Potent and selective activity of a new carbocyclic nucleoside analog (Carbovir: NSC 614846) against human immunodeficiency virus In vitro
Open Access
- 1 October 1988
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 156 (2), 1046-1053
- https://doi.org/10.1016/s0006-291x(88)80950-1
Abstract
No abstract availableFunding Information
- National Institutes of Health (NO1-CA-74102, R01 CA23263)
- U.S. Army Medical Research Institute of Infectious Diseases (DAMD17-86-C-6013)
This publication has 19 references indexed in Scilit:
- The synthesis of XTT: A new tetrazolium reagent that is bioreducible to a water‐soluble formazanJournal of Heterocyclic Chemistry, 1988
- PHASE I STUDIES OF 2',3'-DIDEOXYCYTIDINE IN SEVERE HUMAN IMMUNODEFICIENCY VIRUS INFECTION AS A SINGLE AGENT AND ALTERNATING WITH ZIDOVUDINE (AZT)The Lancet, 1988
- Synthesis and antiviral activity of carbocyclic analogs of xylofuranosides of 2-amino-6-substituted-purines and 2-amino-6-substituted-8-azapurinesJournal of Medicinal Chemistry, 1987
- The Toxicity of Azidothymidine (AZT) in the Treatment of Patients with AIDS and AIDS-Related ComplexNew England Journal of Medicine, 1987
- The Efficacy of Azidothymidine (AZT) in the Treatment of Patients with AIDS and AIDS-Related ComplexNew England Journal of Medicine, 1987
- Potent and selective anti-HTLV-IIILAV activity of 2′,3′-dideoxycytidinene, the 2′,3′-unsaturated derivative of 2′,3′-dideoxycytidineBiochemical and Biophysical Research Communications, 1986
- Carbocyclic analogs of xylofuranosylpurine nucleosides. Synthesis and antitumor activityJournal of Medicinal Chemistry, 1984
- Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for Acquired Immune Deficiency Syndrome (AIDS)Science, 1983
- Facile synthesis of carbocyclic lyxo- and ribonucleosidesThe Journal of Organic Chemistry, 1980
- Synthesis of carbocyclic aminonucleosidesThe Journal of Organic Chemistry, 1978