Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5133813

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

Binding
Binding affinity to BTK (unknown origin) assessed as dissociation constant by KINOMEscan analysis
6
Total Activities
6
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 BTK (CHEMBL5251)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Optimization of a novel piperazinone series as potent selective peripheral covalent BTK inhibitors.
Ma B, Metrick CM, Gu C, Hoemberger M, Bajrami B, Bame E, Huang J, Mingueneau M, Murugan P, Santoro JC, Tang H, Wang T, Hopkins BT.
Bioorg Med Chem Lett (2022) 60 : 128549 -128549
PubMed 35041943 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 6 9.07 9.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4483575 REMIBRUTINIB 3.0 1 9.62
CHEMBL4066176 1 9.62
CHEMBL1873475 IBRUTINIB 4.0 1 9.19
CHEMBL5188786 1 9.04
CHEMBL3707348 ACALABRUTINIB 4.0 1 8.59
CHEMBL3936761 ZANUBRUTINIB 4.0 1 8.34

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4483575 REMIBRUTINIB Kd = 0.24 nM 9.62
CHEMBL4066176 Kd = 0.24 nM 9.62
CHEMBL1873475 IBRUTINIB Kd = 0.64 nM 9.19
CHEMBL5188786 Kd = 0.91 nM 9.04
CHEMBL3707348 ACALABRUTINIB Kd = 2.6 nM 8.59
CHEMBL3936761 ZANUBRUTINIB Kd = 4.6 nM 8.34