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Assay Detail

CHEMBL4700043

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

Binding
Inhibition of wild-type human ABL2 (A248 to G542 residues) expressed in bacterial expression system by Kinomescan 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 ABL2 (CHEMBL4014)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Understanding the mechanism of action of pyrrolo[3,2-b]quinoxaline-derivatives as kinase inhibitors
Unzue, Andrea, Jessen-Trefzer, Claudia, Spiliotopoulos, Dimitrios, Gaudio, Eugenio, Tarantelli, Chiara, Dong, Jing, Zhao, Hongtao, Pachmayr, Johanna, Zahler, Stefan, Bernasconi, Elena, Sartori, Giulio, Cascione, Luciano, Bertoni, Francesco, Sledz, Pawel, Caflisch, Amedeo, Nevado, Cristina
RSC Med Chem (2020) 11 : 665 -675
PubMed 33479666 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 2 7.55 7.58

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4776609 1 7.58
CHEMBL4792853 1 7.51

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4776609 Kd = 26.0 nM 7.58
CHEMBL4792853 Kd = 31.0 nM 7.51