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  • YHO-13351 free base
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YHO-13351 free base

YHO-13351(freebase)是YHO-13177的水溶性前体药物,YHO-13177是腺癌耐药蛋白多药转运通道(BCRP)高效特异性抑制剂。

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YHO-13351 free base的二维码
  • 库存: 现货
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  • 5mg
    ¥1112.00
    890.00
    - +
  • 10mg
    ¥1612.00
    1290.00
    - +
  • 50mg
    ¥5350.00
    4280.00
    - +
  • 100mg
    ¥9087.00
    7270.00
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  • 货号: ajce50354
  • CAS: 912288-64-3
  • 别名:
  • 分子式: C26H33N3O4S
  • 分子量: 483.62
  • 纯度: >98%
  • 溶解度: DMSO : ≥ 30 mg/mL (62.03 mM)
  • 储存: Store at -20°C
  • 库存: 现货

Background

YHO-13351 (free base) is the water-soluble prodrug of YHO-13177, which is a potent and specific inhibitor of BCRP.IC50 value:Target: BCRP inhibitorin vitro: YHO-13177 potentiates the cytotoxicity of SN-38, mitoxantrone, and topotecan in both BCRP-transduced human colon cancer HCT116 (HCT116/BCRP) cells and SN-38-resistant human lung cancer A549 (A549/SN4) cells that express BCRP, but had little effect in the parental cells. In addition, YHO-13177 potentiates the cytotoxicity of SN-38 in human lung cancer NCI-H460 and NCI-H23, myeloma RPMI-8226, and pancreatic cancer AsPC-1 cells that intrinsically expressed BCRP. YHO-13177 increases the intracellular accumulation of Hoechst 33342, a substrate of BCRP, at 30 minutes and partially suppresses the expression of BCRP protein at more than 24 hours after its treatment in both HCT116/BCRP and A549/SN4 cells [1].in vivo: In mice, YHO-13351 is rapidly converted into YHO-13177 after its oral or intravenous administration. Coadministration of irinotecan with YHO-13351 significantly increases the survival time of mice inoculated with BCRP-transduced murine leukemia P388 cells and suppressed the tumor growth in an HCT116/BCRP xenograft model, whereas irinotecan alone has little effect in these tumor models [1].



[1]. Yamazaki R, et al. Novel acrylonitrile derivatives, YHO-13177 and YHO-13351, reverse BCRP/ABCG2-mediated drug resistance in vitro and in vivo. Mol Cancer Ther. 2011 Jul;10(7):1252-63. [2]. Shishido Y, et al. ABCG2 inhibitor YHO-13351 sensitizes cancer stem/initiating-like side population cells to irinotecan. Anticancer Res. 2013 Apr;33(4):1379-86.

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