Article
A mutation in reverse transcriptase of bis(heteroaryl)piperazine-resistant human immunodeficiency virus type 1 that confers increased sensitivity to other nonnucleoside inhibitors.
Proceedings of the National Academy of Sciences of the United States of America - 15 May 1993
Dueweke T J, Pushkarskaya T, Poppe S M, Swaney S M, Zhao J Q, Chen I S, Stevenson M, Tarpley W G
Abstract excerpt
Several nonnucleoside inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) have been described, including Nevirapine, thiobenzimidazolone (TIBO) derivatives, pyridinone derivatives such as L-697,661, and the bis(heteroaryl)piperazines (BHAPs). HIV-1 resistant to L-...
Topics
- Antiviral Agents
- Base Sequence
- Benzodiazepines
- Benzoxazoles
- Cloning, Molecular
- Delavirdine
- Drug Resistance
- HIV Reverse Transcriptase
- Imidazoles
- Indoles
- Molecular Sequence Data
- Mutation
- Nevirapine
- Oligodeoxyribonucleotides