Certain heteroaryl-substituted spirocyclic diamine urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, energy metabolism disorders, and movement disorders (e.g., multiple sclerosis).
描述了某些杂环取代的螺环二胺
脲化合物,这些化合物可用作
FAAH
抑制剂。这些化合物可用于制药组合物和治疗由
脂肪酸酰胺水解酶(
FAAH)活性介导的疾病状态、紊乱和条件的方法,如焦虑、疼痛、炎症、睡眠紊乱、进食紊乱、能量代谢紊乱和运动紊乱(例如多发性硬化)。