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Assay Detail

CHEMBL3226837

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

Binding
Inhibition of JNK in rat INS cells assessed as inhibition of c-jun phosphorylation
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Synthesis and SAR of 2,4-diaminopyrimidines as potent c-jun N-terminal kinase inhibitors
Song X, He Y, Koenig M, Shin Y, Noel R, Chen W, Ling YY, Feurstein D, Lin L, Ruiz CH, Cameron MD, Duckett DR, Kamenecka TM
Medchemcomm (2012) 3 : 238 -243
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 7.42 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3220495 1 8.52
CHEMBL458997 1 6.31
CHEMBL3040440 VS-4718 1.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3220495 IC50 = 3.0 nM 8.52
CHEMBL458997 IC50 = 485.0 nM 6.31
CHEMBL3040440 VS-4718 IC50 > 3000.0 nM -