ChemicalBook Product Catalog Biochemical Engineering Amino Acids and Derivatives Proline derivatives GLYCYL-L-PROLINE

GLYCYL-L-PROLINE

GLYCYL-L-PROLINE Basic information
Product Name:GLYCYL-L-PROLINE
Synonyms:1-(Aminoacetyl)proline;Glycylproline;L-Proline, 1-glycyl-;N-Glycyl-L-proline;Proline, 1-glycyl-, L-;H-GLY-PRO-OH;GLYCYL-L-PROLINE;GLY-PRO
CAS:704-15-4
MF:C7H12N2O3
MW:172.18
EINECS:211-880-2
Product Categories:PYRROLE;Biochemistry;Oligopeptides;Peptide Synthesis;Dipeptides;Dipeptides and Tripeptides;Peptides
Mol File:704-15-4.mol
GLYCYL-L-PROLINE Structure
GLYCYL-L-PROLINE Chemical Properties
Melting point 185℃
Boiling point 411.3±40.0 °C(Predicted)
density 1.356±0.06 g/cm3(Predicted)
refractive index -114 ° (C=4, H2O)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility Water (Slightly)
pka3.18±0.20(Predicted)
form Solid
color White to Off-White
Water Solubility very faint turbidity
InChIKeyKZNQNBZMBZJQJO-YFKPBYRVSA-N
CAS DataBase Reference704-15-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36
Safety Statements 26
WGK Germany 3
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
GLYCYL-L-PROLINE Usage And Synthesis
Chemical PropertiesCrystalline
UsesN-Glycylproline was found to exhibit anti-ischemic effects on the metabolism of neuroactive amino acids and indices of energy turnover in the neocortex of rats after experimental brain ischemia.
UsesSubstrate for Prolidase.
DefinitionChEBI: A dipeptide consisting of L-proline having a glycyl residue attached to its alpha-amino group.
Purification MethodsCrystallise glycyl-L-proline from water at 50-60o by addition of EtOH. [Saidel J Am Chem Soc 77 3893 1955, Bergmann et al. Z Physiol Chem 212 79 1932, Beilstein 22 IV 49.]
GLYCYL-L-PROLINE Preparation Products And Raw materials
SAR-PRO-OH TRH H-LEU-PRO-OH HCL H-SER-PRO-OH Z-GLYCYL-L-PROLINE,Z-L-GLYCYL-L-PROLINE,1-[N-[(phenylmethoxy)carbonyl]glycyl]-L-proline H-PRO-HYP-OH H-PRO-PRO-PRO-OH H-GLY-PRO-PRO-OH ABZ-GLY-4-NITRO-PHE-PRO-OH GLYCYL-L-PROLINE H-GLY-HYP-OH H-GLY-PRO-HYP-OH L-Alanyl-L-proline PHE-PRO L-PRO-PRO H-ILE-PRO-OH HCL Z-PHE-PRO-OH Z-ILE-PRO-OH
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