C[C@@H]1C(=O)O[C@H]2C[C@@]34[C@H]5C[C@@H](C(C)(C)C)[C@]33[C@@H](OC(=O)[C@@H]3O)O[C@@]4(C(=O)O5)[C@@]12O[C@@H]1O[C@H](O)[C@@H](O)[C@H](O)[C@H]1O

InChIKey=OIAKSUXPJZKIAN-FOESXVIZSA-N

C25H32O14

556.517

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Terpene lactones

Diterpene lactones

Ginkgolides and bilobalides

Diterpenoids O-glycosyl compounds Tricarboxylic acids and derivatives Furofurans Gamma butyrolactones Monosaccharides Oxanes Oxolanes Hemiacetals Secondary alcohols Carboxylic acid esters Acetals Polyols Oxacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides

Aliphatic heteropolycyclic compounds

Ginkgolide-skeleton - Diterpenoid - Glycosyl compound - O-glycosyl compound - Tricarboxylic acid or derivatives - Furofuran - Gamma butyrolactone - Monosaccharide - Oxane - Oxolane - Secondary alcohol - Carboxylic acid ester - Hemiacetal - Lactone - Polyol - Carboxylic acid derivative - Organoheterocyclic compound - Acetal - Oxacycle - Organic oxygen compound - Organooxygen compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Alcohol - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as ginkgolides and bilobalides. These are diterpene lactones with a structure based either on the gingkolide or the bilobalide skeleton. The ginkgolide skeleton is a very rigid structure consisting of hexacyclic C20 trilactone. The cis-fused F/A/D/C ring junction forms an empty semi-ball hole, the D ring contains a cage form tetrahydrofuran ring which occupies the center of the empty hole, and the oxygen atoms of the D,C and F ring and 10-hydroxyl group consist of an analogous crown ether structure.

Not available