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Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(CC2NC(=O)C34OC(=O)OCCC(C)(O)C(=O)C(C)C\C=C\C3C3OC3(C)C(C)C24)C=C1

InChIKey

InChIKey=STPONZNLANXPID-SOFGYWHQSA-N

Formula

C29H37NO8

Mass

527.614

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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 - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Oxepane - Acyloin - Monocyclic benzene moiety - 2-pyrrolidone - Pyrrolidone - Benzenoid - Carbonic acid diester - Pyrrolidine - Tertiary alcohol - Carboxamide group - Cyclic ketone - Secondary carboxylic acid amide - Ketone - Lactam - Carbonic acid derivative - Ether - Oxirane - Dialkyl ether - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Alcohol - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organic oxide - Organonitrogen compound - Hydrocarbon derivative - 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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