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Assay Detail

CHEMBL5131304

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

Binding
Inhibition of human Nav1.7 T1398M-I1399D mutant expressed in CHO cells at -100 mV holding potential by electrophysiology whole cell patch clamp technique
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type CHO
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Discovery of Selective Inhibitors of Na<sub>V</sub>1.7 Templated on Saxitoxin as Therapeutics for Pain.
Pajouhesh H, Delwig A, Beckley JT, Klas S, Monteleone D, Zhou X, Luu G, Du Bois J, Hunter JC, Mulcahy JV.
ACS Med Chem Lett (2022) 13 : 1763 -1768
PubMed 36385936 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.64 8.64

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL501134 SAXITOXIN 1 8.64

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL501134 SAXITOXIN IC50 = 2.3 nM 8.64