P0880
Pro-Gly
≥98% (TLC), suitable for cell culture
Synonym(s):
L-prolyl-glycine
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About This Item
Empirical Formula (Hill Notation):
C7H12N2O3
CAS Number:
Molecular Weight:
172.18
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.26
MDL number:
Product Name
Pro-Gly,
SMILES string
OC(=O)CNC(=O)[C@@H]1CCCN1
InChI
1S/C7H12N2O3/c10-6(11)4-9-7(12)5-2-1-3-8-5/h5,8H,1-4H2,(H,9,12)(H,10,11)/t5-/m0/s1
InChI key
RNKSNIBMTUYWSH-YFKPBYRVSA-N
assay
≥98% (TLC)
form
powder
technique(s)
cell culture | mammalian: suitable
color
white
application(s)
cell analysis
storage temp.
−20°C
Quality Level
Related Categories
Biochem/physiol Actions
PRO-GLY is a dipeptide that has previously been shown to prevent progression of diabetes.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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L A Andreeva et al.
Bulletin of experimental biology and medicine, 153(5), 651-654 (2012-11-01)
Intranasal administration of regulatory peptide PRG to rats against the background of persistent hyperglycemia improves blood antiplatelet and anticoagulant-fibrinolytic potential and normalizes blood sugar in comparison with the corresponding parameters in control animals that did not receive the peptide. The
V E Pastorova et al.
Izvestiia Akademii nauk. Seriia biologicheskaia, (5)(5), 593-596 (2005-06-02)
In our study of the effect of proline-containing linear di- and tri-peptides (Pro-Gly, Pro-Gly-Pro) and cyclic peptide cPro-Gly in vitro, we have found that they show depolymerizing activity towards the nonstabilized form of fibrin in the presence and in the
Feng-Chun Wu et al.
The Journal of organic chemistry, 74(13), 4812-4818 (2009-05-23)
Tetrapeptides, containing a terminated primary amine and conformationally restricted D-Pro-Gly or D-Pro-Aib (2-aminoisobutanoic acid) segment as a strongly beta-turn-nucleating element, were designed and synthesized with condensation of N-module dipeptides with C-module dipeptides in solution. They were first applied to catalyze
Shigeo Hayakawa et al.
Journal of the American Chemical Society, 129(25), 7936-7949 (2007-06-07)
We report a combined experimental and computational study of the proline effect in model dipeptides Pro-Gly and Gly-Pro. Gas-phase protonated peptide ions were discharged by glancing collisions with potassium or cesium atoms at 3 keV collision energies, and the peptide
Y-H Chen et al.
Amino acids, 38(3), 839-845 (2009-04-17)
A series of dipeptides of L-proline-L-amino acid and L-proline-D-amino acid were synthesized to evaluate the catalytic effect for asymmetric direct aldol reactions. In the direct aldol reaction, a catalyst of L-proline-L-amino acid achieves better enantioselectivity than the corresponding L-proline-D-amino acid
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