lazertinib [Ligand Id: 10136] activity data from GtoPdb

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  • epidermal growth factor receptor in Human [GtoPdb: 1797] [UniProtKB: P00533]
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  • kinase insert domain receptor in Human [GtoPdb: 1813] [UniProtKB: P35968]
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  • Janus kinase 3 in Human [GtoPdb: 2049] [UniProtKB: P52333]
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  • spleen associated tyrosine kinase in Human [GtoPdb: 2230] [UniProtKB: P43405]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
epidermal growth factor receptor in Human [GtoPdb: 1797] [UniProtKB: P00533]
GtoPdb Measuring inhibition of mutant EGFR kinase activities in biochemical assays (equivalent potency against Del19, L858R, L858R/T790M and Del19/T790M EGFR mutants). NOTE lazertinib is inactive vs. wild type EGFR. - 7.7 pIC50 <20 nM IC50 WO2016060443A2. Compounds and compositions for modulating EGFR mutant kinase activities. (2016)
kinase insert domain receptor in Human [GtoPdb: 1813] [UniProtKB: P35968]
GtoPdb In a biochemical enzyme activity assay. - 6 pIC50 >1000 nM IC50 WO2016060443A2. Compounds and compositions for modulating EGFR mutant kinase activities. (2016)
Janus kinase 3 in Human [GtoPdb: 2049] [UniProtKB: P52333]
GtoPdb In a biochemical enzyme activity assay. - 7.7 pIC50 <20 nM IC50 WO2016060443A2. Compounds and compositions for modulating EGFR mutant kinase activities. (2016)
spleen associated tyrosine kinase in Human [GtoPdb: 2230] [UniProtKB: P43405]
GtoPdb In a biochemical enzyme activity assay. - 6.7 pIC50 201 nM IC50 WO2016060443A2. Compounds and compositions for modulating EGFR mutant kinase activities. (2016)

Our curators have not yet identified this ligand in ChEMBL, but you may find additional data by searching on the ChEMBL site using the ligand's name or structure.