Weight | 228.298 g/mol |
---|---|
Formula | C8H8N2O2S2 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
Thiolutin (87-11-6)
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- The structures of thiolutin and aureothricin, antibiotics containing a unique pyrrolinonodithiole nucleus (Journal of the American Chemical Society, 1955)
- Mode of action of thiolutin, an inhibitor of macromolecular synthesis in Saccharomyces cerevisiae. (Antimicrobial Agents and Chemotherapy, 1973)
- Inhibition of Yeast Ribonucleic Acid Polymerases by Thiolutin (Journal of Bacteriology, 1973)
- Thiolutin, an inhibitor of HUVEC adhesion to vitronectin, reduces paxillin in HUVECs and suppresses tumor cell-induced angiogenesis (International Journal of Cancer, 2001)
- The transcriptional inhibitor thiolutin blocks mRNA degradation in yeast. (Yeast, 2008)
- Isolation ofiso-butyropyrrothine along with thiolutin and aureothricin from aStreptomyces sp. (Cellular and Molecular Life Sciences, 1960)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)NC1=C2C(=CSS2)N(C1=O)C
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InChIKeyMHMRAFONCSQAIA-UHFFFAOYSA-N
- Pubchem - Thiolutin
- Wikipedia - thiolutin
Thiolutin is a sulfur-containing antibiotic, which is a potent inhibitor of bacterial and yeast RNA polymerases. It was found to inhibit in vitro RNA synthesis directed by all three yeast RNA polymerases (I, II, and III). Thiolutin is also an inhibitor of mannan and glucan formation in Saccharomyces cerevisiae and used for the analysis of mRNA stability.
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