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The design and synthesis of diaryl ether second generation HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) with enhanced potency versus key clinical mutations.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2008 May 01; Vol. 18 (9), pp. 2959-66. Date of Electronic Publication: 2008 Mar 25. - Publication Year :
- 2008
-
Abstract
- Using a combination of traditional Medicinal Chemistry/SAR analysis, crystallography, and molecular modeling, we have designed and synthesized a series of novel, highly potent NNRTIs that possess broad antiviral activity against a number of key clinical mutations.
- Subjects :
- Anti-HIV Agents chemical synthesis
Binding Sites
Crystallography, X-Ray
Drug Resistance, Viral
HIV-1 enzymology
HIV-1 genetics
Models, Chemical
Mutation
Nucleosides chemistry
Reverse Transcriptase Inhibitors chemical synthesis
Structure-Activity Relationship
Virus Replication physiology
Anti-HIV Agents pharmacology
Drug Design
Ethers chemistry
HIV-1 drug effects
Reverse Transcriptase Inhibitors pharmacology
Virus Replication drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 18
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 18396399
- Full Text :
- https://doi.org/10.1016/j.bmcl.2008.03.064