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Chelvam Venkatesh

Affiliations: 
2012- IIT Indore 
Area:
Bio-organic chemistry, natural products chemistry
Website:
http://www.iiti.ac.in/people/~cvenkat/
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"Chelvam Venkatesh"
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Publications

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Venkatesh C, Shen J, Putt KS, et al. (2021) Evaluation of the reducing potential of PSMA-containing endosomes by FRET imaging. Cancer Drug Resistance (Alhambra, Calif.). 4: 223-232
Venkatesh C, Doorneweerd DD, Xia W, et al. (2021) Folate-targeted verrucarin A reduces the number of activated macrophages in a mouse model of acute peritonitis. Bioorganic & Medicinal Chemistry Letters. 128091
Pandit A, Sengupta S, Krishnan MA, et al. (2018) First report on 3D-QSAR and molecular dynamics based docking studies of GCPII inhibitors for targeted drug delivery applications Journal of Molecular Structure. 1159: 179-192
Roy J, Nguyen TX, Kanduluru AK, et al. (2015) DUPA conjugation of a cytotoxic indenoisoquinoline topoisomerase I inhibitor for selective prostate cancer cell targeting. Journal of Medicinal Chemistry. 58: 3094-103
Johnson EO, Chang KH, Ghosh S, et al. (2012) LIMK2 is a crucial regulator and effector of Aurora-A-kinase-mediated malignancy. Journal of Cell Science. 125: 1204-16
Khan TA, Kumar S, Venkatesh C, et al. (2011) Regioselective rapid analog synthesis of 1,3-(or 1,5-)diphenyl-4-aryl/heteroaryl-5-(or 3-)(methylthio)pyrazoles via Suzuki cross-coupling Tetrahedron. 67: 2961-2968
Khan TA, Kumar S, Venkatesh C, et al. (2011) ChemInform Abstract: Regioselective Rapid Analogue Synthesis of 1,3-(or 1,5-)Diphenyl-4-aryl/heteroaryl-5-(or 3-)(methylthio)pyrazoles via Suzuki Cross-Coupling. Cheminform. 42: no-no
Kularatne SA, Venkatesh C, Santhapuram HK, et al. (2010) Synthesis and biological analysis of prostate-specific membrane antigen-targeted anticancer prodrugs. Journal of Medicinal Chemistry. 53: 7767-77
Venkatesh C, Reissig HU. (2008) Model studies for the synthesis of heliquinomycin: Preparation of new spiroketals Synthesis. 3605-3614
Sundaram GS, Singh B, Venkatesh C, et al. (2007) Dipolar cycloaddition of ethyl isocyanoacetate to 3-chloro-2-(methylthio)/2-(methylsulfonyl)quinoxalines: highly regio- and chemoselective synthesis of substituted imidazo[1,5-a]quinoxaline-3-carboxylates. The Journal of Organic Chemistry. 72: 5020-3
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