5'-Hydrogenphosphonates and 5'-methylphosphonates of sugar modified pyrimidine nucleosides as potential anti-HIV-1 agents Journal Article


Authors: Krayevsky, A. A.; Tarussova, N. B.; Zhu, Q. Y.; Vidal, P.; Chou, T. C.; Baron, P.; Polsky, B.; Jiang, X. J.; Matulič-Adamič, J.; Rosenberg, I.; Watanabe, K. A.
Article Title: 5'-Hydrogenphosphonates and 5'-methylphosphonates of sugar modified pyrimidine nucleosides as potential anti-HIV-1 agents
Abstract: A number of nucleoside 5‘;-hydrogenphosphonates and nucleoside 5‘;-ioethylphosphonates were prepared, to study their ability to inhibit replication of HIV-1. Two compounds, the 5’-hydrogenphosphonate of 3’;-azido-3‘; -deoxythymidine (AZT-HP, IVc) and of 3‘; -deoxy-3‘; -fluorothymidine (FLT-HP, IVa), exhibit potent anti-HIV-1 activity with selectivity indices similar to or better than those of their parent nucleosides. © 1992, Taylor & Francis Group, LLC. All rights reserved.
Keywords: unclassified drug; human cell; nonhuman; mass spectrometry; enzyme inhibition; cytotoxicity; drug synthesis; antivirus agent; virus replication; nuclear magnetic resonance; antiviral activity; human immunodeficiency virus 1; nucleoside; zidovudine; phosphonic acid derivative; 3' fluorothymidine; pyrimidine nucleoside; rna directed dna polymerase; article; zalcitabine; ultraviolet spectrophotometry; 2',3' dideoxyadenosine; 2',3' dideoxythymidine; 3' deoxy 3' fluorothymidine 5' hydrogenphosphonate; zidovudine 5' hydrogenphosphonate
Journal Title: Nucleosides & Nucleotides
Volume: 11
Issue: 2-4
ISSN: 0732-8311
Publisher: Taylor & Francis Inc.  
Date Published: 1992-01-01
Start Page: 177
End Page: 196
Language: English
DOI: 10.1080/07328319208021696
PROVIDER: scopus
DOI/URL:
Notes: Source: Scopus
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  1. Bruce Polsky
    69 Polsky
  2. Ting-Chao Chou
    319 Chou
  3. Kyoichi A Watanabe
    125 Watanabe
  4. Penny A Baron
    27 Baron