Record Information Version
1.0 Update Date
1/22/2018 11:54:54 AM
Metabolite ID PAMDB110096
Identification Name:
(R )-1-amino-2-propanol O -2-phosphate Description: Not Available
Structure
Synonyms:
(R )-1-aminopropan-2-yl phosphate
Chemical Formula:
C3 H9 NO4 P
Average Molecular Weight:
156.0425693567 Monoisotopic Molecular
Weight:
156.0425693567 InChI Key:
YBOLZUJJGUZUDC-GSVOUGTGSA-M InChI:
InChI=1S/C3H10NO4P/c1-3(2-4)8-9(5,6)7/h3H,2,4H2,1H3,(H2,5,6,7)/p-1/t3-/m1/s1 CAS
number:
Not Available IUPAC Name: Not Available
Traditional IUPAC Name:
Not Available SMILES: CC(C[N+])OP(=O)([O-])[O-]
Chemical Taxonomy
Taxonomy Description This compound belongs to the class of organic compounds known as alkyl phosphates. These are organic compounds containing a phosphate group that is linked to one or more alkyl chains.
Kingdom
Organic compounds Super Class Organic acids and derivatives
Class
Organic phosphoric acids and derivatives Sub Class Phosphate esters
Direct Parent
Alkyl phosphates Alternative Parents
Substituents
Alkyl phosphate Organic nitrogen compound Organic oxygen compound Organopnictogen compound Organic oxide Hydrocarbon derivative Organooxygen compound Organonitrogen compound Organic anion Aliphatic acyclic compound Molecular Framework
Aliphatic acyclic compounds External Descriptors
Not Available
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:
adenosylcobalamin biosynthesis II (late cobalt incorporation)P381-PWY adenosylcobalamin biosynthesis from cobyrinate a,c -diamide IPWY-5509 adenosylcobalamin biosynthesis from cobyrinate a,c -diamide IIPWY-5508
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.
