Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(NCC(=N2)C(O)C(O)COP(O)(=O)OP(O)(=O)OP(O)(O)=O)N1

InChIKey

InChIKey=DGGUVLXVLHAAGT-UHFFFAOYSA-N

Formula

C9H16N5O13P3

Mass

495.17

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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

Not available

Direct Parent

Biopterins and derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Biopterin - Aminopyrimidine - Pyrimidone - Secondary aliphatic/aromatic amine - Monoalkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Heteroaromatic compound - Vinylogous amide - 1,2-diol - Ketimine - Secondary alcohol - Azacycle - Organic 1,3-dipolar compound - Secondary amine - Propargyl-type 1,3-dipolar organic compound - Amine - Hydrocarbon derivative - Primary amine - Organic oxide - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Alcohol - Imine - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as biopterins and derivatives. These are coenzymes containing a 2-amino-pteridine-4-one derivative. They are mainly synthesized in several parts of the body, including the pineal gland.

External Descriptors

Not available

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