Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(CO[C@@H]([C@H](C)O)C2=CN=C3N=C(\N=C\N(C)C)N(CCC4=CC=C(C=C4)[N+]([O-])=O)C(=O)C3=N2)C=C1

InChIKey

InChIKey=IFHPYGZPFPBNBY-SNZSVNCMSA-N

Formula

C28H31N7O6

Mass

561.599

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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 - Benzylether - Nitrobenzene - Phenoxy compound - Anisole - Nitroaromatic compound - Phenol ether - Methoxybenzene - Alkyl aryl ether - Pyrimidone - Monocyclic benzene moiety - Pyrazine - Pyrimidine - Benzenoid - Heteroaromatic compound - Organic nitro compound - Secondary alcohol - C-nitro compound - Lactam - Allyl-type 1,3-dipolar organic compound - Formamidine - Azacycle - Amidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid amidine - Organic oxoazanium - Dialkyl ether - Ether - Organic zwitterion - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organic oxygen compound - Alcohol - Organooxygen compound - Organic nitrogen compound - Organic salt - 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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