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Assay Detail

CHEMBL3705617

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Binding
Radioligand Binding Assay: Radioligand Binding Studies: Saturation experiments. A representative compound of formula (I) was tritiated. Three tritiums were incorporated in place of methyl hydrogens to generate [3H]compound. Binding of this radioligand was preformed in 5 mL borosilicate glass test tubes at room temperature. Binding was initiated by adding membranes to increasing concentrations of [3H]compound in 100 mM NaCl, 20 mM Tris HCl, pH 7.4 buffer containing 0.01% w/v bovine serum albumin (BSA) for 18 h. Non-specific binding was determined in the presence of 1 uM unlabelled compound. After 18 h, the reactants were filtered through GF/C glass fiber filters presoaked in 0.5% w/v polyethylene imine. Filters were washed with 15 mL ice cold 100 mM NaCl, 20 mM Tris HCl, pH7.4 buffer containing 0.25% BSA to separate bound from free ligand. [3H]compound bound to filters was quantified by liquid scintillation counting.Competitive binding experiments.
436
Total Activities
398
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Sodium channel protein type 9 subunit alpha (CHEMBL4296)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

N-substituted benzamides and methods of use thereof
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 436 7.34 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3657932 1 9.00
CHEMBL3657934 1 9.00
CHEMBL3657937 1 9.00
CHEMBL3657947 1 9.00
CHEMBL3657972 1 9.00
CHEMBL3657851 1 9.00
CHEMBL3662229 1 8.80
CHEMBL3657992 1 8.70
CHEMBL3662218 1 8.70
CHEMBL3657955 3 8.70
CHEMBL3657942 1 8.70
CHEMBL3657855 1 8.70
CHEMBL3657854 1 8.68
CHEMBL3657940 1 8.52
CHEMBL3662220 2 8.52
CHEMBL3662219 1 8.52
CHEMBL3662204 1 8.52
CHEMBL3662191 1 8.52
CHEMBL3662190 1 8.52
CHEMBL3662135 1 8.52
CHEMBL3662122 3 8.52
CHEMBL3662090 1 8.52
CHEMBL3658016 1 8.52
CHEMBL3658002 1 8.52
CHEMBL3657953 1 8.52
CHEMBL3657948 1 8.52
CHEMBL3657877 1 8.52
CHEMBL3657840 1 8.52
CHEMBL3657971 1 8.51
CHEMBL3657938 1 8.40

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3657851 IC50 = 1.0 nM 9.00
CHEMBL3657972 IC50 = 1.0 nM 9.00
CHEMBL3657932 IC50 = 1.0 nM 9.00
CHEMBL3657937 IC50 = 1.0 nM 9.00
CHEMBL3657934 IC50 = 1.0 nM 9.00
CHEMBL3657947 IC50 = 1.0 nM 9.00
CHEMBL3662229 IC50 = 1.6 nM 8.80
CHEMBL3657955 IC50 = 2.0 nM 8.70
CHEMBL3662218 IC50 = 2.0 nM 8.70
CHEMBL3657992 IC50 = 2.0 nM 8.70
CHEMBL3657942 IC50 = 2.0 nM 8.70
CHEMBL3657955 IC50 = 2.0 nM 8.70
CHEMBL3657855 IC50 = 2.0 nM 8.70
CHEMBL3657854 IC50 = 2.1 nM 8.68
CHEMBL3658002 IC50 = 3.0 nM 8.52
CHEMBL3657940 IC50 = 3.0 nM 8.52
CHEMBL3658016 IC50 = 3.0 nM 8.52
CHEMBL3662220 IC50 = 3.0 nM 8.52
CHEMBL3657948 IC50 = 3.0 nM 8.52
CHEMBL3662122 IC50 = 3.0 nM 8.52
CHEMBL3662219 IC50 = 3.0 nM 8.52
CHEMBL3662204 IC50 = 3.0 nM 8.52
CHEMBL3657953 IC50 = 3.0 nM 8.52
CHEMBL3662090 IC50 = 3.0 nM 8.52
CHEMBL3657840 IC50 = 3.0 nM 8.52
CHEMBL3662135 IC50 = 3.0 nM 8.52
CHEMBL3662190 IC50 = 3.0 nM 8.52
CHEMBL3662191 IC50 = 3.0 nM 8.52
CHEMBL3657877 IC50 = 3.0 nM 8.52
CHEMBL3657971 IC50 = 3.1 nM 8.51
CHEMBL3662217 IC50 = 4.0 nM 8.40
CHEMBL3662122 IC50 = 4.0 nM 8.40
CHEMBL3657954 IC50 = 4.0 nM 8.40
CHEMBL3662214 IC50 = 4.0 nM 8.40
CHEMBL3662228 IC50 = 4.0 nM 8.40
CHEMBL3662128 IC50 = 4.0 nM 8.40
CHEMBL3662137 IC50 = 4.0 nM 8.40
CHEMBL3662140 IC50 = 4.0 nM 8.40
CHEMBL3657963 IC50 = 4.0 nM 8.40
CHEMBL3662228 IC50 = 4.0 nM 8.40
CHEMBL3662183 IC50 = 4.0 nM 8.40
CHEMBL3662155 IC50 = 4.0 nM 8.40
CHEMBL3639610 IC50 = 4.0 nM 8.40
CHEMBL4113528 IC50 = 4.0 nM 8.40
CHEMBL3657954 IC50 = 4.0 nM 8.40
CHEMBL3662166 IC50 = 4.0 nM 8.40
CHEMBL3662177 IC50 = 4.0 nM 8.40
CHEMBL3662231 IC50 = 4.0 nM 8.40
CHEMBL3662220 IC50 = 4.0 nM 8.40
CHEMBL3662170 IC50 = 4.0 nM 8.40