位置:首页 > 产品库 > AZD1940
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
AZD1940
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
AZD1940图片
规格:98%
分子量:413.52
包装与价格:
包装价格(元)
5mg询价
10mg询价
25mg询价
50mg询价

AZD1940 是一种具有口服活性,高亲和力的大麻素 CB1/CB2 受体激动剂,对 CB1R 和 CB2R 的 pKi 值分别为 7.93 和 9.06,并具有强大的镇痛作用。
货号:ajcx34544
CAS:881413-29-2
分子式:C20H29F2N3O2S
分子量:413.52
溶解度:DMSO : 100 mg/mL (241.83 mM; Need ultrasonic)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

AZD1940 is an orally active, high affinity cannabinoid CB1/CB2 receptor agonist with pKi values of 7.93 and 9.06 for human CB1R and CB2R, respectively. AZD1940 shows a robust analgesia action[1][2].

AZD1940 binds with high affinity to human, rat and mouse CB1 and CB2 receptors and displays full agonism at both receptors in all three species[1][2].

When given orally to rats, AZD1940 produces a robust analgesia in different models of inflammatory and neuropathic pain[1][2].For AZD1940, low brain uptake at analgesic doses has been demonstrated in both rats and primates[1].

[1]. Jarkko KalliomÄki, et al. Evaluation of the analgesic efficacy and psychoactive effects of AZD1940, a novel peripherally acting cannabinoid agonist, in human capsaicin-induced pain and hyperalgesia. Clin Exp Pharmacol Physiol. 2013 Mar;40(3):212-8.
[2]. Magnus Schou, et al. Radiolabeling of the cannabinoid receptor agonist AZD1940 with carbon-11 and PET microdosing in non-human primate. Nucl Med Biol. 2013 Apr;40(3):410-4.

 
 
维奥蛋白资源库 - 中文蛋白资源 CopyRight © 2010-2024