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Bioorganic and Medicinal Chemistry Letters

Volumn 15, Issue 16, 2005, Pages 3767-3770

Hydrophobicity in the design of P2/P2′ tetrahydropyrimidinone HIV protease inhibitors

(2) Garg, Rajni a Patel, Disha a

a CLARKSON UNIVERSITY (United States)

Author keywords

C log P; Hydrophobicity; MR; P2 P2 tetrahydropyrimidinone; QSAR

Indexed keywords

ALUVIRAN; AMPRENAVIR; INDINAVIR; NELFINAVIR; PROTEINASE INHIBITOR; PYRIMIDINONE DERIVATIVE; RITONAVIR; SAQUINAVIR; VIRUS ENZYME;

ARTICLE; DRUG DESIGN; DRUG STRUCTURE; HYDROPHOBICITY; POLARIZATION; QUANTITATIVE STRUCTURE ACTIVITY RELATION;

DRUG DESIGN; HIV PROTEASE; HIV PROTEASE INHIBITORS; HYDROPHOBICITY; LIGANDS; MOLECULAR CONFORMATION; PYRIMIDINONES; QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 22844449003 PISSN: 0960894X EISSN: None Source Type: Journal
DOI: 10.1016/j.bmcl.2005.05.087 Document Type: Article

Times cited : (14)

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