Synthesis and Anti-Human Immunodeficiency Virus(HIV-1) Activity of 3'-Deoxy-3'- (Triazol-1-Ly)thymidines and 2',3'-Dideoxy-3'-(Triazol-1-Yl)uridines, and Inhibition of Reverse Transcriptase by Their 5'-Triphosphates.

Chemical and Pharmaceutical Bulletin- Japan

doi 10.1248/cpb.38.2597

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January 1, 1990

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Pharmaceutical Society of Japan

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Synthesis and Anti-Human Immunodeficiency Virus(HIV-1) Activity of 3'-Deoxy-3'- (Triazol-1-Ly)thymidines and 2',3'-Dideoxy-3'-(Triazol-1-Yl)uridines, and Inhibition of Reverse Transcriptase by Their 5'-Triphosphates.

Chemical and Pharmaceutical Bulletin- Japan

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Abstract

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Authors

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3-Phenyl-1h-1,2,4-Triazol-5-Amine–5-Phenyl-1h-1,2,4-Triazol-3-Amine (1/1)

Biological Activity of Novel N-Substituted Amides of Endo-3-(3-Methylthio-1,2,4-Triazol-5-Yl)bicyclo[2.2.1]hept-5-Ene-2-Carboxylic Acid and N-Substituted Amides of 1-(5-Methylthio-1,2,4-Triazol-3-Yl)cyclohexane-2-Carboxylic Acids

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Synthesis and Reactions of 3-(1,2,4-Triazol-5-Yl)methylene-2-Oxo-1,2,3,4-Tetrahydroquinoxalines.

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