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CAS RN: 1101854-58-3 | 產品號碼: J0038
JZL 184
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產品號碼 | J0038 |
純度/分析方法 | >95.0%(HPLC)(qNMR) |
分子式 / 分子量 | C__2__7H__2__4N__2O__9 = 520.49 |
外觀與形狀(20°C) | Solid |
儲存條件 | Refrigerated (0-10°C) |
儲存在惰性氣體下 | Store under inert gas |
應避免的情況 | Air Sensitive,Heat Sensitive |
CAS RN | 1101854-58-3 |
Reaxys-RN | 20284487 |
MDL編號 | MFCD11976911 |
產品規格
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 95.0 area% |
Purity(qNMR) | min. 95.0 % |
Melting point | 127.0 to 131.0 °C |
NMR | confirm to structure |
性質
熔點 | 129 °C |
GHS
相關法規
RTECS # | TM6127800 |
運輸資料
HS編碼* | 2934.99-000 |
Application
JZL 184: A Potent and Selective Inhibitor of Monoacylglycerol Lipase (MAGL)
Endogenous cannabinoids, such as anandamide [A3448] and 2-arachidonoyl glycerol (2-AG) [A3490], are biologically active lipids that activate the cannabinoid receptors CB1 and CB2. Cannabinoid receptors, located throughout the body, are part of the endocannabinoid system (ECS) which is involved in a variety of physiological processes. Endocannabinoid signaling is terminated by enzymatic hydrolysis, a process that for anandamide is mediated by fatty acid amide hydrolase (FAAH), and for 2-AG is thought to involve monoacylglycerol lipase (MAGL). JZL 184 is a potent and selective inhibitor of MAGL and has been reported to raise mice brain 2-AG levels by eight-fold without altering anandamide and to attenuate neuropathic pain. (The product is for research purpose only.)
References
- Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects
- Characterization of Monoacylglycerol Lipase Inhibition Reveals Differences in Central and Peripheral Endocannabinoid Metabolism
- Blockade of endocannabinoid-degrading enzymes attenuates neuropathic pain
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