934282-55-0
中文名称
AZD 2066
英文名称
(R)-5-(3-chlorophenyl)-3-(1-((4-Methyl-5-(pyridin-4-yl)-4H-1,2,4-triazol-3-yl)oxy)ethyl)isoxazole
CAS
934282-55-0
分子式
C19H16ClN5O2
分子量
381.82
MOL 文件
934282-55-0.mol

基本信息
中文别名
化合物 T10430 英文别名
AZD2066)AZD 2066 (AZD-2066
4-[5-[(1R)-1-[5-(3-Chlorophenyl)-3-isoxazolyl]ethoxy]-4-methyl-4H-1,2,4-triazol-3-yl]pyridine
Pyridine, 4-[5-[(1R)-1-[5-(3-chlorophenyl)-3-isoxazolyl]ethoxy]-4-methyl-4H-1,2,4-triazol-3-yl]-
(R)-5-(3-chlorophenyl)-3-(1-((4-Methyl-5-(pyridin-4-yl)-4H-1,2,4-triazol-3-yl)oxy)ethyl)isoxazole
物理化学性质
熔点140-142°C
沸点626.3±65.0 °C(Predicted)
密度1.39±0.1 g/cm3(Predicted)
储存条件-20°C Freezer, Under inert atmosphere
溶解度可溶于氯仿(轻微)、Dmso(轻微)、甲醇(轻微)
酸度系数(pKa)1.91±0.10(Predicted)
形态固体
颜色白色至灰白色
AZD 2066价格(试剂级)
报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
2025/02/08 | HY-110255 | AZD 2066 | 934282-55-0 | 1 mg | 2340元 |
2025/02/08 | HY-110255 | AZD 2066 AZD 2066 | 934282-55-0 | 5mg | 5850元 |
常见问题列表
生物活性
AZD 2066 是一种选择性的,具有口服活性和可透过血脑屏障的 mGluR5 的拮抗剂。AZD 2066 具有镇痛作用。靶点
mGluR5
|
体外研究
AZD 2066 (1-10 μM) inhibits Ca
2+
response, with IC
50
s of 27.2±9.1, 3.56±0.52, 96.2±17.8, and 380±78.0 nM in mGlu5/HEK cells and striatal, hippocampal, and cortical cultures respectively.
AZD 2066 (1-10 μM) inhibits the oscillatory Ca
2+
response which induced by bath application of DHPG, and blocks either DHPG or Quis effects in mGlu5/HEK cells.
AZD 2066 (1-10 μM) has less effective in striatal neurons.
体内研究
AZD 2066 (0.3-30 mg/kg; p.o.) shows discriminative effects in rats.
Animal Model: | Male Wistar rats (weighing 240-250 g) |
Dosage: | 0.03, 0.1, 0.3, 1, 3, 10, 30 mg/kg |
Administration: | P.o. (60 minutes after administration) |
Result: | Caused full and dose-dependent AZD9272-appropriate responding. |