2. Cell Cycle/DNA Damage Vitamin D Related/Nuclear Receptor Metabolic Enzyme/Protease
  3. PPAR
  4. Mavodelpar free acid

Mavodelpar free acid  (Synonyms: REN001 free acid; HPP593 free acid; Pparδ agonist)

目录号: HY-112597
产品使用指南

摩尔计算器

Mavodelpar free acid 是 PPARδ 的激动剂，来自专利US20180071304， 化合物实例10。

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Mavodelpar free acid Chemical Structure

Mavodelpar free acid Chemical Structure

CAS No. : 942594-93-6

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规格 是否有货
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Mavodelpar free acid 的其他形式现货产品:

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Mavodelpar free acid 相关抗体

Top Publications Citing Use of Products

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PPARα PPARβ/δ PPARγ PPAR PPARδ

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Mavodelpar free acid is a PPARδ agonist extracted from patent US20180071304, compound example 10. Mavodelpar (free acid) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

IC50 & Target

PPARδ[1]
Clinical Trial
分子量

515.57

Formula

C31H30FNO5
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

Mavodelpar free acid 相关分类

  • 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.

Keywords:

Mavodelpar942594-93-6REN001HPP593 Pparδ agonistREN 001REN-001HPP 593HPP-593PPARPeroxisome proliferator-activated receptorsInhibitorinhibitorinhibit

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目录号：
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