CC(O)C(OCCC1=CC(=O)OC1)\C=C\C=C\C(=O)O[C@@H]1C[C@@H]2O[C@H]3C=C(C)CC[C@@]3(CO)[C@@]1(C)[C@]21CO1

InChIKey=JGIYRVDWRBKREW-ACKIIABYSA-N

C29H38O9

530.614

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Sesquiterpenoids

Not available

Trichothecenes

Fatty alcohols Oxepanes Fatty acid esters Butenolides Dicarboxylic acids and derivatives Oxanes Enoate esters Secondary alcohols Lactones Oxacyclic compounds Epoxides Dialkyl ethers Hydrocarbon derivatives Organic oxides Primary alcohols Carbonyl compounds

Aliphatic heteropolycyclic compounds

Trichothecene skeleton - Fatty alcohol - Fatty acid ester - Oxepane - 2-furanone - Dicarboxylic acid or derivatives - Fatty acyl - Oxane - Dihydrofuran - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Secondary alcohol - Carboxylic acid ester - Lactone - Carboxylic acid derivative - Organoheterocyclic compound - Dialkyl ether - Oxirane - Ether - Oxacycle - Organic oxide - Primary alcohol - Alcohol - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain.

Not available