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Assay Detail

CHEMBL655465

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

Binding
[Ca2+] channel binding affinity was evaluated by its ability to displace [3H]-PN-200-110 in rat brain synaptosomes
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Preparation and in vitro biological evaluation of the enantiomers of the diydropyridine BMY 20014, a combination calcium and 1-adrenoreceptor antagonist
Lawson JE, Poindexter GS, Owens DA, Cavanagh RL, Goggins GD, Sarmiento J, Bleiberg BB, Weselcouch EO
Bioorg Med Chem Lett (1993) 3 : 561 -564
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 7 7.64 9.28

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL193 NIFEDIPINE 4.0 1 9.28
CHEMBL2111202 1 8.11
CHEMBL3301661 1 7.80
CHEMBL151910 1 7.46
CHEMBL2111260 1 6.74
CHEMBL2115538 1 6.47
CHEMBL2 PRAZOSIN 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL193 NIFEDIPINE Ki = 0.53 nM 9.28
CHEMBL2111202 Ki = 7.8 nM 8.11
CHEMBL3301661 Ki = 16.0 nM 7.80
CHEMBL151910 Ki = 35.0 nM 7.46
CHEMBL2111260 Ki = 181.0 nM 6.74
CHEMBL2115538 Ki = 338.0 nM 6.47
CHEMBL2 PRAZOSIN Ki > 1000.0 nM -