Structure Information
Structure

Compound Identification

SMILES

C[C@H]1C\C=C\[C@H]2[C@H](O)C(C)=C(C)[C@H]3[C@H](CC4=CC=CC=C4)NC(=O)[C@]23[C@H](O)\C=C\[C@@](C)(O)C1=O

InChIKey

InChIKey=AOIKFORBJLUJGZ-PKFSBTPPSA-N

Formula

C28H35NO5

Mass

465.59

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Cytochalasans

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Cytochalasans

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Cytochalasan - Carbocyclic cytochalasan skeleton - Isoindolone - Isoindole or derivatives - Isoindole - Isoindoline - Benzenoid - 2-pyrrolidone - Pyrrolidone - Monocyclic benzene moiety - Acyloin - Tertiary alcohol - Pyrrolidine - Cyclic ketone - Secondary carboxylic acid amide - Secondary alcohol - Lactam - Ketone - Carboxamide group - Azacycle - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as cytochalasans. These are fungal metabolites structurally characterized by the presence of an isoindolone nucleus fused to a macrocyclic ring, which can either a lactone, as in cytochalasin B, a carbonate, as in cytochalasin E, or a carbocycle, as in cytochalasin D, H, and K.

External Descriptors

Not available

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