Structure Information
Structure

Compound Identification

SMILES

CN(CC1=CN=C2N=C(N)N=C(N)C2=N1)C1=CC=C(C=C1)C(=O)NC(CCC(=O)OC1=CC=CC(CO[N+]([O-])=O)=C1)C(=O)OC1=CC=CC(CO[N+]([O-])=O)=C1

InChIKey

InChIKey=LGGOKSLGLHEJPI-UHFFFAOYSA-N

Formula

C34H32N10O11

Mass

756.689

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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

Glutamic acid and derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Glutamic acid or derivatives - Alpha-amino acid ester - N-acyl-alpha amino acid or derivatives - Hippuric acid or derivatives - Pteridine - Aminobenzamide - Aminobenzoic acid or derivatives - Phenol ester - Benzamide - Benzoic acid or derivatives - Tertiary aliphatic/aromatic amine - Phenoxy compound - Benzoyl - Aniline or substituted anilines - Dialkylarylamine - Aminopyrimidine - Fatty acid ester - Aralkylamine - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Fatty acyl - Imidolactam - Pyrazine - Pyrimidine - Benzenoid - Heteroaromatic compound - Alkyl nitrate - Organic nitrate - Tertiary amine - Secondary carboxylic acid amide - Organic nitro compound - Carboxamide group - Carboxylic acid ester - Organic nitric acid or derivatives - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic salt - Amine - Carbonyl group - Organic zwitterion - Organic nitrogen compound - Primary amine - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as glutamic acid and derivatives. These are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid 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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