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Assay Detail

CHEMBL4431265

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

Binding
Inhibition of human recombinant JAK1 using Ulight-CAGAGAIETDKEYYTVKD as substrate by LANCE assay
2
Total Activities
2
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 JAK1 (CHEMBL2835)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, Synthesis, and Antitumor Evaluation of 4-Amino-(1<i>H</i>)-pyrazole Derivatives as JAKs Inhibitors.
Liang X, Zang J, Zhu M, Gao Q, Wang B, Xu W, Zhang Y.
ACS Med Chem Lett (2016) 7 : 950 -955
PubMed 27774135 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 8.50 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL388978 STAUROSPORINE 1 8.52
CHEMBL4453646 1 8.47

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL388978 STAUROSPORINE IC50 = 3.0 nM 8.52
CHEMBL4453646 IC50 = 3.4 nM 8.47