Khan KM - Search Results

1

An effort to find new α-amylase inhibitors as potent antidiabetics compounds based on indole-based-thiadiazole analogs.

Taha M, Uddin N, Saad SM, Iqbal N, Fareed G, Anouar EH, Hassan MH, Almandil NB, Salahuddin M, Khan KM, Wadood A, Rahman AU. Taha M, et al. Among authors: khan km. J Biomol Struct Dyn. 2022;40(23):13103-13114. doi: 10.1080/07391102.2021.1982774. Epub 2021 Sep 27. J Biomol Struct Dyn. 2022. PMID: 34569449

2

Leishmanicidal potential of N-substituted morpholine derivatives: synthesis and structure-activity relationships.

Khan KM, Khan MZ, Taha M, Maharvi GM, Saify ZS, Parveen S, Choudhary MI. Khan KM, et al. Among authors: khan mz. Nat Prod Res. 2009;23(5):479-84. doi: 10.1080/14786410802090359. Nat Prod Res. 2009. PMID: 19296393

3

Synthesis of bis-Schiff bases of isatins and their antiglycation activity.

Khan KM, Khan M, Ali M, Taha M, Rasheed S, Perveen S, Choudhary MI. Khan KM, et al. Among authors: khan m. Bioorg Med Chem. 2009 Nov 15;17(22):7795-801. doi: 10.1016/j.bmc.2009.09.028. Epub 2009 Sep 19. Bioorg Med Chem. 2009. PMID: 19837595

4

Synthesis and DPPH radical scavenging activity of 5-arylidene-N,N-dimethylbarbiturates.

Khan KM, Khan M, Ali M, Taha M, Hameed A, Ali S, Perveen S, Choudhary MI. Khan KM, et al. Among authors: khan m. Med Chem. 2011 May;7(3):231-6. doi: 10.2174/157340611795564231. Med Chem. 2011. PMID: 21486204

5

Synthesis of novel inhibitors of β-glucuronidase based on benzothiazole skeleton and study of their binding affinity by molecular docking.

Khan KM, Rahim F, Halim SA, Taha M, Khan M, Perveen S, Zaheer-Ul-Haq, Mesaik MA, Iqbal Choudhary M. Khan KM, et al. Among authors: khan m. Bioorg Med Chem. 2011 Jul 15;19(14):4286-94. doi: 10.1016/j.bmc.2011.05.052. Epub 2011 Jun 2. Bioorg Med Chem. 2011. PMID: 21684753

6

Molecular modeling-based antioxidant arylidene barbiturates as urease inhibitors.

Khan KM, Ali M, Wadood A, Zaheer-ul-Haq, Khan M, Lodhi MA, Perveen S, Choudhary MI, Voelter W. Khan KM, et al. Among authors: khan m. J Mol Graph Model. 2011 Sep;30:153-6. doi: 10.1016/j.jmgm.2011.07.001. Epub 2011 Jul 7. J Mol Graph Model. 2011. PMID: 21816644

7

Synthesis of 2,4,6-trichlorophenyl hydrazones and their inhibitory potential against glycation of protein.

Khan KM, Shah Z, Ahmad VU, Khan M, Taha M, Rahim F, Jahan H, Perveen S, Choudhary MI. Khan KM, et al. Among authors: khan m. Med Chem. 2011 Nov;7(6):572-80. doi: 10.2174/157340611797928415. Med Chem. 2011. PMID: 22313297

8

Synthesis and in vitro leishmanicidal activity of disulfide derivatives.

Khan KM, Taha M, Naz F, Khan M, Rahim F, Samreen, Perveen S, Choudhary MI. Khan KM, et al. Among authors: khan m. Med Chem. 2011 Nov;7(6):704-10. doi: 10.2174/157340611797928460. Med Chem. 2011. PMID: 22313310

9

2,4,6-Trichlorophenylhydrazine Schiff bases as DPPH radical and super oxide anion scavengers.

Khan KM, Shah Z, Ahmad VU, Khan M, Taha M, Rahim F, Ali S, Ambreen N, Perveen S, Choudhary MI, Voelter W. Khan KM, et al. Among authors: khan m. Med Chem. 2012 May;8(3):452-61. doi: 10.2174/1573406411208030452. Med Chem. 2012. PMID: 22530900

10

Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers.

Khan KM, Taha M, Naz F, Siddiqui S, Ali S, Rahim F, Perveen S, Choudhary MI. Khan KM, et al. Med Chem. 2012 Jul;8(4):705-10. doi: 10.2174/157340612801216111. Med Chem. 2012. PMID: 22571188

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