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  2. Dopamine Receptor Histamine Receptor Bacterial Amyloid-β
  3. Thiethylperazine

Thiethylperazine 是一种吩噻嗪衍生物,是一种口服有效的多巴胺 D2 受体和组胺 H1 受体拮抗剂。Thiethylperazine 也是一种选择性的 ABCC1 激活剂,可减少小鼠中的淀粉样 β (Aβ) 负荷。Thiethylperazine 具有止吐,抗精神病和抗菌作用。

MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Thiethylperazine Chemical Structure

Thiethylperazine Chemical Structure

CAS No. : 1420-55-9

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     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

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Customer Review

Other Forms of Thiethylperazine:

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

Thiethylperazine, a phenothiazine derivate, is an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. Thiethylperazine is also a selective ABCC1activator that reduces amyloid-β (Aβ) load in mice. Thiethylperazine has anti-emetic, antipsychotic and antimicrobial effects[1][2][3].

IC50 & Target

D2 Receptor

 

H1 Receptor

 

体外研究
(In Vitro)

Thiethylperazine can enhance the antibiotic (Vancomycin) activity at a concentration as low as 2 μg/mL. Thiethylperazine inhibits Vancomycin-sensitive E. faecalis ATCC 29212, Vancomycin-resistant E. faecalis ATCC 51299 and vancomycin-resistant E. faecalis (VREF) isolates with MIC values of 8 μg/mL, 16 μg/mL and 8 μg/mL, respectively[3].

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

体内研究
(In Vivo)

Thiethylperazine (3 mg/kg; intramuscular injection; twice daily; for 30 days) significantly reduces Aβ42 levels in young APP/PS1 mice[2].

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

Animal Model: Young Aβ precursor protein (APPswe) and mutant presenilin-1 (PS1) (APP/PS1) mice[2]
Dosage: 3 mg/kg
Administration: Intramuscular injection; twice daily; for 30 days
Result: Significantly reduced Aβ42 levels in APP/PS1 mice.
分子量

399.62

Formula

C22H29N3S2

CAS 号
性状

固体

颜色

Light brown to gray

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
细胞实验: 

DMSO 中的溶解度 : 100 mg/mL (250.24 mM; 超声助溶; 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 2.5024 mL 12.5119 mL 25.0238 mL
5 mM 0.5005 mL 2.5024 mL 5.0048 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 (protect from 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 (protect from 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 2.5024 mL 12.5119 mL 25.0238 mL 62.5594 mL
5 mM 0.5005 mL 2.5024 mL 5.0048 mL 12.5119 mL
10 mM 0.2502 mL 1.2512 mL 2.5024 mL 6.2559 mL
15 mM 0.1668 mL 0.8341 mL 1.6683 mL 4.1706 mL
20 mM 0.1251 mL 0.6256 mL 1.2512 mL 3.1280 mL
25 mM 0.1001 mL 0.5005 mL 1.0010 mL 2.5024 mL
30 mM 0.0834 mL 0.4171 mL 0.8341 mL 2.0853 mL
40 mM 0.0626 mL 0.3128 mL 0.6256 mL 1.5640 mL
50 mM 0.0500 mL 0.2502 mL 0.5005 mL 1.2512 mL
60 mM 0.0417 mL 0.2085 mL 0.4171 mL 1.0427 mL
80 mM 0.0313 mL 0.1564 mL 0.3128 mL 0.7820 mL
100 mM 0.0250 mL 0.1251 mL 0.2502 mL 0.6256 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:
Thiethylperazine
目录号:
HY-B1794
需求量: