CCC(C)(O)C(=O)OC1C2C(C)C(O)C3(O)OCC22C3C3(C)C(O)C(=O)CC(C)C3CC2OC1=O

InChIKey=QRDCRPATTGGLFS-UHFFFAOYSA-N

C25H36O10

496.553

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Terpene lactones

Not available

Quassinoids

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

Aliphatic heteropolycyclic compounds

C-20 quassinoid skeleton - Quassinoid - Naphthopyran - Naphthalene - Delta valerolactone - Fatty acid ester - Delta_valerolactone - Oxepane - Dicarboxylic acid or derivatives - Fatty acyl - Oxane - Pyran - Tertiary alcohol - Tetrahydrofuran - Cyclic alcohol - Secondary alcohol - Cyclic ketone - Carboxylic acid ester - Hemiacetal - Ketone - Lactone - Polyol - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Organic oxide - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - 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