Name | lazertinib |
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Synonyms |
4A2Y23XK11
N-{5-[(4-{4-[(Dimethylamino)methyl]-3-phenyl-1H-pyrazol-1-yl}-2-pyrimidinyl)amino]-4-methoxy-2-(4-morpholinyl)phenyl}acrylamide 2-Propenamide, N-[5-[[4-[4-[(dimethylamino)methyl]-3-phenyl-1H-pyrazol-1-yl]-2-pyrimidinyl]amino]-4-methoxy-2-(4-morpholinyl)phenyl]- lazertinib |
Description | Lazertinib is a potent, highly mutant-selective, blood-brain barrier permeable, orally available and irreversible third-generation EGFR tyrosine kinase inhibitor, and can be used in the research of non-small cell lung cancer. |
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Related Catalog | |
Target |
EGFRT790M |
In Vitro | Lazertinib (YH25448) is a potent, highly mutant-selective, blood-brain barrier permeable, orally available and irreversible third-generation EGFR tyrosine kinase inhibitor, and can be used in the research of non-small cell lung cancer. Lazertinib targets both T790M mutation and activating EGFR mutations (EGFRm) while sparing wild type[1]. |
References |
Density | 1.3±0.1 g/cm3 |
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Molecular Formula | C30H34N8O3 |
Molecular Weight | 554.643 |
Exact Mass | 554.275391 |
LogP | 2.72 |
Index of Refraction | 1.647 |
Storage condition | -20℃ |