CC(=O)[C@@]12CC\C=C/C(=O)O[C@@H]3C[C@H]4O[C@@H]5C=C(C)CC[C@]5(COC(=O)\C=C(/CCO1)[C@H]2O)[C@]3(C)C41CO1

InChIKey=LXIQXFWXXPJPEE-SSIJUUGUSA-N

C29H36O9

528.598

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Sesquiterpenoids

Not available

Trichothecenes

Macrolides and analogues Oxepanes Oxanes Dicarboxylic acids and derivatives Enoate esters Secondary alcohols Lactones Ketones Oxacyclic compounds Epoxides Dialkyl ethers Organic oxides Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Trichothecene skeleton - Macrolide - Oxepane - Dicarboxylic acid or derivatives - Oxane - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Secondary alcohol - Ketone - Lactone - Carboxylic acid derivative - Organoheterocyclic compound - Dialkyl ether - Oxirane - Ether - Oxacycle - Organic oxygen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - 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