H-Gly-Leu-Tyr-OH

Names

[ CAS No. ]:
4306-24-5

[ Name ]:
H-Gly-Leu-Tyr-OH

[Synonym ]:
glycyl-leucyl-tyrosine
GLY-LEU-TYR
Glycyl-L-leucyl-l-tyrosine
Gly-Leu-Tyr
Glycyl-L-leucyl-L-tyrosin

Biological Activity

[Description]:

Gly-Leu-Tyr is a Glycine (HY-Y0966) derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[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

[ Density]:
1.252g/cm3

[ Boiling Point ]:
693.5ºC at 760 mmHg

[ Molecular Formula ]:
C₁₇H₂₅N₃O₅

[ Molecular Weight ]:
351.39800

[ Flash Point ]:
373.2ºC

[ Exact Mass ]:
351.17900

[ PSA ]:
141.75000

[ LogP ]:
1.47580

[ Index of Refraction ]:
1.566

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

Articles

Effect of protein structure on laccase-catalyzed protein oligomerization.

J. Agric. Food Chem. 54(23) , 8883-90, (2006)

Laccase-catalyzed oligomerization of proteins was studied using Trametes hirsuta laccase (ThL) and coactosin as a model system. The reaction mechanism was elucidated using free amino acids and the tri...

Glycyl-L-leucyl-L-tyrosine dihydrate 2-propanol solvate.

Acta Crystallogr. C 52 ( Pt 8) , 2087-90, (1996)

The asymmetric unit (C17H25N3O5.C3H8O.2H2O) consists of two crystallographically independent peptide molecules, A and B, with different conformations, chi 1(2) being trans and gauche- for the Leu resi...