1. Membrane Transporter/Ion Channel
  2. P-glycoprotein BCRP
  3. CP-100356

CP-100356 是一种具有口服活性的 MDR1 (P-gp)/BCRP 双重抑制剂,可以抑制 MDR1 介导的 Calcein-AM 转运 (IC50 = 0.5 μM) 和 BCRP 介导的 Prazosin 转运 (IC50 = 1.5 μM)。CP-100356 也是 OATP1B1 的弱抑制剂 (IC50 = ~66 μM)。CP-100356 对 MRP2 和主要的人 P450 酶没有抑制作用 (IC50 > 15 μM)。

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CP-100356

CP-100356 Chemical Structure

CAS No. : 142716-85-6

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CP-100356 的其他形式现货产品:

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Other Forms of CP-100356:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

CP-100356 is an orally active dual MDR1 (P-gp)/BCRP inhibitor, with an IC50s of 0.5 and 1.5 µM for inhibiting MDR1-mediated Calcein-AM transport and BCRP-mediated Prazosin transport, respectively. CP-100356 is also a weak inhibitor of OATP1B1 (IC50 = ∼66 µM). CP-100356 is devoid of inhibition against MRP2 and major human P450 enzymes (IC50 > 15 µM)[1].

分子量

560.64

Formula

C31H36N4O6

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.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
CP-100356
目录号:
HY-108347A
需求量: