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Assay Detail

CHEMBL755878

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

Functional
The compound was tested for antagonist activity by selective inhibition of [35S]GTP-gamma-S, binding in Guinea pig caudate stimulated by SMC-80 (Opioid receptor delta 1)
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Cavia porcellus
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Delta-type opioid receptor (CHEMBL236)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Investigation of the N-substituent conformation governing potency and mu receptor subtype-selectivity in (+)-(3R, 4R)-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonists.
Thomas JB, Mascarella SW, Rothman RB, Partilla JS, Xu H, McCullough KB, Dersch CM, Cantrell BE, Zimmerman DM, Carroll FI.
J Med Chem (1998) 41 : 1980 -1990
PubMed 9599247 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 5 8.89 9.51

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL300662 1 9.51
CHEMBL52451 1 9.45
CHEMBL50594 1 8.97
CHEMBL51838 1 8.83
CHEMBL19019 NALTREXONE 4.0 1 7.71

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL300662 Ki = 0.312 nM 9.51
CHEMBL52451 Ki = 0.355 nM 9.45
CHEMBL50594 Ki = 1.07 nM 8.97
CHEMBL51838 Ki = 1.48 nM 8.83
CHEMBL19019 NALTREXONE Ki = 19.3 nM 7.71