1. Cell Cycle/DNA Damage Vitamin D Related/Nuclear Receptor Metabolic Enzyme/Protease
  2. PPAR
  3. Timcodar

Timcodar 是一种大环内酯类试剂,在脂肪生成过程中,Timcodar 能显著抑制脂肪积累,效果与雷帕霉素相似。但与雷帕霉素不同的是,Timcodar 不会引起免疫抑制和葡萄糖抵抗。Timcodar 能有效抑制脂肪生成转录调节因子 PPAR 和 C/EBP,从而抑制涉及脂肪积累的基因。

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Timcodar

Timcodar Chemical Structure

CAS No. : 179033-51-3

1.  客户无需承担相应的运输费用。

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。

3.  试用装只面向终端客户

规格 是否有货
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Other Forms of Timcodar:

查看 PPAR 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

Timcodar is a macrolide agent that can significantly inhibit fat accumulation during adipogenesis, with an effect similar to rapamycin. However, unlike rapamycin, Timcodar does not cause immunosuppression and glucose resistance. Timcodar can effectively inhibit adipogenesis transcriptional regulators PPAR and C/EBP, thereby inhibiting genes involved in fat accumulation.

Clinical Trial
分子量

749.29

Formula

C43H45ClN4O6

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 *
= × ×

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:
Timcodar
目录号:
HY-13766
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