方案
≥99% (HPLC)
质量水平
表单
solid
效能
0.009 μM IC50
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
protect from light
颜色
white
溶解性
H2O: 25 mM
储存温度
2-8°C
InChI
1S/C22H29NO2/c1-17(22(25)20-7-9-21(24)10-8-20)16-23-13-11-19(12-14-23)15-18-5-3-2-4-6-18/h2-10,17,19,22,24-25H,11-16H2,1H3/t17-,22+/m0/s1
InChI key
WVZSEUPGUDIELE-HTAPYJJXSA-N
一般描述
A potent, activity-dependent antagonist highly selective for GluN1/NR2B subtype NMDA receptors (IC50 = 0.009 and 52 µM for NR2B and NR2A subtype receptors respectively). Commonly used for studying brain functions and disorders involving neurotransmissions mediated by GluN1/NR2B subtype NMDA receptors (learning and memory, neuroplasticity, neurotoxicity, neuropathic pain, addiction, and neurogenesis enhancement).
生化/生理作用
Primary Target
GluN1/NR2B receptors
GluN1/NR2B receptors
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
Qi, Y., et al. 2013. Cereb. Cortex.23, 932.
Soloviova, A., et al. 2012. Exp. Biol. & Med.153, 764.
Solovyeva, A., et al. 2012. Neurosci. & Behav. Physiol.42, 456.
Chazot, L., et al. 2004. Curr. Med. Chem.11, 389.
Lynch, R., et al. 2001. Eur. J. Pharmacol.416, 185.
Fischer, G., et al. 1997. J. Pharmacol. Exp. Ther.283, 1285.
Soloviova, A., et al. 2012. Exp. Biol. & Med.153, 764.
Solovyeva, A., et al. 2012. Neurosci. & Behav. Physiol.42, 456.
Chazot, L., et al. 2004. Curr. Med. Chem.11, 389.
Lynch, R., et al. 2001. Eur. J. Pharmacol.416, 185.
Fischer, G., et al. 1997. J. Pharmacol. Exp. Ther.283, 1285.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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