These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
217 related articles for article (PubMed ID: 29653432)
21. Synthesis, preliminarily biological evaluation and molecular docking study of new Olaparib analogues as multifunctional PARP-1 and cholinesterase inhibitors. Gao CZ; Dong W; Cui ZW; Yuan Q; Hu XM; Wu QM; Han X; Xu Y; Min ZL J Enzyme Inhib Med Chem; 2019 Dec; 34(1):150-162. PubMed ID: 30427217 [TBL] [Abstract][Full Text] [Related]
22. New piperidine-hydrazone derivatives: Synthesis, biological evaluations and molecular docking studies as AChE and BChE inhibitors. Karaman N; Sıcak Y; Taşkın-Tok T; Öztürk M; Karaküçük-İyidoğan A; Dikmen M; Koçyiğit-Kaymakçıoğlu B; Oruç-Emre EE Eur J Med Chem; 2016 Nov; 124():270-283. PubMed ID: 27592396 [TBL] [Abstract][Full Text] [Related]
23. Synthesis, molecular docking studies, and biological evaluation of novel alkyl bis(4-amino-5-cyanopyrimidine) derivatives. Boualia I; Derabli C; Boulcina R; Bensouici C; Yildirim M; Birinci Yildirim A; Mokrani EH; Debache A Arch Pharm (Weinheim); 2019 Nov; 352(11):e1900027. PubMed ID: 31448454 [TBL] [Abstract][Full Text] [Related]
24. Synthesis and in vitro evaluation of novel rhodanine derivatives as potential cholinesterase inhibitors. Krátký M; Štěpánková Š; Vorčáková K; Vinšová J Bioorg Chem; 2016 Oct; 68():23-9. PubMed ID: 27428597 [TBL] [Abstract][Full Text] [Related]
25. Tricyclic pyrazolo[1,5-d][1,4]benzoxazepin-5(6H)-one scaffold derivatives: Synthesis and biological evaluation as selective BuChE inhibitors. Chen SC; Qiu GL; Li B; Shi JB; Liu XH; Tang WJ Eur J Med Chem; 2018 Mar; 147():194-204. PubMed ID: 29438888 [TBL] [Abstract][Full Text] [Related]
26. Cholinesterase inhibitory activity versus aromatic core multiplicity: a facile green synthesis and molecular docking study of novel piperidone embedded thiazolopyrimidines. Basiri A; Murugaiyah V; Osman H; Kumar RS; Kia Y; Hooda A; Parsons RB Bioorg Med Chem; 2014 Jan; 22(2):906-16. PubMed ID: 24369842 [TBL] [Abstract][Full Text] [Related]
27. Discovery of new butyrylcholinesterase inhibitors via structure-based virtual screening. Atatreh N; Al Rawashdah S; Al Neyadi SS; Abuhamdah SM; Ghattas MA J Enzyme Inhib Med Chem; 2019 Dec; 34(1):1373-1379. PubMed ID: 31347933 [TBL] [Abstract][Full Text] [Related]
28. Discovery of New Selective Butyrylcholinesterase (BChE) Inhibitors with Anti-Aβ Aggregation Activity: Structure-Based Virtual Screening, Hit Optimization and Biological Evaluation. Jiang CS; Ge YX; Cheng ZQ; Wang YY; Tao HR; Zhu K; Zhang H Molecules; 2019 Jul; 24(14):. PubMed ID: 31311169 [TBL] [Abstract][Full Text] [Related]
29. Synthesis of novel 5-(aroylhydrazinocarbonyl)escitalopram as cholinesterase inhibitors. Nisa MU; Munawar MA; Iqbal A; Ahmed A; Ashraf M; Gardener QA; Khan MA Eur J Med Chem; 2017 Sep; 138():396-406. PubMed ID: 28688279 [TBL] [Abstract][Full Text] [Related]
30. Cholinesterases inhibition and molecular modeling studies of piperidyl-thienyl and 2-pyrazoline derivatives of chalcones. Shah MS; Khan SU; Ejaz SA; Afridi S; Rizvi SUF; Najam-Ul-Haq M; Iqbal J Biochem Biophys Res Commun; 2017 Jan; 482(4):615-624. PubMed ID: 27865835 [TBL] [Abstract][Full Text] [Related]
31. Design, synthesis and biological evaluation of acridone glycosides as selective BChE inhibitors. Ma W; Bi J; Zhao C; Gao Y; Zhang G Carbohydr Res; 2020 May; 491():107977. PubMed ID: 32169593 [TBL] [Abstract][Full Text] [Related]
32. Synthesis and evaluation of 4-substituted coumarins as novel acetylcholinesterase inhibitors. Razavi SF; Khoobi M; Nadri H; Sakhteman A; Moradi A; Emami S; Foroumadi A; Shafiee A Eur J Med Chem; 2013 Jun; 64():252-9. PubMed ID: 23644208 [TBL] [Abstract][Full Text] [Related]
33. Potent acetylcholinesterase inhibitors: design, synthesis, biological evaluation, and docking study of acridone linked to 1,2,3-triazole derivatives. Mohammadi-Khanaposhtani M; Saeedi M; Zafarghandi NS; Mahdavi M; Sabourian R; Razkenari EK; Alinezhad H; Khanavi M; Foroumadi A; Shafiee A; Akbarzadeh T Eur J Med Chem; 2015 Mar; 92():799-806. PubMed ID: 25636055 [TBL] [Abstract][Full Text] [Related]
34. 4-Aryl-4-oxo-N-phenyl-2-aminylbutyramides as acetyl- and butyrylcholinesterase inhibitors. Preparation, anticholinesterase activity, docking study, and 3D structure-activity relationship based on molecular interaction fields. Vitorović-Todorović MD; Juranić IO; Mandić LM; Drakulić BJ Bioorg Med Chem; 2010 Feb; 18(3):1181-93. PubMed ID: 20061157 [TBL] [Abstract][Full Text] [Related]
35. In-silico identification of the binding mode of synthesized adamantyl derivatives inside cholinesterase enzymes. Al-Aboudi A; Al-Qawasmeh RA; Shahwan A; Mahmood U; Khalid A; Ul-Haq Z Acta Pharmacol Sin; 2015 Jul; 36(7):879-86. PubMed ID: 25937631 [TBL] [Abstract][Full Text] [Related]
36. SAR based in-vitro anticholinesterase and molecular docking studies of nitrogenous progesterone derivatives. Amin MJ; Miana GA; Rashid U; Rahman KM; Khan HU; Sadiq A Steroids; 2020 Jun; 158():108599. PubMed ID: 32126219 [TBL] [Abstract][Full Text] [Related]
37. Pharmacological evaluations of amide carboxylates as potential anti-Alzheimer agents: anti-radicals, enzyme inhibition, simulation and behavioral studies in animal models. Mahnashi MH; Ali S; M Alshehri O; Almazni IA; Asiri SA; Sadiq A; Zafar R; Jan MS J Biomol Struct Dyn; 2024 Oct; 42(17):9249-9268. PubMed ID: 37642974 [TBL] [Abstract][Full Text] [Related]
38. Synthesis, Characterization and Cholinesterase Inhibition Studies of New Arylidene Aminothiazolylethanone Derivatives. Channar PA; Shah MS; Saeed A; Khan SU; Larik FA; Shabir G; Iqbal J Med Chem; 2017; 13(7):648-653. PubMed ID: 28266279 [TBL] [Abstract][Full Text] [Related]
39. Design, synthesis, docking study and biological evaluation of some novel tetrahydrochromeno [3',4':5,6]pyrano[2,3-b]quinolin-6(7H)-one derivatives against acetyl- and butyrylcholinesterase. Khoobi M; Alipour M; Moradi A; Sakhteman A; Nadri H; Razavi SF; Ghandi M; Foroumadi A; Shafiee A Eur J Med Chem; 2013 Oct; 68():291-300. PubMed ID: 23988412 [TBL] [Abstract][Full Text] [Related]
40. Alkynyl and β-ketophosphonates: Selective and potent butyrylcholinesterase inhibitors. Cavallaro V; Moglie YF; Murray AP; Radivoy GE Bioorg Chem; 2018 Apr; 77():420-428. PubMed ID: 29427857 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]