C\C=C(/C)C(=O)O[C@H]1[C@H]2OC(=O)[C@H](O)[C@H]3[C@@H](C)[C@@H](O)C4(O)OC[C@]23[C@H]4[C@@]2(C)[C@H](O)[C@@H](O)C=C(C)[C@H]12

InChIKey=OMOJVYZMOHWBDG-SCCYAIPWSA-N

C25H34O10

494.537

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Terpene lactones

Not available

Quassinoids

Triterpenoids Naphthopyrans Naphthalenes Oxepanes Fatty acid esters Delta valerolactones Pyrans Oxanes Dicarboxylic acids and derivatives Tetrahydrofurans Enoate esters Secondary alcohols Hemiacetals Cyclic alcohols and derivatives Polyols Oxacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteropolycyclic compounds

Polycyclic triterpenoid - Triterpenoid - C-20 quassinoid skeleton - Quassinoid - Naphthopyran - Naphthalene - Oxepane - Delta_valerolactone - Fatty acid ester - Delta valerolactone - Fatty acyl - Pyran - Oxane - Dicarboxylic acid or derivatives - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Tetrahydrofuran - Cyclic alcohol - Secondary alcohol - Lactone - Hemiacetal - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.

Not available