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Substance
ID:378557
Structure
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Functional Group
Text
ID:128489
Nε-(1-Carboxymethyl)-L-lysine
Toronto Research Chemicals
ID: C180075
Names and Identifiers
IUPAC name
(2S)-2-amino-6-[(carboxymethyl)amino]hexanoic acid
IUPAC Traditional name
N(6)-carboxymethyllysine
Synonyms
2-Amino-6-(carboxymethyl-amino)-hexanoic Acid
N6-(Carboxymethyl)lysine
N6-(Carboxymethyl)-L-lysine
CML
Nε-(1-Carboxymethyl)-L-lysine
Registration numbers
CAS Number
5746-04-3
Properties
Physical Property
Melting Point
>260°C (dec.)
Solubility
Water
Apperance
Off-White Solid
Product Information
Certificate of Analysis
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Safety Information
Storage Condition
Hygroscopic, -20°C Freezer, Under Inert Atmosphere
MSDS Link
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Molecule Details
CEL and CML are two stable, nonenzymatic chemical modifications of protein lysine residues resulting from glycation and oxidation reactions.
Molecular Spectra
No Data Available
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References
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Ahmed M.U., et al.: Biochem.J., 324, 565 (1996)
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Fu, M.X., et al.: J. Biol. Chem., 271, 9982 (1996)
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Schleicher, E.D., et al.: J. Clin. Invest., 99, 457 (1996)
•
Shibayama, R., et al.: Diabetes, 48, 1842 (1996)
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