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O-Desmethyl gefitinib D8 Size:Contact [email protected] for quotation R406 bound to the ATP

SKU: 5984817322

4.4
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Description

R406 bound to the ATP binding pocket of Syk and inhibited its kinase activity as an ATP-competitive inhibitor (K(i) = 30 nM)

PubMed PMID: 30755068

org/wiki/TRV130)

ISRIB (trans-isomer)

O-Desmethyl gefitinib D8 Size:Contact [email protected] for quotation R406 bound to the ATPO Desmethyl gefitinib D8 is a deuterium labeled O Desmethyl gefitinib. O Desmethyl gefitinib is an active metabolite of Gefitinib in human plasma. The formation of O desmethyl gefitinib is dependent on CYP2D6 activity. O desmethyl gefitinib inhibits EGFR with an IC50 of 36 nM in subcellular assays. Product information Molecular Weight: 440. 93 Formula: C21H22ClFN4O3 Chemical Name: 4 [(3 chloro 4 fluorophenyl)amino] 6 {3 [(2, 2, 3, 3, 5, 5, 6, 6

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