Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL754713

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Binding affinity towards human cloned Opioid receptor mu 1 using [3H]DAMGO
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Mu-type opioid receptor (CHEMBL233)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Identification of (3R)-7-hydroxy-N-((1S)-1-[[(3R,4R)-4-(3-hydroxyphenyl)- 3,4-dimethyl-1-piperidinyl]methyl]-2-methylpropyl)-1,2,3,4-tetrahydro- 3-isoquinolinecarboxamide as a novel potent and selective opioid kappa receptor antagonist.
Thomas JB, Atkinson RN, Vinson NA, Catanzaro JL, Perretta CL, Fix SE, Mascarella SW, Rothman RB, Xu H, Dersch CM, Cantrell BE, Zimmerman DM, Carroll FI.
J Med Chem (2003) 46 : 3127 -3137
PubMed 12825951 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 6 8.09 9.02

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL415247 JDTIC 1.0 1 9.02
CHEMBL2112473 1 8.42
CHEMBL575508 1 8.05
CHEMBL2112474 1 7.88
CHEMBL573214 NORBINALTORPHIMINE 1 7.68
CHEMBL10872 1 7.48

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL415247 JDTIC Ki = 0.96 nM 9.02
CHEMBL2112473 Ki = 3.8 nM 8.42
CHEMBL575508 Ki = 8.86 nM 8.05
CHEMBL2112474 Ki = 13.2 nM 7.88
CHEMBL573214 NORBINALTORPHIMINE Ki = 21.0 nM 7.68
CHEMBL10872 Ki = 33.1 nM 7.48