首页
订购/客服:400-666-5481

Befiradol hydrochloride

    
≥99%

Befiradol hydrochloride

源叶(MedMol)
V38620 一键复制产品信息
2436760-81-3
C20H23Cl2F2N3O
430.32
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V38620-1mg
≥99%

¥1480.00

货期:3-5天 - - - -
V38620-5mg
≥99%

¥3790.00

货期:3-5天 - - - -
V38620-10mg
≥99%

¥5390.00

货期:3-5天 - - - -
V38620-25mg
≥99%

¥8130.00

货期:3-5天 - - - -
V38620-50mg
≥99%

¥10900.00

货期:3-5天 - - - -
V38620-100mg
≥99%

¥14700.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
体内研究: Befiradol (F13640; NLX-112) reduces the activity of dorsal raphe serotonergic neurons at 0.2-18.2 μg/kg, i.v. (cumulative doses; ED50=0.69 μg/kg, i.v.) and increases the discharge rate of 80% of mPFC pyramidal neurons in the same dose range (ED50=0.62 μg/kg, i.v.). Both effects are reversed by the subsequent administration of the 5-HT1A receptor antagonist (±)WAY100635. In microdialysis studies, Befiradol (F13640; NLX-112) (0.04-0.63 mg/kg, i.p.) dose-dependently decreases extracellular 5-HT in the hippocampus and mPFC. Likewise, Befiradol (F13640; NLX-112) (0.01-2.5 mg/kg, i.p.) dose-dependently increases extracellular DA in mPFC, an effect dependent on the activation of postsynaptic 5-HT1A receptors in mPFC. Local perfusion of Befiradol in mPFC (1-1,000 μM) also increases extracellular DA in a concentration-dependent manner. Both the systemic and local effects of Befiradol are prevented by prior (±)WAY100635 administration.
参考文献: 1. Lladó-Pelfort L, et al. In vivo electrophysiological and neurochemical effects of the selective 5-HT1A receptor agonist, F13640, at pre- and postsynaptic 5-HT1A receptors in the rat. Psychopharmacology (Berl). 2012 May;221(2):261-72.
保存条件: 2-8°C,RT,干燥
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.324 ml 11.619 ml 23.239 ml
5 mM 0.465 ml 2.324 ml 4.648 ml
10 mM 0.232 ml 1.162 ml 2.324 ml
50 mM 0.046 ml 0.232 ml 0.465 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

如何获取质检证书(COA)?
请输入货号和一个与之匹配的批号。
例如:
批号:JS298415 货号:S20001-25g
在货品标签上如何找到货号和批号?

摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

=
×
×