Design and synthesis of uracil urea derivatives as potent and selective fatty acid amide hydrolase inhibitors
Design and synthesis of uracil urea derivatives as potent and selective fatty acid amide hydrolase inhibitors
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作为有效和选择性脂肪酸酰胺水解酶抑制剂的尿嘧啶脲衍生物的设计和合成
DOI:
10.1039/c7ra02237a
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发表时间:
2017-04
期刊:
影响因子:
3.9
通讯作者:
Li Yuhang
中科院分区:
文献类型:
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作者:
Qiu Yan;Ren Jie;Ke Hongwei;Zhang Yang;Gao Qi;Yang Longhe;Lu Canzhong;Li Yuhang
Fatty acid amide hydrolase (FAAH) is one of the key enzymes involved in the biological degradation of endocannabinoids, especially anandamide. Pharmacological blockage of FAAH restores the levels of endocannabinoids, providing therapeutic benefits in the
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影响因子:
2
作者:
R. Dmochowski
通讯作者:
R. Dmochowski
影响因子:
7.3
作者:
Mor, Marco;Lodola, Alessio;Piomelli, Daniele
通讯作者:
Piomelli, Daniele
DOI:
10.1016/j.respe.2020.09.004
发表时间:
2020-10-10
期刊:
Revue D'Epidemiologie et De Sante Publique
影响因子:
--
作者:
La rédaction
通讯作者:
La rédaction
影响因子:
9.3
作者:
通讯作者:
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