Khan MT - Search Results

1

Tyrosinase inhibition studies of cycloartane and cucurbitane glycosides and their structure-activity relationships.

Khan MT, Choudhary MI, Atta-ur-Rahman, Mamedova RP, Agzamova MA, Sultankhodzhaev MN, Isaev MI. Khan MT, et al. Bioorg Med Chem. 2006 Sep 1;14(17):6085-8. doi: 10.1016/j.bmc.2006.05.002. Epub 2006 May 23. Bioorg Med Chem. 2006. PMID: 16716596

2

New tyrosinase inhibitors selected by atomic linear indices-based classification models.

Casañola-Martín GM, Khan MT, Marrero-Ponce Y, Ather A, Sultankhodzhaev MN, Torrens F. Casañola-Martín GM, et al. Among authors: khan mt. Bioorg Med Chem Lett. 2006 Jan 15;16(2):324-30. doi: 10.1016/j.bmcl.2005.09.085. Epub 2005 Nov 3. Bioorg Med Chem Lett. 2006. PMID: 16275084

3

Oxazolones: new tyrosinase inhibitors; synthesis and their structure-activity relationships.

Khan KM, Mughal UR, Khan MT, Zia-Ullah, Perveen S, Choudhary MI. Khan KM, et al. Among authors: khan mt. Bioorg Med Chem. 2006 Sep 1;14(17):6027-33. doi: 10.1016/j.bmc.2006.05.014. Epub 2006 Jun 5. Bioorg Med Chem. 2006. PMID: 16750372

4

Structure-activity relationships of tyrosinase inhibitory combinatorial library of 2,5-disubstituted-1,3,4-oxadiazole analogues.

Khan MT, Choudhary MI, Khan KM, Rani M, Atta-ur-Rahman. Khan MT, et al. Among authors: khan km. Bioorg Med Chem. 2005 May 16;13(10):3385-95. doi: 10.1016/j.bmc.2005.03.012. Bioorg Med Chem. 2005. PMID: 15934142

5

Tyrosinase inhibition studies of diterpenoid alkaloids and their derivatives: structure-activity relationships.

Sultankhodzhaev MN, Khan MT, Moin M, Choudhary MI, Atta-ur-Rahman. Sultankhodzhaev MN, et al. Among authors: khan mt. Nat Prod Res. 2005 Jul;19(5):517-22. doi: 10.1080/14786410512331330585. Nat Prod Res. 2005. PMID: 15938198

6

Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure-activity relationship.

Khan MT, Khan SB, Ather A. Khan MT, et al. Among authors: khan sb. Bioorg Med Chem. 2006 Feb 15;14(4):938-43. doi: 10.1016/j.bmc.2005.09.010. Epub 2005 Oct 3. Bioorg Med Chem. 2006. PMID: 16202612

7

Prediction of tyrosinase inhibition activity using atom-based bilinear indices.

Marrero-Ponce Y, Khan MT, Casañola Martín GM, Ather A, Sultankhodzhaev MN, Torrens F, Rotondo R. Marrero-Ponce Y, et al. Among authors: khan mt. ChemMedChem. 2007 Apr;2(4):449-78. doi: 10.1002/cmdc.200600186. ChemMedChem. 2007. PMID: 17366651

8

Tetraketones: a new class of tyrosinase inhibitors.

Khan KM, Maharvi GM, Khan MT, Jabbar Shaikh A, Perveen S, Begum S, Choudhary MI. Khan KM, et al. Among authors: khan mt. Bioorg Med Chem. 2006 Jan 15;14(2):344-51. doi: 10.1016/j.bmc.2005.08.029. Epub 2005 Sep 28. Bioorg Med Chem. 2006. PMID: 16198580

9

Synthesis of methyl ether analogues of sildenafil (Viagra) possessing tyrosinase inhibitory potential.

Khan KM, Maharvi GM, Perveen S, Khan MT, Abdel-Jalil RJ, Shah ST, Fecker M, Choudhary MI; Atta-ur-Rahman; Voelter W. Khan KM, et al. Among authors: khan mt. Chem Biodivers. 2005 Apr;2(4):470-6. doi: 10.1002/cbdv.200590027. Chem Biodivers. 2005. PMID: 17191995

10

Tyrosinase inhibitors from Rhododendron collettianum and their structure-activity relationship (SAR) studies.

Ahmad VU, Ullah F, Hussain J, Farooq U, Zubair M, Khan MT, Choudhary MI. Ahmad VU, et al. Among authors: khan mt. Chem Pharm Bull (Tokyo). 2004 Dec;52(12):1458-61. doi: 10.1248/cpb.52.1458. Chem Pharm Bull (Tokyo). 2004. PMID: 15577244 Free article.

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