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DY3002是一种选择性且高效的EGFR抑制剂,具有克服T790M介导的非小细胞肺癌耐药性的活性。DY3002在激酶实验中对EGFR T790M突变体表现出优越的抑制效果(IC50 = 0.71 nM),相比之下,对野生型EGFR的抑制效果较弱(IC50 = 448.7 nM)。DY3002在选择性上显著优于rociletinib和osimertinib,显示出极高的选择性指数(SI = 632.0)。在细胞实验中,DY3002针对H1975细胞的IC50值为0.037 μM,表现出增强的抑制效力。此外,DY3002在生物学性质方面优于其他替代化合物,且不引起高血糖。

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DY3002 Chemical Structure

DY3002 Chemical Structure

CAS No. : 2020015-37-4

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生物活性

DY3002 is a selective and highly potent EGFR inhibitor with activity in overcoming T790M-mediated drug resistance in non-small cell lung cancer. DY3002 exhibited superior inhibitory effects against EGFR T790M mutants in kinase assays (IC50 = 0.71 nM), compared to weaker inhibitory effects against wild-type EGFR (IC50 = 448.7 nM). DY3002 was significantly superior to rociletinib and osimertinib in selectivity, showing an extremely high selectivity index (SI = 632.0). In cell experiments, DY3002 had an IC50 value of 0.037 μM against H1975 cells, showing enhanced inhibitory potency. In addition, DY3002 was superior to other alternative compounds in terms of biological properties and did not cause hyperglycemia[1].

分子量

464.95

Formula

C24H25ClN6O2

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
DY3002
目录号:
HY-119396
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