1. Metabolic Enzyme/Protease
  2. Phosphodiesterase (PDE)
  3. Dovramilast

Dovramilast  (Synonyms: CC-11050)

目录号: HY-147263 纯度: 99.83%
COA 产品使用指南

Dovramilast (CC-11050) 是一种磷酸二酯酶 4 (PDE4) 抑制剂,具有口服活性,可以减少炎症反应,改善 Isoniazid (HY-B0329) 介导的肺部细菌清除。Dovramilast 作为辅助试剂,可用于结核病的研究。

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Dovramilast Chemical Structure

Dovramilast Chemical Structure

CAS No. : 340019-69-4

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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。

3.  试用装只面向终端客户

规格 价格 是否有货 数量
1 mg ¥1727
In-stock
5 mg ¥3800
In-stock
10 mg ¥6000
In-stock
50 mg   询价  
100 mg   询价  

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Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Dovramilast (CC-11050) is an orally active phosphodiesterase 4 (PDE4) inhibitor and can reduce the inflammatory response and improves Isoniazid (INH)-mediated bacillary clearance from the lungs. Dovramilast, as an adjunct, is used for the research of tuberculosis (TB)[1].

IC50 & Target

PDE4

 

体内研究
(In Vivo)

Dovramilast (oral gavage, 5, 25, or 50 mg/kg, single) significantly improves antibiotic-mediated bacterial killing and reduces lung pathology[2].
Pharmacokinetic Parameters of Dovramilast in B6D2F1 mice[2].

Sampling time(h) Concentration(ng/ml)
CC-11050 only CC-11050+INH
1 1,331.6±136.97 905.35±594.23
2 1,409.47±140.85 1,309.39±214.08
5 948.85±128.7 1,609.18±167.2
8 820.6±265.98 1,271.73±249.18
24 1.27±1.1 4.96±1.85
Tmax(h) 2.0 5.0
Cmax(ng/ml) 1,410 1,610
AUClast(ng × h/ml) 10,200 13,900

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: B6D2F1 mice[2]
Dosage: 5, 25, or 50 mg/kg
Administration: oral, 5, 25, or 50 mg/kg, single
Result: Reduced PDE4 expression in mtb-infected mouse lungs.
Animal Model: B6D2F1 mice[2]
Dosage: 5, 25, or 50 mg/kg
Administration: oral gavage, 5, 25, or 50 mg/kg, single
Result: Improved antibiotic-mediated bacterial killing and reduced lung pathology.
Clinical Trial
分子量

472.55

Formula

C24H28N2O6S

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

4°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

溶解性数据
In Vitro: 

DMSO 中的溶解度 : 25 mg/mL (52.90 mM; 超声助溶 (<60°C); 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.1162 mL 10.5809 mL 21.1618 mL
5 mM 0.4232 mL 2.1162 mL 4.2324 mL
查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 摩尔计算器

  • 稀释计算器

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

质量
=
浓度
×
体积
×
分子量 *

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料
参考文献

完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.1162 mL 10.5809 mL 21.1618 mL 52.9045 mL
5 mM 0.4232 mL 2.1162 mL 4.2324 mL 10.5809 mL
10 mM 0.2116 mL 1.0581 mL 2.1162 mL 5.2904 mL
15 mM 0.1411 mL 0.7054 mL 1.4108 mL 3.5270 mL
20 mM 0.1058 mL 0.5290 mL 1.0581 mL 2.6452 mL
25 mM 0.0846 mL 0.4232 mL 0.8465 mL 2.1162 mL
30 mM 0.0705 mL 0.3527 mL 0.7054 mL 1.7635 mL
40 mM 0.0529 mL 0.2645 mL 0.5290 mL 1.3226 mL
50 mM 0.0423 mL 0.2116 mL 0.4232 mL 1.0581 mL
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:
Dovramilast
目录号:
HY-147263
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