木霉菌素
外观
(重定向自C17H24O4)
| 木霉菌素 | |
|---|---|
| IUPAC命名法 12,13-Epoxytrichothec-9-en-4β-yl acetate | |
| 系统IUPAC名 (2R,2′S,4R,5S,5aR,9aR)-5,5a,8-Trimethyl-2,3,4,5,5a,6,7,9a-octahydrospiro[[2,5]methano[1]benzoxepine-10,2′-oxiran]-4-yl acetate | |
| 识别 | |
| CAS号 | 4682-50-2 |
| PubChem | 20806 |
| ChemSpider | 19582 |
| SMILES |
|
| Beilstein | 6868411 |
| ChEBI | 9688 |
| KEGG | C09741 |
| 性质 | |
| 化学式 | C17H24O4 |
| 摩尔质量 | 292.37 g/mol g·mol⁻¹ |
| 若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 | |
木霉菌素(英語:Trichodermin或称为木霉素)是一种有机化合物,化学式C
17H
24O
4,为一种存在于木霉属(Trichoderma)真菌中的单端孢霉烯[1],可作为真核细胞蛋白质合成抑制剂[2]。
参考文献
[编辑]- ^ Wei, Cha-mer; Hansen, Bent S.; Vaughan, Maurice H.; McLaughlin, Calvin S. Mechanism of Action of the Mycotoxin Trichodermin, a 12,13-Epoxytrichothecene. Proceedings of the National Academy of Sciences. March 1974, 71 (3): 713–717. Bibcode:1974PNAS...71..713W. PMC 388083
. PMID 4522785. doi:10.1073/pnas.71.3.713
.
- ^ Carrasco, L.; Barbacid, M.; Vazquez, D. The trichodermin group of antibiotics, inhibitors of peptide bond formation by eukaryotic ribosomes. Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis. June 1973, 312 (2): 368–376. PMID 4579233. doi:10.1016/0005-2787(73)90381-X.