CC[C@](C)(O)C(=O)O[C@@H]1[C@H]2[C@@H](C)[C@@H](O)C3(O)OC[C@@]22[C@H]3[C@@]3(C)[C@H](O)[C@@H](O)C=C(C)[C@@H]3C[C@H]2OC1=O

InChIKey=LZKVXMYVBSNXER-JYUFQXQPSA-N

C25H36O10

496.553

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Terpene lactones

Not available

Quassinoids

Triterpenoids Depsipeptides Naphthopyrans Fatty alcohol esters Naphthalenes Oxepanes Fatty acid esters Delta valerolactones Pyrans Oxanes Hemiketals Dicarboxylic acids and derivatives Tetrahydrofurans Tertiary alcohols Secondary alcohols Cyclic alcohols and derivatives Carboxylic acid esters Oxacyclic compounds Organic oxides Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Polycyclic triterpenoid - Triterpenoid - C-20 quassinoid skeleton - Depsipeptide - Quassinoid - Naphthopyran - Fatty alcohol ester - Naphthalene - Oxepane - Delta_valerolactone - Fatty acid ester - Delta valerolactone - Fatty acyl - Pyran - Oxane - Hemiketal - Dicarboxylic acid or derivatives - Tetrahydrofuran - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Lactone - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - 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 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