Structure Information
Structure

Compound Identification

SMILES

Cl.NC(CC1=CC=C(NC2=C3C=CC(=CC3=NC3=CC=CC=C23)[N+]([O-])=O)C=C1)C(O)=O

InChIKey

InChIKey=QOYWFIBYAGFQHX-UHFFFAOYSA-N

Formula

C22H19ClN4O4

Mass

438.87

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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 heteropolycyclic compounds

Substituents

Phenylalanine or derivatives - Acridine - Benzoquinoline - Nitroquinoline - Aminoquinoline - 4-aminoquinoline - 3-phenylpropanoic-acid - Alpha-amino acid - Amphetamine or derivatives - Quinoline - Nitroaromatic compound - Aniline or substituted anilines - Aralkylamine - Aminopyridine - Primary aromatic amine - Benzenoid - Monocyclic benzene moiety - Pyridine - Heteroaromatic compound - Organic nitro compound - C-nitro compound - Amino acid - Azacycle - Secondary amine - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxoazanium - Organoheterocyclic compound - Hydrochloride - Hydrocarbon derivative - Organonitrogen compound - Primary aliphatic amine - Organooxygen compound - Carbonyl group - Primary amine - Organic zwitterion - Organic oxide - Organic oxygen compound - Organic salt - Amine - Organic nitrogen compound - Aromatic heteropolycyclic 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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