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Journal of the American Chemical Society|February 3, 2012
Hydrophobic core flexibility modulates enzyme activity in HIV-1 proteaseSeema Mittal, Yufeng Cai, Madhavi N L Nalam, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 20, 2003
Programming peptidomimetic syntheses by translating genetic codes designed de novoAnthony C Forster, Zhongping Tan, Madhavi N L Nalam, et al.
ACS Chemical Biology|August 20, 2013
Testing the substrate-envelope hypothesis with designed pairs of compoundsYang Shen, Michael D Altman, Akbar Ali, et al.
Journal of Medicinal Chemistry|October 21, 2010
Structure-based design, synthesis, and structure-activity relationship studies of HIV-1 protease inhibitors incorporating phenyloxazolidinonesAkbar Ali, G S Kiran Kumar Reddy, Madhavi N L Nalam, et al.
Journal of Medicinal Chemistry|December 8, 2006
Discovery of HIV-1 protease inhibitors with picomolar affinities incorporating N-aryl-oxazolidinone-5-carboxamides as novel P2 ligandsAkbar Ali, G S Kiran Kumar Reddy, Hong Cao, et al.
Journal of Medicinal Chemistry|June 20, 2012
Design, synthesis, and biological and structural evaluations of novel HIV-1 protease inhibitors to combat drug resistanceMaloy Kumar Parai, David J Huggins, Hong Cao, et al.
Journal of Virology|February 1, 2013
Structural and thermodynamic basis of amprenavir/darunavir and atazanavir resistance in HIV-1 protease with mutations at residue 50Seema Mittal, Rajinthna M Bandaranayake, Nancy M King, et al.
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