H-Gly-DL-Phe-OH

Names

[ CAS No. ]:
721-66-4

[ Name ]:
H-Gly-DL-Phe-OH

[Synonym ]:
EINECS 211-958-6
N-Glycyl-DL-B-phenylalanine
Gly-D-Phe-OH/Gly-L-Phe-OH,(1:1)
Glycylphenylalanine
2-(glycylamino)-3-phenyl-propionic acid
N-glycyl-DL-phenylalanine
N-glycyl-3-phenyl-DL-alanine
H-GLY-DL-PHE-OH
N-glycyl-phenylalanine
MFCD00065109
GLY-DL-PHE
rac-(R*)-N-Glycyl-2-benzylglycine

Biological Activity

[Description]:

Glycyl-DL-phenylalanine is a phenylalanine 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):1793-807.

Chemical & Physical Properties

[ Density]:
1.259 g/cm3

[ Boiling Point ]:
492.2ºC at 760 mmHg

[ Melting Point ]:
273-275℃ (Decomposition)

[ Molecular Formula ]:
C₁₁H₁₄N₂O₃

[ Molecular Weight ]:
222.24000

[ Flash Point ]:
251.5ºC

[ Exact Mass ]:
222.10000

[ PSA ]:
92.42000

[ LogP ]:
0.84840

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Riboflavin-binding protein is a novel bitter inhibitor.

Chem. Senses 33(1) , 57-63, (2008)

Riboflavin-binding protein (RBP) from chicken egg, which was recently reported to be a selective sweet inhibitor for protein sweeteners, was also found to be a bitter inhibitor. RBP elicited broadly t...

Molecular mechanism of the inhibition of cytochrome c aggregation by Phe-Gly.

Arch. Biochem. Biophys. 435(1) , 182-9, (2005)

Experimental and computational studies suggest that few general principles govern protein/protein interactions and aggregation. The knowledge of these rules may be exploited to design peptides that ar...

Intrinsic folding of small peptide chains: spectroscopic evidence for the formation of beta-turns in the gas phase.

J. Am. Chem. Soc. 127(2) , 707-12, (2005)

Laser desorption of model peptides coupled to laser spectroscopic techniques enables the gas-phase observation of genuine secondary structures of biology. Spectroscopic evidence for the formation of b...