Compound Identification
SMILES
[H][C@@](O)(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@]([H])(O)C1=NC2([H])C(O)=NC(=N)NC2([H])NC1
InChIKey
InChIKey=NTKATOSHVDZIIF-JEUXIKPASA-N
Formula
C9H18N5O13P3
Mass
497.186
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Pteridines and derivatives
-
Subclass
Pterins and derivatives
- Level 5 Biopterins and derivatives
-
Subclass
Pterins and derivatives
-
Class
Pteridines and derivatives
-
Superclass
Organoheterocyclic compounds
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
Monoalkyl phosphates Hydropyrimidines Secondary alcohols Ketimines 1,2-diols Propargyl-type 1,3-dipolar organic compounds Dialkylamines Carboximidamides Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Biopterin - Monoalkyl phosphate - Hydropyrimidine - 1,2,5,6-tetrahydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - 1,2-diol - Ketimine - Secondary alcohol - Azacycle - Organic 1,3-dipolar compound - Secondary aliphatic amine - Propargyl-type 1,3-dipolar organic compound - Secondary amine - Carboximidamide - Organic oxygen compound - Imine - Alcohol - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Amine - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic 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