Structure Information
Structure

Compound Identification

SMILES

CC1=CC(=C(NC(=O)C(OC(=O)CNC(=O)C2=CC=C(Br)C=C2)C2=CC=CC=C2)C=C1)[N+]([O-])=O

InChIKey

InChIKey=NGRJTTYALWSIMY-UHFFFAOYSA-N

Formula

C24H20BrN3O6

Mass

526.343

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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 homomonocyclic compounds

Substituents

Depsipeptide - Alpha-amino acid ester - Hippuric acid or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - 4-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Phenylacetamide - Benzyloxycarbonyl - Nitrobenzene - Benzamide - Nitrotoluene - Anilide - Benzoic acid or derivatives - N-arylamide - Nitroaromatic compound - Benzoyl - Toluene - Bromobenzene - Halobenzene - Aryl bromide - Aryl halide - Benzenoid - Monocyclic benzene moiety - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organic oxoazanium - Monocarboxylic acid or derivatives - Carbonyl group - Organooxygen compound - Organic zwitterion - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organopnictogen compound - Organobromide - Organic oxide - Organohalogen compound - Hydrocarbon derivative - Aromatic homomonocyclic 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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