Structure Information
Structure

Compound Identification

SMILES

CCCNC1=C(NC(CC2=CC=C(NC(=O)C3=CC=C(C=C3)[N+]([O-])=O)C=C2)C(O)=O)C(=O)C1=O

InChIKey

InChIKey=ZFZMYZCKRATATB-UHFFFAOYSA-N

Formula

C23H22N4O7

Mass

466.45

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Subclass

Amino acids, peptides, and analogues

Intermediate Tree Nodes

Amino acids and derivatives - Alpha amino acids and derivatives

Direct Parent

Phenylalanine and derivatives

Alternative Parents

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

Phenylalanine or derivatives - Benzanilide - Aromatic anilide - 3-phenylpropanoic-acid - Alpha-amino acid - Amphetamine or derivatives - Benzamide - Benzoic acid or derivatives - Nitrobenzene - Nitroaromatic compound - Benzoyl - Aralkylamine - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - Benzenoid - Vinylogous amide - Amino acid - Carboxamide group - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Cyclic ketone - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Secondary amine - Organic oxoazanium - Carboxylic acid - Monocarboxylic acid or derivatives - Organic salt - Organooxygen compound - Organic oxygen compound - Amine - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organopnictogen compound - Organic oxide - Organic cation - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

External Descriptors

Not available

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