| Weight | 283.283 g/mol |
|---|---|
| Formula | C16H13NO4 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Virstatin (88909-96-0)
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- Virstatin inhibits dimerization of the transcriptional activator ToxT (Proceedings of the National Academy of Sciences of the United States of America, 2007)
- Interaction of Virstatin with Human Serum Albumin: Spectroscopic Analysis and Molecular Modeling (PLOS ONE, 2012)
- Virstatin inhibits biofilm formation and motility of Acinetobacter baumannii (BMC Microbiology, 2014)
- Accessory Cholera Enterotoxin, Ace, from Vibrio cholerae: Structure, Unfolding, and Virstatin Binding (Biochemistry, 2011)
- Molecular mechanisms of virstatin resistance by nonO1/nonO139 strains of Vibrio cholerae (Molecular Microbiology, 2007)
- Role of LuxIR Homologue AnoIR in Acinetobacter nosocomialis and the Effect of Virstatin on the Expression of anoR Gene. (Journal of Microbiology and Biotechnology, 2015)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C3C(=C1)C(=O)N(C(=O)C3=CC=C2)CCCC(=O)O
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InChIKeyZHXRDXTYPCPBTI-UHFFFAOYSA-N
- Pubchem - Virstatin
- Wikipedia - Virstatin
Virstatin is a small molecule that inhibits the activity of the cholera protein, ToxT. Its activity in cholera was first published in 2005 in a paper that described the screening of a chemical library in a phenotypic screen and subsequent testing of one of the hits in infected mice. The compound is an isoquinoline alkaloid and can be synthesized by reacting 1,8-napthalic anhydride with 4-amino-n-butyric acid or by a simple two-step synthesis
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Virstatin
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