Salar U - Search Results

1

N-Aryl-3,4-dihydroisoquinoline Carbothioamide Analogues as Potential Urease Inhibitors.

Ali F, Shamim S, Lateef M, Khan KM, Taha M, Salar U, Wadood A, Rehman AU, Nawaz NUA, Perveen S. Ali F, et al. Among authors: salar u. ACS Omega. 2021 Jun 7;6(24):15794-15803. doi: 10.1021/acsomega.1c01182. eCollection 2021 Jun 22. ACS Omega. 2021. PMID: 34179623 Free PMC article.

2

2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors.

Javaid K, Saad SM, Rasheed S, Moin ST, Syed N, Fatima I, Salar U, Khan KM, Perveen S, Choudhary MI. Javaid K, et al. Among authors: salar u. Bioorg Med Chem. 2015 Dec 1;23(23):7417-21. doi: 10.1016/j.bmc.2015.10.038. Epub 2015 Oct 29. Bioorg Med Chem. 2015. PMID: 26552899

3

Synthesis of 6-chloro-2-Aryl-1H-imidazo[4,5-b]pyridine derivatives: Antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies.

Taha M, Ismail NH, Imran S, Rashwan H, Jamil W, Ali S, Kashif SM, Rahim F, Salar U, Khan KM. Taha M, et al. Among authors: salar u. Bioorg Chem. 2016 Apr;65:48-56. doi: 10.1016/j.bioorg.2016.01.007. Epub 2016 Feb 1. Bioorg Chem. 2016. PMID: 26855413

4

Thiadiazole derivatives as New Class of β-glucuronidase inhibitors.

Salar U, Taha M, Ismail NH, Khan KM, Imran S, Perveen S, Wadood A, Riaz M. Salar U, et al. Bioorg Med Chem. 2016 Apr 15;24(8):1909-18. doi: 10.1016/j.bmc.2016.03.020. Epub 2016 Mar 10. Bioorg Med Chem. 2016. PMID: 26994638

5

Dihydropyrimidones: As novel class of β-glucuronidase inhibitors.

Ali F, Khan KM, Salar U, Iqbal S, Taha M, Ismail NH, Perveen S, Wadood A, Ghufran M, Ali B. Ali F, et al. Among authors: salar u. Bioorg Med Chem. 2016 Aug 15;24(16):3624-35. doi: 10.1016/j.bmc.2016.06.002. Epub 2016 Jun 4. Bioorg Med Chem. 2016. PMID: 27325448

6

Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies.

Salar U, Taha M, Khan KM, Ismail NH, Imran S, Perveen S, Gul S, Wadood A. Salar U, et al. Eur J Med Chem. 2016 Oct 21;122:196-204. doi: 10.1016/j.ejmech.2016.06.037. Epub 2016 Jun 24. Eur J Med Chem. 2016. PMID: 27371923

7

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: salar u. Bioorg Chem. 2016 Oct;68:56-63. doi: 10.1016/j.bioorg.2016.07.008. Epub 2016 Jul 18. Bioorg Chem. 2016. PMID: 27454618

8

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives.

Khan KM, Qurban S, Salar U, Taha M, Hussain S, Perveen S, Hameed A, Ismail NH, Riaz M, Wadood A. Khan KM, et al. Among authors: salar u. Bioorg Chem. 2016 Oct;68:245-58. doi: 10.1016/j.bioorg.2016.08.010. Epub 2016 Aug 24. Bioorg Chem. 2016. PMID: 27592296

9

Coumarin sulfonates: As potential leads for ROS inhibition.

Salar U, Khan KM, Jabeen A, Faheem A, Fakhri MI, Saad SM, Perveen S, Taha M, Hameed A. Salar U, et al. Bioorg Chem. 2016 Dec;69:37-47. doi: 10.1016/j.bioorg.2016.09.006. Epub 2016 Sep 19. Bioorg Chem. 2016. PMID: 27669119

10

Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives.

Salar U, Khan KM, Taha M, Ismail NH, Ali B, Qurat-Ul-Ain, Perveen S, Ghufran M, Wadood A. Salar U, et al. Eur J Med Chem. 2017 Jan 5;125:1289-1299. doi: 10.1016/j.ejmech.2016.11.031. Epub 2016 Nov 14. Eur J Med Chem. 2017. PMID: 27886546

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