h-ala-gly-oh

Names

[ CAS No. ]:
687-69-4

[ Name ]:
h-ala-gly-oh

[Synonym ]:
L-ALANYL GLYCINE extrapure
N-L-Alanylglycine
L-ALANYLGLYCINE
Ala-Gly,L-Alanyl-glycine
ALA-GLY
L-Ala-Gly-OH
Glycine,N-L-alanyl
DL-alanylglycine
L-alanine-glycine-OH
N-L-Alanylglycine
H-β-Ala-Gly-OH

Biological Activity

[Description]:

(S)-2-(2-Aminopropanamido)acetic acid is a Glycine (HY-Y0966) derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[Target]

Human Endogenous Metabolite

[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]:
1.263 g/cm3

[ Boiling Point ]:
417.4ºC at 760 mmHg

[ Melting Point ]:
249-255ºC (dec.)

[ Molecular Formula ]:
C₅H₁₀N₂O₃

[ Molecular Weight ]:
146.14400

[ Flash Point ]:
206.2ºC

[ Exact Mass ]:
146.06900

[ PSA ]:
92.42000

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

Differential mobility spectrometry of isomeric protonated dipeptides: modifier and field effects on ion mobility and stability.

Anal. Chem. 83 , 3470-3476, (2011)

The ability to resolve isomeric protonated dipeptides was investigated with the new technique of differential ion mobility mass spectrometry that uses "modifier" molecules to enhance differential mobi...

Infrared spectroscopy of the alanine dipeptide analog in liquid water with DFT-MD. Direct evidence for P(II)/beta conformations.

Phys. Chem. Chem. Phys. 12 , 10198-10209, (2010)

Following our previous work [J. Phys. Chem. B. Lett., 2009, 113, 10059], DFT-based molecular dynamics (DFTMD) simulations of 2-Ala peptide (i.e. Ac-Ala-NHMe dialanine peptide analog with methyl group ...