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Assay Detail

CHEMBL1647727

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

Binding
Inhibition of human recombinant calmodulin assessed as inhibition of calmodulin-sensitive cAMP phosphodiesterase activation after 15 mins by spectrophotometric analysis
16
Total Activities
9
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Calmodulin-1 (CHEMBL6093)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Vasorelaxant effect of flavonoids through calmodulin inhibition: Ex vivo, in vitro, and in silico approaches.
Torres-Piedra M, Figueroa M, Hernández-Abreu O, Ibarra-Barajas M, Navarrete-Vázquez G, Estrada-Soto S, Estrada-Soto S.
Bioorg Med Chem (2011) 19 : 542 -546
PubMed 21129983 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 4.67 5.29
Inhibition 7 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL138649 6-HYDROXYFLAVONE 2 5.29
CHEMBL50 QUERCETIN 3.0 2 4.89
CHEMBL9352 NARINGENIN 2 4.66
CHEMBL117 CHRYSIN 2 4.48
CHEMBL276915 7-HYDROXYFLAVONE 2 4.43
CHEMBL294009 FLAVONOL 2 4.26
CHEMBL275638 FLAVONE 2.0 2 -
CHEMBL14 CARBACHOL 4.0 1 -
CHEMBL193 NIFEDIPINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL138649 6-HYDROXYFLAVONE IC50 = 5170.0 nM 5.29
CHEMBL50 QUERCETIN IC50 = 12970.0 nM 4.89
CHEMBL9352 NARINGENIN IC50 = 22010.0 nM 4.66
CHEMBL117 CHRYSIN IC50 = 33430.0 nM 4.48
CHEMBL276915 7-HYDROXYFLAVONE IC50 = 37100.0 nM 4.43
CHEMBL294009 FLAVONOL IC50 = 55200.0 nM 4.26
CHEMBL275638 FLAVONE IC50 = 102280.0 nM -
CHEMBL14 CARBACHOL IC50 - -
CHEMBL193 NIFEDIPINE IC50 - -
CHEMBL276915 7-HYDROXYFLAVONE Inhibition - % -
CHEMBL138649 6-HYDROXYFLAVONE Inhibition - % -
CHEMBL294009 FLAVONOL Inhibition - % -
CHEMBL275638 FLAVONE Inhibition - % -
CHEMBL117 CHRYSIN Inhibition - % -
CHEMBL50 QUERCETIN Inhibition - % -
CHEMBL9352 NARINGENIN Inhibition - % -