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Adoprazine

    
≥98%

Adoprazine

源叶(MedMol)
S84496 一键复制产品信息
222551-17-9
C24H24FN3O2
405.46
阿哆嗪;Adoprazine; SLV-313;
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S84496-5mg
≥98%

¥1160.00

货期:2-3天 - - - -
S84496-10mg
≥98%

¥1820.00

货期:2-3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
产品描述: Adoprazine (SLV313) is a full 5-HT1A receptor agonist with a pEC50 of 9 at cloned h5-HT1A receptors. Adoprazine (SLV313) is a full D2 and D3 receptor antagonist with pA2s of 9.3 and 8.9 at hD2 and hD3 receptors, respectively. Adoprazine (SLV313) has the characteristics of atypical antipsychotics.
靶点: 5-HT1A Receptor:9 (pEC50);D2 Receptor:9.3 (pA2);D3 Receptor:8.9 (pA2);D4 Receptor:8.0 (pKi);5-HT7 Receptor:7.2 (pKi);5-HT1A Receptor;9.1 (pKi);D2 Receptor:8.4 (pKi);D3 Receptor:8.4 (pKi);Others
体内研究: Adoprazine (SLV313) (0.1-10 mg/kg; p.o.; single) is sufficient to reduce extracellular 5-HT and increase dopamine levels in the nucleus accumbens in a dose- and time-dependent manner Animal Model: Male Wistar rats (275-350 g) Dosage: 0.1 mg/kg, 0.3 mg/kg, 1 mg/kg, 3 mg/kg, 10 mg/kg Administration: p.o.; single Result: Led to a dose- and time-dependent increase in extracellular levels of DA, DOPAC, and HVA. In contrast, led to a reduction in 5-HT levels and no change in 5-HIAA levels.
参考文献: 1. Andrew C McCreary, et al. SLV313 (1-(2,3-dihydro-benzo[1,4]dioxin-5-yl)-4- [5-(4-fluoro-phenyl)-pyridin-3-ylmethyl]-piperazine monohydrochloride): a novel dopamine D2 receptor antagonist and 5-HT1A receptor agonist potential antipsychotic drug. Neuropsych 2. Liesbeth A Bruins Slot, et al. Differential profile of antipsychotics at serotonin 5-HT1A and dopamine D2S receptors coupled to extracellular signal-regulated kinase. Eur J Pharmacol. 2006 Mar 18;534(1-3):63-70.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.466 ml 12.332 ml 24.663 ml
5 mM 0.493 ml 2.466 ml 4.933 ml
10 mM 0.247 ml 1.233 ml 2.466 ml
50 mM 0.049 ml 0.247 ml 0.493 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

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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)

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