Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=C(C(C2=CC(=CC=C2)[N+]([O-])=O)C(C(=O)C2=CC=C(C)C=C2)=C(N1)C(=O)OCC)C(=O)C1=CC=C(C)C=C1

InChIKey

InChIKey=QFVIGIFTYGBDJM-UHFFFAOYSA-N

Formula

C33H30N2O8

Mass

582.609

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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

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Alpha-amino acid or derivatives - Dihydropyridinecarboxylic acid derivative - Nitrobenzene - Nitroaromatic compound - Benzoyl - Aryl ketone - Dihydropyridine - Toluene - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Hydropyridine - Benzenoid - Vinylogous amide - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Organic nitro compound - Carboxylic acid ester - Ketone - C-nitro compound - Organoheterocyclic compound - Azacycle - Organic 1,3-dipolar compound - Secondary aliphatic amine - Propargyl-type 1,3-dipolar organic compound - Enamine - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Amine - Hydrocarbon derivative - Organic salt - Organonitrogen compound - Organooxygen compound - Organic cation - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

External Descriptors

Not available

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