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Assay Detail

CHEMBL4231476

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

Binding
Inhibition of CaV1.2 channel in rat tail artery myocytes assessed as reduction in Ba2+ current at -50 mV holding potential by whole-cell patch-clamp assay
3
Total Activities
2
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Antimalarial agents against both sexual and asexual parasites stages: structure-activity relationships and biological studies of the Malaria Box compound 1-[5-(4-bromo-2-chlorophenyl)furan-2-yl]-N-[(piperidin-4-yl)methyl]methanamine (MMV019918) and analogues.
Vallone A, D'Alessandro S, Brogi S, Brindisi M, Chemi G, Alfano G, Lamponi S, Lee SG, Jez JM, Koolen KJM, Dechering KJ, Saponara S, Fusi F, Gorelli B, Taramelli D, Parapini S, Caldelari R, Campiani G, Gemma S, Butini S.
Eur J Med Chem (2018) 150 : 698 -718
PubMed 29571157 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Inhibition 2 - -
IC50 1 5.48 5.48

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4246869 2 5.48
CHEMBL537152 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4246869 IC50 = 3300.0 nM 5.48
CHEMBL4246869 Inhibition - % -
CHEMBL537152 Inhibition - % -