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Assay Detail

CHEMBL750041

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

Binding
Binding affinity to displace 0.4 nM of [3H]- gallopamil in rat myocardial membranes
4
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Tissue Myocardium
Subcellular Membrane
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Studies on Ca2+ channel antagonists. A 2-diazo-3,3,3-trifluoropropionamide derivative related to verapamil as a potential photoaffinity probe.
Theodore LJ, Nelson WL, Dave B, Giacomini JC.
J Med Chem (1990) 33 : 873 -877
PubMed 2153831 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 4 7.62 7.81

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL51149 GALLOPAMIL 2.0 2 7.81
CHEMBL355473 2 7.42

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL51149 GALLOPAMIL Ki = 15.5 nM 7.81
CHEMBL51149 GALLOPAMIL Ki = 15.5 nM 7.81
CHEMBL355473 Ki = 37.6 nM 7.42
CHEMBL355473 Ki = 37.6 nM 7.42