371 related articles for article (PubMed ID: 24461561)
1. Ionic liquid mediated synthesis of mono- and bis-spirooxindole-hexahydropyrrolidines as cholinesterase inhibitors and their molecular docking studies.
Kia Y; Osman H; Kumar RS; Basiri A; Murugaiyah V
Bioorg Med Chem; 2014 Feb; 22(4):1318-28. PubMed ID: 24461561
[TBL] [Abstract][Full Text] [Related]
2. Synthesis and discovery of highly functionalized mono- and bis-spiro-pyrrolidines as potent cholinesterase enzyme inhibitors.
Kia Y; Osman H; Suresh Kumar R; Basiri A; Murugaiyah V
Bioorg Med Chem Lett; 2014 Apr; 24(7):1815-9. PubMed ID: 24594354
[TBL] [Abstract][Full Text] [Related]
3. Synthesis and cholinesterase inhibitory activity study of new piperidone grafted spiropyrrolidines.
Basiri A; Abd Razik BM; Ezzat MO; Kia Y; Kumar RS; Almansour AI; Arumugam N; Murugaiyah V
Bioorg Chem; 2017 Dec; 75():210-216. PubMed ID: 28987876
[TBL] [Abstract][Full Text] [Related]
4. Ionic liquid-enabled synthesis, cholinesterase inhibitory activity, and molecular docking study of highly functionalized tetrasubstituted pyrrolidines.
Kumar RS; Almansour AI; Arumugam N; Althomili DMQ; Altaf M; Basiri A; D K; Sai Manohar T; S V
Bioorg Chem; 2018 Apr; 77():263-268. PubMed ID: 29421701
[TBL] [Abstract][Full Text] [Related]
5. Spiropyrrolidine/spiroindolizino[6,7-b]indole heterocyclic hybrids: Stereoselective synthesis, cholinesterase inhibitory activity and their molecular docking study.
Arumugam N; Almansour AI; Suresh Kumar R; Altaf M; Padmanaban R; Sureshbabu P; Angamuthu G; Kotresha D; Manohar TS; Venketesh S
Bioorg Chem; 2018 Sep; 79():64-71. PubMed ID: 29723743
[TBL] [Abstract][Full Text] [Related]
6. Synthesis and discovery of novel piperidone-grafted mono- and bis-spirooxindole-hexahydropyrrolizines as potent cholinesterase inhibitors.
Kia Y; Osman H; Kumar RS; Murugaiyah V; Basiri A; Perumal S; Wahab HA; Bing CS
Bioorg Med Chem; 2013 Apr; 21(7):1696-707. PubMed ID: 23454132
[TBL] [Abstract][Full Text] [Related]
7. Design, synthesis and cholinesterase inhibitory activity of novel spiropyrrolidine tethered imidazole heterocyclic hybrids.
Almansour AI; Arumugam N; Kumar RS; Kotresha D; Manohar TS; Venketesh S
Bioorg Med Chem Lett; 2020 Jan; 30(2):126789. PubMed ID: 31753696
[TBL] [Abstract][Full Text] [Related]
8. A facile chemo-, regio- and stereoselective synthesis and cholinesterase inhibitory activity of spirooxindole-pyrrolizine-piperidine hybrids.
Kia Y; Osman H; Kumar RS; Murugaiyah V; Basiri A; Perumal S; Razak IA
Bioorg Med Chem Lett; 2013 May; 23(10):2979-83. PubMed ID: 23570788
[TBL] [Abstract][Full Text] [Related]
9. Ionic liquid mediated synthesis and molecular docking study of novel aromatic embedded Schiff bases as potent cholinesterase inhibitors.
Abd Razik BM; Osman H; Basiri A; Salhin A; Kia Y; Ezzat MO; Murugaiyah V
Bioorg Chem; 2014 Dec; 57():162-168. PubMed ID: 25462993
[TBL] [Abstract][Full Text] [Related]
10. Synthesis and cholinesterase inhibition of cativic acid derivatives.
Alza NP; Richmond V; Baier CJ; Freire E; Baggio R; Murray AP
Bioorg Med Chem; 2014 Aug; 22(15):3838-49. PubMed ID: 25017625
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Novel biphenyl bis-sulfonamides as acetyl and butyrylcholinesterase inhibitors: Synthesis, biological evaluation and molecular modeling studies.
Mutahir S; Jończyk J; Bajda M; Khan IU; Khan MA; Ullah N; Ashraf M; Qurat-ul-Ain ; Riaz S; Hussain S; Yar M
Bioorg Chem; 2016 Feb; 64():13-20. PubMed ID: 26595185
[TBL] [Abstract][Full Text] [Related]
13. A facile ionic liquid promoted synthesis, cholinesterase inhibitory activity and molecular modeling study of novel highly functionalized spiropyrrolidines.
Almansour AI; Kumar RS; Arumugam N; Basiri A; Kia Y; Ali MA; Farooq M; Murugaiyah V
Molecules; 2015 Jan; 20(2):2296-309. PubMed ID: 25642838
[TBL] [Abstract][Full Text] [Related]
14. Microwave assisted synthesis, cholinesterase enzymes inhibitory activities and molecular docking studies of new pyridopyrimidine derivatives.
Basiri A; Murugaiyah V; Osman H; Kumar RS; Kia Y; Ali MA
Bioorg Med Chem; 2013 Jun; 21(11):3022-31. PubMed ID: 23602518
[TBL] [Abstract][Full Text] [Related]
15. Cholinesterase Inhibitory Activity of Some semi-Rigid Spiro Heterocycles: POM Analyses and Crystalline Structure of Pharmacophore Site.
Hadda TB; Talhi O; Silva ASM; Senol FS; Orhan IE; Rauf A; Mabkhot YN; Bachari K; Warad I; Farghaly TA; Althagafi II; Mubarak MS
Mini Rev Med Chem; 2018; 18(8):711-716. PubMed ID: 28714400
[TBL] [Abstract][Full Text] [Related]
16. Dispiropyrrolidinyl-piperidone embedded indeno[1,2-b]quinoxaline heterocyclic hybrids: Synthesis, cholinesterase inhibitory activity and their molecular docking simulation.
Arumugam N; Almansour AI; Kumar RS; Kotresha D; Saiswaroop R; Venketesh S
Bioorg Med Chem; 2019 Jun; 27(12):2621-2628. PubMed ID: 30952387
[TBL] [Abstract][Full Text] [Related]
17. Three-Component Access to Functionalized Spiropyrrolidine Heterocyclic Scaffolds and Their Cholinesterase Inhibitory Activity.
Boudriga S; Haddad S; Murugaiyah V; Askri M; Knorr M; Strohmann C; Golz C
Molecules; 2020 Apr; 25(8):. PubMed ID: 32340203
[TBL] [Abstract][Full Text] [Related]
18. Molecular-docking-guided design and synthesis of new IAA-tacrine hybrids as multifunctional AChE/BChE inhibitors.
Cheng ZQ; Zhu KK; Zhang J; Song JL; Muehlmann LA; Jiang CS; Liu CL; Zhang H
Bioorg Chem; 2019 Mar; 83():277-288. PubMed ID: 30391700
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and biological evaluation of berberine-thiophenyl hybrids as multi-functional agents: Inhibition of acetylcholinesterase, butyrylcholinesterase, and Aβ aggregation and antioxidant activity.
Su T; Xie S; Wei H; Yan J; Huang L; Li X
Bioorg Med Chem; 2013 Sep; 21(18):5830-40. PubMed ID: 23932451
[TBL] [Abstract][Full Text] [Related]
20. Synthesis, structure-activity relationship and molecular docking studies of 3-O-flavonol glycosides as cholinesterase inhibitors.
Mughal EU; Javid A; Sadiq A; Murtaza S; Zafar MN; Khan BA; Sumrra SH; Tahir MN; Kanwal ; Khan KM
Bioorg Med Chem; 2018 Jul; 26(12):3696-3706. PubMed ID: 29886083
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
