dipeptide-9
synthetic peptide consisting of glutamic acid and lysine
 
Notes:
In non-diabetic kidney scarring the protein crosslinking enzyme tissue transglutaminase (tTg) has been implicated in the process by the formation of increased epsilon-(gamma-glutamyl)lysine bonds between ECM components in both experimental and human disease. Changes in tTg and epsilon-(gamma-glutamyl)lysine occur in human Diabetic nephropathy as well, the leading cause of chronic kidney failure. (PMID 15292688) In Parkinson's disease (PD), conformational changes in the alpha-synuclein monomer precede the formation of Lewy bodies. Both tTG and its substrate-characteristic N(epsilon)-(gamma-glutamyl)-lysine crosslink are increased in PD nigral dopamine neurons. (PMID 15001552) Expression of tissue transglutaminase (tTgase) and epsilon-(gamma-glutamyl)-lysine was present in all scarring of the blebs sites, being the main cause of failure in glaucoma filtration surgery. Transglutaminases are calcium-dependent enzymes that catalyze the posttranslational modification of proteins through an acyl transfer reaction between the gamma-carboxamide group of a peptide-bound glutaminyl residue and various amines. Covalent cross-linking using epsilon-(gamma-glutamyl)-lysine bonds is stable and resistant to enzymatic, chemical, and mechanical disruption. (PMID: 16936095) [HMDB]
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Name: (2R)-2-amino-6-[[(4S)-4-amino-4-carboxybutanoyl]amino]hexanoic acid
CAS Number: 17105-15-6Picture of molecule3D/inchi
MDL: MFCD00055787
XlogP3-AA: -6.30 (est)
Molecular Weight: 275.30537000
Formula: C11 H21 N3 O5
NMR Predictor: Predict (works with chrome or firefox)
Category: hair conditioning, humectants, skin conditioning
 
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 1.177e+005 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: hair conditioning
humectants
skin conditioning
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Suppliers:
Sigma-Aldrich: Sigma
For experimental / research use only.
?-Glu-e-Lys
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: hair conditioning, humectants, skin conditioning
Recommendation for dipeptide-9 usage levels up to:
 not for fragrance use.
 
Recommendation for dipeptide-9 flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
National Institute of Allergy and Infectious Diseases: Data
 (2R)-2-amino-6-[[(4S)-4-amino-4-carboxybutanoyl]amino]hexanoic acid
Chemidplus: 0017105156
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References:
 (2R)-2-amino-6-[[(4S)-4-amino-4-carboxybutanoyl]amino]hexanoic acid
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 6427014
Pubchem (sid): 135023015
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): HMDB03869
FooDB: FDB023239
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
(2R)-2-amino-6-[[(4S)-4-amino-4-carboxybutanoyl]amino]hexanoic acid
 synthetic peptide consisting of glutamic acid and lysine
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