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Men 10376 TFA
  • 品牌:Chemstan
  • 产地:中国
  • 货号:CS-P1276A
  • 价格: ¥1950/支
  • 发布日期: 2020-11-24
  • 更新日期: 2025-09-19
产品详请
产地 中国
品牌 Chemstan
货号 CS-P1276A
用途 分析检测
包装规格 1mg
纯度 99%%
CAS编号
是否进口

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Men 10376 TFA 是一种有效的选择性的?tacCSkinin NK-2?受体拮抗剂,对大鼠小肠 NK-2 受体的?Ki?值为 4.4 μM。

Description

Men 10376 TFA is a selective tachykinin NK-2 receptor antagonist, with a Ki of 4.4 μM for rat small intestine NK-2 receptor[1] .

IC50 & Target

Ki: 4.4 μM (NK-2 receptor, rat small intestine)[1]

In Vitro

Men 10376 is a selective tachykinin NK-2 receptor, with a Ki of 4.4 μM, and shows low selectivity for NK-1 and NK-3 receptors (Ki, >10 μM)[1] . Men 10376 shows pA2s of 5.66 and 8.08 for NK-1 (guinea-pig ileum) and NK-2 receptors (endothelium-deprived rabbit pulmonary artery). Men 10376 shows no effect on NK-3 receptor (Ki, >10 μM)[2] .

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

In Vivo

Men 10376 (1 and 3 μmol/kg) antagonizes increase in bladder motility produced by the NK-2 receptor agonist in rats[2] .

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

Molecular Weight

1195.25

Formula

C??H??F?N??O??

Sequence

Asp-Tyr-{d-Trp}-Val-{d-Trp}-{d-Trp}-Lys-NH2

Sequence Shortening

DY-{d-Trp}-V-{d-Trp}{d-Trp}-K-NH2

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Protect from light

Powder-80°C2 years-20°C1 year

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

Solvent & Solubility

In Vitro: 

H2O : 1.43 mg/mL (1.20 mM; Need ultrasonic)

Preparing 
Stock Solutions

ConcentrationSolventMass1 mg5 mg10 mg1 mM0.8366 mL4.1832 mL8.3665 mL5 mM---------10 mM---------

*

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。

References
  • [1]. Quartara L, et al. N-terminal truncated analogs of men 10376 as tachykinin NK-2 receptor antagonists. Life Sci. 1992;51(25):1929-36.

    [2]. Maggi CA, et al. In vivo evidence for tachykininergic transmission using a new NK-2 receptor-selective antagonist, MEN 10,376. J Pharmacol Exp Ther. 1991 Jun;257(3):1172-8.


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