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Aminothiazoles: Hit to lead development to identify antileishmanial agents.
Eur J Med Chem. 2015 Sep 18;102:582-93. doi: 10.1016/j.ejmech.2015.08.013. Epub 2015 Aug 11.
Eur J Med Chem. 2015.
PMID: 26318065
Design, synthesis and biological evaluation of 2-substituted quinolines as potential antileishmanial agents.
Gopinath VS, Pinjari J, Dere RT, Verma A, Vishwakarma P, Shivahare R, Moger M, Kumar Goud PS, Ramanathan V, Bose P, Rao MV, Gupta S, Puri SK, Launay D, Martin D.
Gopinath VS, et al.
Eur J Med Chem. 2013 Nov;69:527-36. doi: 10.1016/j.ejmech.2013.08.028. Epub 2013 Sep 15.
Eur J Med Chem. 2013.
PMID: 24095747
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Design, synthesis, ADME characterization and antileishmanial evaluation of novel substituted quinoline analogs.
Gopinath VS, Rao M, Shivahare R, Vishwakarma P, Ghose S, Pradhan A, Hindupur R, Sarma KD, Gupta S, Puri SK, Launay D, Martin D.
Gopinath VS, et al.
Bioorg Med Chem Lett. 2014 May 1;24(9):2046-52. doi: 10.1016/j.bmcl.2014.03.065. Epub 2014 Mar 28.
Bioorg Med Chem Lett. 2014.
PMID: 24726804
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Acridones circumvent P-glycoprotein-associated multidrug resistance (MDR) in cancer cells.
Gopinath VS, Thimmaiah P, Thimmaiah KN.
Gopinath VS, et al.
Bioorg Med Chem. 2008 Jan 1;16(1):474-87. doi: 10.1016/j.bmc.2007.09.020. Epub 2007 Sep 15.
Bioorg Med Chem. 2008.
PMID: 17933543
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Nanomolar affinity small molecule correctors of defective Delta F508-CFTR chloride channel gating.
Yang H, Shelat AA, Guy RK, Gopinath VS, Ma T, Du K, Lukacs GL, Taddei A, Folli C, Pedemonte N, Galietta LJ, Verkman AS.
Yang H, et al. Among authors: gopinath vs.
J Biol Chem. 2003 Sep 12;278(37):35079-85. doi: 10.1074/jbc.M303098200. Epub 2003 Jun 27.
J Biol Chem. 2003.
PMID: 12832418
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