Deping Chai

发表

An efficient, asymmetric solid-phase synthesis of benzothiadiazine-substituted tetramic acids: potent inhibitors of the hepatitis C virus RNA-dependent RNA polymerase.

G. Burton, R. Sarisky, Victor K. Johnston, 2006, Bioorganic & medicinal chemistry letters.

Discovery of the First Potent and Selective Inhibitor of Centromere-Associated Protein E: GSK923295.

J. D. Elliott, Nicholas D. Adams, X. Qian, 2010, ACS medicinal chemistry letters.

Synthesis and biological activity of heteroaryl 3-(1,1-dioxo-2H-(1,2,4)-benzothiadizin-3-yl)-4-hydroxy-2(1H)-quinolinone derivatives as hepatitis C virus NS5B polymerase inhibitors.

Adam T. Gates, R. Sarisky, D. Dhanak, 2009, Bioorganic & medicinal chemistry letters.

Substituted benzothiadizine inhibitors of Hepatitis C virus polymerase.

Dashyant Dhanak, Adam T. Gates, R. Sarisky, 2009, Bioorganic & medicinal chemistry letters.

Synthesis of the aglycone of 26-O-deacetyl pavoninin-5

Deping Chai, W. Solvibile, J. Williams, 2003 .

Studies toward the synthesis of the shark repellent pavoninin-5

Deping Chai, Dominic Wright, Wei Zhao, 2002, Lipids.

3-(1,1-dioxo-2H-(1,2,4)-benzothiadiazin-3-yl)-4-hydroxy-2(1H)-quinolinones, potent inhibitors of hepatitis C virus RNA-dependent RNA polymerase.

Dashyant Dhanak, Adam T. Gates, G. Hofmann, 2006, Journal of medicinal chemistry.

A highly efficient, asymmetric synthesis of benzothiadiazine-substituted tetramic acids: potent inhibitors of hepatitis C virus RNA-dependent RNA polymerase.

K. Duffy, K. Evans, Deping Chai, 2005, Organic letters.

Synthesis of (25R)-26-hydroxycholesterol

Deping Chai, Dominic Wright, J. Williams, 2002, Steroids.

Quinoline 3-sulfonamides inhibit lactate dehydrogenase A and reverse aerobic glycolysis in cancer cells

Jennifer B Dennison, G. Mills, J. Briand, 2013, Cancer & Metabolism.

Quinoline 3-sulfonamides inhibit lactate dehydrogenase A and reverse aerobic glycolysis in cancer cells

Jennifer B Dennison, G. Mills, J. Briand, 2013, Cancer & metabolism.