Record Information Version
1.0 Update Date
1/22/2018 11:54:54 AM
Metabolite ID PAMDB110672
Identification Name:
D-arginine Description: Not Available
Structure
Synonyms:
D-2-Amino-5-guanidinovaleric acid
Chemical Formula:
C6 H15 N4 O2
Average Molecular Weight:
176.1273257786 Monoisotopic Molecular
Weight:
176.1273257786 InChI Key:
ODKSFYDXXFIFQN-SCSAIBSYSA-O InChI:
InChI=1S/C6H14N4O2/c7-4(5(11)12)2-1-3-10-6(8)9/h4H,1-3,7H2,(H,11,12)(H4,8,9,10)/p+1/t4-/m1/s1 CAS
number:
Not Available IUPAC Name: Not Available
Traditional IUPAC Name:
Not Available SMILES: C(NC(N)=[N+])CCC([N+])C([O-])=O
Chemical Taxonomy
Taxonomy Description This compound belongs to the class of organic compounds known as arginine and derivatives. These are compounds containing arginine or a derivative thereof resulting from reaction of arginine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
Kingdom
Organic compounds Super Class Organic acids and derivatives
Class
Carboxylic acids and derivatives Sub Class Amino acids, peptides, and analogues
Direct Parent
Arginine and derivatives Alternative Parents
Substituents
Arginine or derivatives Fatty acid Carboxylic acid salt Carboxylic acid Monocarboxylic acid or derivatives Carbonyl group Organic nitrogen compound Hydrocarbon derivative Organic oxide Organic salt Organooxygen compound Organonitrogen compound Organopnictogen compound Organic oxygen compound Organic cation 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:
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.
