Date published: 2026-5-6

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S-(+)-CBPG

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Alternate Names:
S-(+)-2-(3'-Carboxybicyclo[1.1.1]pentyl)glycine; UPF 596
Application:
S-(+)-CBPG is a structurally new group I mGluR antagonist
Molecular Weight:
185.17
Molecular Formula:
C8H11NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

S-(+)-CBPG is a potent and selective, structurally new group I metabotropic glutamate receptor (mGluR) antagonist.


S-(+)-CBPG References

  1. Metabotropic G-protein-coupled glutamate receptors as therapeutic targets.  |  Pellicciari, R. and Costantino, G. 1999. Curr Opin Chem Biol. 3: 433-40. PMID: 10419848
  2. Biochemical and electrophysiological studies on (S)-(+)-2-(3'-carboxybicyclo(1.1.1)pentyl)-glycine (CBPG), a novel mGlu5 receptor agonist endowed with mGlu1 receptor antagonist activity.  |  Mannaioni, G., et al. 1999. Neuropharmacology. 38: 917-26. PMID: 10428410
  3. Asymmetric synthesis of some substituted-3-phenyl prolines.  |  Micheli, F., et al. 1999. Farmaco. 54: 461-4. PMID: 10486913
  4. Pharmacological agents acting at subtypes of metabotropic glutamate receptors.  |  Schoepp, DD., et al. 1999. Neuropharmacology. 38: 1431-76. PMID: 10530808
  5. Induction of LTD by activation of group I mGluR in the dentate gyrus in vitro.  |  Camodeca, N., et al. 1999. Neuropharmacology. 38: 1597-606. PMID: 10530821
  6. Protection with metabotropic glutamate 1 receptor antagonists in models of ischemic neuronal death: time-course and mechanisms.  |  Pellegrini-Giampietro, DE., et al. 1999. Neuropharmacology. 38: 1607-19. PMID: 10530822
  7. 1-Aminoindan-1,5-dicarboxylic acid and (S)-(+)-2-(3'-carboxybicyclo[1.1.1] pentyl)-glycine, two mGlu1 receptor-preferring antagonists, reduce neuronal death in in vitro and in vivo models of cerebral ischaemia.  |  Pellegrini-Giampietro, DE., et al. 1999. Eur J Neurosci. 11: 3637-47. PMID: 10564371
  8. (S)-(+)-2-(3'-carboxybicyclo[1.1.1]pentyl)-glycine, a structurally new group I metabotropic glutamate receptor antagonist.  |  Pellicciari, R., et al. 1996. J Med Chem. 39: 2874-6. PMID: 8709120
  9. Presynaptic mGlu1 type receptors potentiate transmitter output in the rat cortex.  |  Moroni, F., et al. 1998. Eur J Pharmacol. 347: 189-95. PMID: 9653880
  10. mGluRs novel ligands and molecular modeling studies[J].  |  Pellicciari R, Costantino G, Marinozzi M. 1996. Neuropharmacology,., 6(35):: A23.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

S-(+)-CBPG, 1 mg

sc-222268
1 mg
$35.00

S-(+)-CBPG, 5 mg

sc-222268A
5 mg
$133.00