C2374
Cyclo-Gly-Pro
≥98% (GC/HPLC)
Synonym(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
Empirical Formula (Hill Notation):
C7H10N2O2
CAS Number:
Molecular Weight:
154.17
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Quality Level
assay
≥98% (GC/HPLC)
form
powder
solubility
DMSO: >10 mg/mL
storage temp.
−20°C
SMILES string
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)
InChI key
OWOHLURDBZHNGG-UHFFFAOYSA-N
Biochem/physiol Actions
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).
Cyclo-Gly-Pro is a neuro-protective compound.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C2374-10MG | 04061833217948 |