A possible improvement for structure-based drug design illustrated by the discovery of a Tat HIV-1 inhibitor-Reference-Cited by-同舟云学术

A possible improvement for structure-based drug design illustrated by the discovery of a Tat HIV-1 inhibitor

Published:2004-03 Issue:6 Volume:14 Page:1543-1546
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Montembault Mickaël,Vo-Thanh Giang,Deyine Abdallah,Fargeas Valérie,Villiéras Monique,Adjou Ané,Dubreuil Didier,Esquieu Didier,Grégoire Catherine,Opi Sandrine,Péloponèse Jean-Marie,Campbell Grant,Watkins Jennifer,de Mareuil Jean,Aubertin Anne-Marie,Bailly Christian,Loret Erwann,Lebreton Jacques

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference19 articles.

1. Strategies in the design of antiviral drugs

2. Approaches to solving the rigid receptor problem by identifying a minimal set of flexible residues during ligand docking11PDB coordinates have been deposited with the RSCB with accession ID: 1F28.

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