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Assay Detail

CHEMBL5131640

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

Binding
Inhibition of JAK 2 (unknown origin)
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Tyrosine-protein kinase JAK2 (CHEMBL2971)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Recent Developments in the Use of Kinase Inhibitors for Management of Viral Infections.
Raghuvanshi R, Bharate SB.
J Med Chem (2022) 65 : 893 -921
PubMed 33539089 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 8.20 9.57

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4303389 NS-018 2.0 1 9.57
CHEMBL603469 LESTAURTINIB 3.0 1 9.05
CHEMBL495727 AT-9283 2.0 1 8.92
CHEMBL4297507 DELGOCITINIB 3.0 1 8.59
CHEMBL1789941 RUXOLITINIB 4.0 1 8.55
CHEMBL1287853 FEDRATINIB 4.0 1 8.52
CHEMBL2107823 GANDOTINIB 2.0 1 8.52
CHEMBL2105759 BARICITINIB 4.0 1 8.24
CHEMBL4116008 CERDULATINIB 2.0 1 8.22
CHEMBL1078178 MOMELOTINIB 4.0 1 7.75
CHEMBL221959 TOFACITINIB 4.0 1 7.70
CHEMBL2035187 PACRITINIB 4.0 1 7.64
CHEMBL3301607 FILGOTINIB 4.0 1 7.55
CHEMBL1944698 ZOTIRACICLIB 2.0 1 7.14
CHEMBL4747591 1 7.11

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4303389 NS-018 IC50 = 0.27 nM 9.57
CHEMBL603469 LESTAURTINIB IC50 = 0.9 nM 9.05
CHEMBL495727 AT-9283 IC50 = 1.2 nM 8.92
CHEMBL4297507 DELGOCITINIB IC50 = 2.6 nM 8.59
CHEMBL1789941 RUXOLITINIB IC50 = 2.8 nM 8.55
CHEMBL1287853 FEDRATINIB IC50 = 3.0 nM 8.52
CHEMBL2107823 GANDOTINIB IC50 = 3.0 nM 8.52
CHEMBL2105759 BARICITINIB IC50 = 5.7 nM 8.24
CHEMBL4116008 CERDULATINIB IC50 = 6.0 nM 8.22
CHEMBL1078178 MOMELOTINIB IC50 = 18.0 nM 7.75
CHEMBL221959 TOFACITINIB IC50 = 20.0 nM 7.70
CHEMBL2035187 PACRITINIB IC50 = 23.0 nM 7.64
CHEMBL3301607 FILGOTINIB IC50 = 28.0 nM 7.55
CHEMBL1944698 ZOTIRACICLIB IC50 = 73.0 nM 7.14
CHEMBL4747591 IC50 = 77.0 nM 7.11