Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC=CC=C1OCC(=O)OCC(=O)NC1=CC=C(C=C1)S(=O)(=O)N1CCOCC1

InChIKey

InChIKey=IJZQCJPERWYLSH-UHFFFAOYSA-N

Formula

C20H21N3O9S

Mass

479.46

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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

Depsipeptides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Depsipeptide - Nitrophenyl ether - Phenoxyacetate - Benzenesulfonamide - Benzenesulfonyl group - Nitrobenzene - Anilide - Phenoxy compound - Nitroaromatic compound - N-arylamide - Phenol ether - Alkyl aryl ether - Oxazinane - Morpholine - Organosulfonic acid amide - Monocyclic benzene moiety - Benzenoid - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Carboxamide group - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Oxacycle - Organic oxoazanium - Azacycle - Organoheterocyclic compound - Organic zwitterion - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound

Description

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

External Descriptors

Not available

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