Fluoxetine hydrochloride 英文名称: Fluoxetine hydrochloride | |||||||||||||||||||||||||||||||||||||||||||||
型号:null 产品货号: INS1005-0025MG | |||||||||||||||||||||||||||||||||||||||||||||
价格:请致电:010-57128832,18610462672 | |||||||||||||||||||||||||||||||||||||||||||||
品牌: gene operation | |||||||||||||||||||||||||||||||||||||||||||||
INS1005-Fluoxetine hydrochloride Fluoxetine hydrochloride,≥98% 【英文同义名】:Fluoxetine HCl, LY110140HCl, LY110140HCl, LY110140 hydrochloride, LY-110,140HCl, Prozac®, Sarafem®, Ladose®andFontex® 【中文同义名】:盐酸氟西汀 订购信息:(原装进口,常备现货)
产品描述 Fluoxetine hydrochloride (同义名: Fluoxetine HCl, LY110140HCl, LY110140HCl, LY110140 hydrochloride, LY-110,140HCl, Prozac®, Sarafem®, Ladose®andFontex®) ,氟西汀游离碱的盐酸盐形式是一种非常强效的选择性血清素再吸收的抑制剂[1-2],而且作为临床有用的抗抑郁药,机理是通过增加与神经传递相关的血清素含量发挥作用[3]。氟西汀可以与人的5-HT转运体结合(Ki值为0.9-20 nM),其选择性结合效率比5-HT1A,5-HT 2A,H 1,α1,α2-***能和毒蕈碱受体高约150-900倍[4]。,它一般作为Prozac®,Sarafem®,Ladose®和Fontex®品牌销售药品的活性成分,对重度抑郁症,强迫性神经症,神经性贪食症,恐慌症和经前烦躁症的具有疗效。
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结构式使用浓度(仅作参考)Fluoxetine hydrochloride的具体使用浓度请参考相关文献,并根据自身实验条件(如实验目的,细胞种类,培养特性等)进行摸索和优化。 参考文献[1] Wong DT, et al. A selective inhibitor of serotonin uptake: Lilly 110140, 3-(p-trifluoromethyl- phenoxy)-N-methyl-3-phenylpropylamine. Life Sci. 15(3):471-9 (1974). [2] Fuller RW, et al. Fluoxetine, a selective inhibitor of serotonin uptake. Med Res Rev.11(1): 17-34 (1991). [3] Benfield P, et al. Fluoxetine. A review of its pharmacodynamic and pharmacokinetic properties,and therapeutic efficacy in depressive illness. Drugs. 32(6):481-508 (1986). [4] Owens MJ, et al. Neurotransmitter receptor and transporter binding profile of antidepressants and their metabolites.J PharmacolExpTher. 283(3):1305-22 (1997). [5] Chang EA, et al. Increased cellular turnover in response to fluoxetine in neuronal precursors derived from human embryonic stem cells. Int J Dev Biol. 54(4):707-15 (2010). |