Additivity in the Analysis and Design of HIV Protease Inhibitors-Reference-Cited by-同舟云学术

Additivity in the Analysis and Design of HIV Protease Inhibitors

Published:2009-01-07 Issue:3 Volume:52 Page:737-754
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Jorissen Robert N.¹,Reddy G. S. Kiran Kumar¹,Ali Akbar¹,Altman Michael D.¹,Chellappan Sripriya¹,Anjum Saima G.¹,Tidor Bruce¹,Schiffer Celia A.¹,Rana Tariq M.¹,Gilson Michael K.¹

Affiliation:

1. Center for Advanced Research in Biotechnology, UMBI, 9600 Gudelsky Drive, Rockville, Maryland 20850, Chemical Biology Program, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts, Department of Biological Engineering and Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge,...

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm8009525

Reference31 articles.

1. Joint United Nations Programme on HIV/AIDS (UNAIDS) and World Health Organization (WHO). AIDS Epidemic Update: December, 2007;2007;http://www.unaids.org.

2. HIV chemotherapy

3. New non-nucleoside reverse transcriptase inhibitors (NNRTIs) in development for the treatment of HIV infections

4. Discovery of HIV-1 Protease Inhibitors with Picomolar Affinities Incorporating N-Aryl-oxazolidinone-5-carboxamides as Novel P2 Ligands

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