CC[C@H](C)C(=O)O[C@H]1C[C@H](O)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)OC3=C(OP(O)(=O)OC4CC[C@@]5(C)[C@@H](CC[C@H]6[C@@H]7CCC([C@H](C)CC[C@@H](C)C(C)C)[C@@]7(C)CC[C@H]56)C4)C(=O)OC3C(O)CO)[C@@H]12

InChIKey=GULRJLPGAWCCLY-FTDHRZTMSA-N

C57H91O15P

1047.314

Organic compounds

Lipids and lipid-like molecules

Steroids and steroid derivatives

Ergostane steroids

Not available

Ergostane steroids

Steroid lactones Tricarboxylic acids and derivatives Monoalkyl phosphates Beta hydroxy acids and derivatives Butenolides Enol esters Enoate esters Secondary alcohols Lactones Oxacyclic compounds Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteropolycyclic compounds

Ergostane-skeleton - Steroid lactone - Tricarboxylic acid or derivatives - Beta-hydroxy acid - Monoalkyl phosphate - 2-furanone - Hydroxy acid - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Dihydrofuran - Enol ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Lactone - Carboxylic acid ester - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Organooxygen compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Primary alcohol - Organic oxygen compound - Organic oxide - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position.

Not available