Structure Information
Structure

Compound Identification

SMILES

C[C@H](OC(=O)C(OC(C)(C)C)C(=O)OC(C)(C)C)[C@H](O)[C@H]1CNC2=C(N1C(=O)OC(C)(C)C)C(=O)N=C(N2)\N=C\N(C)C

InChIKey

InChIKey=FWJQXHKZGPIBOI-PLABOJISSA-N

Formula

C28H46N6O9

Mass

610.709

Export to:

JSON SDF CSV

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 - Pterin-5-carboxylate - Pyrimidone - Secondary aliphatic/aromatic amine - Dicarboxylic acid or derivatives - Monosaccharide - Pyrimidine - 1,3-dicarbonyl compound - Heteroaromatic compound - Vinylogous amide - Carbamic acid ester - Amino acid or derivatives - Carboxylic acid ester - Tertiary amine - Secondary alcohol - Amidine - Formamidine - Carboxylic acid amidine - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Secondary amine - Organic oxide - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Amine - Organic nitrogen compound - Organic oxygen 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

Previous Back Next