Potent and selective activity of a new carbocyclic nucleoside analog (carbovir: NSC 614846) against human immunodeficiency virus in vitro

Biochem Biophys Res Commun. 1988 Oct 31;156(2):1046-53. doi: 10.1016/s0006-291x(88)80950-1.

Abstract

Carbocyclic 2',3'-didehydro-2',3'-dideoxyguanosine (Carbovir: NSC 614846), a novel nucleoside analog, emerged as a potent and selective anti-HIV agent from a large screening program conducted by the National Cancer Institute and its contractors. Its hydrolytic stability and its ability to inhibit the infectivity and replication of HIV in T-cells at concentrations of approximately 200- to 400-fold below toxic concentrations make carbovir a top-priority candidate for development as a potential antiretroviral agent in the treatment of AIDS patients.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acquired Immunodeficiency Syndrome / drug therapy
  • Antiviral Agents
  • Cytopathogenic Effect, Viral / drug effects
  • Dideoxynucleosides / pharmacology*
  • HIV / drug effects*
  • HIV / physiology
  • Molecular Structure
  • Structure-Activity Relationship
  • Virus Replication / drug effects
  • Zalcitabine
  • Zidovudine / pharmacology

Substances

  • Antiviral Agents
  • Dideoxynucleosides
  • carbovir
  • Zidovudine
  • Zalcitabine