CC1OC2CC(C)=CC(=O)OCC34CCC5(C)OC5C3OC3CC(OC(=O)C=CC=CC1O2)C4(C)C31CO1

InChIKey=ZIYCBQPVLHOKPQ-UHFFFAOYSA-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 1,3-dioxolanes Lactones Oxacyclic compounds Epoxides Dialkyl ethers Acetals Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteropolycyclic compounds

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