产品详情 |
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Product Name | Afatinib dimaleate |
Description | Potent dual specificity EGFR/HER2 inhibitor (IC50 are 0.4, 0.5, 10, 14, 1 nM for EGFRL858R, EGFRwt, EGFR L858R/T790M, ErbB2 (HER2) and ErbB4 (HER4), respectively). 100-fold more active than Gefitinib in L858R-T790M EGFR double mutant cell line. Irreversibly binds EGFR and HER2. Suppresses the kinase activity of wild-type and activated EGFR and HER2 mutants, including erlotinib-resistant isoforms. Induces tumor regression in xenograft and transgenic lung cancer models. Purity 98%. MW (observed): 718.08 |
Size | 10 mg |
Concentration | n/a |
Applications | n/a |
Other Names | (2E)-N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-[[(3S)-tetrahydro-3-furanyl]oxy]-6-quinazolinyl]-4-(dimethylamino)-2-butenamide dimaleate. BIBW2992 |
Gene, Accession, CAS # | CAS: 850140-73-7 |
Catalog # | 6812/10 |
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Order / More Info | Afatinib dimaleate from TOCRIS BIOSCIENCE
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Product Specific References | n/a |
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