Emivirin
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Non-proprietary name | Emivirin | |||||||||||||||
other names |
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Molecular formula | C 17 H 22 N 2 O 3 | |||||||||||||||
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Drug information | ||||||||||||||||
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Mechanism of action |
allosteric inhibition of reverse transcriptase |
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properties | ||||||||||||||||
Molar mass | 302.37 g mol −1 | |||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Emivirin (Coactinon, MKC-442) is a non-nucleoside reverse transcriptase inhibitor . However, work on the active ingredient was discontinued by Triangle Pharmaceuticals as no improved effectiveness could be demonstrated. The drug should be used to treat HIV .
pharmacology
Emivirin attaches itself to a region of reverse transcriptase that is adjacent to the catalytic center and allosterically inhibits the enzyme .
literature
- Tanaka, Takashima, Journal of Medicinal Chemistry 1995, Vol 38, No 15, p. 2864
- Szczech, Furman, Painter, et al. a., Antimicrobial agents and chemotherapy , 44 (1), 123-130 dAN 2000
Individual evidence
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.