1143577-13-2Relevant academic research and scientific papers
Design, synthesis, and biological evaluation of a series of piperazine ureas as fatty acid amide hydrolase inhibitors
Kono, Mitsunori,Matsumoto, Takahiro,Imaeda, Toshihiro,Kawamura, Toru,Fujimoto, Shinji,Kosugi, Yohei,Odani, Tomoyuki,Shimizu, Yuji,Matsui, Hideki,Shimojo, Masato,Kori, Masakuni
, p. 1468 - 1478 (2014/03/21)
A series of piperazine ureas were designed, synthesized, and evaluated for their potential as novel orally efficacious fatty acid amide hydrolase (FAAH) inhibitors for the treatment of neuropathic and inflammatory pain. We carried out an optimization stud
AMIDE COMPOUND
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Page/Page column 17, (2009/07/10)
An object of the present invention is to provide a novel fused-ring compound which has a FAAH inhibitory effect and is useful as an analgesic. The present invention relates to a compound represented by formula (I): wherein symbols are as defined in the specification, or salt thereof.
