G2752
Gly-Phe
≥97.0% (TLC)
Sinônimo(s):
Glycyl-L-phenylalanine
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1 G
R$ 580,00
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1 G
R$ 580,00
About This Item
Fórmula linear:
NH2CH2CONHCH(COOH)CH2C6H5
Número CAS:
Peso molecular:
222.24
Beilstein:
2279318
Número CE:
Número MDL:
Código UNSPSC:
12352209
ID de substância PubChem:
NACRES:
NA.26
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Nome do produto
Gly-Phe,
Ensaio
≥97.0% (TLC)
Nível de qualidade
Formulário
crystalline
cor
white
pf
264 °C
temperatura de armazenamento
−20°C
cadeia de caracteres SMILES
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
chave InChI
JBCLFWXMTIKCCB-VIFPVBQESA-N
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Categorias relacionadas
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Resolution of chiral compounds by HPLC using mobile phase additives and a porous graphitic carbon stationary phase.
B J Clark et al.
Journal of pharmaceutical and biomedical analysis, 7(12), 1883-1888 (1989-01-01)
T Takarada et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 6(21), 3906-3913 (2000-12-29)
Oligopeptides are efficiently hydrolyzed by Ce(IV) to the corresponding amino acids under mild conditions. The pseudo first-order rate constants for the hydrolysis of H-Gly-Phe-OH and H-Gly-Gly-OH at pH 7.0 and 50 degrees C are 3.5 x 10(-1) and 2.8 x
Susan Weng Larsen et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 22(5), 399-408 (2004-07-22)
Oil-based depot formulations may constitute a future delivery method for small peptides. Thus, a requirement is attainment of sufficient oil solubility for such active compounds. A model dipeptide (Gly-Phe) has been converted into lipophilic prodrugs by esterification at the C-terminal
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
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