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Assay Detail

CHEMBL5733291

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

Binding
Rubidium efflux assay: HEK-293 cells overexpressing the channel of interest were seeded in a 96-well plate at a density of 30000 cells/well and incubated at 37° C./5% CO2 for 48 hr. The assay was carried out using the Red Membrane Potential Dye (Molecular Devices) following the manufacturer's instructions. Briefly, the cells were incubated with 1× red membrane potential dye for 1.5 hour. The cells were then treated with various concentrations of the test compounds for 15-20 min followed by depolarization with 10-30 μM Veratridine. The fluorescence was read following excitation at 510-545 nm and emission at 565-625 nm in FLIPR. The “max-min” fluorescence values were used to calculate the % inhibition. IC50 values were calculated by plotting % inhibition against concentration and curve fitting into a sigmoidal dose response.Through the use of the above described assay procedure, compounds were found to exhibit functional activity against Nav 1.7 in vitro and particularly well suited for the treatment of diseases or disorders as described herein above.
684
Total Activities
226
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Sulfonamide compounds as voltage-gated sodium channel modulators
(2019)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 228 7.06 10.40
kon 228 - -
k_off 228 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4640389 3 10.40
CHEMBL5822353 3 9.70
CHEMBL4639872 3 9.70
CHEMBL4633361 3 9.52
CHEMBL4636970 3 9.52
CHEMBL5969083 3 9.30
CHEMBL4649472 3 9.30
CHEMBL5808125 3 9.15
CHEMBL5800639 3 9.15
CHEMBL5987817 3 9.05
CHEMBL5786465 3 9.05
CHEMBL4634870 3 9.00
CHEMBL4644542 3 9.00
CHEMBL4647620 3 9.00
CHEMBL4640134 3 9.00
CHEMBL4641925 3 9.00
CHEMBL4644526 3 8.70
CHEMBL6057917 3 8.70
CHEMBL4647267 3 8.52
CHEMBL5770334 3 8.52
CHEMBL5933833 3 8.52
CHEMBL4648205 3 8.52
CHEMBL5861156 3 8.40
CHEMBL5809035 3 8.40
CHEMBL5936312 3 8.40
CHEMBL4639765 3 8.40
CHEMBL5940262 3 8.30
CHEMBL4637586 3 8.30
CHEMBL5914530 3 8.30
CHEMBL4638356 3 8.22

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4640389 IC50 = 0.04 nM 10.40
CHEMBL5822353 IC50 = 0.2 nM 9.70
CHEMBL4639872 IC50 = 0.2 nM 9.70
CHEMBL4633361 IC50 = 0.3 nM 9.52
CHEMBL4636970 IC50 = 0.3 nM 9.52
CHEMBL4649472 IC50 = 0.5 nM 9.30
CHEMBL5969083 IC50 = 0.5 nM 9.30
CHEMBL5808125 IC50 = 0.7 nM 9.15
CHEMBL5800639 IC50 = 0.7 nM 9.15
CHEMBL5987817 IC50 = 0.9 nM 9.05
CHEMBL5786465 IC50 = 0.9 nM 9.05
CHEMBL4647620 IC50 = 1.0 nM 9.00
CHEMBL4644542 IC50 = 1.0 nM 9.00
CHEMBL4634870 IC50 = 1.0 nM 9.00
CHEMBL4641925 IC50 = 1.0 nM 9.00
CHEMBL4640134 IC50 = 1.0 nM 9.00
CHEMBL4644526 IC50 = 2.0 nM 8.70
CHEMBL6057917 IC50 = 2.0 nM 8.70
CHEMBL5933833 IC50 = 3.0 nM 8.52
CHEMBL4648205 IC50 = 3.0 nM 8.52
CHEMBL4647267 IC50 = 3.0 nM 8.52
CHEMBL5770334 IC50 = 3.0 nM 8.52
CHEMBL5861156 IC50 = 4.0 nM 8.40
CHEMBL5809035 IC50 = 4.0 nM 8.40
CHEMBL5936312 IC50 = 4.0 nM 8.40
CHEMBL4639765 IC50 = 4.0 nM 8.40
CHEMBL5940262 IC50 = 5.0 nM 8.30
CHEMBL5914530 IC50 = 5.0 nM 8.30
CHEMBL4637586 IC50 = 5.0 nM 8.30
CHEMBL4638356 IC50 = 6.0 nM 8.22
CHEMBL5875251 IC50 = 7.0 nM 8.15
CHEMBL4635396 IC50 = 7.0 nM 8.15
CHEMBL5979061 IC50 = 8.0 nM 8.10
CHEMBL5976850 IC50 = 8.0 nM 8.10
CHEMBL5921722 IC50 = 8.0 nM 8.10
CHEMBL4640506 IC50 = 8.0 nM 8.10
CHEMBL5811377 IC50 = 8.0 nM 8.10
CHEMBL5970651 IC50 = 10.0 nM 8.00
CHEMBL5853482 IC50 = 10.0 nM 8.00
CHEMBL6030794 IC50 = 11.0 nM 7.96
CHEMBL5947139 IC50 = 11.0 nM 7.96
CHEMBL5851755 IC50 = 11.0 nM 7.96
CHEMBL5766501 IC50 = 11.0 nM 7.96
CHEMBL5802978 IC50 = 11.0 nM 7.96
CHEMBL4632408 IC50 = 11.0 nM 7.96
CHEMBL6026887 IC50 = 12.0 nM 7.92
CHEMBL6056998 IC50 = 12.0 nM 7.92
CHEMBL4637917 IC50 = 12.0 nM 7.92
CHEMBL5785104 IC50 = 12.0 nM 7.92
CHEMBL5944449 IC50 = 12.0 nM 7.92