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FL442作为一种Androgen Receptor(AR) 调节剂,在AR依赖性前列腺癌细胞中展现出显著的抑制活性,其效率与Bicalutamide和Enzalutamide这类传统抗雄激素药物相似。此外,FL442针对于对Enzalutamide显示较强耐药性的AR突变体F876L也保持了抗雄激素活性。在小鼠模型中,FL442的药代动力学特征表明该化合物具有较长的半衰期(8小时)、针对前列腺组织的良好定向性及优异的代谢稳定性,且在低血浆浓度(30 ng/mL)下依然能有效抑制LNCaP肿瘤生长。

FL442作为一种Androgen Receptor(AR) 调节剂,在AR依赖性前列腺癌细胞中展现出显著的抑制活性,其效率与Bicalutamide和Enzalutamide这类传统抗雄激素药物相似。此外,FL442针对于对Enzalutamide显示较强耐药性的AR突变体F876L也保持了抗雄激素活性。在小鼠模型中,FL442的药代动力学特征表明该化合物具有较长的半衰期(8小时)、针对前列腺组织的良好定向性及优异的代谢稳定性,且在低血浆浓度(30 ng/mL)下依然能有效抑制LNCaP肿瘤生长。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 25 mg | ¥ 10,600  | 4-6周 | |
| 50 mg | ¥ 13,800  | 4-6周 | |
| 100 mg | ¥ 17,500  | 4-6周 | 
FL442 相关产品
| 产品描述 | FL442 is an Androgen Receptor (AR) modulator. This compound exhibits potent inhibitory effects in AR-dependent prostate cancer cells, showing similar suppression efficiency to the traditional antiandrogen drugs Bicalutamide and Enzalutamide. It also maintains antiandrogen activity against the Enzalutamide-resistant AR mutant F876L. The pharmacokinetic properties of FL442 in mice reveal a longer half-life (8 hours), excellent targeting (prostate tissue), and metabolic stability. Additionally, it is effective at inhibiting LNCaP tumor growth at low plasma concentrations (30 ng/mL).  | 
| 分子量 | 294.27 | 
| 分子式 | C15H13F3N2O | 
| CAS No. | 1431166-12-9 | 
| 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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