Wadood A - Search Results

1

Octahydrocyclopenta[c]pyridine and octahydrocyclopenta[c]pyran analogues as a protease activated receptor 1 (PAR1) antagonist.

Wadood A, Kim H, Park CM, Song JH, Lee S. Wadood A, et al. Arch Pharm Res. 2015 Nov;38(11):2029-41. doi: 10.1007/s12272-015-0623-6. Epub 2015 Jun 12. Arch Pharm Res. 2015. PMID: 26068939

2

Synthesis, in vitro urease inhibitory potential and molecular docking study of Benzimidazole analogues.

Zaman K, Rahim F, Taha M, Ullah H, Wadood A, Nawaz M, Khan F, Wahab Z, Shah SAA, Rehman AU, Kawde AN, Gollapalli M. Zaman K, et al. Among authors: wadood a. Bioorg Chem. 2019 Aug;89:103024. doi: 10.1016/j.bioorg.2019.103024. Epub 2019 May 31. Bioorg Chem. 2019. PMID: 31176853

3

Hybrid benzothiazole analogs as antiurease agent: Synthesis and molecular docking studies.

Taha M, Ismail NH, Imran S, Wadood A, Rahim F, Khan KM, Riaz M. Taha M, et al. Among authors: wadood a. Bioorg Chem. 2016 Jun;66:80-7. doi: 10.1016/j.bioorg.2016.03.010. Epub 2016 Mar 24. Bioorg Chem. 2016. PMID: 27038849

4

Synthesis, β-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs.

Taha M, Ismail NH, Imran S, Rahim F, Wadood A, Khan H, Ullah H, Salar U, Khan KM. Taha M, et al. Among authors: wadood a. Bioorg Chem. 2016 Oct;68:56-63. doi: 10.1016/j.bioorg.2016.07.008. Epub 2016 Jul 18. Bioorg Chem. 2016. PMID: 27454618

5

Synthesis of potent urease inhibitors based on disulfide scaffold and their molecular docking studies.

Taha M, Ismail NH, Imran S, Wadood A, Rahim F, Riaz M. Taha M, et al. Among authors: wadood a. Bioorg Med Chem. 2015 Nov 15;23(22):7211-8. doi: 10.1016/j.bmc.2015.10.017. Epub 2015 Oct 22. Bioorg Med Chem. 2015. PMID: 26507431

6

Synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory potential of hydrazide based Schiff bases.

Rahim F, Ullah H, Taha M, Wadood A, Javed MT, Rehman W, Nawaz M, Ashraf M, Ali M, Sajid M, Ali F, Khan MN, Khan KM. Rahim F, et al. Among authors: wadood a. Bioorg Chem. 2016 Oct;68:30-40. doi: 10.1016/j.bioorg.2016.07.005. Epub 2016 Jul 15. Bioorg Chem. 2016. PMID: 27441832

7

In silico binding analysis and SAR elucidations of newly designed benzopyrazine analogs as potent inhibitors of thymidine phosphorylase.

Taha M, Ismail NH, Imran S, Rahim F, Wadood A, Al Muqarrabun LM, Khan KM, Ghufran M, Ali M. Taha M, et al. Among authors: wadood a. Bioorg Chem. 2016 Oct;68:80-9. doi: 10.1016/j.bioorg.2016.07.010. Epub 2016 Jul 25. Bioorg Chem. 2016. PMID: 27474803

8

Dihydropyrimidine based hydrazine dihydrochloride derivatives as potent urease inhibitors.

Khan A, Hashim J, Arshad N, Khan I, Siddiqui N, Wadood A, Ali M, Arshad F, Khan KM, Choudhary MI. Khan A, et al. Among authors: wadood a. Bioorg Chem. 2016 Feb;64:85-96. doi: 10.1016/j.bioorg.2015.12.007. Epub 2015 Dec 31. Bioorg Chem. 2016. PMID: 26771129

9

1-[(4'-Chlorophenyl) carbonyl-4-(aryl) thiosemicarbazide derivatives as potent urease inhibitors: Synthesis, in vitro and in silico studies.

Ali B, Khan KM, Salar U, Kanwal, Hussain S, Ashraf M, Riaz M, Wadood A, Taha M, Perveen S. Ali B, et al. Among authors: wadood a. Bioorg Chem. 2018 Sep;79:363-371. doi: 10.1016/j.bioorg.2018.05.017. Epub 2018 May 23. Bioorg Chem. 2018. PMID: 29859384

10

Synthesis of benzotriazoles derivatives and their dual potential as α-amylase and α-glucosidase inhibitors in vitro: Structure-activity relationship, molecular docking, and kinetic studies.

Hameed S, Kanwal, Seraj F, Rafique R, Chigurupati S, Wadood A, Rehman AU, Venugopal V, Salar U, Taha M, Khan KM. Hameed S, et al. Among authors: wadood a. Eur J Med Chem. 2019 Dec 1;183:111677. doi: 10.1016/j.ejmech.2019.111677. Epub 2019 Sep 5. Eur J Med Chem. 2019. PMID: 31514061

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