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Antitumor agent-174 (Compound 10) 通过直接结合Hsp90的N端位点,促进β-catenin降解,以抑制Wnt/β-catenin信号传导。该化合物有效抑制结肠癌(CRC)细胞增殖,诱导S和G2/M期停滞,并阻断细胞的克隆形成能力。它能下调CDK1、Cyclin D1、c-Myc、Cyclin B1和Cyclin A2,并上调P21蛋白。Antitumor agent-174 对结直肠癌(CRC)显示出显著的抗肿瘤活性,具备优异的药代动力学特性及低毒性。
Antitumor agent-174 (Compound 10) 通过直接结合Hsp90的N端位点,促进β-catenin降解,以抑制Wnt/β-catenin信号传导。该化合物有效抑制结肠癌(CRC)细胞增殖,诱导S和G2/M期停滞,并阻断细胞的克隆形成能力。它能下调CDK1、Cyclin D1、c-Myc、Cyclin B1和Cyclin A2,并上调P21蛋白。Antitumor agent-174 对结直肠癌(CRC)显示出显著的抗肿瘤活性,具备优异的药代动力学特性及低毒性。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
Antitumor agent-174 相关产品
| 产品描述 | Antitumor agent-174 (Compound 10) directly binds to the N-terminal site of Hsp90, promoting the degradation of β-catenin and thereby inhibiting Wnt/β-catenin signaling. This compound effectively suppresses the proliferation of colorectal cancer (CRC) cells, induces S and G2/M phase arrest, and prevents cell colony formation. It downregulates proteins such as CDK1, Cyclin D1, c-Myc, Cyclin B1, and Cyclin A2, while upregulating P21. Antitumor agent-174 exhibits significant antitumor activity against CRC, offering excellent pharmacokinetics and low toxicity. |
| 分子式 | C20H18Cl2N2 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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