CC(=O)OC[C@]12[C@H](OC(C)=O)C(=O)C(C)=C[C@H]1OC1[C@H](O)C[C@@]2(C)C11CO1

InChIKey=LRARZSDWZXRWLZ-RXMAYRRKSA-N

C19H24O8

380.393

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Sesquiterpenoids

Not available

Trichothecenes

Fatty alcohol esters Iridoids and derivatives Oxepanes Cyclohexenones Alpha-acyloxy ketones Oxanes Monosaccharides Dicarboxylic acids and derivatives Alpha-branched alpha,beta-unsaturated ketones Enones Acryloyl compounds Secondary alcohols Cyclic alcohols and derivatives Carboxylic acid esters Oxacyclic compounds Epoxides Dialkyl ethers Organic oxides Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Trichothecene skeleton - Fatty alcohol ester - Secoiridoid-skeleton - Monoterpenoid - Cyclohexenone - Alpha-acyloxy ketone - Oxepane - Alpha-branched alpha,beta-unsaturated-ketone - Oxane - Monosaccharide - Dicarboxylic acid or derivatives - Alpha,beta-unsaturated ketone - Enone - Cyclic alcohol - Acryloyl-group - Cyclic ketone - Secondary alcohol - Ketone - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Alcohol - 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