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C2374

Sigma-Aldrich

Cyclo-Gly-Pro

≥98% (GC/HPLC)

Synonyme(s) :

(S)-3,6-Dioxohexahydropyrrolo[1,2-a]pyrazine, Glycyl-L-proline lactam, cyclo-GP, cyclo-Glycyl-L-Proline, cyclo-L-prolylglycine

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About This Item

Formule empirique (notation de Hill):
C7H10N2O2
Numéro CAS:
3705-27-9
Poids moléculaire :
154.17
Numéro MDL:
MFCD01083707
Code UNSPSC :
12352200
ID de substance PubChem :
329774997
Nomenclature NACRES :
NA.32

Niveau de qualité

100

Pureté

≥98% (GC/HPLC)

Forme

powder

Solubilité

DMSO: >10 mg/mL

Température de stockage

−20°C

Chaîne SMILES 

O=C1CNC(=O)C2CCCN12

InChI

1S/C7H10N2O2/c10-6-4-8-7(11)5-2-1-3-9(5)6/h5H,1-4H2,(H,8,11)

Clé InChI

OWOHLURDBZHNGG-UHFFFAOYSA-N

Actions biochimiques/physiologiques

Cyclo-Gly-Pro is a neuro-protective compound, an endogenous diketopiperazine, which enhances memory. In the animal model of PD, the compound improved functional recovery when administered after the onset of dyskinesia. It appears that the compound recovery function may result from non-proliferative neurogenesis that results from the inhibition of apoptosis of stem cells and/or the promotion of neuronal-orientated proliferation in the SVZ (subventricular zone).

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

J Guan et al.
Neuropharmacology, 53(6), 749-762 (2007-10-02)
The current study describes the neuroprotective effects of an endogenous diketopiperazine, cyclo-glycyl-proline (cyclic GP), in rats with hypoxic-ischemic brain injury and the pre-clinical development of an analogue, cyclo-L-glycyl-L-2-allylproline (NNZ 2591), modified for improved bioavailability. The compounds were given either intracerebroventricularly
J Tritt-Goc et al.
International journal of peptide and protein research, 34(4), 299-305 (1989-10-01)
The complexation of cyclo(Pro17O-Gly15N) and cyclo(Gly17O-Pro) with Co2+ ions has been studied by 17O, 14N and 15N n.m.r. spectroscopy in aqueous solution. 17O, 14N and 15N transverse relaxation times and chemical shifts were measured as a function of temperature. The
Douglas R Houston et al.
Journal of medicinal chemistry, 47(23), 5713-5720 (2004-10-29)
Family 18 chitinases play an essential role in a range of pathogens and pests. Several inhibitors are known, including the potent inhibitors argadin and allosamidin, and the structures of these in complex with chitinases have been elucidated. Recent structural analysis
F Sussman et al.
Proceedings of the National Academy of Sciences of the United States of America, 86(20), 7880-7884 (1989-10-01)
Calcium plays a crucial role in many cellular processes. Its functions are directly dependent on the high specificity for Ca2+ exhibited by the proteins and ion carriers that bind divalent ions. To elucidate the basis for this specificity we have
Z-F Wu et al.
Scandinavian journal of immunology, 76(2), 131-140 (2012-05-23)
This study was undertaken to isolate active secondary metabolites from immunostimulatory Alcaligenes faecalis FY-3 and evaluate their activities using grass carp Ctenopharyngodon idella kidney (CIK) cells. By applying chromatography techniques and successive recrystallization, three purified metabolites were obtained and identified

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