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

CHEMBL654579

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

Binding
Inhibition of [3H]nitrendipine binding to L-type calcium channel receptor(CCR) in rat cerebral cortex homogenate
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Voltage-gated L-type calcium channel (CHEMBL2095177)
Type PROTEIN FAMILY
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
Ki 2 8.70 9.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL277363 1 9.72
CHEMBL23 DILTIAZEM 4.0 1 7.68

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL277363 Ki = 0.19 nM 9.72
CHEMBL23 DILTIAZEM Ki = 21.0 nM 7.68