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  3. WB-308

WB-308是一种的小分子,通过体外EGFR激酶活性系统被鉴定为EGFR的抑制剂。WB-308能够降低NSCLC细胞的增殖和克隆形成,引起G2/M期阻滞和凋亡。此外,WB-308在两种体内动物模型中(肺原位移植模型和患者来源的克隆小鼠模型)抑制了肿瘤的生长。WB-308损害了EGFR、AKT和ERK1/2蛋白的磷酸化。与Gefitinib相比,WB-308的细胞毒性较低。本研究表明,WB-308是一种新的EGFR-TKI,可能被考虑用于替代Gefitinib在NSCLC临床抑制中。

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WB-308 Chemical Structure

WB-308 Chemical Structure

CAS No. : 1373764-87-4

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生物活性

WB-308 is a novel small molecule that was identified as an inhibitor of EGFR by an in vitro EGFR kinase activity system. WB-308 was able to reduce the proliferation and clonogenicity of NSCLC cells, causing G2/M phase arrest and apoptosis. In addition, WB-308 inhibited tumor growth in two in vivo animal models (lung orthotopic transplantation model and patient-derived clonal mouse model). WB-308 impaired the phosphorylation of EGFR, AKT, and ERK1/2 proteins. Compared with Gefitinib, WB-308 had lower cytotoxicity. This study showed that WB-308 is a new EGFR-TKI that may be considered as an alternative to Gefitinib in the clinical treatment of NSCLC.

分子量

308.35

Formula

C19H17FN2O

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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产品名称:
WB-308
目录号:
HY-116504
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