Structure Information
Structure

Compound Identification

SMILES

CNC1=C(C=C(C=C1)S(=O)(=O)NCC(=O)OCC(=O)NC1=CC2=C(OCCO2)C=C1)[N+]([O-])=O

InChIKey

InChIKey=UURVHMWNSHYDTD-UHFFFAOYSA-N

Formula

C19H20N4O9S

Mass

480.45

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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 heteropolycyclic compounds

Substituents

Depsipeptide - Alpha-amino acid ester - Benzodioxane - Benzo-1,4-dioxane - Benzenesulfonamide - Alpha-amino acid or derivatives - Nitrobenzene - Nitroaromatic compound - Phenylalkylamine - N-arylamide - Secondary aliphatic/aromatic amine - Alkyl aryl ether - Benzenoid - Para-dioxin - Monocyclic benzene moiety - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic nitro compound - C-nitro compound - Carboxylic acid ester - Carboxamide group - Amino acid or derivatives - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Secondary amine - Organic oxoazanium - Monocarboxylic acid or derivatives - Ether - Secondary aliphatic amine - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic hyponitrite - Amine - Aromatic heteropolycyclic 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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