YK-4-279CAS号： 1037184-44-3分子式： C17H13Cl2NO4分子量： 366.2描述纯度储存/保存方法别名外观可溶性/溶解性靶点In vitro(体外研究)In vivo(体内研究)
| 产品描述 | |
| 描述 |
YK 4-279 is an inhibitor of RNA Helicase A (RHA) binding to the oncogenic transciption factor EWS-FLI1. YK-4-279 inhibits Ewing’s sarcoma family tumor (ESFT) cell growth; YK-4-279 induces apoptosis.
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| 纯度 |
≥98%
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| 储存/保存方法 |
Store at -20℃ for one year（Powder）；Store at 2-4℃ for two weeks；Store at -20℃ for six months after dissolution.
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| 基本信息 | |
| 别名 |
YK 4-279
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| 外观 |
White or off white solid
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| 可溶性/溶解性 |
DMSO : 25 mg/mL (68.27 mM)
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| 生物活性 | |
| 靶点 |
RNA helicase A
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| In vitro(体外研究) |
YK-4-279 eliminates cyclin D levels by blocking the interaction of EWS-FLI1 with RHA in EWS-FLI1-containing TC32 cells. YK-4-279 also specifically inhibits ESFT cell growth and induces apoptosis. YK-4-279 also inhibits ERG and ETV1 biological activity in fusion-positive prostate cancer cells, and further decreases cell motility and invasion.
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| In vivo(体内研究) |
In vivo, YK-4-279 (1.5 mg/dose i.p.) inhibits the growth of ESFT xenograft tumors. In mouse model, YK-4-279 selectively prevents prostate cancer growth and metastasis in fusion-positive LNCaP-luc-M6 tumors.
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| 参考文献 |
分子结构图
