The DOI matches its Crossref record; 203 of the 210 references it cites were found in a registry or an index.
Acetylcholinesterase inhibitors as Alzheimer therapy: From nerve toxins to neuroprotection
Abstract
Acetylcholinesterase is a member of the α/β hydrolase protein super family, with a significant role in acetylcholine-mediated neurotransmission. Research in the modulators of AChEs has moved from a potent poison (Sarin, Soman) in war times to the potent medicine (physostigmine) in peaceful times. Natural anti-AChE includes carbamates, glycoalkaloids, anatoxins derived from green algae; synthetic anti-AChE includes highly poisonous organophosphates used as nerve gases and insecticides. Recently, the role of anti-AChE was reassessed from neurotoxins to neuron-protective in the diseases characterized by impaired acetylcholine-mediated neurotransmission like Alzheimer's disease (AD). So, the AChE has been proven to be the most viable therapeutic target for the symptomatic treatment of AD. This review article gives a spectrum of strategies to design AChE inhibitors used in the Alzheimer therapy.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In addition, the enzyme plays a role in the production of amyloid plaques and neurofibrillary tangles.”
From An update on the novel and approved drugs for Alzheimer disease (2022) · cites this paper as Singh et al., 2013
In the citing paper
“the positive effect of galantamine in restoring certain normal behavioral traits could result from its acetylcholinesterase inhibitor activity.”
From Galantamine Slows Down Plaque Formation and Behavioral Decline in the 5XFAD Mouse Model of Alzheimer’s Disease (2014) · cites this paper as [54]
In the citing paper
“acetylcholinesterase has been shown to promote the aggregation of β-amyloid peptide fragments by forming a complex with the growing fibrils [54].”
From Galantamine Slows Down Plaque Formation and Behavioral Decline in the 5XFAD Mouse Model of Alzheimer’s Disease (2014) · cites this paper as [54]
In the citing paper
“According to the cholinergic hypothesis, a decreased production of acetylcholine or an amplified acetylcholinesterase activity results in impairment of the cholinergic transmission, in turn leading to the loss of intellectual abilities [54].”
From Galantamine Slows Down Plaque Formation and Behavioral Decline in the 5XFAD Mouse Model of Alzheimer’s Disease (2014) · cites this paper as [54]
Citations
Cites
The Amyloid Hypothesis of Alzheimer’s Disease: Progress and Problems on the Road to Therapeutics
Hardy, J., & Selkoe, D. J. (2002) · Science · doi:10.1126/science.1072994 · Cited by 13,864
Glenner, G. G., & Wong, C. W. (1984) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(84)80190-4 · Cited by 5,404
Memory systems of the brain: A brief history and current perspective
Squire, L. R. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.06.005 · Cited by 2,269
Diabetes mellitus and the risk of dementia: The Rotterdam Study
Ott, A., Stolk, R. P., van Harskamp, F., Pols, H. A. P., Hofman, A., & Breteler, M. M. B. (1999) · Neurology · doi:10.1212/wnl.53.9.1937 · Cited by 2,175
A Century of Alzheimer's Disease
Goedert, M., & Spillantini, M. G. (2006) · Science · doi:10.1126/science.1132814 · Cited by 2,153
Memantine in Moderate-to-Severe Alzheimer's Disease
Reisberg, B., Doody, R., Stöffler, A., Schmitt, F., Ferris, S., & Möbius, H. J. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa013128 · Cited by 2,043
General Nature of the Genetic Code for Proteins
Crick, F. H. C., Barnett, L., Brenner, S., & Watts-Tobin, R. J. (1961) · Nature · doi:10.1038/1921227a0 · Cited by 1,392
Oral Tetrahydroaminoacridine in Long-Term Treatment of Senile Dementia, Alzheimer Type
Summers, W. K., Majovski, L. V., Marsh, G. M., Tachiki, K. H., & Kling, A. S. (1986) · New England Journal of Medicine · doi:10.1056/nejm198611133152001 · Cited by 1,161
Inestrosa, N. C., Alvarez, A. R., Pérez, C. A., Moreno, R. D., Vicente, M., Linker, C., Casanueva, O. I., Soto, C. A., & Garrido, J. (1996) · Neuron · doi:10.1016/s0896-6273(00)80108-7 · Cited by 1,117
Microglia: Intrinsic immuneffector cell of the brain
Gehrmann, J., Matsumoto, Y., & Kreutzberg, G. W. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(94)00015-h · Cited by 1,111
Research works printed but not linked: 4
- Alzheimer, 1907, Over a eigenartigo disease of the cerebral cortex, Allg. Z. Psychiat., 64, 146
- Proskurnina, 1957, Oral solution containing galanthamine and a sweetening agent, J. Gen. Chem., 22, 1899
- Bores, 1996, Galanthamine derivatives for the treatment of Alzheimer's disease, Drugs Future, 21, 621
- Zhan, 2011, Synthesis of physostigmine analogues and evaluation of their anticholinesterase activities, Bioorg. Med. Chem. Lett., 20, 1532, 10.1016/j.bmcl.2010.01.097 · DOI
Cited by
Sorted by citations
Items 101–200 of 390
Emerging treatments for the behavioral and psychological symptoms of dementia
Anand, A., Khurana, P., Chawla, J. S., Sharma, N., & Khurana, N. (2017) · CNS Spectrums · doi:10.1017/s1092852917000530 · Cited by 36
Recent Advances in Excimer-Based Fluorescence Probes for Biological Applications
Chen, Y. (2022) · Molecules · doi:10.3390/molecules27238628 · Cited by 33
Rafique, H., Hu, X., Ren, T., Dong, R., Aadil, R. M., Zou, L., Sharif, M. K., & Li, L. (2023) · Nutrients · doi:10.3390/nu16010117 · Cited by 33
Kandasamy, S., Kalaiarasi, C., & Kumaradhas, P. (2016) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2016.1264891 · Cited by 33
Thiazole‐substituted benzoylpiperazine derivatives as acetylcholinesterase inhibitors
Şahin, Z., Ertaş, M., Bender, C., Bülbül, E. F., Berk, B., Biltekin, S. N., Yurttaş, L., & Demirayak, Ş. (2018) · Drug Development Research · doi:10.1002/ddr.21481 · Cited by 33
Effect of pesticides on phosphorylation of tau protein, and its influence on Alzheimer’s disease
Torres-Sánchez, E. D., Ortíz, G. G., Reyes-Uribe, E., Torres-Jasso, J. H., & Flores, J. S. (2023) · World Journal of Clinical Cases · doi:10.12998/wjcc.v11.i24.5628 · Cited by 33
Su, G., Chen, J., Huang, L., Zhao, M., Huang, Q., Zhang, J., Zeng, X. B., Zhang, Y., Deng, L., & Zhao, T. (2023) · Food Chemistry · doi:10.1016/j.foodchem.2023.137905 · Cited by 32
Anti-amnesic effects of Ganoderma species: A possible cholinergic and antioxidant mechanism
Kaur, R., Singh, V., & Shri, R. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.06.029 · Cited by 32
Jiang, Y., & Gao, H. (2018) · Phytomedicine · doi:10.1016/j.phymed.2018.09.199 · Cited by 32
Qi, C., Zhou, Q. Y., Gao, W., Liu, M., Chen, C., Li, X., Lai, Y., Zhou, Y., Li, D., Hu, Z., et al. (2019) · Phytochemistry · doi:10.1016/j.phytochem.2019.05.014 · Cited by 32
Zhan, G., Miao, R., Zhang, F., Hao, X., Zheng, X., Zhang, H., Zhang, X., & Guo, Z. (2020) · Phytochemistry · doi:10.1016/j.phytochem.2020.112450 · Cited by 32
Lotfi, S., Rahmani, T., Hatami, M., Pouramiri, B., Kermani, E. T., Rezvannejad, E., Mortazavi, M., Hafshejani, S. F., Askari, N., Pourjamali, N., et al. (2020) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2020.104457 · Cited by 33
Krátký, M., Štěpánková, Š., Vorčáková, K., & Vinšová, J. (2016) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2016.07.004 · Cited by 32
Song, S. H., Choi, S. M., Kim, J. E., Sung, J. E., Lee, H. A., Choi, Y. H., Bae, C. J., Choi, Y. W., & Hwang, D. Y. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.12.012 · Cited by 31
Khan, W. U., Salman, M., Ali, M., Majid, H., Yar, M. S., Akhtar, M., Parvez, S., & Najmi, A. K. (2024) · Neurochemistry International · doi:10.1016/j.neuint.2024.105839 · Cited by 33
Singh, M., Kaur, M., Singh, N., & Silakari, O. (2017) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2017.09.012 · Cited by 30
Monjas, L., Arce, M. P., Leon, R. M., Egea, J., Pérez, C., Villarroya, M., López, M. G., Gil, C., Conde, S., & Rodrı́guez-Franco, M. I. (2017) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2017.02.034 · Cited by 30
Chadha, N., Tiwari, A. K., Kumar, V., Lal, S., Milton, M. D., & Mishra, A. K. (2014) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2014.921793 · Cited by 29
Effects of aryl methanesulfonate derivatives on acetylcholinesterase and butyrylcholinesterase
Zilbeyaz, K., Stellenboom, N., Güney, M., Öztekіn, A., & Şentürk, M. (2018) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.22210 · Cited by 29
Li, X., Li, T., Zhang, P., Li, X., Lu, L., Sun, Y., Zhang, B., Allen, S., White, L. J., Phillips, J. B., et al. (2022) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2022.114841 · Cited by 29
Wang, Y., Wang, K., Yan, J., Zhou, Q., & Wang, X. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232213886 · Cited by 32
da Silva, C. B., Pott, A., Elífio-Esposito, S., Dalarmi, L., do Nascimento, K. F., Burci, L. M., de Oliveira, M., Dias, J. D. F. G., Zanin, S. M. W., Miguel, O. G., et al. (2016) · Molecules · doi:10.3390/molecules21010053 · Cited by 29
Aly, S. H., Uba, A. İ., Nilofar, N., Majrashi, T. A., Hassab, M. A. E., Eldehna, W. M., Zengin, G., & Eldahshan, O. A. (2025) · PLoS ONE · doi:10.1371/journal.pone.0319147 · Cited by 28
Spiazzi, C. C., Soares, M. B., Izaguirry, A. P., Vargas, L., Zanchi, M. M., Pavin, N. F., Affeldt, R. F., Lüdtke, D. S., Prigol, M., & Cibin, F. W. S. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/976908 · Cited by 28
Zhou, B., Li, H., Cui, Z., Li, D., Geng, H., Gao, J., & Zhou, L. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.112415 · Cited by 28
Xavier, N. M., Schwarz, Š., Vaz, P. D., Csük, R., & Rauter, A. P. (2014) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201301913 · Cited by 28
Durgun, M., Akocak, S., Lolak, N., Topal, F., Koçyiğit, Ü. M., Türkeş, C., Işık, M., & Beydemir, Ş. (2023) · Chemistry & Biodiversity · doi:10.1002/cbdv.202301824 · Cited by 27
García, M. E., Borioni, J. L., Cavallaro, V., Puiatti, M., Pierini, A. B., Murray, A. P., & Peñéñory, A. B. (2015) · Steroids · doi:10.1016/j.steroids.2015.09.001 · Cited by 27
Oluwagunwa, O. A., Alashi, A. M., Taiwo, K. A., Oyedele, D. J., Adebooye, O. C., & Aluko, R. E. (2018) · Journal of Food Biochemistry · doi:10.1111/jfbc.12566 · Cited by 27
Bowroju, S. K., Penthala, N. R., Lakkaniga, N. R., Balasubramaniam, M., Ayyadevara, S., Reis, R. J. S., & Crooks, P. A. (2021) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2021.116311 · Cited by 27
Cahlíková, L., Pérez, D. I., Štěpánková, Š., Chlebek, J., Šafratová, M., Hošťálková, A., & Opletal, L. (2015) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5b00191 · Cited by 27
Burilova, E. A., Pashirova, T. N., Zueva, I. V., Гибадуллина, Э. М., Lushchekina, S. V., Sapunova, А. S., Kayumova, R. M., Rogov, A. M., Evtugyn, V. G., Sudakov, I. A., et al. (2020) · Nanoscale · doi:10.1039/d0nr04037a · Cited by 27
Yadav, M. K., Singh, S. K., Singh, M., Mishra, S. S., Singh, A. K., Tripathi, J. S., & Tripathi, Y. B. (2019) · Open Access Macedonian Journal of Medical Sciences · doi:10.3889/oamjms.2019.247 · Cited by 26
Self-citationVandeput, M., Parsajoo, C., Vanheuverzwijn, J., Patris, S., Yardım, Y., le Jeune, A., Sarakbi, A., Mertens, D., & Kauffmann, J. (2014) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2014.09.012 · Cited by 28
Marcinkowska, M., Bucki, A., Panek, D., Siwek, A., Fajkis-Zajączkowska, N., Bednarski, M., Zygmunt, M., Godyń, J., Valdivieso, Á. D. R., Kotańska, M., et al. (2019) · Archiv der Pharmazie · doi:10.1002/ardp.201900041 · Cited by 26
Gupta, S. M., Behera, A., Jain, N. K., Kumar, D., Tripathi, A., Tripathi, S. M., Mujwar, S., Patra, J., & Negi, A. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics15010094 · Cited by 26
Yadav, E., Singh, D., Yadav, P. S., & Verma, A. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00549 · Cited by 26
Organoruthenium Prodrugs as a New Class of Cholinesterase and Glutathione‐S‐Transferase Inhibitors
Ristovski, S., Uzelac, M., Kljun, J., Lipec, T., Uršič, M., Jokhadar, Š. Z., Žužek, M. C., Trobec, T., Frangež, R., Sepčić, K., et al. (2018) · ChemMedChem · doi:10.1002/cmdc.201800432 · Cited by 26
Lan, T. T., Anh, D. T., Pham‐The, H., Dung, D. T. M., Hương, L. T. T., Park, E. J., Jeon, H. W., Kang, J. S., Thuần, N. T. D., Han, S., et al. (2019) · Medicinal Chemistry Research · doi:10.1007/s00044-019-02488-1 · Cited by 26
Vrabec, R., Maříková, J., Ločárek, M., Korábečný, J., Hulcová, D., Hošťálková, A., Kuneš, J., Chlebek, J., Kučera, T., Hrabinová, M., et al. (2021) · Phytochemistry · doi:10.1016/j.phytochem.2021.113017 · Cited by 25
Kumar, N., Jangid, K., Kumar, V., Yadav, R. P., Mishra, J., Upadhayay, S., Kumar, V., Devi, B., Kumar, V., Dwivedi, A. R., et al. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00007 · Cited by 25
Mohammadbaghban, E., Taravati, A., Najafzadehvarzi, H., Khaleghzadeh‐Ahangar, H., & Tohidi, F. (2024) · Physiological Reports · doi:10.14814/phy2.16095 · Cited by 28
Synthesis and cholinesterase inhibition of cativic acid derivatives
Alza, N. P., Richmond, V., Baier, C. J., Freire, E., Baggio, R., & Murray, A. P. (2014) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2014.06.030 · Cited by 24
Singh, M., Kaur, M., Vyas, B., & Silakari, O. (2017) · Medicinal Chemistry Research · doi:10.1007/s00044-017-2078-4 · Cited by 24
Zeng, Y. B., Nie, L., Liu, L., Niu, C., Li, Y., Bozorov, K. A., Zhao, J., Shen, J., & Aisa, H. A. (2022) · Journal of Heterocyclic Chemistry · doi:10.1002/jhet.4452 · Cited by 25
Discovery of butyrylcholinesterase inhibitors among derivatives of azaphenothiazines
Lodarski, K., Jończyk, J., Szałaj, N., Bajda, M., Gładysz, J., Walczyk, J., Jeleń, M., MORAK-MŁODAWSKA, B. I., Pluta, K., & Malawska, B. (2014) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.3109/14756366.2014.889127 · Cited by 24
Avram, S., Mernea, M., Limban, C., Borcan, F., & Chifiriuc, M. C. (2019) · Current Neuropharmacology · doi:10.2174/1570159x18666191230120053 · Cited by 24
Menéndez, C. A., Biscussi, B., Accordino, S. R., Murray, A. P., Gerbino, D. C., & Appignanesi, G. A. (2017) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2017.09.012 · Cited by 23
1,8-Naphthyridine Derivatives: A Privileged Scaffold for Versatile Biological Activities
Ojha, M., Yadav, D., Kumar, A., Dasgupta, S., & Yadav, R. (2020) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557520666201009162804 · Cited by 22
Baussanne, I., Firstova, O., Botezatu, A. V. D., Larosa, C., Furdui, B., Ghinea, I. O., Thomas, A. M., Chierici, S., Dinică, R. M., & Demeunynck, M. (2021) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2021.105390 · Cited by 22
Liu, Q., Wu, J., Li, F., Cai, P., Yang, X., Kong, L., & Wang, X. (2017) · MedChemComm · doi:10.1039/c7md00199a · Cited by 23
Neuropharmacology of altered brain oscillations in schizophrenia
Koch, M., Schmiedt‐Fehr, C., & Mathes, B. (2015) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2015.02.014 · Cited by 21
Buckler, J. N., Taher, E. S., Fraser, N. J., Willis, A. C., Carr, P. D., Jackson, C. J., & Banwell, M. G. (2017) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.7b01062 · Cited by 22
Aster glehni Extract Ameliorates Scopolamine-Induced Cognitive Impairment in Mice
Liao, Y., Bae, H. J., Park, J. H., Zhang, J., Koo, B., Lim, M. K., Han, E. H., Lee, S. H., Jung, S. Y., Lew, J. H., et al. (2019) · Journal of Medicinal Food · doi:10.1089/jmf.2018.4302 · Cited by 21
Ayoup, M. S., Barakat, M. R., Abdel‐Hamid, H., Emam, E., Al-Faiyz, Y. S., Masoud, A. A., Ghareeb, D. A., Sonousi, A. S. M., & Kassab, A. E. (2024) · RSC Medicinal Chemistry · doi:10.1039/d4md00113c · Cited by 21
Yokota, S.-I., Nakamura, K., Ando, M., Kamei, H., Hakuno, F., Takahashi, S., & Shibata, S. (2014) · FEBS Open Bio · doi:10.1016/j.fob.2014.10.009 · Cited by 20
Zhou, B., Zhang, B., Li, X., Liu, X., Li, H., Li, D., Cui, Z., Geng, H., & Zhou, L. (2018) · Scientific Reports · doi:10.1038/s41598-018-19999-3 · Cited by 21
Dinca, V. C., Viespe, C., Brajnicov, S., Constantinoiu, I., Moldovan, A., Bonciu, A. F., Toader, C., Ginghină, R. E., Grigoriu, N., Dinescu, M., et al. (2018) · Sensors · doi:10.3390/s18124265 · Cited by 21
Zhang, Y., Zhang, S., Xu, G., Yan, H., Pu, Y., & Zuo, Z. (2016) · Molecular BioSystems · doi:10.1039/c6mb00661b · Cited by 20
Computational Studies on Acetylcholinesterase Inhibitors: From Biochemistry to Chemistry
Bagri, K., Kumar, A., Manisha, M., & Kumar, P. P. (2019) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557520666191224144346 · Cited by 21
Misík, J., Korábečný, J., Nepovimová, E., Cabelova, P., & Kassa, J. (2015) · Biomedical Papers · doi:10.5507/bp.2015.006 · Cited by 20
Chronic administration of isocarbophos induces vascular cognitive impairment in rats
Li, P., Yin, Y., Zhu, M., Pan, G., Zhao, F., Lu, J., Liu, Z., Wang, S., & Hu, C. (2016) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12775 · Cited by 20
Wu, D., Xu, X., Sun, N., Li, D., Zhu, B., & Lin, S. (2020) · Food & Function · doi:10.1039/d0fo02570d · Cited by 19
Pant, S., Ranjith Kumar, K., Rana, P., Anthwal, T., Ali, S. M., Gupta, M., Chauhan, M., & Nain, S. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.3c00662 · Cited by 20
Vilela, A. F. L., Cardoso, C. L., & Mateo, C. (2018) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2018.09.071 · Cited by 20
Ma, Z., Zhou, X., Chen, L., Chen, X., & Feng, X. (2025) · Food Research International · doi:10.1016/j.foodres.2025.117721 · Cited by 20
Ayvaz, M. Ç., Aksu, F., & Kır, F. (2019) · British Food Journal · doi:10.1108/bfj-06-2018-0399 · Cited by 19
Kumar, H., Goyal, A., Kumar, N., & Garg, P. (2022) · Medicinal Chemistry Research · doi:10.1007/s00044-022-02953-4 · Cited by 18
Wang, J., Yu, Z., Ye, P., & Xu, B. (2023) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2023.109397 · Cited by 18
Gupta, M., Ojha, M., Yadav, D., Pant, S., & Yadav, R. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00403 · Cited by 19
The Evolution of AChE Inhibitors in Alzheimer's Disease: From Single‐Target to Multi‐Target Ligands
Mehta, N. V., Kapadia, A., Khambete, M., & Abhyankar, A. N. (2025) · ChemBioChem · doi:10.1002/cbic.202500053 · Cited by 20
Roumiani, M. E., & Dorosti, N. (2019) · Ultrasonics Sonochemistry · doi:10.1016/j.ultsonch.2019.01.025 · Cited by 17
Schaduangrat, N., Prachayasittikul, V., Choomwattana, S., Wongchitrat, P., Phopin, K., Suwanjang, W., Malik, A. A., Vincent, B., & Nantasenamat, C. (2019) · Medicinal Research Reviews · doi:10.1002/med.21563 · Cited by 17
Yassa, N. W., Khalil, S., Saleh, S. R., Ghareeb, D. A., Demellawy, M. E., & El-Sayed, M. M. (2020) · PLoS ONE · doi:10.1371/journal.pone.0237929 · Cited by 17
RetractedMariki, A., Anaeigoudari, A., Zahedifar, M., Pouramiri, B., Ayati, A., & Lotfi, S. (2021) · Polycyclic aromatic compounds · doi:10.1080/10406638.2021.1933102 · Cited by 17
Bamboo leaf extract improves spatial learning ability in a rat model with senile dementia
Liu, J., Min-ying, Z., Feng, C.-Y., Ding, H.-B., Zhan, Y., Zhao, Z., & Ding, Y. (2015) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1400249 · Cited by 17
Asetilkolinesteraz ve Bütirilkolinesteraz Enzimlerinin Alzheimer Hastalığı ile İlişkisi
DEMİR, Z., & Türkan, F. (2022) · Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi · doi:10.21597/jist.1161271 · Cited by 16
Zhang, Z., Lv, J., Wang, Y., Yu, H., Guo, B., Zhai, J., Wang, C., Zhao, Y., Fan, F., & Luo, W. (2023) · Chemistry - A European Journal · doi:10.1002/chem.202203363 · Cited by 16
Borioni, J. L., Cavallaro, V., Murray, A. P., Peñéñory, A. B., Puiatti, M., & García, M. E. (2021) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2021.104893 · Cited by 16
da Silva, G. S., Figueiró, M., Tormena, C. F., Coelho, F., & Almeida, W. P. (2016) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.3109/14756366.2016.1144597 · Cited by 16
Fatty acid profile and bioactivity from Annona hypoglauca seeds oil
Ricardo, C. D. S., Antonio, A. D. M. F., Edvan, A. C., Jacqueline, A. T., Vany, P. F., Ane, K. P. C., de Melo, C. G. A. A. R., Fernández, I. M., & Pedro, R. E. R. (2015) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb2015.14714 · Cited by 15
Mohamed, E. M., Elmaidomy, A. H., Alaaeldin, R., Alsenani, F., Altemani, F. H., Algehainy, N. A., Alanazi, M. A., Bagalagel, A. A., Althagafi, A. A., Elrehany, M. A., et al. (2023) · Metabolites · doi:10.3390/metabo13060732 · Cited by 15
Aydin, B. O., Anıl, D. A., Demir, Y., & Alagöz, M. A. (2024) · Molecular Diversity · doi:10.1007/s11030-023-10774-9 · Cited by 15
Macan, M., Vukšić, A., Žunec, S., Konjevoda, P., Lovrić, J., Kelava, M., Štambuk, N., Vrkić, N., & Bradamante, V. (2015) · Pharmacological Reports · doi:10.1016/j.pharep.2015.02.005 · Cited by 15
Adedayo, B. C., Jesubowale, O. S., Adebayo, A. A., & Oboh, G. (2020) · Journal of Food Biochemistry · doi:10.1111/jfbc.13280 · Cited by 15
Anand, A., Khurana, N., Ali, N., Alasmari, A. F., Alharbi, M., Waseem, M., & Sharma, N. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1005972 · Cited by 15
Krátký, M., Štěpánková, Š., Vorčáková, K., & Vinšová, J. (2018) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2018.07.017 · Cited by 15
Potential of tropical macroalgae from French Polynesia for biotechnological applications
Zubia, M., Thomas, O., Soulet, S., Demoy, M., Saulnier, D., Connan, S., Murphy, E., Tintillier, F., Stiger‐Pouvreau, V., & Petek, S. (2019) · Journal of Applied Phycology · doi:10.1007/s10811-019-01920-8 · Cited by 16
Semenov, V. E., Giniyatullin, R., Lushchekina, S. V., Kots, E. D., Petrov, K. A., Nikitashina, A. D., Minnekhanova, O. A., Васильевич, З. В., Nikolsky, E. E., Masson, P., et al. (2014) · MedChemComm · doi:10.1039/c4md00225c · Cited by 15
dos Santos, R. C., Filho, A. A. D. M., Chagas, E. A., Fernández, I. M., Takahashi, J. A., & Ferraz, V. P. (2019) · Journal of Essential Oil Research · doi:10.1080/10412905.2018.1555102 · Cited by 14
Fungal Metabolites as Promising New Drug Leads for the Treatment of Alzheimer's Disease
Takahashi, J. A., Sande, D., Lima, G. D. S., Moura, M. A. F. E., & Lima, M. T. N. S. (2019) · Studies in natural products chemistry · doi:10.1016/b978-0-444-64185-4.00001-0 · Cited by 14
García-García, A., Rojas, S., Rivas‐García, L., Navarro‐Hortal, M. D., Romero‐Márquez, J. M., Fernández‐Bolaños, J. G., Choquesillo‐Lazarte, D., Salinas‐Castillo, A., López, Ó., Quiles, J. L., et al. (2021) · Chemical Communications · doi:10.1039/d1cc04404d · Cited by 14
Kumar, B., Kumar, N., Thakur, A., Kumar, V., Kumar, R., & Kumar, V. (2022) · Current Drug Targets · doi:10.2174/1389450123666220117104038 · Cited by 14
Fonseca, A., Matos, M. J., Reis, J., Duarte, Y., Gutiérrez, M., Santana, L., Uriarte, E., & Borges, F. (2016) · RSC Advances · doi:10.1039/c6ra05262b · Cited by 14
Ricardo, C. D. S., Antonio, A. D. M. F., Edvan, A. C., Jacqueline, A. T., Vany, P. F., Ismael, M. F. A. N., Pedro, R. E. R., Ana, C. G. C., & Holanda, L. C. (2015) · Journal of Medicinal Plants Research · doi:10.5897/jmpr2015.5919 · Cited by 14
In silico, NMR and pharmacological evaluation of an hydroxyoxindole cholinesterase inhibitor
Bacalhau, P., Fernandes, L., Martins, M. R., Candeias, F., Carreiro, E. P., López, Ó., Caldeira, A. T., Totobenazara, J., Guedes, R. C., & Burke, A. J. (2018) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2018.12.007 · Cited by 14
Siopa, F., Frade, R. F. M., Diniz, A., Andrade, J. M., Nicolai, M., Meirinhos, A., Lucas, S. D., Marcelo, F., Afonso, C. A. M., & Rijo, P. M. (2018) · ACS Omega · doi:10.1021/acsomega.8b02347 · Cited by 14
Arshad, A. S. M., Chear, N. J., Ezzat, M. O., Hanapi, N. A., Meesala, R., Suhana Arshad, B., Mansor, S. M., & Mordi, M. N. (2019) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2019.127070 · Cited by 14
Computer-aided Design of Chalcone Derivatives as Lead Compounds Targeting Acetylcholinesterase
Riswanto, F. D. O., Hariono, M., Yuliani, S. H., & Istyastono, E. P. (2017) · INDONESIAN JOURNAL OF PHARMACY · doi:10.14499/indonesianjpharm28iss2pp100 · Cited by 13
Love Wave Surface Acoustic Wave Sensor with Laser-Deposited Nanoporous Gold Sensitive Layer
Viespe, C., Dinca, V. C., Popescu‐Pelin, G., & Miu, D. M. (2019) · Sensors · doi:10.3390/s19204492 · Cited by 13
Metadata
- Authors
- Singh, M., Kaur, M., Kukreja, H., Chugh, R., Silakari, O., & Singh, D.
- Affiliations
- Panjab University (IN)
- Corresponding author
- Singh, Dhandeep
- Venue
- European Journal of Medicinal Chemistry
- Publisher
- Elsevier BV
- Published
- 2013-12
- Volume
- 70
- Pages
- 165-188
- ISSN
- 0223-5234 (ISSN-L)
- OpenAlex
- W1994264985
- Cited by
- 364
- References
- 210
- Citations by year
- 2026: 12 · 2025: 30 · 2024: 31 · 2023: 34 · 2022: 35 · 2021: 29 · 2020: 32 · 2019: 36 · 2018: 30 · 2017: 31 · 2016: 21 · 2015: 23 · 2014: 17 · 2013: 1
- FWCI
- 2.90
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Medicinal Chemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pharmacology (medical) › Cholinesterase and Neurodegenerative Diseases
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Pesticide Exposure and Toxicity
- Keywords
- acetylcholinesterase inhibitors, Alzheimer's disease, acetylcholinesterase, cholinergic neurotransmission, organophosphorus nerve agents, carbamate insecticides, physostigmine, glycoalkaloids, anatoxin, neuroprotection, drug design strategies, alpha/beta hydrolase superfamily
- MeSH terms
- Acetylcholinesterase, Alzheimer Disease, Animals, Cholinesterase Inhibitors, Humans, Drug Design, Molecular Structure
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review