CC1=CC(O)=CC(O)=C1C(=O)O[C@@H]1C[C@]2(C)[C@H]3[C@@H](O)C(C)(C)C[C@@]3(O)C=C(C=O)[C@]12O

InChIKey=BYWJNFQCWYEWHX-KLMFUOAUSA-N

C23H28O8

432.469

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Sesquiterpenoids

Illudanes and illudins

Melleolides and analogues

p-Hydroxybenzoic acid alkyl esters o-Hydroxybenzoic acid esters Salicylic acid and derivatives Resorcinols Benzoyl derivatives Meta cresols Toluenes 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Vinylogous acids Tertiary alcohols Secondary alcohols Carboxylic acid esters Cyclic alcohols and derivatives Polyols Monocarboxylic acids and derivatives Organic oxides Aldehydes Hydrocarbon derivatives

Aromatic homopolycyclic compounds

Melleolide-skeleton - P-hydroxybenzoic acid alkyl ester - P-hydroxybenzoic acid ester - O-hydroxybenzoic acid ester - Dihydroxybenzoic acid - Salicylic acid or derivatives - Benzoate ester - Benzoic acid or derivatives - M-cresol - Resorcinol - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Toluene - Phenol - Monocyclic benzene moiety - Benzenoid - Vinylogous acid - Cyclic alcohol - Tertiary alcohol - Secondary alcohol - Cyclobutanol - Carboxylic acid ester - Carboxylic acid derivative - Polyol - Monocarboxylic acid or derivatives - Aldehyde - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic homopolycyclic compound

This compound belongs to the class of organic compounds known as melleolides and analogues. These are compounds with a structure characterized by the presence of a 2-hydroxy-4-methoxy-6-methylbenzoic acid derivative linked to a 3,6,6,7b-tetramethyl-cyclobuta[e]indene moiety.

Not available