Structure-activity and cross-resistance evaluations of a series of human immunodeficiency virus type-1-specific compounds related to oxathiin carboxanilide.
@article{Buckheit1995StructureactivityAC, title={Structure-activity and cross-resistance evaluations of a series of human immunodeficiency virus type-1-specific compounds related to oxathiin carboxanilide.}, author={R. Buckheit and T. Kinjerski and V. Fliakas-Boltz and J. Russell and T. L. Stup and L. Pallansch and W. G. Brouwer and D. Dao and W. Harrison and R. J. Schultz}, journal={Antimicrobial agents and chemotherapy}, year={1995}, volume={39}, pages={2718 - 2727} }
A series of compounds related to the nonnucleoside reverse transcriptase (RT) inhibitor (NNRTI) oxathiin carboxanilide (UC84) were evaluated for activity against the human immunodeficiency virus (HIV) to determine structural requirements for anti-HIV activity. Twenty-seven compounds representative of the more than 400 Uniroyal Chemical Company (UC) compounds were evaluated for structure-activity relationships. Several of the compounds evaluated were highly active, with 50% effective… CONTINUE READING
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References
SHOWING 1-10 OF 49 REFERENCES
Viral resistance to the thiazolo-iso-indolinones, a new class of nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase.
- Biology, Medicine
- Antimicrobial Agents and Chemotherapy
- 1993
- 57
- PDF
Biological and biochemical anti-HIV activity of the benzothiadiazine class of nonnucleoside reverse transcriptase inhibitors.
- Biology, Medicine
- Antiviral research
- 1994
- 66
Differential antiviral activity of two TIBO derivatives against the human immunodeficiency and murine leukemia viruses alone and in combination with other anti-HIV agents.
- Biology, Medicine
- AIDS research and human retroviruses
- 1993
- 17
Suppression of the breakthrough of human immunodeficiency virus type 1 (HIV-1) in cell culture by thiocarboxanilide derivatives when used individually or in combination with other HIV-1-specific inhibitors (i.e., TSAO derivatives).
- Biology, Medicine
- Proceedings of the National Academy of Sciences of the United States of America
- 1995
- 40
- PDF
Carboxanilide derivative non-nucleoside inhibitors of HIV-1 reverse transcriptase interact with different mechanistic forms of the enzyme.
- Chemistry, Medicine
- Biochemistry
- 1995
- 28
Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives
- Biology, Medicine
- Nature
- 1990
- 652
In vitro selection and molecular characterization of human immunodeficiency virus-1 resistant to non-nucleoside inhibitors of reverse transcriptase.
- Biology, Medicine
- Molecular pharmacology
- 1992
- 122
Identification of the human immunodeficiency virus reverse transcriptase residues that contribute to the activity of diverse nonnucleoside inhibitors.
- Biology, Medicine
- Antimicrobial Agents and Chemotherapy
- 1992
- 65
- PDF