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P0880

L-Prolylglycin

≥98% (TLC), suitable for cell culture

Synonym(e):

L-prolyl-glycine

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Über diesen Artikel

Empirische Formel (Hill-System):
C7H12N2O3
CAS-Nummer:
Molekulargewicht:
172.18
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.26
MDL number:

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Unterstützung erhalten

Produktname

L-Prolylglycin,

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

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Dieser Artikel
G3915M4139A0878
form

powder

form

powder

form

powder

form

powder

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

-

assay

≥98% (TLC)

assay

≥99%

assay

>98% (TLC)

assay

≥99% (TLC)

storage temp.

−20°C

storage temp.

-

storage temp.

2-8°C

storage temp.

−20°C

Quality Level

200

Quality Level

400

Quality Level

200

Quality Level

200

color

white

color

white

color

white

color

white

Biochem/physiol Actions

PRO-GLY is a dipeptide that has previously been shown to prevent progression of diabetes.

Lagerklasse

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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Die Dokumentenbibliothek aufrufen

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
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
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
Z Dzakula et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 135(2), 454-465 (1999-01-08)
Analytical expressions have been derived that translate uncertainties in distance constraints (obtained from NMR investigations) into uncertainties in atom positions in the maximum likelihood (ML) structure consistent with these inputs. As a test of this approach, a comparison was made
A Hagting et al.
The Journal of biological chemistry, 269(15), 11391-11399 (1994-04-15)
Lactococcus lactis takes up di- and tripeptides via a proton motive force-dependent carrier protein. The gene (dtpT) encoding the di-tripeptide transport protein of L. lactis was cloned by complementation of a dipeptide transport-deficient and proline auxotrophic Escherichia coli strain. Functional

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