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PBS磷酸盐缓冲液(20×) 三苯基硫氯甲烷,≥96% Regorafenib (BAY 73-4506) 1-氨基芘
AZ 5104 is an inhibitor of mutant EGFRs (IC50 = 2 nM for EGFRL858R/T790M and EGFRT790M for both) and an active metabolite of AZD 9291 (Item No. 16237).1 It is selective for these mutant EGFRs over wild-type EGFR (IC50 = 33 nM). AZ 5104 is formed from AZD 9291 by the cytochrome P450 (CYP) isoform CYP3A.2 It decreases proliferation of H1975 non-small cell lung cancer (NSCLC) cells containing the L858R activating and T790M resistance mutations (GI50 = 24 nM). AZ 5104 (2.5-10 mg/kg per day) reduces tumor growth in an H1975 mouse xenograft model.
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