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 |