3390/molecules24213984 31689976
    [Google Scholar]
  75. ZhanY. TaW. TangW. HuaR. WangJ. WangC. LuW. Potential antiviral activity of isorhamnetin against SARS-CoV-2 spike pseudotyped virus in vitro.Drug Dev. Res.20218281124113010.1002/ddr.21815 33847382
    [Google Scholar]
  76. Antunes-RicardoM. Gutiérrez-UribeJ.A. Martínez-VitelaC. Serna-SaldívarS.O. Topical anti-inflammatory effects of isorhamnetin glycosides isolated from Opuntia ficus-indica.BioMed Res. Int.201520151910.1155/2015/847320 25821823
    [Google Scholar]
  77. Farias-PereiraR. SavareseJ. YueY. LeeS.H. ParkY. Fat-lowering effects of isorhamnetin are via NHR-49-dependent pathway in Caenorhabditis elegans.Curr. Res. Food Sci.20202707610.1016/j.crfs.2019.11.002 32914113
    [Google Scholar]
  78. PatelR. PakradooniR. OakC. BhaskaranN. ShuklaS. Abstract 3507: Rhamnetin enhances anti-proliferative and apoptotic effects on prostate cancer cells.Cancer Res.20167614_Supplement350710.1158/1538‑7445.AM2016‑3507
    [Google Scholar]
  79. LeeH. KrishnanM. KimM. YoonY.K. KimY. Rhamnetin, a natural flavonoid, ameliorates organ damage in a mouse model of carbapenem-resistant Acinetobacter baumannii-induced sepsis.Int. J. Mol. Sci.202223211289510.3390/ijms232112895 36361685
    [Google Scholar]
  80. NisariM. BozkurtÖ. ErtekinT. CeylanD. İnançN. AlÖ. GülerH. UnurE. Rhamnetin improves antioxidant status in the liver of Ehrlich solid tumor bearing mice.Med. Sci. Discov20207549450010.36472/msd.v7i5.380
    [Google Scholar]
  81. GaeteL. TchernitchinA.N. BustamanteR. VillenaJ. LemusI. GidekelM. CabreraG. AstorgaP. Daidzein-estrogen interaction in the rat uterus and its effect on human breast cancer cell growth.J. Med. Food201215121081109010.1089/jmf.2011.0322 23216111
    [Google Scholar]
  82. PengY. ShiY. ZhangH. MineY. TsaoR. Anti-inflammatory and anti-oxidative activities of daidzein and its sulfonic acid ester derivatives.J. Funct. Foods20173563564010.1016/j.jff.2017.06.027
    [Google Scholar]
  83. ZhengM. ZhouM. ChenM. LuY. ShiD. WangJ. LiuC. Neuroprotective effect of daidzein extracted from Pueraria lobate radix in a stroke model via the Akt/mTOR/BDNF channel.Front. Pharmacol.20221277248510.3389/fphar.2021.772485 35095491
    [Google Scholar]
  84. PharmawatiM. WrasiatiL.P. Phytochemical screening and FTIR spectroscopy on crude extract from Enhalus acoroides leaves.Malays. J. Anal. Sci.20202417077
    [Google Scholar]
  85. SiddiqueH.R. SaleemM. Beneficial health effects of lupeol triterpene: A review of preclinical studies.Life Sci.2011887-828529310.1016/j.lfs.2010.11.020 21118697
    [Google Scholar]
  86. LimaV.N. Oliveira-TintinoC.D.M. SantosE.S. MoraisL.P. TintinoS.R. FreitasT.S. GeraldoY.S. PereiraR.L.S. CruzR.P. MenezesI.R.A. CoutinhoH.D.M. Antimicrobial and enhancement of the antibiotic activity by phenolic compounds: Gallic acid, caffeic acid and pyrogallol.Microb. Pathog.201699566110.1016/j.micpath.2016.08.004 27497894
    [Google Scholar]
  87. GuptaJ. Preliminary phytochemical investigation, antioxidant and antimicrobial activity of Jasminumpubescence leaves extracts.Res. J. Pharm. Technol.202013126073607610.5958/0974‑360X.2020.01058.6
    [Google Scholar]
  88. PalR.S. MishraA. Quality control assaessment of Dhatryadi Ghrita with HPTLC method.Curr. Biotechnol.20208210410810.2174/2211550108666190902123809
    [Google Scholar]
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