U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C26H40N4
Molecular Weight 408.6226
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MCOPPB

SMILES

CC1(CCCCCCC1)N2CCC(CC2)N3C(=NC4=CC=CC=C34)[C@@H]5CCCNC5

InChI

InChIKey=CYYNMPPFEJPBJD-OAQYLSRUSA-N
InChI=1S/C26H40N4/c1-26(15-7-3-2-4-8-16-26)29-18-13-22(14-19-29)30-24-12-6-5-11-23(24)28-25(30)21-10-9-17-27-20-21/h5-6,11-12,21-22,27H,2-4,7-10,13-20H2,1H3/t21-/m1/s1

HIDE SMILES / InChI

Molecular Formula C26H40N4
Molecular Weight 408.6226
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

MCOPPB trihydrochloride (MCOPPB) is a nonpeptide agonist of the NOP receptor, an anxiolytic agent. MCOPPB has a high affinity for the human NOP receptor (pKi = 10.07 +/- 0.01) and 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 it penetrated into the brain after it was orally administered. MCOPPB - a compound with few adverse effects on the central nervous system - is a potential therapeutic agent for the treatment of anxiety.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
10.07 null [pKi]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Pharmacological characterization of the newly synthesized nociceptin/orphanin FQ-receptor agonist 1-[1-(1-methylcyclooctyl)-4-piperidinyl]-2-[(3R)-3-piperidinyl]-1H-benzimidazole as an anxiolytic agent.
2008 Mar
Novel non-peptide nociceptin/orphanin FQ receptor agonist, 1-[1-(1-Methylcyclooctyl)-4-piperidinyl]-2-[(3R)-3-piperidinyl]-1H-benzimidazole: design, synthesis, and structure-activity relationship of oral receptor occupancy in the brain for orally potent antianxiety drug.
2009 Feb 12
Quantitative Signaling and Structure-Activity Analyses Demonstrate Functional Selectivity at the Nociceptin/Orphanin FQ Opioid Receptor.
2015 Sep
Patents

Sample Use Guides

Mice: In the mouse Vogel conflict test, MCOPPB trihydrochloride (10 mg/kg, p.o.) and diazepam (3 mg/kg, p.o.) elicited anxiolytic-like effects, although MCOPPB trihydrochloride produced a bell-shaped response curve. In addition, MCOPPB (10 mg/kg, p.o.) was still effective as an anxiolytic agent even after repeated administration for 5 days.
Route of Administration: Oral
EC50 value of the MCOPPB trihydrochloride (MCOPPB) for the activity of [35S]GTPγS binding in response to the respective agonist–hNOP receptor binding in HEK293 cells was 0.0858 nM.
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:33:21 GMT 2023
Edited
by admin
on Sat Dec 16 15:33:21 GMT 2023
Record UNII
8NMK0UG3HV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MCOPPB
Common Name English
1-(1-(1-METHYLCYCLOOCTYL)-4-PIPERIDINYL)-2-(3R)-3-PIPERIDINYL-1H-BENZIMIDAZOLE
Systematic Name English
1-(1-(1-METHYLCYCLOOCTYL)-4-PIPERIDINYL)-2-((3R)-3-PIPERIDINYL)-1H-BENZIMIDAZOLE
Systematic Name English
1H-BENZIMIDAZOLE, 1-(1-(1-METHYLCYCLOOCTYL)-4-PIPERIDINYL)-2-(3R)-3-PIPERIDINYL-
Systematic Name English
Code System Code Type Description
FDA UNII
8NMK0UG3HV
Created by admin on Sat Dec 16 15:33:22 GMT 2023 , Edited by admin on Sat Dec 16 15:33:22 GMT 2023
PRIMARY
CAS
1028969-49-4
Created by admin on Sat Dec 16 15:33:22 GMT 2023 , Edited by admin on Sat Dec 16 15:33:22 GMT 2023
PRIMARY
PUBCHEM
24800108
Created by admin on Sat Dec 16 15:33:22 GMT 2023 , Edited by admin on Sat Dec 16 15:33:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID401018254
Created by admin on Sat Dec 16 15:33:22 GMT 2023 , Edited by admin on Sat Dec 16 15:33:22 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY