Synthesis of analogues of the benzodiazepine Ro 5-3335, antagonist of Tat HIV-1. Biological evaluation by Luciferase transactivation and anti-viral assay
- 31 December 1996
- journal article
- research article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 31 (6) , 497-505
- https://doi.org/10.1016/0223-5234(96)85171-3
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Bicyclic imidazo derivatives, a new class of highly selective inhibitors for the human immunodeficiency virus type 1Antiviral Research, 1994
- A Tat antagonist inhibits HIV-1 induction in naturally infected and experimentally infected T cellsBiochemical and Biophysical Research Communications, 1992
- Inhibition of HIV Replication in Acute and Chronic Infections in Vitro by a Tat AntagonistScience, 1991
- Systematic Synthesis and Antiviral Evaluation of α-L-Arabinofuranosyl and 2′-Deoxy-α-L-Erythro-Pento-Furanosyl Nucleosides of the Five Naturally Occurring Nucleic Acid BasesNucleosides and Nucleotides, 1991
- The HIV-1 Tat protein: An RNA sequence-specific processivity factor?Cell, 1990
- Fragments of the HIV-1 Tat Protein Specifically Biand TAR RNAScience, 1990
- Inhibition of Antigen-Induced Lymphocyte Proliferation by Tat Protein from HIV-1Science, 1989
- The HIV tat gene induces dermal lesions resembling Kaposi's sarcoma in transgenic miceNature, 1988
- Location of the Trans -Activating Region on the Genome of Human T-Cell Lymphotropic Virus Type IIIScience, 1985
- Trans -Activator Gene of Human T-Lymphotropic Virus Type III (HTLV-III)Science, 1985