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MCOPPB trihydrochloride_Molecular_structure_CAS_1028969-49-4)
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MCOPPB trihydrochloride

Catalog No. S2223 Name Selleck Chemicals
CAS Number 1028969-49-4 Website http://www.selleckchem.com
M. F. C26H43Cl3N4 Telephone (877) 796-6397
M. W. 518.00542 Fax (832) 582-8590
Purity Email sales@selleckchem.com
Storage -20°C Chembase ID: 72909

SYNONYMS

IUPAC name
1-[1-(1-methylcyclooctyl)piperidin-4-yl]-2-[(3R)-piperidin-3-yl]-1H-1,3-benzodiazole trihydrochloride
IUPAC Traditional name
1-[1-(1-methylcyclooctyl)piperidin-4-yl]-2-[(3R)-piperidin-3-yl]-1,3-benzodiazole trihydrochloride

DATABASE IDS

CAS Number 1028969-49-4

PROPERTIES

Target Opioid recepotor
Salt Data trihydrochlorid
Storage Condition -20°C

DETAILS

Description (English)
Biological Activity:
MCOPPB trihydrochloride is a trihydrochloride form of MCOPPB that is a new nonpeptide nociceptin/orphanin FQ peptide (NOP)-receptor agonist with a pKi of 10.07 ± 0.01 for the human NOP receptor. MCOPPB exhibits anxiolytic effects with no effect on memory or locomotion. MCOPPB was regarded as one of the most potent, non-peptide NOP full agonists in vitro. MCOPPB has a high affinity for the human NOP receptor. MCOPPB has a high selectivity for the NOP receptor over other members of the opioid receptor family: 12-, 270- and >1000-fold more selective for the NOP receptor than for the micro-, kappa-, and delta-receptor, respectively. In an ex vivo binding study, MCOPPB (10 mg/kg, p.o.) inhibited signaling through the NOP receptor in the mouse brain, suggesting that MCOPPB penetrated into the brain after MCOPPB was orally administered. In the mouse Vogel conflict test, MCOPPB (10 mg/kg, p.o.) and diazepam (3 mg/kg, p.o.) elicited anxiolytic-like effects, although MCOPPB produced a bell-shaped response curve. MCOPPB at an oral dose of 10 mg/kg did not affect locomotor activity or memory, nor did MCOPPB contribute to ethanol-induced hypnosis. [1][2]References on MCOPPB 3HCl[1] J. Med. Chem, 2009, 52:610–625[2] J Pharmacol Sci, 2008, 106:361 – 368

REFERENCES

  • Hayashi S et al. J Med Chem. 2009 Feb 12; 52(3):610-25.