Compound Identification
SMILES
C[C@H](O)[C@H](O)C1CN=C2NC(N)NC(=O)C2=N1
InChIKey
InChIKey=XFYMOOIPEIPRLU-NURNDFSTSA-N
Formula
C9H15N5O3
Mass
241.251
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Pteridines and derivatives
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Subclass
Pterins and derivatives
- Level 5 Biopterins and derivatives
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Subclass
Pterins and derivatives
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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
Diazinanes Imidolactams 1,2-diols Amino acids and derivatives Secondary carboxylic acid amides Secondary alcohols Ketimines Lactams Ortho amides Orthocarboxylic acid derivatives Carboxamidines Carboximidamides Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives Primary amines
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Biopterin - 1,3-diazinane - Imidolactam - 1,2-diol - Ketimine - Lactam - Carboxamide group - Ortho amide - Orthocarboxylic acid derivative - Secondary alcohol - Amino acid or derivatives - Secondary carboxylic acid amide - Carboxylic acid amidine - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Amidine - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Imine - Organonitrogen compound - Organooxygen compound - Primary amine - Carbonyl group - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Alcohol - 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