P0880
Pro-Gly
≥98% (TLC), suitable for cell culture
Synonym(s):
L-prolyl-glycine
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C7H12N2O3
CAS Number:
Molecular Weight:
172.18
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.26
Recommended Products
Product Name
Pro-Gly,
Assay
≥98% (TLC)
Quality Level
form
powder
technique(s)
cell culture | mammalian: suitable
color
white
application(s)
cell analysis
storage temp.
−20°C
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
Biochem/physiol Actions
PRO-GLY is a dipeptide that has previously been shown to prevent progression of diabetes.
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
T A Gudasheva et al.
European journal of drug metabolism and pharmacokinetics, 22(3), 245-252 (1997-07-01)
The metabolism of a new piracetam analogue, the dipeptide cognitive enhancer N-phenylacetyl-L-prolylglycine ethyl ester (GVS-111) was studied in vivo. GVS-111 itself was not found in rat brain 1 h after 5 mg/kg i.p. administration up to limit of detection (LOD)
Daisuke Motooka et al.
Biopolymers, 98(2), 111-121 (2011-10-25)
Extensive studies on the structure of collagen have revealed that the hydroxylation of Pro residues in a variety of model peptides with the typical (X-Y-Gly)(n) repeats (X and Y: Pro and its analogues) represents one of the major factors influencing
[Effects of dipeptides Gly-Pro, Pro-Gly, glycine, and proline on the cardiotropic effect of acetylcholine].
N E Babskaia et al.
Biulleten' eksperimental'noi biologii i meditsiny, 126(8), 139-141 (1998-10-20)
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
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service