Record Information Version
1.0 Update Date
1/22/2018 11:54:54 AM
Metabolite ID PAMDB110733
Identification Name:
4α-hydroxy-tetrahydrobiopterin Description: Not Available
Structure
Synonyms:
4α-hydroxy-5,6,7,8-tetrahydrobiopterin
4α-hydroxy-tetrahydropterin
6R )-6-(L-erythro -1,2-dihydroxypropyl)-5,6,7,8-tetrahydro-4α-hydroxypterin
Chemical Formula:
C9 H15 N5 O4
Average Molecular Weight:
257.1124039959 Monoisotopic Molecular
Weight:
257.1124039959 InChI Key:
KJKIEFUPAPPGBC-ATDKUNPGSA-N InChI:
InChI=1S/C9H15N5O4/c1-3(15)5(16)4-2-11-6-9(18,14-4)7(17)13-8(10)12-6/h3-5,14-16,18H,2H2,1H3,(H3,10,11,12,13,17)/t3?,4-,5?,9+/m1/s1 CAS
number:
Not Available IUPAC Name: Not Available
Traditional IUPAC Name:
Not Available SMILES: CC(O)C(O)[CH]1(CNC2(=NC(N)=NC(=O)C(O)(N1)2))
Chemical Taxonomy
Taxonomy 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.
Kingdom
Organic compounds Super Class Organoheterocyclic compounds
Class
Pteridines and derivatives Sub Class Pterins and derivatives
Direct Parent
Biopterins and derivatives Alternative Parents
Substituents
Biopterin Hydropyrimidine 1,2,5,6-tetrahydropyrimidine Imidolactam 1,2-diol Secondary alcohol Alkanolamine Amidine Carboxylic acid amidine Secondary aliphatic amine Azacycle Secondary amine Carboximidamide Propargyl-type 1,3-dipolar organic compound Organic 1,3-dipolar compound Organopnictogen compound Hydrocarbon derivative Imine Organonitrogen compound Organooxygen compound Alcohol Amine Organic oxygen compound Organic nitrogen compound Aliphatic heteropolycyclic compound Molecular Framework
Aliphatic heteropolycyclic compounds External Descriptors
tetrahydropterin (CHEBI:15374) a small molecule (CPD-5881)
Physical Properties State:
Not Available Charge: Not Available
Melting point:
Not Available Experimental Properties:
Not Available Predicted Properties
Biological Properties Cellular Locations:
Not Available Reactions:
Pathways:
Spectra Spectra:
Not Available
References References:
Not Available Synthesis Reference:
Not Available Material Safety Data Sheet (MSDS)
Not Available
Links External Links:
This project is supported by
the University of Maryland ,
School of Pharmacy ,
Mass Spectrometry Center , a Waters Center of Excellence. The center is an NIH-investigator funded research and core facility that supports a wide range of cutting-edge metabolomic studies. The Center is supported through a center grant from the University of Maryland and NIH grants to its members. The PAMDB project is affiliated with
The Metabolomics Innovation Centre (TMIC) a leading metabolomics research and service center funded through Genome Alberta, Genome British Columbia and Genome Canada.
