CC1OC2OC1\C=C/C=C\C(=O)O[C@@H]1C[C@H]3O[C@@H]4C=C(C)CC[C@]4(COC(=O)\C=C(C)/C2O)[C@]1(C)C31CO1

InChIKey=MCGWYAODOJPYQT-QUOOWUKISA-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 Secondary alcohols 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 - Secondary alcohol - Lactone - Carboxylic acid ester - Oxacycle - Acetal - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Oxirane - Dialkyl ether - Alcohol - Organic oxygen compound - Organic oxide - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - 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