CAS NO: | 176199-48-7 |
包装 | 价格(元) |
10 mM * 1 mL in Water | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
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 |
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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 |
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溶解性数据 | In Vitro: H2O : 6.33 mg/mL(34.18 mM;Need ultrasonic and warming) 配制储备液
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以下溶剂前显示的百
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