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Assay Detail

CHEMBL4362319

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

Binding
Inhibition of BLK (unknown origin) using KVEKIGEGTYGVVYK as substrate in presence of [gamma33P]ATP as substrate in presence of [gamma33P]ATP by scintillation counting method
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 Blk (CHEMBL2250)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Identification of a new family of pyrazolo[3,4-d]pyrimidine derivatives as multitarget Fyn-Blk-Lyn inhibitors active on B- and T-lymphoma cell lines.
Fallacara AL, Passannanti R, Mori M, Iovenitti G, Musumeci F, Greco C, Crespan E, Kissova M, Maga G, Tarantelli C, Spriano F, Gaudio E, Bertoni F, Botta M, Schenone S.
Eur J Med Chem (2019) 181 : 111545 -111545
PubMed 31400706 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 2 6.75 6.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4452230 1 6.77
CHEMBL3578214 1 6.72

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4452230 Ki = 170.0 nM 6.77
CHEMBL3578214 Ki = 190.0 nM 6.72