Synthesis and HIV inhibition activity of 2′,3′-dideoxy-3′-C-hydroxymethyl nucleosides

Journal of Medicinal Chemistry

Volumn 39, Issue 26, 1996, Pages 5276-5280

  Lee Ruff, E ^a   Ostrowski, Mario ^b   Ladha, Azim ^b   Stynes, Dennis V ^a   Vernik, Isaak ^a   Jiang, Ji Long ^a   Wan, Wei Qin ^c   Ding, Shi Fa ^b   Joshi, Sadhna ^b  

^a YORK UNIVERSITY   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c School of Pharmacy Second Military Medical University Guohe Road 325   (China)

Author keywords

[No Author keywords available]

Indexed keywords

6 (HEXYLOXY) 9 [2',3' DIDEOXY 3' C (HYDROXYMETHYL) BETA D ERYTHRO PENTOFURANOSYL]PURINE; 9 [2',3' DIDEOXY 3' C (HYDROXYMETHYL) BETA D ERYTHRO PENTOFURANOSYL]ADENINE; ADENINE DERIVATIVE; NUCLEOSIDE DERIVATIVE; PURINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIVIRAL ACTIVITY; ARTICLE; DRUG EFFECT; DRUG SYNTHESIS; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS 1; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; VIRUS REPLICATION;

ANTI-HIV AGENTS; CELL LINE; HIV-1; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; PURINE NUCLEOSIDES; SPECTROMETRY, MASS, FAST ATOM BOMBARDMENT;

EID: 0030462245     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm950822k     Document Type: Article

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