Phenylac-Gly-Lys-OH

Modify Date: 2024-01-08 16:32:20

Phenylac-Gly-Lys-OH Structure
Phenylac-Gly-Lys-OH structure
Common Name Phenylac-Gly-Lys-OH
CAS Number 113969-25-8 Molecular Weight 321.37200
Density N/A Boiling Point N/A
Molecular Formula C16H23N3O4 Melting Point N/A
MSDS Chinese USA Flash Point N/A

 Use of Phenylac-Gly-Lys-OH


(S)-6-Amino-2-(2-(2-phenylacetamido)acetamido)hexanoic acid is a lysine derivative[1].

 Names

Name N-Phenylacetyl-Gly-Lys
Synonym More Synonyms

 Phenylac-Gly-Lys-OH Biological Activity

Description (S)-6-Amino-2-(2-(2-phenylacetamido)acetamido)hexanoic acid is a lysine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

Molecular Formula C16H23N3O4
Molecular Weight 321.37200
Exact Mass 321.16900
PSA 121.52000
LogP 1.52580

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles4

More Articles
3-hydroxykynurenine-mediated modification of human lens proteins: structure determination of a major modification using a monoclonal antibody.

J. Biol. Chem. 280 , 22154-22164, (2005)

Tryptophan can be oxidized in the eye lens by both enzymatic and non-enzymatic mechanisms. Oxidation products, such as kynurenines, react with proteins to form yellow-brown pigments and cause covalent...

Elucidation of a novel polypeptide cross-link involving 3-hydroxykynurenine.

Biochemistry 38 , 11455-11464, (1999)

3-Hydroxykynurenine, a metabolite of tryptophan, is a powerful antioxidant and neurotoxin. The neurotoxicity results from the oxidation of 3-hydroxykynurenine, and hydroxyl radicals, formed via H(2)O(...

Polypeptide modification and cross-linking by oxidized 3-hydroxykynurenine.

Biochemistry 39 , 16176-16184, (2000)

3-Hydroxykynurenine (3OHKyn) is present in the mammalian lens as a UV filter and is formed from kynurenine in the tryptophan metabolic pathway. 3OHKyn is a readily autoxidized o-aminophenol which bind...

 Synonyms

6-amino-2-[[2-[(2-phenylacetyl)amino]acetyl]amino]hexanoic acid