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Assay Detail

CHEMBL757329

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

Binding
Inhibition of [3H]diprenorphine binding to rat brain membrane opioid receptors;(T= total opioid receptor family)
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Opioid receptor (CHEMBL2094129)
Type PROTEIN FAMILY
Organism Rattus norvegicus

Publication

Photoactivatable opiate derivatives as irreversible probes of the mu-opioid receptor.
Galzi JL, Mejean A, Ilien B, Mollereau C, Meunier JC, Goeldner M, Hirth C.
J Med Chem (1990) 33 : 2456 -2464
PubMed 2167979 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 12 8.46 9.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL290429 CARFENTANIL 2.0 1 9.60
CHEMBL314209 1 9.30
CHEMBL19019 NALTREXONE 4.0 1 9.26
CHEMBL312040 ETONITAZENE 2.0 1 9.22
CHEMBL311995 NALTREXONEDIAZONIUM 1 8.77
CHEMBL310829 1 8.40
CHEMBL312046 1 8.30
CHEMBL81328 1 8.10
CHEMBL312281 1 8.00
CHEMBL81465 1 7.75
CHEMBL309542 1 7.57
CHEMBL84237 1 7.21

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL290429 CARFENTANIL Ki = 0.25 nM 9.60
CHEMBL314209 Ki = 0.5 nM 9.30
CHEMBL19019 NALTREXONE Ki = 0.55 nM 9.26
CHEMBL312040 ETONITAZENE Ki = 0.6 nM 9.22
CHEMBL311995 NALTREXONEDIAZONIUM Ki = 1.7 nM 8.77
CHEMBL310829 Ki = 4.0 nM 8.40
CHEMBL312046 Ki = 5.0 nM 8.30
CHEMBL81328 Ki = 8.0 nM 8.10
CHEMBL312281 Ki = 10.0 nM 8.00
CHEMBL81465 Ki = 18.0 nM 7.75
CHEMBL309542 Ki = 27.0 nM 7.57
CHEMBL84237 Ki = 62.0 nM 7.21