2. Others Membrane Transporter/Ion Channel Neuronal Signaling Metabolic Enzyme/Protease
  3. Isotope-Labeled Compounds GABA Receptor Endogenous Metabolite
  4. Tetrahydrodeoxycorticosterone-d3

Tetrahydrodeoxycorticosterone-d3  (Synonyms: Tetrahydro-11-deoxycorticosterone-d3)

目录号: HY-113346S 纯度: 98.50%
COA 产品使用指南

摩尔计算器

Tetrahydrodeoxycorticosterone-d3 是 Tetrahydrodeoxycorticosterone 氘代物。Tetrahydrodeoxycorticosterone 是一种神经类固醇，是一种有效的 GABAA 受体正变构调节剂 (PAM)。Tetrahydrodeoxycorticosterone 具有有效的神经抑制特性。

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Tetrahydrodeoxycorticosterone-d<sub>3</sub> Chemical Structure

Tetrahydrodeoxycorticosterone-d3 Chemical Structure

CAS No. : 72205-58-4

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规格 价格 是否有货 数量
500 μg ￥2900
In-stock
1 mg ￥4800
In-stock
5 mg   询价  
10 mg   询价  

* Please select Quantity before adding items.

Other Forms of Tetrahydrodeoxycorticosterone-d3:

Tetrahydrodeoxycorticosterone-d3 相关抗体

Top Publications Citing Use of Products

MCE 顾客使用本产品发表的 1 篇科研文献

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Tetrahydrodeoxycorticosterone-d3 is the deuterium labeled Tetrahydrodeoxycorticosterone. Tetrahydrodeoxycorticosterone, an neurosteroid, is a potent positive allosteric modulator (PAM) of GABAA receptor. Tetrahydrodeoxycorticosterone has potent neuroinhibitory properties[1][2][3].

体外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

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

Tetrahydrodeoxycorticosterone-d3 相关抗体:
分子量

337.51

Formula

C21H31D3O3
CAS 号
非标记 CAS

567-03-3
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
溶解性数据
细胞实验： 

DMSO 中的溶解度 : 100 mg/mL (296.29 mM; 超声加热助溶; 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 2.9629 mL 14.8144 mL 29.6287 mL
5 mM 0.5926 mL 2.9629 mL 5.9258 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。-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

只
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

Tetrahydrodeoxycorticosterone-d3 相关分类

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。-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 2.9629 mL 14.8144 mL 29.6288 mL 74.0719 mL
5 mM 0.5926 mL 2.9629 mL 5.9258 mL 14.8144 mL
10 mM 0.2963 mL 1.4814 mL 2.9629 mL 7.4072 mL
15 mM 0.1975 mL 0.9876 mL 1.9753 mL 4.9381 mL
20 mM 0.1481 mL 0.7407 mL 1.4814 mL 3.7036 mL
25 mM 0.1185 mL 0.5926 mL 1.1852 mL 2.9629 mL
30 mM 0.0988 mL 0.4938 mL 0.9876 mL 2.4691 mL
40 mM 0.0741 mL 0.3704 mL 0.7407 mL 1.8518 mL
50 mM 0.0593 mL 0.2963 mL 0.5926 mL 1.4814 mL
60 mM 0.0494 mL 0.2469 mL 0.4938 mL 1.2345 mL
80 mM 0.0370 mL 0.1852 mL 0.3704 mL 0.9259 mL
100 mM 0.0296 mL 0.1481 mL 0.2963 mL 0.7407 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.

Keywords:

Tetrahydrodeoxycorticosterone-d372205-58-4Tetrahydro-11-deoxycorticosterone-d3Isotope-Labeled CompoundsGABA ReceptorEndogenous MetaboliteGamma-aminobutyric acid Receptorγ-Aminobutyric acid ReceptorInhibitorinhibitorinhibit

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目录号：
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