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Xanomeline oxalate (LY246708 oxalate), a potent and selective muscarinic receptor agonist (SMRA), effectively stimulates in vivo phosphoinositide hydrolysis. It is a valuable compound for Alzheimer's disease research.
Xanomeline oxalate (LY246708 oxalate), a potent and selective muscarinic receptor agonist (SMRA), effectively stimulates in vivo phosphoinositide hydrolysis. It is a valuable compound for Alzheimer's disease research.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 143 | 现货 | |
5 mg | ¥ 320 | 现货 | |
10 mg | ¥ 533 | 现货 | |
25 mg | ¥ 1,050 | 现货 | |
50 mg | ¥ 1,690 | 现货 | |
100 mg | ¥ 2,530 | 现货 | |
200 mg | ¥ 3,580 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 352 | 现货 |
产品描述 | Xanomeline oxalate (LY246708 oxalate), a potent and selective muscarinic receptor agonist (SMRA), effectively stimulates in vivo phosphoinositide hydrolysis. It is a valuable compound for Alzheimer's disease research. |
体外活性 | Xanomeline在A9 L m1细胞中促进磷脂酰肌醇(PI)水解。此外,Xanomeline对大鼠脑部的[3H]-pirenzepine([3H]-PZ)和[3H]-oxotremorine-M([3H]-OXO-M)结合具有抑制作用,其Kis分别为7 nM和3 nM[1]。 |
体内活性 | Xanomeline 在活体内强效激活PI水解,并且该效应被毒蕈碱拮抗剂所阻断,证明其通过毒蕈碱受体介导。在小鼠中,Xanomeline诱导的[3H]-IP累积的ED100为54 μmole/kg,作用部位为海马。在大鼠中,Xanomeline诱导的[3H]-IP累积的ED100为8.1 μmole/kg, 作用部位同为海马[1]。 |
别名 | 诺美林草酸盐, LY246708 oxalate |
分子量 | 371.45 |
分子式 | C16H25N3O5S |
CAS No. | 141064-23-5 |
Smiles | OC(=O)C(O)=O.CCCCCCOc1nsnc1C1=CCCN(C)C1 |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 45 mg/mL (121.1 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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