CC1=CC2OC3C(=O)C(OC(=O)CCl)C(C)(C33CO3)C2(COC(=O)CCl)CC1

InChIKey=QTWLIYSPGOWHAJ-UHFFFAOYSA-N

C19H22Cl2O7

433.28

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Sesquiterpenoids

Not available

Trichothecenes

Oxepanes Alpha-acyloxy ketones Oxanes Dicarboxylic acids and derivatives Alpha-halocarboxylic acid derivatives Ketones Carboxylic acid esters Oxacyclic compounds Epoxides Dialkyl ethers Organochlorides Organic oxides Hydrocarbon derivatives Alkyl chlorides

Aliphatic heteropolycyclic compounds

Trichothecene skeleton - Oxepane - Alpha-acyloxy ketone - Dicarboxylic acid or derivatives - Oxane - Alpha-halocarboxylic acid derivative - Alpha-halocarboxylic acid or derivatives - Carboxylic acid ester - Ketone - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Organooxygen compound - Organochloride - Organohalogen compound - Alkyl chloride - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Alkyl halide - 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