方案
≥98% (TLC)
质量水平
表单
solid
效能
0.55 nM IC50
0.34 nM Ki
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
protect from light
颜色
white to off-white
溶解性
DMSO: 25 mM
储存温度
2-8°C
一般描述
An extremely potent, non-competitive antagonist for mGlu receptor subtype 1 (Ki = 0.34 nM; IC50 = 0.55 nM). 400-fold more selective for mGlu1 than for mGlu5 and no interaction with mGlu2, mGlu3, mGlu4, mGlu6, AMPA or NMDA receptors (IC50 >10 µM). Centrally active following systemic administration. Widely used for studying substance abuse, learning and memory, and neural plasticity.
生化/生理作用
Primary Target
mGlu₁
mGlu₁
警告
Toxicity: Standard Handling (A)
重悬
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
其他说明
Lavreysen, H., et al. 2004. Neuropharmacology.47, 961.
Steckler, T., et al. 2005. Psychopharmacology.179, 198.
Steckler, T., et al. 2005. Behav. Brain. Res.164, 52.
Mabire, D., et al. 2005. J. Med. Chem.48, 2134.
Fukunaga, I., et al. 2007. Br. J. Pharmacol.151, 870.
Knopfel, T., et al. 2007. Br. J. Pharmacol.151, 723.
Achat-Mendes, C., et al. 2012. J. Pharmacol. Exp. Ther.343, 214.
Steckler, T., et al. 2005. Psychopharmacology.179, 198.
Steckler, T., et al. 2005. Behav. Brain. Res.164, 52.
Mabire, D., et al. 2005. J. Med. Chem.48, 2134.
Fukunaga, I., et al. 2007. Br. J. Pharmacol.151, 870.
Knopfel, T., et al. 2007. Br. J. Pharmacol.151, 723.
Achat-Mendes, C., et al. 2012. J. Pharmacol. Exp. Ther.343, 214.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
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