欢迎光临源叶生物,登录 | 注册 |
当前位置: 首页 > 小分子抑制剂 > Neuroscience > Xanomeline (oxalate)

浏览历史

S83161

Xanomeline (oxalate)

源叶(MedMol) ≥98%
  • 英文名:
  • Xanomeline (oxalate)
  • 别名:
  • XANOMELINE OXALATE; UNII-JF5A0PK3G5;
  • CAS号:
  • 141064-23-5
  • 分子式:
  • C16H25N3O5S
  • 分子量:
  • 371.4518
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S83161-10mg ≥98% ¥430.00元 10 - - - EA 加入购物车
源叶(MedMol) S83161-50mg ≥98% ¥1440.00元 10 - - - EA 加入购物车
源叶(MedMol) S83161-100mg ≥98% ¥2470.00元 10 - - - EA 加入购物车
源叶(MedMol) S83161-250mg ≥98% ¥4737.00元 7 - - - EA 加入购物车
大包装询价

提交您的电话号码并同意《个人信息授权与保护申明》,到货后将短信提示。
提交

产品介绍

参考文献

质检证书(COA)

摩尔浓度计算器

相关产品

  • 提示:详情请下载说明书。
  • 产品描述: Xanomeline oxalate (LY246708 oxalate) is a potent and selective muscarinic receptor agonist (SMRA) and stimulates phosphoinositide hydrolysis in vivo. Xanomeline oxalate can be used for the research of Alzheimer’s disease
  • 靶点: muscarinic receptor;AChR
  • 体外研究:
    Xanomeline stimulates phosphoinositide (PI) hydrolysis in the A9 L m1 cells. Xanomeline inhibits [3H]-pirenzepine ([3H]-PZ) and [3H]-oxotremorine-M ([3H]-OXO-M) binding to rat brain with Kis of 7 and 3 nM, respectively
  • 体内研究:
    Xanomeline robustly stimulates in vivo PI hydrolysis and the effect is blocked by muscarinic antagonists, demonstrating mediation by muscarinic receptors. In mice the ED100 for Xanomeline-induced stimulation of [3H]-IP accumulation is 54 μmole/kg in hippocampus. And in rats the ED100 for Xanomeline-induced stimulation of [3H]-IP accumulation is 8.1 μmole/kg in hippocampus. Animal Model: Male CF1 mice weighing 18-20 g are injected [3H]-myoinositol Dosage: 8.1-81 μmole/kg Administration: S.c. injections; 1 h prior to killing and 1 h after the administration Result: Increased accumulation in a dose-related manner up to 130%, 75%, 60% above lithium levels in hippocampus, cortex and neostriatum, respectively. And did not increase accumulation of [3H]-IP in the brain stem. Induced salivation, tremor and hypothermia in mice with the ED50 of 13.7±0.8 μmole/kg. Animal Model: Rats are injected [3H]-myoinositol Dosage: 2.7-81 μmole/kg Administration: S.c. injections; 1 h prior to killing and 1 h after the administration Result: Increased [3H]-IP formation dose dependently in hippocampus up to 221% above lithium control.
  • 参考文献:
    1. F P Bymaster, et al. Xanomeline Compared to Other Muscarinic Agents on Stimulation of Phosphoinositide Hydrolysis in Vivo and Other Cholinomimetic Effects. Brain Res. 1998 Jun 8; 795(1-2):179-90.
  • 溶解性: soluble  in  DMSO
  • 保存条件: 2-8℃;充氩;干燥
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.692 ml 13.461 ml 26.921 ml
    5 mM 0.538 ml 2.692 ml 5.384 ml
    10 mM 0.269 ml 1.346 ml 2.692 ml
    50 mM 0.054 ml 0.269 ml 0.538 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。
输入产品批号:

本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:


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


  • =
    *
    *


源叶所有产品仅用作科学研究,销售产品行为均适用于我司网上所列通用销售条款。