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Assay Detail

CHEMBL654574

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

Binding
Ability to inhibit [3H]nitrendipine binding to the L-type calcium channel receptor(CCR) in rat heart homogenate
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Tissue Heart
Confidence 9 — Direct single protein target
Curated By Expert

Target

Voltage-dependent L-type calcium channel subunit alpha-1C (CHEMBL3762)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Cardiovascular characterization of pyrrolo[2,1-d][1,5]benzothiazepine derivatives binding selectively to the peripheral-type benzodiazepine receptor (PBR): from dual PBR affinity and calcium antagonist activity to novel and selective calcium entry blockers.
Campiani G, Fiorini I, De Filippis MP, Ciani SM, Garofalo A, Nacci V, Giorgi G, Sega A, Botta M, Chiarini A, Budriesi R, Bruni G, Romeo MR, Manzoni C, Mennini T.
J Med Chem (1996) 39 : 2922 -2938
PubMed 8709127 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.77 7.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL277363 1 7.77

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL277363 IC50 = 17.0 nM 7.77