1. Cell Cycle/DNA Damage Epigenetics
  2. Aurora Kinase
  3. DBPR728

DBPR728 是一种 6K465 的酰基前药,携带较少的氢键供体,6K465 作为 Aurora 激酶抑制剂,可以破坏 MYC 家族癌蛋白的稳定性,并已显示出抗肿瘤功效。DBPR728 具有抑制过表达 C-MYC 和 N-MYC 的癌症的潜力,且口服生物利用度较 6K465 提高了 10 倍。

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DBPR728 Chemical Structure

DBPR728 Chemical Structure

CAS No. : 2702965-64-6

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2.  同一机构(单位)同一产品试用装仅限申领一次,同一机构(单位)一年内

     可免费申领三个不同产品的试用装。

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规格 价格 是否有货 数量
5 mg ¥2850
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10 mg ¥4740
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查看 Aurora Kinase 亚型特异性产品:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

DBPR728 is an acyl prodrug of 6K465 that carries fewer hydrogen bond donors. 6K465 acts as an Aurora kinase inhibitor that destabilizes MYC family cancer proteins and has antitumor efficacy. DBPR728 has the potential to inhibit cancers that overexpress C-MYC and N-MYC, with a 10-fold increase in oral bioavailability compared to 6K465[1].

分子量

598.11

Formula

C29H37ClFN9O2

CAS 号
性状

固体

颜色

White to off-white

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
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 *
= × ×

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
Help & FAQs
  • 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:
DBPR728
目录号:
HY-162470
需求量: