350 related articles for article (PubMed ID: 26943478)
21. Galantamine derivatives with indole moiety: Docking, design, synthesis and acetylcholinesterase inhibitory activity.
Atanasova M; Stavrakov G; Philipova I; Zheleva D; Yordanov N; Doytchinova I
Bioorg Med Chem; 2015 Sep; 23(17):5382-9. PubMed ID: 26260334
[TBL] [Abstract][Full Text] [Related]
22. Design and synthesis of novel coumarin-pyridinium hybrids: In vitro cholinesterase inhibitory activity.
Vafadarnejad F; Mahdavi M; Karimpour-Razkenari E; Edraki N; Sameem B; Khanavi M; Saeedi M; Akbarzadeh T
Bioorg Chem; 2018 Apr; 77():311-319. PubMed ID: 29421707
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Synthesis, biological activity and molecular modeling studies on 1H-benzimidazole derivatives as acetylcholinesterase inhibitors.
Alpan AS; Parlar S; Carlino L; Tarikogullari AH; Alptüzün V; Güneş HS
Bioorg Med Chem; 2013 Sep; 21(17):4928-37. PubMed ID: 23891231
[TBL] [Abstract][Full Text] [Related]
26. Synthesis and anti-cholinesterase activity of new 7-hydroxycoumarin derivatives.
Alipour M; Khoobi M; Moradi A; Nadri H; Homayouni Moghadam F; Emami S; Hasanpour Z; Foroumadi A; Shafiee A
Eur J Med Chem; 2014 Jul; 82():536-44. PubMed ID: 24941128
[TBL] [Abstract][Full Text] [Related]
27. Rational design of carbamate-based dual binding site and central AChE inhibitors by a "biooxidisable" prodrug approach: Synthesis, in vitro evaluation and docking studies.
Ţînţaş ML; Gembus V; Alix F; Barré A; Coadou G; Truong L; Sebban M; Papamicaël C; Oulyadi H; Levacher V
Eur J Med Chem; 2018 Jul; 155():171-182. PubMed ID: 29886321
[TBL] [Abstract][Full Text] [Related]
28. Synthesis, biological evaluation and molecular modeling of aloe-emodin derivatives as new acetylcholinesterase inhibitors.
Shi DH; Huang W; Li C; Wang LT; Wang SF
Bioorg Med Chem; 2013 Mar; 21(5):1064-73. PubMed ID: 23380475
[TBL] [Abstract][Full Text] [Related]
29. Novel coumarin derivatives bearing N-benzyl pyridinium moiety: potent and dual binding site acetylcholinesterase inhibitors.
Alipour M; Khoobi M; Foroumadi A; Nadri H; Moradi A; Sakhteman A; Ghandi M; Shafiee A
Bioorg Med Chem; 2012 Dec; 20(24):7214-22. PubMed ID: 23140986
[TBL] [Abstract][Full Text] [Related]
30. Solanocapsine derivatives as potential inhibitors of acetylcholinesterase: Synthesis, molecular docking and biological studies.
García ME; Borioni JL; Cavallaro V; Puiatti M; Pierini AB; Murray AP; Peñéñory AB
Steroids; 2015 Dec; 104():95-110. PubMed ID: 26362598
[TBL] [Abstract][Full Text] [Related]
31. Novel donepezil-like N-benzylpyridinium salt derivatives as AChE inhibitors and their corresponding dihydropyridine "bio-oxidizable" prodrugs: Synthesis, biological evaluation and structure-activity relationship.
Azzouz R; Peauger L; Gembus V; Ţînţaş ML; Sopková-de Oliveira Santos J; Papamicaël C; Levacher V
Eur J Med Chem; 2018 Feb; 145():165-190. PubMed ID: 29324339
[TBL] [Abstract][Full Text] [Related]
32. Acetylcholinesterase inhibitory activity of scopolin and scopoletin discovered by virtual screening of natural products.
Rollinger JM; Hornick A; Langer T; Stuppner H; Prast H
J Med Chem; 2004 Dec; 47(25):6248-54. PubMed ID: 15566295
[TBL] [Abstract][Full Text] [Related]
33. Design, synthesis and anticholinesterase activity of a novel series of 1-benzyl-4-((6-alkoxy-3-oxobenzofuran-2(3H)-ylidene) methyl) pyridinium derivatives.
Nadri H; Pirali-Hamedani M; Shekarchi M; Abdollahi M; Sheibani V; Amanlou M; Shafiee A; Foroumadi A
Bioorg Med Chem; 2010 Sep; 18(17):6360-6. PubMed ID: 20673725
[TBL] [Abstract][Full Text] [Related]
34. Synthesis, biological evaluation, and molecular modeling of berberine derivatives as potent acetylcholinesterase inhibitors.
Huang L; Shi A; He F; Li X
Bioorg Med Chem; 2010 Feb; 18(3):1244-51. PubMed ID: 20056426
[TBL] [Abstract][Full Text] [Related]
35. Synthesis, in vitro acetylcholinesterase inhibitory activity and molecular docking of new acridine-coumarin hybrids.
Hamulakova S; Janovec L; Soukup O; Jun D; Kuca K
Int J Biol Macromol; 2017 Nov; 104(Pt A):333-338. PubMed ID: 28601645
[TBL] [Abstract][Full Text] [Related]
36. Design, synthesis and preliminary structure-activity relationship investigation of nitrogen-containing chalcone derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors: a further study based on Flavokawain B Mannich base derivatives.
Liu H; Fan H; Gao X; Huang X; Liu X; Liu L; Zhou C; Tang J; Wang Q; Liu W
J Enzyme Inhib Med Chem; 2016 Aug; 31(4):580-9. PubMed ID: 26186269
[TBL] [Abstract][Full Text] [Related]
37. Novel tacrine derivatives exhibiting improved acetylcholinesterase inhibition: Design, synthesis and biological evaluation.
Reddy EK; Remya C; Mantosh K; Sajith AM; Omkumar RV; Sadasivan C; Anwar S
Eur J Med Chem; 2017 Oct; 139():367-377. PubMed ID: 28810188
[TBL] [Abstract][Full Text] [Related]
38. Converting maslinic acid into an effective inhibitor of acylcholinesterases.
Schwarz S; Loesche A; Lucas SD; Sommerwerk S; Serbian I; Siewert B; Pianowski E; Csuk R
Eur J Med Chem; 2015 Oct; 103():438-45. PubMed ID: 26383128
[TBL] [Abstract][Full Text] [Related]
39. Identification of novel acetylcholinesterase inhibitors: Indolopyrazoline derivatives and molecular docking studies.
Chigurupati S; Selvaraj M; Mani V; Selvarajan KK; Mohammad JI; Kaveti B; Bera H; Palanimuthu VR; Teh LK; Salleh MZ
Bioorg Chem; 2016 Aug; 67():9-17. PubMed ID: 27231830
[TBL] [Abstract][Full Text] [Related]
40. Design, synthesis and evaluation of flavonoid derivatives as potent AChE inhibitors.
Sheng R; Lin X; Zhang J; Chol KS; Huang W; Yang B; He Q; Hu Y
Bioorg Med Chem; 2009 Sep; 17(18):6692-8. PubMed ID: 19692250
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]