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Assay Detail

CHEMBL4055573

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

Binding
Binding affinity to partial length human SIK expressed in Escherichia coli BL21 by active-site-dependent competition assay
1
Total Activities
1
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

Serine/threonine-protein kinase SIK1 (CHEMBL6082)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure Based Design of N-(3-((1H-Pyrazolo[3,4-b]pyridin-5-yl)ethynyl)benzenesulfonamides as Selective Leucine-Zipper and Sterile-α Motif Kinase (ZAK) Inhibitors.
Chang Y, Lu X, Shibu MA, Dai YB, Luo J, Zhang Y, Li Y, Zhao P, Zhang Z, Xu Y, Tu ZC, Zhang QW, Yun CH, Huang CY, Ding K.
J Med Chem (2017) 60 : 5927 -5932
PubMed 28586211 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 1 7.35 7.35

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4098896 1 7.35

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4098896 Kd = 45.0 nM 7.35