220 related articles for article (PubMed ID: 29175588)
1. Modification of Bischler-Möhlau indole derivatives through palladium catalyzed Suzuki reaction as effective cholinesterase inhibitors, their kinetic and molecular docking studies.
Parveen S; Shah MS; Zaib S; Gul T; Khan KM; Iqbal J; Hassan A
Bioorg Chem; 2018 Feb; 76():166-176. PubMed ID: 29175588
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Investigating 1,2,3,4,5,6-hexahydroazepino[4,3-b]indole as scaffold of butyrylcholinesterase-selective inhibitors with additional neuroprotective activities for Alzheimer's disease.
Purgatorio R; de Candia M; Catto M; Carrieri A; Pisani L; De Palma A; Toma M; Ivanova OA; Voskressensky LG; Altomare CD
Eur J Med Chem; 2019 Sep; 177():414-424. PubMed ID: 31158754
[TBL] [Abstract][Full Text] [Related]
5. Identification of New Chromenone Derivatives as Cholinesterase Inhibitors and Molecular Docking Studies.
Iqbal J; Abbasi MSA; Zaib S; Afridi S; Furtmann N; Bajorath J; Langer P
Med Chem; 2018; 14(8):809-817. PubMed ID: 29473519
[TBL] [Abstract][Full Text] [Related]
6. Synthesis and anticholinesterase activity of new substituted benzo[d]oxazole-based derivatives.
Pouramiri B; Moghimi S; Mahdavi M; Nadri H; Moradi A; Tavakolinejad-Kermani E; Firoozpour L; Asadipour A; Foroumadi A
Chem Biol Drug Des; 2017 May; 89(5):783-789. PubMed ID: 27863021
[TBL] [Abstract][Full Text] [Related]
7. Tetrahydroquinoline-Isoxazole/Isoxazoline Hybrid Compounds as Potential Cholinesterases Inhibitors: Synthesis, Enzyme Inhibition Assays, and Molecular Modeling Studies.
Rodríguez Núñez YA; Gutíerrez M; Alzate-Morales J; Adasme-Carreño F; Güiza FM; Bernal CC; Bohórquez ARR
Int J Mol Sci; 2019 Dec; 21(1):. PubMed ID: 31861333
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Quinoline containing chalcone derivatives as cholinesterase inhibitors and their in silico modeling studies.
Shah MS; Najam-Ul-Haq M; Shah HS; Farooq Rizvi SU; Iqbal J
Comput Biol Chem; 2018 Oct; 76():310-317. PubMed ID: 30142564
[TBL] [Abstract][Full Text] [Related]
11. Synthesis and biological evaluation of indoloquinoline alkaloid cryptolepine and its bromo-derivative as dual cholinesterase inhibitors.
Nuthakki VK; Mudududdla R; Sharma A; Kumar A; Bharate SB
Bioorg Chem; 2019 Sep; 90():103062. PubMed ID: 31220673
[TBL] [Abstract][Full Text] [Related]
12. Experimental and Computational Evaluation of Piperonylic Acid Derived Hydrazones Bearing Isatin Moieties as Dual Inhibitors of Cholinesterases and Monoamine Oxidases.
Vishnu MS; Pavankumar V; Kumar S; Raja AS
ChemMedChem; 2019 Jul; 14(14):1359-1376. PubMed ID: 31177620
[TBL] [Abstract][Full Text] [Related]
13. Design and synthesis of N-substituted-2-hydroxyiminoacetamides and interactions with cholinesterases.
Maraković N; Knežević A; Vinković V; Kovarik Z; Šinko G
Chem Biol Interact; 2016 Nov; 259(Pt B):122-132. PubMed ID: 27238725
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Efficient Synthesis and Discovery of Schiff Bases as Potent Cholinesterase Inhibitors.
Razik BM; Osman H; Ezzat MO; Basiri A; Salhin A; Kia Y; Murugaiyah V
Med Chem; 2016; 12(6):527-36. PubMed ID: 26833077
[TBL] [Abstract][Full Text] [Related]
16. Synthesis of physostigmine analogues and evaluation of their anticholinesterase activities.
Zhan ZJ; Bian HL; Wang JW; Shan WG
Bioorg Med Chem Lett; 2010 Mar; 20(5):1532-4. PubMed ID: 20144867
[TBL] [Abstract][Full Text] [Related]
17. Synthesis, structure-activity relationship and molecular docking of 3-oxoaurones and 3-thioaurones as acetylcholinesterase and butyrylcholinesterase inhibitors.
Mughal EU; Sadiq A; Murtaza S; Rafique H; Zafar MN; Riaz T; Khan BA; Hameed A; Khan KM
Bioorg Med Chem; 2017 Jan; 25(1):100-106. PubMed ID: 27780618
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Isolation of cholinesterase and β-secretase 1 inhibiting compounds from Lycopodiella cernua.
Nguyen VT; To DC; Tran MH; Oh SH; Kim JA; Ali MY; Woo MH; Choi JS; Min BS
Bioorg Med Chem; 2015 Jul; 23(13):3126-34. PubMed ID: 26003344
[TBL] [Abstract][Full Text] [Related]
20. 1,2,3,4-Tetrahydrobenzo[h][1,6]naphthyridines as a new family of potent peripheral-to-midgorge-site inhibitors of acetylcholinesterase: synthesis, pharmacological evaluation and mechanistic studies.
Di Pietro O; Viayna E; Vicente-García E; Bartolini M; Ramón R; Juárez-Jiménez J; Clos MV; Pérez B; Andrisano V; Luque FJ; Lavilla R; Muñoz-Torrero D
Eur J Med Chem; 2014 Feb; 73():141-52. PubMed ID: 24389509
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
