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Structure Information
Structure

Compound Identification

SMILES

CC1[C@H]2[C@H](CC3=CC=CC=C3)NC(=O)[C@]22OC(=O)O\C=C\[C@@](C)(O)C(=O)[C@@H](C)C\C=C\[C@H]2[C@@H]2O[C@]12C

InChIKey

InChIKey=LAJXCUNOQSHRJO-UZWUCFIWSA-N

Formula

C28H33NO7

Mass

495.572

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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

Cytoglobosin skeleton - Cytochalasan - Macrolactam - Isoindolone - Isoindoline - Isoindole or derivatives - Oxepane - Monocyclic benzene moiety - Carbonic acid diester - Benzenoid - 2-pyrrolidone - Pyrrolidone - Acyloin - Enol ester - Tertiary alcohol - Pyrrolidine - Carboxamide group - Cyclic ketone - Secondary carboxylic acid amide - Ketone - Lactam - Carbonic acid derivative - Organoheterocyclic compound - Ether - Oxirane - Azacycle - Dialkyl ether - Carboxylic acid derivative - Oxacycle - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Organonitrogen compound - 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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