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G2752

Sigma-Aldrich

Gly-Phe

≥97.0% (TLC)

Synonym(s):

Glycyl-L-phenylalanine

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About This Item

Linear Formula:
NH2CH2CONHCH(COOH)CH2C6H5
CAS Number:
3321-03-7
Molecular Weight:
222.24
Beilstein:
2279318
EC Number:
222-027-9
MDL number:
MFCD00065110
UNSPSC Code:
12352209
PubChem Substance ID:
24895100
NACRES:
NA.26

product name

Gly-Phe,

Assay

≥97.0% (TLC)

form

crystalline

color

white

mp

264 °C

storage temp.

−20°C

SMILES string

NCC(=O)N[C@@H](Cc1ccccc1)C(O)=O

InChI

1S/C11H14N2O3/c12-7-10(14)13-9(11(15)16)6-8-4-2-1-3-5-8/h1-5,9H,6-7,12H2,(H,13,14)(H,15,16)/t9-/m0/s1

InChI key

JBCLFWXMTIKCCB-VIFPVBQESA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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S J Reshkin et al.
The American journal of physiology, 260(3 Pt 2), R563-R569 (1991-03-01)
The transport mechanisms for the dipeptide glycyl-L-phenylalanine (Gly-Phe) and L-phenylalanine (Phe) were characterized in fish intestinal brush-border membrane vesicles (BBMV). Gly-Phe was rapidly hydrolyzed only intravesicularly with almost total hydrolysis occurring even at 10 s. Dipeptide uptake was not stimulated
Roderick Y H Lim et al.
Proceedings of the National Academy of Sciences of the United States of America, 103(25), 9512-9517 (2006-06-14)
Natively unfolded phenylalanine-glycine (FG)-repeat domains are alleged to form the physical constituents of the selective barrier-gate in nuclear pore complexes during nucleocytoplasmic transport. Presently, the biophysical mechanism behind the selective gate remains speculative because of a lack of information regarding
Kuniyo Inouye et al.
Bioscience, biotechnology, and biochemistry, 71(8), 2083-2086 (2007-08-11)
The aim of this study was to improve the performance of affinity gels containing glycyl-D-phenylalanine (Gly-D-Phe) as a ligand to thermolysin. Gly-D-Phe was immobilized to the resin through spacers of varying chain lengths. The resulting affinity gels had spacer chain
Wutharath Chin et al.
Journal of the American Chemical Society, 127(2), 707-712 (2005-01-13)
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 beta-turns in gas-phase peptide chains containing glycine and phenylalanine residues establishes the intrinsic stability
Kenji Maehashi et al.
Chemical senses, 33(1), 57-63 (2007-09-12)
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 tuned inhibition of various bitter substances including quinine-HCl, naringin, theobromine
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