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Eglumegad
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Eglumegad图片
CAS NO:176199-48-7

LY354740
Eglumetad
Eglumegad (LY354740) 是一种有效,选择性的group II (mGlu2/3) receptor激动剂,对人mGlu2和mGlu3受体的IC50分别为5和24 nM。
生物活性

Eglumegad (LY354740) is a highly potent and selectivegroup II (mGlu2/3) receptoragonist withIC50s of 5 and 24 nM on transfected human mGlu2 and mGlu3 receptors, respectively.

IC50& Target

mGluR2R

5 nM (IC50)

mGluR3R

24 nM (IC50)

体外研究
(In Vitro)

Eglumegad (LY354740) down-regulates spots 1014, 1822 (hypoxia up-regulated protein 1), 4513 (an isoform of protein disulfide isomerase 3), 6204, 6312, 7306 (26S proteasome non-ATPase regulatory subunit 7) and protein spots 1013 and 6005 (destrin), and up-regulates spot 6507 (collapsin response mediator protein 1) in mouse cortical neurons[2].

体内研究
(In Vivo)

Eglumegad (LY354740) (15 or 30 mg/kg, i.p.) has no effect on spatial working memory performance in Gria1–/–or WT mice, and it has no effect on rewarded alternation testing with a short inter-trial interval in Gria1–/–and WT mice at concentration of 30 mg/kg. Eglumegad (LY354740) (15 or 30 mg/kg, i.p.) reduces spontaneous locomotor activity in wild-type and Gria1–/–mice[1]. Eglumegad (LY354740) (15 mg/kg, i.p.) dreases novelty-induced hyperlocomotion in naive GluA1-KO and pre-handled GluA1-KO males, but not in females. Eglumegad (LY354740) (15 mg/kg, i.p.) significantly reduces the increased c-Fos expression of GluA1-KO males to the level of WT males, but not in of females[3]. Eglumegad (LY354740) (10 mg/kg, i.p.) attenuates the immobilization stress-induced increase in BDNF mRNA expression in the rat mPFC[4].

分子量

185.18

性状

Solid

Formula

C8H11NO4

CAS 号

176199-48-7

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

H2O : 6.33 mg/mL(34.18 mM;Need ultrasonic and warming)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM5.4002 mL27.0008 mL54.0015 mL
5 mM1.0800 mL5.4002 mL10.8003 mL
10 mM0.5400 mL2.7001 mL5.4002 mL
*

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℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: PBS

    Solubility: 2.86 mg/mL (15.44 mM); Clear solution; Need ultrasonic and warming and heat to 60℃

*以上所有助溶剂都可在本网站选购。
 
 
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