Structure Information
Structure

Compound Identification

SMILES

NC1=[NH+]C(=O)C2=NC(C[NH2+]C3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O)=CN=C2N1

InChIKey

InChIKey=OVBPIULPVIDEAO-UHFFFAOYSA-P

Formula

C19H21N7O6

Mass

443.419

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Pteridines and derivatives

Subclass

Pterins and derivatives

Intermediate Tree Nodes

Pteroic acids and derivatives - Folic acids and derivatives

Direct Parent

Folic acids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Folic acid - Glutamic acid or derivatives - Hippuric acid or derivatives - Hippuric acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Aminobenzamide - Aminobenzoic acid or derivatives - Benzamide - Benzoic acid or derivatives - Benzoyl - Phenylalkylamine - Aniline or substituted anilines - Pyrimidone - Aminopyrimidine - Aralkylamine - Pyrimidine - Pyrazine - Benzenoid - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Vinylogous amide - Heteroaromatic compound - Secondary carboxylic acid amide - Amino acid - Carboxamide group - Amino acid or derivatives - Lactam - Carboxylic acid derivative - Carboxylic acid - Azacycle - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Primary amine - Organooxygen compound - Organic oxygen compound - Organic oxide - Amine - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as folic acids. These are heterocyclic compounds based on the 4-[(pteridin-6-ylmethyl)amino]benzoic acid skeleton conjugated with one or more L-glutamate units.

External Descriptors

Not available

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