Record Information Version
1.0 Update Date
1/22/2018 12:54:54 PM
Metabolite ID PAMDB110811
Identification Name:
α-D-glucosamine 6-phosphate Description: Not Available
Structure
Synonyms:
α-D-glucosamine phosphate
α-D-glucosamine 6-phosphate
α-α-D-glucosamine-6-P
Chemical Formula:
C6 H13 NO8 P
Average Molecular Weight:
260.0535279735 Monoisotopic Molecular
Weight:
260.0535279735 InChI Key:
XHMJOUIAFHJHBW-UKFBFLRUSA-M InChI:
InChI=1S/C6H14NO8P/c7-3-5(9)4(8)2(15-6(3)10)1-14-16(11,12)13/h2-6,8-10H,1,7H2,(H2,11,12,13)/p-1/t2-,3-,4-,5-,6+/m1/s1 CAS
number:
Not Available IUPAC Name: Not Available
Traditional IUPAC Name:
Not Available SMILES: C(OP([O-])(=O)[O-])C1(OC(O)C([N+])C(O)C(O)1)
Chemical Taxonomy
Taxonomy Description This compound belongs to the class of organic compounds known as hexose phosphates. These are carbohydrate derivatives containing a hexose substituted by one or more phosphate groups.
Kingdom
Organic compounds Super Class Organic oxygen compounds
Class
Organooxygen compounds Sub Class Carbohydrates and carbohydrate conjugates
Direct Parent
Hexose phosphates Alternative Parents
Substituents
Hexose phosphate Monosaccharide phosphate Amino saccharide Organic phosphoric acid derivative Oxane Phosphoric acid ester Alkyl phosphate 1,2-diol Hemiacetal Secondary alcohol Oxacycle Organoheterocyclic compound Polyol Organonitrogen compound Organic nitrogen compound Hydrocarbon derivative Organic oxide Organopnictogen compound Alcohol Organic anion Aliphatic heteromonocyclic compound Molecular Framework
Aliphatic heteromonocyclic 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:
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.
