Khan KM - Search Results

1

3-substituted coumarin derivatives over-activate the HslV protease: A potential drug target for antibacterial activity.

Aurangzeb S, Hamid M, Salar U, Rashid Y, Khan KM, Azim MK, Bashir S. Aurangzeb S, et al. Among authors: khan km. Pak J Pharm Sci. 2022 Jul;35(4(Special)):1241-1250. Pak J Pharm Sci. 2022. PMID: 36218103

2

Synthesis of coumarin derivatives with cytotoxic, antibacterial and antifungal activity.

Khan KM, Saify ZS, Khan MZ, Zia-Ullah, Choudhary IM, Atta-Ur-Rahman, Perveen S, Chohan ZH, Supuran CT. Khan KM, et al. Among authors: khan mz. J Enzyme Inhib Med Chem. 2004 Aug;19(4):373-9. doi: 10.1080/14756360409162453. J Enzyme Inhib Med Chem. 2004. PMID: 15558956

3

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: khan km. 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

4

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: khan km. Bioorg Chem. 2016 Apr;65:48-56. doi: 10.1016/j.bioorg.2016.01.007. Epub 2016 Feb 1. Bioorg Chem. 2016. PMID: 26855413

5

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. Among authors: khan km. 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

6

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: khan km. 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

7

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. Among authors: khan km. 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

8

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: khan km, khan h. Bioorg Chem. 2016 Oct;68:56-63. doi: 10.1016/j.bioorg.2016.07.008. Epub 2016 Jul 18. Bioorg Chem. 2016. PMID: 27454618

9

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. Bioorg Chem. 2016 Oct;68:245-58. doi: 10.1016/j.bioorg.2016.08.010. Epub 2016 Aug 24. Bioorg Chem. 2016. PMID: 27592296

10

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. Among authors: khan km. Bioorg Chem. 2016 Dec;69:37-47. doi: 10.1016/j.bioorg.2016.09.006. Epub 2016 Sep 19. Bioorg Chem. 2016. PMID: 27669119

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