Similar articles for PMID: 28126287

Year	Number of Results
1988	1
1990	2
1991	1
1993	1
1995	2
1996	3
1997	1
1999	1
2001	2
2002	1
2003	2
2005	3
2007	1
2008	1
2009	3
2010	8
2011	9
2012	7
2013	16
2014	23
2015	16
2016	41
2017	51
2018	73
2019	68
2020	67
2021	46
2022	38
2023	9
2024	0

1

Synthesis, biological evaluation and docking studies of 2,3-dihydroquinazolin-4(1H)-one derivatives as inhibitors of cholinesterases.

Sarfraz M, Sultana N, Rashid U, Akram MS, Sadiq A, Tariq MI. Sarfraz M, et al. Bioorg Chem. 2017 Feb;70:237-244. doi: 10.1016/j.bioorg.2017.01.004. Epub 2017 Jan 17. Bioorg Chem. 2017. PMID: 28126287 Free article.

2

Synthesis, crystal structure determination, biological screening and docking studies of N¹-substituted derivatives of 2,3-dihydroquinazolin-4(1H)-one as inhibitors of cholinesterases.

Sultana N, Sarfraz M, Tanoli ST, Akram MS, Sadiq A, Rashid U, Tariq MI. Sultana N, et al. Bioorg Chem. 2017 Jun;72:256-267. doi: 10.1016/j.bioorg.2017.04.009. Epub 2017 Apr 17. Bioorg Chem. 2017. PMID: 28495556

3

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. Shah MS, et al. Biochem Biophys Res Commun. 2017 Jan 22;482(4):615-624. doi: 10.1016/j.bbrc.2016.11.082. Epub 2016 Nov 16. Biochem Biophys Res Commun. 2017. PMID: 27865835

4

Syntheses, cholinesterases inhibition, and molecular docking studies of pyrido[2,3-b]pyrazine derivatives.

Hameed A, Zehra ST, Shah SJ, Khan KM, Alharthy RD, Furtmann N, Bajorath J, Tahir MN, Iqbal J. Hameed A, et al. Chem Biol Drug Des. 2015 Nov;86(5):1115-20. doi: 10.1111/cbdd.12579. Epub 2015 May 28. Chem Biol Drug Des. 2015. PMID: 25951978

5

Pyridine sulfonamide as a small key organic molecule for the potential treatment of type-II diabetes mellitus and Alzheimer's disease: In vitro studies against yeast α-glucosidase, acetylcholinesterase and butyrylcholinesterase.

Riaz S, Khan IU, Bajda M, Ashraf M, Qurat-Ul-Ain, Shaukat A, Rehman TU, Mutahir S, Hussain S, Mustafa G, Yar M. Riaz S, et al. Bioorg Chem. 2015 Dec;63:64-71. doi: 10.1016/j.bioorg.2015.09.008. Epub 2015 Sep 30. Bioorg Chem. 2015. PMID: 26451651

6

Design and synthesis of some new carboxamide and propanamide derivatives bearing phenylpyridazine as a core ring and the investigation of their inhibitory potential on in-vitro acetylcholinesterase and butyrylcholinesterase.

Kilic B, Gulcan HO, Aksakal F, Ercetin T, Oruklu N, Umit Bagriacik E, Dogruer DS. Kilic B, et al. Bioorg Chem. 2018 Sep;79:235-249. doi: 10.1016/j.bioorg.2018.05.006. Epub 2018 May 8. Bioorg Chem. 2018. PMID: 29775949

7

Synthesis of novel 5-(aroylhydrazinocarbonyl)escitalopram as cholinesterase inhibitors.

Nisa MU, Munawar MA, Iqbal A, Ahmed A, Ashraf M, Gardener QA, Khan MA. Nisa MU, et al. Eur J Med Chem. 2017 Sep 29;138:396-406. doi: 10.1016/j.ejmech.2017.06.036. Epub 2017 Jun 30. Eur J Med Chem. 2017. PMID: 28688279

8

Biological Evaluation of Azomethine-dihydroquinazolinone Conjugates as Cancer and Cholinesterase Inhibitors.

Iqbal J, Saeed A, Shah SJ, al-Rashida M, Shams-ul Mahmood. Iqbal J, et al. Med Chem. 2016;12(1):74-82. doi: 10.2174/1573406411666150708111417. Med Chem. 2016. PMID: 26152145

9

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. Kumar RS, et al. Bioorg Chem. 2018 Apr;77:263-268. doi: 10.1016/j.bioorg.2018.01.019. Epub 2018 Feb 3. Bioorg Chem. 2018. PMID: 29421701

10

A Series of New Hydrazone Derivatives: Synthesis, Molecular Docking and Anticholinesterase Activity Studies.

Bozbey İ, Özdemir Z, Uslu H, Özçelik AB, Şenol FS, Orhan İE, Uysal M. Bozbey İ, et al. Mini Rev Med Chem. 2020;20(11):1042-1060. doi: 10.2174/1389557519666191010154444. Mini Rev Med Chem. 2020. PMID: 31660824

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