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Assay Detail

CHEMBL931283

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

Binding
Inhibition of human Nav1.7 channel expressed in HEK293 cells at -60 mV by patch clamp method
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HEK293
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

A-803467, a potent and selective Nav1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat.
Jarvis MF, Honore P, Shieh CC, Chapman M, Joshi S, Zhang XF, Kort M, Carroll W, Marron B, Atkinson R, Thomas J, Liu D, Krambis M, Liu Y, McGaraughty S, Chu K, Roeloffs R, Zhong C, Mikusa JP, Hernandez G, Gauvin D, Wade C, Zhu C, Pai M, Scanio M, Shi L, Drizin I, Gregg R, Matulenko M, Hakeem A, Gross M, Johnson M, Marsh K, Wagoner PK, Sullivan JP, Faltynek CR, Krafte DS.
Proc Natl Acad Sci U S A (2007) 104 : 8520 -8525
PubMed 17483457 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 5.17 5.17

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL250699 1 5.17

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL250699 IC50 = 6740.0 nM 5.17