C[13C@H]1[13CH2]\[13CH]=[13CH]\[13C@H]2[13C@@H]3O[13C@]3(C)[13C@@H]([13CH3])[C@H]3[C@H](CC4=CNC5=CC=CC=C45)N[13C](=O)[13C@@]23[13C](=O)\[13CH]=[13CH]\[13CH2][13CH2]\[13C](C)=[13CH]\1

InChIKey=WDTVRLZSWNFOOH-GRWXZSFHSA-N

C32H38N2O3

516.529

Organic compounds

Alkaloids and derivatives

Cytochalasans

Chaetoglobosins

Not available

Chaetoglobosins

Macrolactams 3-alkylindoles Isoindolones Oxepanes Substituted pyrroles Pyrrolidine-2-ones Benzenoids Heteroaromatic compounds Secondary carboxylic acid amides Lactams Ketones Oxacyclic compounds Azacyclic compounds Dialkyl ethers Epoxides Organonitrogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Chaetoglobosin skeleton - Macrolactam - Isoindolone - 3-alkylindole - Indole - Indole or derivatives - Isoindoline - Isoindole or derivatives - Oxepane - Benzenoid - Substituted pyrrole - 2-pyrrolidone - Pyrrolidone - Heteroaromatic compound - Pyrrolidine - Pyrrole - Carboxamide group - Ketone - Lactam - Secondary carboxylic acid amide - Azacycle - Oxacycle - Carboxylic acid derivative - Ether - Oxirane - Dialkyl ether - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as chaetoglobosins. These are cytochalasans with a structure in which the hydrogenated isoindole bears an (indol-3-yl)methyl group.

Not available