Structure Information
Structure

Compound Identification

SMILES

COC1=C(Cl)C=C(C[C@H]2NC(=O)\C=C\C[C@H](OC(=O)[C@H](CC(C)C)OC(=O)[C@H](CC(C)C)NC2=O)[C@H](C)[C@H]2O[C@@H]2C2=CC=CC=C2)C=C1

InChIKey

InChIKey=YDFQQEDILSXYKT-ABWCHRGGSA-N

Formula

C37H47ClN2O8

Mass

683.24

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Peptidomimetics

Subclass

Depsipeptides

Intermediate Tree Nodes

Not available

Direct Parent

Cyclic depsipeptides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Cyclic depsipeptide - Macrolide lactam - Macrolide - Alpha-amino acid ester - Macrolactam - Alpha-amino acid or derivatives - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Chlorobenzene - Halobenzene - Benzenoid - Aryl chloride - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Aryl halide - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Lactam - Lactone - Ether - Oxirane - Oxacycle - Dialkyl ether - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organochloride - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

External Descriptors

Not available

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