Plant extracts and phytochemicals targeting Alzheimer’s through acetylcholinesterase inhibition

Deepa A V , Dennis Thomas T

Exploration of Neuroscience ›› 2025, Vol. 4 ›› Issue (1) : 100697

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Exploration of Neuroscience ›› 2025, Vol. 4 ›› Issue (1) :100697 DOI: 10.37349/en.2025.100697
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Plant extracts and phytochemicals targeting Alzheimer’s through acetylcholinesterase inhibition
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Abstract

Alzheimer’s disease (AD) is a progressive neurodegenerative disease and the most common type of dementia, characterized by cognitive decline in later years of life. Among various hypotheses explaining AD pathology, the cholinergic hypothesis is one of the most studied. Though there are Food and Drug Administration (FDA) approved drugs (donepezil, galantamine, rivastigmine and tacrine) for AD treatment, their adverse effects make it urgent to develop new drugs with minimal side effects. This review focuses on the acetylcholinesterase (AChE) inhibitory potential of plant extracts and phytochemicals that could aid in preventing and mitigating AD. From the literature search, extracts of 28 species were found to have strong inhibition against AChE, with IC50 values ranging from 0.08 μg/mL to 10.0 μg/mL. The highest number of species with AChE inhibition belongs to the Amaryllidacea family, followed by Fabaceae, Lycopodiaceae, Amaranthaceae and Anacardiaceae. Several phytochemicals, including alkaloids, terpenoids and phenolics, show a multitarget approach in AD therapy, exhibiting more than one of the following activities such as inhibition of AChE, butyrylcholinesterase (BuChE), MAO-A, beta site amyloid precursor protein cleaving enzyme 1 (BACE-1), β-amyloid (Aβ) aggregation, tau phosphorylation, and an ability to cross blood-brain barrier (BBB). With a multitarget approach and minimal side effects, they could revolutionise the treatment of AD. Many phytochemicals and their derivatives are under clinical and pre-clinical trials, potentially serving as prospective therapeutic drug candidates for treating AD. This review briefly discusses the findings and advances in knowledge about plant-derived bioactive compounds as potential new drugs acting as AChE inhibitors.

Keywords

Alzheimer’s / acetylcholinesterase / plant extract / phytochemicals / alkaloids / phenolics / flavonoids / terpenoids

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Deepa A V, Dennis Thomas T. Plant extracts and phytochemicals targeting Alzheimer’s through acetylcholinesterase inhibition. Exploration of Neuroscience, 2025, 4 (1) : 100697 DOI:10.37349/en.2025.100697

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References

[1]

Santos TCD,Gomes TM,Pinto BAS,Camara AL,Paes AMdA.Naturally Occurring Acetylcholinesterase Inhibitors and Their Potential Use for Alzheimer’s Disease Therapy.Front Pharmacol.2018;9:1192.

[2]

Fiest KM,Roberts JI,Maxwell CJ,Hogan DB,Smith EE,Frolkis A,et al.The Prevalence and Incidence of Dementia Due to Alzheimer’s Disease: a Systematic Review and Meta-Analysis.Can J Neurol Sci.2016;43:S51-82.

[3]

Scheltens P,Blennow K,Breteler MMB,Strooper Bd,Frisoni GB,Salloway S,et al.Alzheimer’s disease.Lancet.2016;388:505-17.

[4]

Prince M,Wimo A,Guerchet M,Ali GC,Prina M.World Alzheimer Report 2015. The Global Impact of Dementia. An Analysis of Prevalence, Incidence, Cost and Trends.Alzheimer’s Dis Int.2015

[5]

2021 Alzheimer’s disease facts and figures.Alzheimers Dement.2021;17:327-406.

[6]

Abubakar MB,Sanusi KO,Ugusman A,Mohamed W,Kamal H,Ibrahim NH,Khoo CS,Kumar J.Alzheimer’s Disease: An Update and Insights Into Pathophysiology.Front Aging Neurosci.2022;14:742408.

[7]

Savelieff MG,Lee S,Liu Y,Lim MH.Untangling amyloid-β, tau, and metals in Alzheimer’s disease.ACS Chem Biol.2013;8:856-65.

[8]

Trippier PC,Labby KJ,Hawker DD,Mataka JJ,Silverman RB.Target- and mechanism-based therapeutics for neurodegenerative diseases: strength in numbers.J Med Chem.2013;56:3121-47.

[9]

Agis-Torres A,Sölhuber M,Fernandez M,Sanchez-Montero JM.Multi-Target-Directed Ligands and other Therapeutic Strategies in the Search of a Real Solution for Alzheimer’s Disease.Curr Neuropharmacol.2014;12:2-36.

[10]

Blaikie L,Kay G,Lin PKT.Current and emerging therapeutic targets of alzheimer’s disease for the design of multi-target directed ligands.Medchemcomm.2019;10:2052-72.

[11]

Taqui R,Debnath M,Ahmed S,Ghosh A.Advances on plant extracts and phytocompounds with acetylcholinesterase inhibition activity for possible treatment of Alzheimer’s disease.Phytomed Plus.2022;2:100184.

[12]

Sutherland GT,Siebert GA,Kril JJ,Mellick GD.Knowing me, knowing you: can a knowledge of risk factors for Alzheimer’s disease prove useful in understanding the pathogenesis of Parkinson’s disease?J Alzheimers Dis.2011;25:395-415.

[13]

Selkoe DJ,Hardy J.The amyloid hypothesis of Alzheimer’s disease at 25 years.EMBO Mol Med.2016;8:595-608.

[14]

K P,Prasanth DSNBK,Shadakshara MKR,Ahmad SF,Seemaladinne R,Rudrapal M,et al.Citronellal as a Promising Candidate for Alzheimer’s Disease Treatment: A Comprehensive Study on In Silico and In Vivo Anti-Acetylcholine Esterase Activity.Metabolites.2023;13:1133.

[15]

Murray AP,Faraoni MB,Castro MJ,Alza NP,Cavallaro V.Natural AChE Inhibitors from Plants and their Contribution to Alzheimer’s Disease Therapy.Curr Neuropharmacol.2013;11:388-413.

[16]

Anand R,Gill KD,Mahdi AA.Therapeutics of Alzheimer’s disease: Past, present and future.Neuropharmacology.2014;76:27-50.

[17]

Masondo NA,Stafford GI,Aremu AO,Makunga NP.Acetylcholinesterase inhibitors from southern African plants: An overview of ethnobotanical, pharmacological potential and phytochemical research including and beyond Alzheimer’s disease treatment.S Afr J Bot.2019;120:39-64.

[18]

Khan H,MaryaAmin S,Kamal MA,Patel S.Flavonoids as acetylcholinesterase inhibitors: Current therapeutic standing and future prospects.Biomed Pharmacother.2018;101:860-70.

[19]

Reid GA,Darvesh S.Interaction of exogenous acetylcholinesterase and butyrylcholinesterase with amyloid-β plaques in human brain tissue.Chem Biol Interact.2024;395:111012.

[20]

Xu H,Ferreira D,Londos E,Eriksdotter M.Cholinesterase inhibitors, cognitive decline, major cardiovascular events, and mortality in dementia with Lewy bodies.Alzheimer’s Dement.2023;19:e078017.

[21]

Patel A,Shah D,Patel Y,Patel S,Mehta M,Bambharoliya T.A Review on Recent Development of Novel Heterocycles as Acetylcholinesterase Inhibitor for the Treatment of Alzheimer’s Disease.Curr Drug Targets.2023;24:225-46.

[22]

Vecchio I,Sorrentino L,Paoletti A,Marra R,Arbitrio M.The State of The Art on Acetylcholinesterase Inhibitors in the Treatment of Alzheimer’s Disease.J Cent Nerv Syst Dis.2021;13:11795735211029113.

[23]

Gao Y,Liu Y,Li Y.Safety and efficacy of acetylcholinesterase inhibitors for Alzheimer’s disease: A systematic review and meta-analysis.Adv Clin Exp Med.2024;33:1179-87.

[24]

Yun Y,Miao Y,Sun X,Sun J,Wang X.Synthesis and biological evaluation of 2-arylbenzofuran derivatives as potential anti-Alzheimer’s disease agents.J Enzyme Inhib Med Chem.2021;36:1346-56.

[25]

Howes MJR,Houghton PJ.Acetylcholinesterase inhibitors of natural origin.Int J Biomed Pharm Sci.2009;3:67-86.

[26]

Fadaeinasab M,Basiri A,Kia Y,Karimian H,Ali HM,Murugaiyah V.New Indole Alkaloids from the Bark of Rauvolfia Reflexa and their Cholinesterase Inhibitory Activity.Cell Physiol Biochem.2015;37:1997-2011.

[27]

Majolo F,Hoffmann LF,Ana WLPS,Alves C,Silva J,Martins A,et al.Recent Drugs Tested in Clinical Trials for Alzheimer’s and Parkinson’s Diseases Treatment: Current Approaches in Tracking New Drugs.Front Clin Drug Res: CNS Neurol Disord.2024;12:1-58.

[28]

Pratap GK,Shantaram M.An Alternative Approach for Anti-Alzheimer’s Compounds from Plant ExtractsPhytomedicine and Alzheimer’s Disease. CRC Press; 2020.

[29]

Nguyen K,Hoffman H,Chakkamparambil B,Grossberg GT.Evaluation of rivastigmine in Alzheimer’s disease.Neurodegener Dis Manag.2021;11:35-48.

[30]

Polinsky RJ.Clinical pharmacology of rivastigmine: a new-generation acetylcholinesterase inhibitor for the treatment of Alzheimer’s disease.Clin Ther.1998;20:634-47.

[31]

Haake A,Nguyen K,Friedman L,Chakkamparambil B,Grossberg GT.An update on the utility and safety of cholinesterase inhibitors for the treatment of Alzheimer’s disease.Expert Opin Drug Saf.2020;19:147-57.

[32]

Farlow MR,Grossberg GT,Sadowsky CH,Meng X,Somogyi M.A 24-week, randomized, controlled trial of rivastigmine patch 13.3 mg/24 h versus 4.6 mg/24 h in severe Alzheimer’s dementia.CNS Neurosci Ther.2013;19:745-52.

[33]

Shamsi A,Mohammad T,Anwar S,Alajmi MF,Hussain A,Hassan MI,et al.Probing the interaction of Rivastigmine Tartrate, an important Alzheimer’s drug, with serum albumin: Attempting treatment of Alzheimer’s disease.Int J Biol Macromol.2020;148:533-42.

[34]

Ray B,Maloney B,Sambamurti K,Karnati HK,Nelson PT,Greig NH,et al.Rivastigmine modifies the α-secretase pathway and potentially early Alzheimer’s disease.Transl Psychiatry.2020;10:47Erratum in: Transl Psychiatry. 2020;10:81.

[35]

Mohsin NA,Ahmad M.Donepezil: A review of the recent structural modifications and their impact on anti-Alzheimer activity.Braz J Pharm Sci.2020;56:e18325.

[36]

Colović MB,Krstić DZ,Lazarević-Pašti TD,Bondžić AM,Vasić VM.Acetylcholinesterase inhibitors: pharmacology and toxicology.Curr Neuropharmacol.2013;11:315-35.

[37]

Jelic V,Darreh-Shori T.Donepezil: A Review of Pharmacological Characteristics and Role in the Management of Alzheimer Disease.Clin Med Insights: Ther.2010;2:CMT.S5410.

[38]

Sharma K.Cholinesterase inhibitors as Alzheimer’s therapeutics (Review).Mol Med Rep.2019;20:1479-87.

[39]

Pooladgar P,Sakhabakhsh M,Taghva A,Soleiman-Meigooni S.Donepezil Beyond Alzheimer’s Disease? A Narrative Review of Therapeutic Potentials of Donepezil in Different Diseases.Iran J Pharm Res.2022;21:e128408.

[40]

Du H,Liu X,Xie J,Ma F.Novel Deoxyvasicinone-Donepezil Hybrids as Potential Multitarget Drug Candidates for Alzheimer’s Disease.ACS Chem Neurosci.2019;10:2397-407.

[41]

Zhang H,Zhao Y,Yu M,Zhao Z,Liu P,Cheng H,et al.Reassembly of native components with donepezil to execute dual-missions in Alzheimer’s disease therapy.J Control Release.2019;296:14-28.

[42]

Krishna KV,Saha RN,Dubey SK.Biophysical, Biochemical, and Behavioral Implications of ApoE3 Conjugated Donepezil Nanomedicine in a Aβ1-42 Induced Alzheimer’s Disease Rat Model.ACS Chem Neurosci.2020;11:4139-51.

[43]

Kho J,Ioannou A,Mandal AKJ,Missouris CG.Donepezil induces ventricular arrhythmias by delayed repolarisation.Naunyn Schmiedebergs Arch Pharmacol.2021;394:559-60.

[44]

Hsieh C,Tseng P,Chen T,Lin P,Chen Y,Ho B,et al.The association of changes of sleep architecture related to donepezil: A systematic review and meta-analysis.J Formos Med Assoc.2022;121:1466-77.

[45]

Wang H,Liou L,Hsu C,Lin H.Letter to the editor: Donepezil-induced parkinsonism in end-stage renal disease.Neurol Sci.2021;42:4809-12.

[46]

Sutthapitaksakul L,Dass CR,Sriamornsak P.Donepezil—an updated review of challenges in dosage form design.J Drug Deliv Sci Technol.2021;63:102549.

[47]

Adlimoghaddam A,Neuendorff M,Roy B,Albensi BC.A review of clinical treatment considerations of donepezil in severe Alzheimer’s disease.CNS Neurosci Ther.2018;24:876-88.

[48]

Marucci G,Buccioni M,Ben DD,Lambertucci C,Volpini R,Amenta F.Efficacy of acetylcholinesterase inhibitors in Alzheimer’s disease.Neuropharmacology.2021;190:108352.

[49]

Saito T,Hisahara S,Iwahara N,Emoto MC,Yokokawa K,Suzuki H,et al.Early administration of galantamine from preplaque phase suppresses oxidative stress and improves cognitive behavior in APPswe/PS1dE9 mouse model of Alzheimer’s disease.Free Radic Biol Med.2019;145:20-32.

[50]

Simoni E,Daniele S,Bottegoni G,Pizzirani D,Trincavelli ML,Goldoni L,et al.Combining galantamine and memantine in multitargeted, new chemical entities potentially useful in Alzheimer’s disease.J Med Chem.2012;55:9708-21.

[51]

Singhal M,Merino V,Rosini M,Cavalli A,Kalia YN.Controlled Iontophoretic Delivery in Vitro and in Vivo of ARN14140-A Multitarget Compound for Alzheimer’s Disease.Mol Pharm.2019;16:3460-8.

[52]

Varadharajan A,Davis AD,Ghosh A,Jagtap T,Xavier A,Menon AJ,et al.Guidelines for pharmacotherapy in Alzheimer’s disease - A primer on FDA-approved drugs.J Neurosci Rural Pract.2023;14:566-73.

[53]

Lima E,Medeiros J.Terpenes as Potential Anti-Alzheimer’s Disease Agents.Appl Sci.2024;14:3898.

[54]

Shah H,Patel A,Parikh V,Nagani A,Bhimani B,Shah U,et al.The β-Secretase Enzyme BACE1: A Biochemical Enigma for Alzheimer’s Disease.CNS Neurol Disord Drug Targets.2020;19:184-94.

[55]

Liu W,Liu X,Tian L,Gao Y,Liu W,Chen H,et al.Design, synthesis and biological evaluation of harmine derivatives as potent GSK-3β/DYRK1A dual inhibitors for the treatment of Alzheimer’s disease.Eur J Med Chem.2021;222:113554.

[56]

Patel SS,Raghuwanshi R,Masood M,Acharya A,Jain SK.Medicinal plants with acetylcholinesterase inhibitory activity.Rev Neurosci.2018;29:491-529.

[57]

Saad SA,Abd-Alla HI,Aly HF,Shalaby NMM,Afify AEMMR,Ali HFM,et al.Citharexylum spinosum promotes antioxidant, anti-inflammatory, and anti-acetylcholinesterase activities.Egypt J Chem.2024;67:63-75.

[58]

da Silva Barbosa DC,Holanda VN,de Assis CRD,de Oliveira Farias de Aguiar JCR,doNascimento PH,da Silva WV,et al.Chemical composition and acetylcholinesterase inhibitory potential, in silico, of Myrciaria floribunda (H. West ex Willd.) O. Berg fruit peel essential oil.Ind Crops Prod.2020;151:112372.

[59]

Nwidu LL,Elmorsy E,Thornton J,Wijamunige B,Wijesekara A,Tarbox R,et al.Anti-acetylcholinesterase activity and antioxidant properties of extracts and fractions of Carpolobia lutea.Pharm Biol.2017;55:1875-83.

[60]

Adewusi EA,Steenkamp V.In vitro screening for acetylcholinesterase inhibition and antioxidant activity of medicinal plants from southern Africa.Asian Pac J Trop Med.2011;4:829-35.

[61]

Armijos C,Gilardoni G,Amay L,Lozano A,Bracco F,Ramirez J,et al.Phytochemical and ethnomedicinal study of Huperzia species used in the traditional medicine of Saraguros in Southern Ecuador; AChE and MAO inhibitory activity.J Ethnopharmacol.2016;193:546-54.

[62]

Cardoso-Lopes EM,Maier JA,Silva MRd,Regasini LO,Simote SY,Lopes NP,et al.Alkaloids from stems of Esenbeckia leiocarpa Engl. (Rutaceae) as potential treatment for Alzheimer disease.Molecules.2010;15:9205-13.

[63]

Aazza S,El-Guendouz S,Miguel M.Screening for acetylcholinesterase inhibition, lipid peroxidation inhibition and antioxidant activity of medicinal plants from Morocco.Bol Latinoam Caribe Plant Med Aromat.2023;22:1-18.

[64]

Kuk EB,Jo AR,Oh SI,Sohn HS,Seong SH,Roy A,et al.Anti-Alzheimer’s disease activity of compounds from the root bark of Morus alba L.Arch Pharm Res.2017;40:338-49.

[65]

Ali MY,Jung HA,Choi JS.Anti-diabetic and anti-Alzheimer’s disease activities of Angelica decursiva.Arch Pharm Res.2015;38:2216-27.

[66]

Fawole OA,Amoo SO,Ndhlala AR,Light ME,Finnie JF,Staden JV.Anti-inflammatory, anticholinesterase, antioxidant and phytochemical properties of medicinal plants used for pain-related ailments in South Africa.J Ethnopharmacol.2010;127:235-41.

[67]

Lima JA,Costa RS,Epifânio RA,Castro NG,Rocha MS,Pinto AC.Geissospermum vellosii stembark: anticholinesterase activity and improvement of scopolamine-induced memory deficits.Pharmacol Biochem Behav.2009;92:508-13.

[68]

Penumala M,Zinka RB,Shaik JB,Mallepalli SKR,Vadde R,Amooru DG.Phytochemical profiling and in vitro screening for anticholinesterase, antioxidant, antiglucosidase and neuroprotective effect of three traditional medicinal plants for Alzheimer’s Disease and Diabetes Mellitus dual therapy.BMC Complement Altern Med.2018;18:77.

[69]

Lin HQ,Ho MT,Lau LS,Wong KK,Shaw PC,Wan DCC.Anti-acetylcholinesterase activities of traditional Chinese medicine for treating Alzheimer’s disease.Chem Biol Interact.2008;175:352-4.

[70]

Ohba T,Yoshino Y,Ishisaka M,Abe N,Tsuruma K,Shimazawa M,et al.Japanese Huperzia serrata extract and the constituent, huperzine A, ameliorate the scopolamine-induced cognitive impairment in mice.Biosci Biotechnol Biochem.2015;79:1838-44.

[71]

Suciati, Poerwantoro D, Widyawaruyanti A, Ingkaninan K. Acetylcholinesterase inhibitory activity of extract and fractions from the root of Rauvolfia serpentina(L.) Bth.ex Kurz.J Basic Clin Physiol Pharmacol.2021;32:313-7.

[72]

Idris M,Parumasivam T,Awang K,Zahari A,Litaudon M,Apel C,et al.Bioassay-guided isolation of acetylcholinesterase and butyrylcholinesterase inhibitors from Horsfieldia tomentosa fruits (Myristicaceae).Phytochem Lett.2025;65:133-40.

[73]

da Silva Lopes FF,Luís Eloi Silva J,de Morais Pereira Eloi N,Moreira Rodrigues AL,da Silva MVF,Montes RA,et al.Chemical Characterization, Phenolic Compounds Quantification, and Assessment of Antioxidant and Anti-Acetylcholinesterase Activities of Byrsonima sericea DC fruits.Chem Biodivers.2024;21:e202301760.

[74]

Bonesi M,Loizzo MR,Conforti F,Passalacqua NG,Saab A,Menichini F,et al.Berberis aetnensis and B. libanotica: a comparative study on the chemical composition, inhibitory effect on key enzymes linked to Alzheimer’s disease and antioxidant activity.J Pharm Pharmacol.2013;65:1726-35.

[75]

Jung HA,Ali MY,Jung HJ,Jeong HO,Chung HY,Choi JS.Inhibitory activities of major anthraquinones and other constituents from Cassia obtusifolia against β-secretase and cholinesterases.J Ethnopharmacol.2016;191:152-60.

[76]

Yang Z,Zhang D,Ren J,Yang M,Li S.Acetylcholinesterase inhibitory activity of the total alkaloid from traditional Chinese herbal medicine for treating Alzheimer’s disease.Med Chem Res.2012;21:734-8.

[77]

Yaman C,Erenler R,Atalar MN,Adem Ş,Çalişkan UK.Phytochemical Properties, Antioxidant and in Vitro/in Silico Anti-Acetylcholinesterase Activities of Hypericum heterophyllum Leaf from Türkiye.Brazilian Arch Biol Technol.2024;67:e24230043.

[78]

Yang Z,Zhang X,Du J,Ma Z,Guo F,Li S,et al.An aporphine alkaloid from Nelumbo nucifera as an acetylcholinesterase inhibitor and the primary investigation for structure-activity correlations.Nat Prod Res.2012;26:387-92.

[79]

Hlila MB,Omri A,Jannet HB,Lamari A,Aouni M,Selmi B.Phenolic composition, antioxidant and anti-acetylcholinesterase activities of the Tunisian Scabiosa arenaria.Pharm Biol.2013;51:525-32.

[80]

Penumala M,Zinka RB,Shaik JB,Gangaiah DA.In Vitro Screening of Three Indian Medicinal Plants for Their Phytochemicals, Anticholinesterase, Antiglucosidase, Antioxidant, and Neuroprotective Effects.Biomed Res Int.2017;2017:5140506.

[81]

Cortes N,Posada-Duque RA,Alvarez R,Alzate F,Berkov S,Cardona-Gómez GP,et al.Neuroprotective activity and acetylcholinesterase inhibition of five Amaryllidaceae species: a comparative study.Life Sci.2015;122:42-50.

[82]

Sher N,Ahmed M,Mushtaq N.Phytochemical analysis, antioxidant, acetylcholinesterase, and α-amylase inhibitors from Hippeastrum hybridum extract.J Tradit Chin Med.2024;44:496-504.

[83]

Leite DOD,Camilo CJ,Nonato CFA,Carvalho NKG,Salazar GJT,de Morais SM,et al.Chemical Profile and Evaluation of the Antioxidant and Anti-Acetylcholinesterase Activities of Annona squamosa L. (Annonaceae) Extracts.Foods.2021;10:2343.

[84]

Moyo M,Ndhlala AR,Finnie JF,Van Staden J.Phenolic composition, antioxidant and acetylcholinesterase inhibitory activities of Sclerocarya birrea and Harpephyllum caffrum (Anacardiaceae) extracts.Food Chem.2010;123:69-76.

[85]

Ahmad S,Ullah F,Ayaz M,Sadiq A,Imran M.Antioxidant and anticholinesterase investigations of Rumex hastatus D. Don: potential effectiveness in oxidative stress and neurological disorders.Biol Res.2015;48:20.

[86]

Tung BT,Hai NT,Thu DK.Antioxidant and acetylcholinesterase inhibitory activities in vitro of different fraction of Huperzia squarrosa (Forst.) Trevis extract and attenuation of scopolamine-induced cognitive impairment in mice.J Ethnopharmacol.2017;198:24-32.

[87]

da Silva Mendes JW,Camilo CJ,de Carvalho NKG,Alves Nonato CdF,Pereira de Lima RD,Alves DR,et al.In vitro antioxidant and acetylcholinesterase inhibitory properties of the alkaloid fraction of Cissampelos sympodialis Eichler.S Afr J Bot.2021;141:99-104.

[88]

Zhao Y,Dou J,Wu T,Aisa HA.Investigating the antioxidant and acetylcholinesterase inhibition activities of Gossypium herbaceam.Molecules.2013;18:951-62.

[89]

Atolani O,Adewara J,Onojah J.In-vitro Cholinesterase Inhibition Potential and Fatty Acid Profiling of Lipids Obtained via Direct Trans-esterification from Sarcocephalus latifolius (sm.) Fruits and Leaves.Al-Bahir.2025;6:1-5.

[90]

Tundis R,Menichini F,Conforti F,Loizzo MR,Bonesi M,Statti G,et al.A potential role of alkaloid extracts from Salsola species (Chenopodiaceae) in the treatment of Alzheimer’s disease.J Enzyme Inhib Med Chem.2009;24:818-24.

[91]

Ahmad S,Ullah F,Sadiq A,Ayaz M,Imran M,Ali I,et al.Chemical composition, antioxidant and anticholinesterase potentials of essential oil of Rumex hastatus D. Don collected from the North West of Pakistan.BMC Complement Altern Med.2016;16:29.

[92]

Jung HA,Karki S,Kim JH,Choi JS.BACE1 and cholinesterase inhibitory activities of Nelumbo nucifera embryos.Arch Pharm Res.2015;38:1178-87.

[93]

Ovais M,Ayaz M,Khalil AT,Shah SA,Jan MS,Raza A,et al.HPLC-DAD finger printing, antioxidant, cholinesterase, and α-glucosidase inhibitory potentials of a novel plant Olax nana.BMC Complement Altern Med.2018;18:1.

[94]

Ayaz M,Junaid M,Ahmed J,Ullah F,Sadiq A,Ahmad S,et al.Phenolic contents, antioxidant and anticholinesterase potentials of crude extract, subsequent fractions and crude saponins from Polygonum hydropiper L.BMC Complement Altern Med.2014;14:145.

[95]

Zavala-Ocampo LM,López-Camacho PY,Aguirre-Hernández E,Cárdenas-Vázquez R,Bonilla-Jaime H,Basurto-Islas G.Neuroprotective effects of Petiveria alliacea on scopolamine-induced learning and memory impairment mouse model.J Ethnopharmacol.2024;318:116881.

[96]

Cahlíková L,Valterová I,Macáková K,Opletal L.Analysis of Amaryllidaceae alkaloids from Zephyranthes grandiflora by GC/MS and their cholinesterase activity.Rev bras farmacogn.2011;21:575-80.

[97]

Bhadra S,Mukherjee PK,Kumar NS,Bandyopadhyay A.Anticholinesterase activity of standardized extract of Illicium verum Hook. f. fruits.Fitoterapia.2011;82:342-6.

[98]

Islam MA,Zaman S,Biswas K,Al-Amin MY,Hasan MK,Alam AHMK,et al.Evaluation of cholinesterase inhibitory and antioxidant activity of Wedelia chinensis and isolation of apigenin as an active compound.BMC Complement Med Ther.2021;21:204.

[99]

Imran M,Ullah F,Ayaz M,Sadiq A,Shah MR,Jan MS,et al.Anticholinesterase and antioxidant potentials of Nonea micrantha Bioss. & Reut along with GC-MS analysis.BMC Complement Altern Med.2017;17:499.

[100]

Nazir N,Zahoor M,Uddin F,Nisar M.Chemical composition, in vitro antioxidant, anticholinesterase, and antidiabetic potential of essential oil of Elaeagnus umbellata Thunb.BMC Complement Med Ther.2021;21:73.

[101]

Feitosa CM,Freitas RM,Luz NNN,Bezerra MZB,Trevisan MTS.Acetylcholinesterase inhibition by somes promising Brazilian medicinal plants.Braz J Biol.2011;71:783-9.

[102]

Bonesi M,Menichini F,Tundis R,Loizzo MR,Conforti F,Passalacqua NG,et al.Acetylcholinesterase and butyrylcholinesterase inhibitory activity of Pinus species essential oils and their constituents.J Enzyme Inhib Med Chem.2010;25:622-8.

[103]

Tuzimski T,Petruczynik A.Application of HPLC-DAD for In Vitro Investigation of Acetylcholinesterase Inhibition Activity of Selected Isoquinoline Alkaloids from Sanguinaria canadensis Extracts.Molecules.2021;26:230.

[104]

Kamal Z,Ullah F,Ayaz M,Sadiq A,Ahmad S,Zeb A,et al.Anticholinesterase and antioxidant investigations of crude extracts, subsequent fractions, saponins and flavonoids of atriplex laciniata L.: potential effectiveness in Alzheimer’s and other neurological disorders.Biol Res.2015;48:21.

[105]

Fatima I,Safdar N,Akhtar W,Munir A,Saqib S,Ayaz A,et al.Evaluation of potential inhibitory effects on acetylcholinesterase, pancreatic lipase, and cancer cell lines using raw leaves extracts of three fabaceae species.Heliyon.2023;9:e15909.

[106]

Carpinella MC,Andrione DG,Ruiz G,Palacios SM.Screening for acetylcholinesterase inhibitory activity in plant extracts from Argentina.Phytother Res.2010;24:259-63.

[107]

Eltahawy NA,Ali AI,Ibrahim SA,Nafie MS,Sindi AM,Alkharobi H,et al.Analysis of Marrubiin in Marrubium alysson L. Extract Using Advanced HPTLC: Chemical Profiling, Acetylcholinesterase Inhibitory Activity, and Molecular Docking.Metabolites.2023;14:27.

[108]

Jan H,Usman H,Shah M,Zaman G,Mushtaq S,Drouet S,et al.Phytochemical analysis and versatile in vitro evaluation of antimicrobial, cytotoxic and enzyme inhibition potential of different extracts of traditionally used Aquilegia pubiflora Wall. Ex Royle.BMC Complement Med Ther.2021;21:165.

[109]

Saleem H,Ahmad I,Shahid MN,Gill MSA,Nadeem MF,Mahmood W,et al.In Vitro Acetylcholinesterase and Butyrylcholinesterase Inhibitory Potentials of Jatropha Gossypifolia Plant Extracts.Acta Pol Pharm.2016;73:419-23Erratum in: Acta Pol Pharm. 2016;73:808.

[110]

Lai D,Yang Z,Xue W,Sheng J,Shi Y,Yao X.Isolation, characterization and acetylcholinesterase inhibitory activity of alkaloids from roots of Stemona sessilifolia.Fitoterapia.2013;89:257-64.

[111]

Mukherjee PK,Kumar V,Houghton PJ.Screening of Indian medicinal plants for acetylcholinesterase inhibitory activity.Phytother Res.2007;21:1142-5.

[112]

Chen X,He X,Sun J,Wang Z.Phytochemical Composition, Antioxidant Activity, α-Glucosidase and Acetylcholinesterase Inhibitory Activity of Quinoa Extract and Its Fractions.Molecules.2022;27:2420.

[113]

Ayaz M,Junaid M,Ullah F,Sadiq A,Khan MA,Ahmad W,et al.Comparative chemical profiling, cholinesterase inhibitions and anti-radicals properties of essential oils from Polygonum hydropiper L: a preliminary anti- Alzheimer’s study.Lipids Health Dis.2015;14:141.

[114]

Chaiyana W,Okonogi S.Inhibition of cholinesterase by essential oil from food plant.Phytomedicine.2012;19:836-9.

[115]

Uddin MJ,Russo D,Rahman MM,Uddin SB,Halim MA,Zidorn C,et al.Anticholinesterase Activity of Eight Medicinal Plant Species: In Vitro and In Silico Studies in the Search for Therapeutic Agents against Alzheimer’s Disease.Evid Based Complement Alternat Med.2021;2021:9995614.

[116]

Sahoo AK,Dandapat J,Dash UC,Kanhar S.Features and outcomes of drugs for combination therapy as multi-targets strategy to combat Alzheimer’s disease.J Ethnopharmacol.2018;215:42-73.

[117]

Jin Z,Yao G.Amaryllidaceae and Sceletium alkaloids.Nat Prod Rep.2019;36:1462-88.

[118]

Berkov S,Atanasova M,Georgiev B,Bastida J,Doytchinova I.The Amaryllidaceae alkaloids: an untapped source of acetylcholinesterase inhibitors.Phytochem Rev.2022;21:1415-43.

[119]

Sahiner M,Yilmaz AS,Gungor B,Sahiner N.A Review on Phyto-Therapeutic Approaches in Alzheimer’s Disease.J Funct Biomater.2023;14:50.

[120]

Gajendra K,Pratap GK,Poornima DV,Shantaram M,Ranjita G.Natural acetylcholinesterase inhibitors: A multi-targeted therapeutic potential in Alzheimer’s disease.Eur J Med Chem Rep.2024;11:100154.

[121]

Pratap GK,Ashwini S,Shantaram M.Alzheimer’s Disease: A Challenge In Managing with Certain Medicinal Plants – A Review.Int J Pharm Sci Res.2017;8:4960-72.

[122]

Pratap GK,Jayakar V,Lokapur V,Shantaram M.Role of Functional Foods in the Amelioration of Alzheimer’s and Related Diseases.Functional Foods for Health Maintenance:Understanding their Role in Cancer Prevention. Bentham Science Publishers2023.pp. 433–49.

[123]

Orhan IE,Orhan G,Gurkas E.An overview on natural cholinesterase inhibitors--a multi-targeted drug class--and their mass production.Mini Rev Med Chem.2011;11:836-42.

[124]

Ahmed F,Ghalib RM,Sasikala P,Ahmed KKM.Cholinesterase inhibitors from botanicals.Pharmacogn Rev.2013;7:121-30.

[125]

Heinrich M,Mah J,Amirkia V.Alkaloids Used as Medicines: Structural Phytochemistry Meets Biodiversity—An Update and Forward Look.Molecules.2021;26:1836.

[126]

Mukherjee PK,Kumar V,Mal M,Houghton PJ.Acetylcholinesterase inhibitors from plants.Phytomedicine.2007;14:289-300.

[127]

Dall’Acqua S.Plant-derived acetylcholinesterase inhibitory alkaloids for the treatment of Alzheimer’s disease.Bot: Targets Ther.2013;3:19-28.

[128]

Williams P,Sorribas A,Howes MR.Natural products as a source of Alzheimer’s drug leads.Nat Prod Rep.2011;28:48-77.

[129]

Loizzo MR,Tundis R,Menichini F,Menichini F.Natural products and their derivatives as cholinesterase inhibitors in the treatment of neurodegenerative disorders: an update.Curr Med Chem.2008;15:1209-28.

[130]

Yarnell E,Abascal K.Treating Hypertension Botanically.Altern Complementary Ther.2001;7:284-90.

[131]

Dey P,Kundu A,Kumar A,Gupta M,Lee BM,Bhakta T.Chapter 15 - Analysis of alkaloids (indole alkaloids, isoquinoline alkaloids, tropane alkaloids). In: Sanches Silva A,Nabavi SF,Saeedi M,Nabavi SM. editors.Recent Advances in Natural Products AnalysisElsevier; 2020. pp. 505–67.

[132]

Kashyap P,Kalaiselvan V,Kumar R,Kumar S.Ajmalicine and Reserpine: Indole Alkaloids as Multi-Target Directed Ligands Towards Factors Implicated in Alzheimer’s Disease.Molecules.2020;25:1609.

[133]

Wiatrak B,Kubis-Kubiak A,Piwowar A,Barg E.PC12 Cell Line: Cell Types, Coating of Culture Vessels, Differentiation and Other Culture Conditions.Cells.2020;9:958.

[134]

Jiang B,Meng L,Zou N,Wang H,Li S,Huang L,et al.Mechanism-based pharmacokinetics-pharmacodynamics studies of harmine and harmaline on neurotransmitters regulatory effects in healthy rats: Challenge on monoamine oxidase and acetylcholinesterase inhibition.Phytomedicine.2019;62:152967.

[135]

Zhang L,Li D,Yu S.Pharmacological effects of harmine and its derivatives: a review.Arch Pharm Res.2020;43:1259-75.

[136]

Li S,Wang Y,Qi S,Zhang Y,Deng G,Ding W,et al.Analogous β-Carboline Alkaloids Harmaline and Harmine Ameliorate Scopolamine-Induced Cognition Dysfunction by Attenuating Acetylcholinesterase Activity, Oxidative Stress, and Inflammation in Mice.Front Pharmacol.2018;9:346.

[137]

Puri B,Hall A.Phytochemical Dictionary: A Handbook of Bioactive Compounds from PlantsIn: Baxter H, Harborne JB, Moss GP. 2 nd ed. London: CRC Press; 1998.

[138]

Mak S,Luk WWK,Cui W,Hu S,Tsim KWK,Han Y.Synergistic inhibition on acetylcholinesterase by the combination of berberine and palmatine originally isolated from Chinese medicinal herbs.J Mol Neurosci.2014;53:511-6.

[139]

Imenshahidi M,Hosseinzadeh H.Berberis Vulgaris and Berberine: An Update Review.Phytother Res.2016;30:1745-64.

[140]

Imenshahidi M,Hosseinzadeh H.Berberine and barberry (Berberis vulgaris): A clinical review.Phytother Res.2019;33:504-23.

[141]

Hostalkova A,Marikova J,Opletal L,Korabecny J,Hulcova D,Kunes J,et al.Isoquinoline Alkaloids from Berberis vulgaris as Potential Lead Compounds for the Treatment of Alzheimer’s Disease.J Nat Prod.2019;82:239-48.

[142]

Carradori S,D’Ascenzio M,Chimenti P,Secci D,Bolasco A.Selective MAO-B inhibitors: a lesson from natural products.Mol Divers.2014;18:219-43.

[143]

Cai Z,Wang C,Yang W.Role of berberine in Alzheimer’s disease.Neuropsychiatr Dis Treat.2016;12:2509-20.

[144]

Hung TM,Na M,Dat NT,Ngoc TM,Youn U,Kim HJ,et al.Cholinesterase inhibitory and anti-amnesic activity of alkaloids from Corydalis turtschaninovii.J Ethnopharmacol.2008;119:74-80.

[145]

Seidl C,Correia BL,Stinghen AEM,Santos CAM.Acetylcholinesterase inhibitory activity of uleine from Himatanthus lancifolius.Z Naturforsch C J Biosci.2010;65:440-4.

[146]

Brunhofer G,Fallarero A,Karlsson D,Batista-Gonzalez A,Shinde P,Mohan CG,et al.Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.Bioorg Med Chem.2012;20:6669-79.

[147]

Zhang Y,Wang Q,Liu R,Zhou H,Crommen J,Moaddel R,et al.Rapid screening and identification of monoamine oxidase-A inhibitors from Corydalis Rhizome using enzyme-immobilized magnetic beads based method.J Chromatogr A.2019;1592:1-8.

[148]

Wang Y,Pei H,Chen W,Du R,Li J,He Z.Palmatine Protects PC12 Cells and Mice from Aβ25-35-Induced Oxidative Stress and Neuroinflammation via the Nrf2/HO-1 Pathway.Molecules.2023;28:7955.

[149]

Long J,Song J,Zhong L,Liao Y,Liu L,Li X.Palmatine: A review of its pharmacology, toxicity and pharmacokinetics.Biochimie.2019;162:176-84.

[150]

Wianowska D,Garbaczewska S,Cieniecka–Roslonkiewicz A,Typek R,Dawidowicz AL.Chemical composition and antifungal activity of Chelidonium majus extracts – antagonistic action of chelerythrine and sanguinarine against Botrytis cinerea.Chemistry and Ecology.2018;34:582-94.

[151]

Baek SC,Ryu HW,Kang M,Lee H,Park D,Cho M,et al.Selective inhibition of monoamine oxidase A by chelerythrine, an isoquinoline alkaloid.Bioorg Med Chem Lett.2018;28:2403-7.

[152]

Plazas E,Hagenow S,Murillo MA,Stark H,Cuca LE.Isoquinoline alkaloids from the roots of Zanthoxylum rigidum as multi-target inhibitors of cholinesterase, monoamine oxidase A and Aβ1-42 aggregation.Bioorg Chem.2020;98:103722.

[153]

Jung HA,Min B,Yokozawa T,Lee J,Kim YS,Choi JS.Anti-Alzheimer and antioxidant activities of Coptidis Rhizoma alkaloids.Biol Pharm Bull.2009;32:1433-8.

[154]

Masi M,Mubaiwa B,Mabank T,Karakoyun Ç,Cimmino A,Van Otterlo WAL,et al.Alkaloids isolated from indigenous South African Amaryllidaceae: Crinum buphanoides (Welw. ex Baker), Crinum graminicola (I. Verd.), Cyrtanthus mackenii (Hook. f) and Brunsvigia grandiflora (Lindl).S Afr J Bot.2018;118:188-91.

[155]

Dasari R,Banuls LMY,Masi M,Pelly SC,Mathieu V,Green IR,et al.C1,C2-ether derivatives of the Amaryllidaceae alkaloid lycorine: retention of activity of highly lipophilic analogues against cancer cells.Bioorg Med Chem Lett.2014;24:923-7.

[156]

Nair JJ,Staden Jv.Pharmacological and toxicological insights to the South African Amaryllidaceae.Food Chem Toxicol.2013;62:262-75.

[157]

Kohelová E,Peřinová R,Maafi N,Korábečný J,Hulcová D,Maříková J,et al.Derivatives of the β-Crinane Amaryllidaceae Alkaloid Haemanthamine as Multi-Target Directed Ligands for Alzheimer’s Disease.Molecules.2019;24:1307.

[158]

Choo CY,Hirasawa Y,Karimata C,Koyama K,Sekiguchi M,Kobayashi J,et al.Carinatumins A–C, new alkaloids from Lycopodium carinatum inhibiting acetylcholinesterase.Bioorg Med Chem.2007;15:1703-7.

[159]

Tang XC,He XC,Bai DL.Huperzine A: A novel acetylcholinesterase inhibitor.Drugs of the Future.1999;24:647-63.

[160]

Tang XC.Huperzine A (shuangyiping): a promising drug for Alzheimer’s disease.Zhongguo Yao Li Xue Bao.1996;17:481-4.

[161]

Tang CX,Han YF.Pharmacological Profile of Huperzine A, a Novel Acetylcholinesterase Inhibitor from Chinese Herb.CNS Drug Rev.1999;5:281-300.

[162]

Zhang H.New insights into huperzine A for the treatment of Alzheimer’s disease.Acta Pharmacol Sin.2012;33:1170-5.

[163]

Zhang HY,Yan H,Tang XC.Non-cholinergic effects of huperzine A: beyond inhibition of acetylcholinesterase.Cell Mol Neurobiol.2008;28:173-83.

[164]

Islam MT,Tabrez S,Jabir NR,Ali M,Kamal MA,Araujo LdS,et al.An Insight into the Therapeutic Potential of Major Coffee Components.Curr Drug Metab.2018;19:544-56.

[165]

Pohanka M,Dobes P.Caffeine inhibits acetylcholinesterase, but not butyrylcholinesterase.Int J Mol Sci.2013;14:9873-82.

[166]

Weng PH,Chen YC,Chen TF,Sun Y,Wen LL,Yip PK,et al.P1-387: Caffeine Intake and Cognitive Response to Acetylcholinesterase Inhibitors in Alzheimer’s Disease.Alzheimer’s Dementia.2014;10:P456.

[167]

Akomolafe SF.The effects of caffeine, caffeic acid, and their combination on acetylcholinesterase, adenosine deaminase and arginase activities linked with brain function.J Food Biochem.2017;41:e12401.

[168]

Lorenzo CD,Colombo F,Biella S,Stockley C,Restani P.Polyphenols and Human Health: The Role of Bioavailability.Nutrients.2021;13:273.

[169]

Tressera-Rimbau A,Arranz S,Eder M,Vallverdú-Queralt A.Dietary Polyphenols in the Prevention of Stroke.Oxid Med Cell Longev.2017;2017:7467962.

[170]

Cheng Y,Sheen J,Hu WL,Hung Y.Polyphenols and Oxidative Stress in Atherosclerosis-Related Ischemic Heart Disease and Stroke.Oxid Med Cell Longev.2017;2017:8526438.

[171]

Katalinić M,Rusak G,Barović JD,Sinko G,Jelić D,Antolović R,et al.Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase.Eur J Med Chem.2010;45:186-92.

[172]

Falé PLV,Ascensão L,Serralheiro ML,Haris PI.Interaction between Plectranthus barbatus herbal tea components and acetylcholinesterase: binding and activity studies.Food Funct.2012;3:1176-84.

[173]

Melrose J.The Potential of Flavonoids and Flavonoid Metabolites in the Treatment of Neurodegenerative Pathology in Disorders of Cognitive Decline.Antioxidants (Basel).2023;12:663.

[174]

Panche AN,Diwan AD,Chandra SR.Flavonoids: an overview.J Nutr Sci.2016;5:e47Erratum in: J Nutr Sci. 2025;14:e11.

[175]

Rajput MS,Sarkar PD.Modulation of neuro-inflammatory condition, acetylcholinesterase and antioxidant levels by genistein attenuates diabetes associated cognitive decline in mice.Chem Biol Interact.2017;268:93-102.

[176]

Hammond R,Gibbs RB.GPR30 is positioned to mediate estrogen effects on basal forebrain cholinergic neurons and cognitive performance.Brain Res.2011;1379:53-60.

[177]

Darbandi N,Ramezani M,Noori M.Mespilus germanica Flavonoids Attenuate Cognitive Dysfunction in the Streptozotocin-induced Rat Model of Alzheimer’s Disease.Indian J Pharm Sci.2018;80:668-75.

[178]

Zhang X,Bai L,Zhang S,Zhou X,Li Y,Bai J.Trx-1 ameliorates learning and memory deficits in MPTP-induced Parkinson’s disease model in mice.Free Radic Biol Med.2018;124:380-7.

[179]

Costa LG,Garrick JM,Roquè PJ,Pellacani C.Mechanisms of Neuroprotection by Quercetin: Counteracting Oxidative Stress and More.Oxid Med Cell Longev.2016;2016:2986796.

[180]

Jung M,Park M.Acetylcholinesterase Inhibition by Flavonoids from Agrimonia pilosa.Molecules.2007;12:2130-9.

[181]

Vila-Nova NS,Morais SM,Falcão MJC,Bevilaqua CML,Rondon FCM,Wilson ME.Leishmanicidal and cholinesterase inhibiting activities of phenolic compounds of Dimorphandra gardneriana and Platymiscium floribundum, native plants from Caatinga biome.Pesq Vet Bras.2012;32:1164-8.

[182]

Dzoyem JP,Eloff JN.Anti-inflammatory, anticholinesterase and antioxidant activity of leaf extracts of twelve plants used traditionally to alleviate pain and inflammation in South Africa.J Ethnopharmacol.2015;160:194-201.

[183]

Balkis A,Tran K,Lee Y,Ng K.Screening flavonoids for inhibition of acetylcholinesterase identified baicalein as the most potent inhibitor.J Agric Sci.2015;7:26-35.

[184]

Sevindik HG,Güvenalp Z,Yerdelen KO,Yuca H,Demirezer LO.The discovery of potential anticholinesterase compounds from Achillea millefolium L.Ind Crops Prod.2015;76:873-9.

[185]

Zhang S,Zhu Q,Chen J,OuYang D,Lu J.The pharmacological activity of epigallocatechin-3-gallate (EGCG) on Alzheimer’s disease animal model: A systematic review.Phytomedicine.2020;79:153316.

[186]

Oladapo OM,Ben-Azu B,Ajayi AM,Emokpae O,Eneni AO,Omogbiya IA,et al.Naringin Confers Protection against Psychosocial Defeat Stress-Induced Neurobehavioral Deficits in Mice: Involvement of Glutamic Acid Decarboxylase Isoform-67, Oxido-Nitrergic Stress, and Neuroinflammatory Mechanisms.J Mol Neurosci.2021;71:431-45.

[187]

Sinha R,Anderson DE,McDonald SS,Greenwald P.Cancer risk and diet in India.J Postgrad Med.2003;49:222-8.

[188]

Abbasi MA,Ilyas M,Aziz-ur-RehmanSonia A,Shahwar D,Raza MA,et al.Curcumin and its derivatives: Moderate inhibitors of acetylcholinesterase, butyrylcholinesterase and trypsin.Sci Iran.2012;19:1580-3.

[189]

Hatcher H,Planalp R,Cho J,Torti FM,Torti SV.Curcumin: from ancient medicine to current clinical trials.Cell Mol Life Sci.2008;65:1631-52.

[190]

Strimpakos AS,Sharma RA.Curcumin: preventive and therapeutic properties in laboratory studies and clinical trials.Antioxid Redox Signal.2008;10:511-45.

[191]

Kalaycıoğlu Z,Gazioğlu I,Erim FB.Comparison of antioxidant, anticholinesterase, and antidiabetic activities of three curcuminoids isolated from Curcuma longa L.Nat Prod Res.2017;31:2914-7.

[192]

Wolkmer P,Silva CB,Paim FC,Duarte MMMF,Castro V,Palma HE,et al.Pre-treatment with curcumin modulates acetylcholinesterase activity and proinflammatory cytokines in rats infected with Trypanosoma evansi.Parasitol Int.2013;62:144-9.

[193]

Akinyemi AJ,Okonkwo PK,Faboya OA,Onikanni SA,Fadaka A,Olayide I,et al.Curcumin improves episodic memory in cadmium induced memory impairment through inhibition of acetylcholinesterase and adenosine deaminase activities in a rat model.Metab Brain Dis.2017;32:87-95.

[194]

Jang MH,Piao XL,Kim JM,Kwon SW,Park JH.Inhibition of cholinesterase and amyloid-β aggregation by resveratrol oligomers from Vitis amurensis.Phytother Res.2008;22:544-9.

[195]

Schmatz R,Mazzanti CM,Spanevello R,Stefanello N,Gutierres J,Corrêa M,et al.Resveratrol prevents memory deficits and the increase in acetylcholinesterase activity in streptozotocin-induced diabetic rats.Eur J Pharmacol.2009;610:42-8.

[196]

Schmatz R,Mazzanti CM,Spanevello R,Stefanello N,Gutierres J,Maldonado PA,et al.Ectonucleotidase and acetylcholinesterase activities in synaptosomes from the cerebral cortex of streptozotocin-induced diabetic rats and treated with resveratrol.Brain Res Bull.2009;80:371-6.

[197]

Yang X,Qiang X,Li Y,Luo L,Xu R,Zheng Y,et al.Pyridoxine-resveratrol hybrids Mannich base derivatives as novel dual inhibitors of AChE and MAO-B with antioxidant and metal-chelating properties for the treatment of Alzheimer’s disease.Bioorg Chem.2017;71:305-14.

[198]

Adisakwattana S.Cinnamic Acid and Its Derivatives: Mechanisms for Prevention and Management of Diabetes and Its Complications.Nutrients.2017;9:163.

[199]

Guzman JD.Natural cinnamic acids, synthetic derivatives and hybrids with antimicrobial activity.Molecules.2014;19:19292-349.

[200]

de Cássia da Silveira E Sá R,Andrade LN,Dos Reis Barreto de Oliveira R,de Sousa DP.A review on anti-inflammatory activity of phenylpropanoids found in essential oils.Molecules.2014;19:1459-80.

[201]

Anantharaju PG,Gowda PC,Vimalambike MG,Madhunapantula SV.An overview on the role of dietary phenolics for the treatment of cancers.Nutr J.2016;15:99.

[202]

Zhao Z,Moghadasian MH.Chemistry, natural sources, dietary intake and pharmacokinetic properties of ferulic acid: A review.Food Chem.2008;109:691-702.

[203]

Elufioye TO,Obuotor EM,Agbedahunsi JM,Adesanya SA.Cholinesterase inhibitory activity and structure elucidation of a new phytol derivative and a new cinnamic acid ester from Pycnanthus angolensis.Rev Bras Farmacogn.2016;26:433-7.

[204]

Lan J,Hou J,Liu Y,Ding Y,Zhang Y,Li L,et al.Design, synthesis and evaluation of novel cinnamic acid derivatives bearing N-benzyl pyridinium moiety as multifunctional cholinesterase inhibitors for Alzheimer’s disease.J Enzyme Inhib Med Chem.2017;32:776-88.

[205]

Bhadra S,Dalai MK,Chanda J,Mukherjee PK.Chapter 13 - Evaluation of Bioactive Compounds as Acetylcholinesterase Inhibitors from Medicinal Plants. Evidence-Based Validation Herb Med. In: Mukherjee PK. editors.Evidence-Based Validation of Herbal Medicine.Boston:Elsevier2015.pp. 273–306.

[206]

Böttger A,Vothknecht U,Bolle C,Wolf A.Terpenes and TerpenoidsLessons on Caffeine, Cannabis & Co. Learning Materials in Biosciences. Cham; Springer International Publishing; 2018. pp.153–70.

[207]

Perveen S.Introductory Chapter: Terpenes and Terpenoids. In: Perveen S,Al-Taweel A. editors.Terpenes and Terpenoids.Rijeka:IntechOpen2018

[208]

Min SLS,Liew SY,Chear NJY,Goh BH,Tan W,Khaw KY.Plant Terpenoids as the Promising Source of Cholinesterase Inhibitors for Anti-AD Therapy.Biology (Basel).2022;11:307.

[209]

Brahmkshatriya PP,Brahmkshatriya PS.Terpenes: Chemistry, biological role, and therapeutic applications. In: Ramawat K,Mérillon JM. editors.Natural Products.Berlin:Springer2013.pp. 2665–91.

[210]

Krishna S,Bustamante L,Haynes RK,Staines HM.Artemisinins: their growing importance in medicine.Trends Pharmacol Sci.2008;29:520-7.

[211]

Wang G,Tang W,Bidigare RR.Terpenoids As Therapeutic Drugs and Pharmaceutical Agents. In: Zhang L,Demain AL. editors.Natural ProductsHumana Press; 2005. pp. 197–227.

[212]

Dohi S,Terasaki M,Makino M.Acetylcholinesterase inhibitory activity and chemical composition of commercial essential oils.J Agric Food Chem.2009;57:4313-8.

[213]

Wojtunik-Kulesza KA,Targowska-Duda K,Klimek K,Ginalska G,Jóźwiak K,Waksmundzka-Hajnos M,et al.Volatile terpenoids as potential drug leads in Alzheimer’s disease.Open Chem.2017;15:332-43.

[214]

Hegazy MF,Ibrahim AY,Mohamed TA,Shahat AA,Halawany AME,Abdel-Azim NS,et al.Sesquiterpene Lactones from Cynara cornigera: Acetyl Cholinesterase Inhibition and In Silico Ligand Docking.Planta Med.2016;82:138-46Erratum in: Planta Med. 2016;82:E3.

[215]

Alarcón J,Cespedes CL,Muñoz E,Balbontin C,Valdes F,Gutierrez M,et al.Dihydroagarofuranoid Sesquiterpenes as Acetylcholinesterase Inhibitors from Celastraceae Plants: Maytenus disticha and Euonymus japonicus.J Agric Food Chem.2015;63:10250-6.

[216]

Chougouo RDK,Nguekeu YMM,Dzoyem JP,Awouafack MD,Kouamouo J,Tane P,et al.Anti-inflammatory and acetylcholinesterase activity of extract, fractions and five compounds isolated from the leaves and twigs of Artemisia annua growing in Cameroon.Springerplus.2016;5:1525.

[217]

Yang D,Li W,Dong W,Wang J,Mei W,Dai H.Five new 5,11-epoxyguaiane sesquiterpenes in agarwood “Qi-Nan” from Aquilaria sinensis.Fitoterapia.2016;112:191-6.

[218]

Zardi-Bergaoui A,Znati M,Harzallah-Skhiri F,Jannet HB.Caryophyllene Sesquiterpenes from Pulicaria vulgaris GAERTN.: Isolation, Structure Determination, Bioactivity and Structure-Activity Relationship.Chem Biodivers.2019;16:e1800483.

[219]

Liu Y,Li J,Li D,Li X,Li D,Zhou G,et al.Anti-cholinesterase activities of constituents isolated from Lycopodiastrum casuarinoides.Fitoterapia.2019;139:104366.

[220]

Murata T,Selenge E,Oikawa S,Ageishi K,Batkhuu J,Sasaki K,et al.Cholinesterase-inhibitory diterpenoids and chemical constituents from aerial parts of Caryopteris mongolica.J Nat Med.2015;69:471-8.

[221]

Senol FS,Ślusarczyk S,Matkowski A,Pérez-Garrido A,Girón-Rodríguez F,Cerón-Carrasco JP,et al.Selective in vitro and in silico butyrylcholinesterase inhibitory activity of diterpenes and rosmarinic acid isolated from Perovskia atriplicifolia Benth. and Salvia glutinosa L.Phytochemistry.2017;133:33-44.

[222]

Nguyen VT,To DC,Tran MH,Oh SH,Kim JA,Ali MY,et al.Isolation of cholinesterase and β-secretase 1 inhibiting compounds from Lycopodiella cernua.Bioorg Med Chem.2015;23:3126-34.

[223]

Ado MA,Maulidiani M,Ismail IS,Ghazali HM,Shaari K,Abas F.Acetylcholinesterase and α-glucosidase inhibitory compounds from Callicarpa maingayi.Nat Prod Res.2021;35:2992-6.

[224]

Jamila N,Khairuddean M,Yeong KK,Osman H,Murugaiyah V.Cholinesterase inhibitory triterpenoids from the bark of Garcinia hombroniana.J Enzyme Inhib Med Chem.2015;30:133-9.

[225]

Liu Y,Chen G,Chen X,Chen S,Gan L,Yuan T.Colocynthenins A–D, Ring-A seco-Cucurbitane Triterpenoids from the Fruits of Citrullus colocynthis.J Nat Prod.2018;81:2115-9.

[226]

Liu J,Peng X,Li X,Li T,Zhang W,Shi L,et al.Norfriedelins A–C with acetylcholinesterase inhibitory activity from acerola tree (Malpighia emarginata).Org Lett.2013;15:1580-3.

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