Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=QOYWFIBYAGFQHX-FERBBOLQSA-N

Formula

C22H19ClN4O4

Mass

438.87

Export to:

JSON SDF CSV

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 - Benzoquinoline - Acridine - Nitroquinoline - Quinoline - Amphetamine or derivatives - Nitroaromatic compound - Hydroxypyridine - Heterocyclic fatty acid - Branched fatty acid - Fatty acyl - Benzenoid - Pyridine - Monocyclic benzene moiety - Heteroaromatic compound - Secondary ketimine - Amino acid - Organic nitro compound - C-nitro compound - Ketimine - Azacycle - 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 - Secondary aliphatic amine - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Hydrochloride - Organic zwitterion - Organooxygen compound - Organonitrogen compound - Organic hyponitrite - Primary aliphatic amine - Imine - Amine - 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

Previous Back Next