COC1=C2C(=O)C3=C(OC2=C2C4CCOC4OC2=C1)C=CC=C3OC(C)=O

InChIKey=PJJWGYZJXVDGSN-UHFFFAOYSA-N

C20H16O7

368.341

Organic compounds

Phenylpropanoids and polyketides

Sterigmatocystins

Not available

Not available

Sterigmatocystins

Xanthones Chromones Coumarans Anisoles Pyranones and derivatives Alkyl aryl ethers Vinylogous esters Tetrahydrofurans Heteroaromatic compounds Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Acetals Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Sterigmatocystin backbone - Xanthone - Xanthene - Dibenzopyran - Chromone - 1-benzopyran - Benzopyran - Coumaran - Anisole - Pyranone - Alkyl aryl ether - Benzenoid - Pyran - Heteroaromatic compound - Vinylogous ester - Tetrahydrofuran - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as sterigmatocystins. These are a group of closely related fungal metabolites chemically characterized by a xanthone moiety fused to a dihydrodifurano or a tetrahydrodifurano moiety. The chemical difference among the various sterigmagocystins are the presence or absence of unsaturation at positions 2 and 3 of the difurano ring system, the substitution pattern on positions 6, 7, and 10 of the xanthone system and/or the substituent on position 3 of the difurano system. They are produced by Aspergilus spp. and Bipolaris spp.

Not available