发明名称 Isoxazolines as inhibitors of fatty acid amide hydrolase
摘要 IP No. 596585 The present disclosure provides isoxazoline FAAH inhibitors of the formula (I): or pharmaceutically acceptable forms thereof, wherein each of G, Ra, Rb, Rc, and Rd are as defined herein. The present invention also provides pharmaceutical compositions comprising a compound of formula (I), or a pharmaceutically acceptable form thereof, and a pharmaceutically acceptable excipient. The present invention also provides methods for treating an FAAH-mediated condition comprising administering a therapeutically effective amount of a compound of formula (I), or pharmaceutically acceptable form thereof, to a subject in need thereof. Conditions treated include a painful condition, an inflammatory condition, an immune disorder, a disorder of the central nervous system, a metabolic disorder, a cardiac disorder, glaucoma, neuropathic pain, central pain, deafferentiation pain, chronic pain, post–operative pain, preoperative pain, nociceptive pain, acute pain, non–inflammatory pain, inflammatory pain, pain associated with cancer, wound pain, burn pain, pain associated with medical procedures, pain resulting from pruritus, painful bladder syndrome, pain associated with premenstrual dysphoric disorder, pain associated with premenstrual syndrome, pain associated with chronic fatigue syndrome, pain associated with pre-term labor, pain associated with withdrawal symptoms from drug addiction, joint pain, arthritic pain, lumbosacral pain, musculo–skeletal pain, headache, migraine, muscle ache, lower back pain, neck pain, toothache dental/maxillofacial pain, visceral pain, a gastrointestinal disorder, a skin condition, neurotoxicity and/or neurotrauma, stroke, multiple sclerosis, spinal cord injury, epilepsy, a mental disorder, a sleep condition, a movement disorder, nausea and/or emesis, amyotrophic lateral sclerosis, Alzheimer’s disease, drug addiction, a wasting condition, an obesity-related condition and complication thereof, hypertension, circulatory shock, myocardial reperfusion injury and atherosclerosis
申请公布号 NZ596585(A) 申请公布日期 2014.01.31
申请号 NZ20100596585 申请日期 2010.05.18
申请人 INFINITY PHARMACEUTICALS INC. 发明人 CHAN LAWRENCE K;CASTRO ALFREDO C;SNYDER DANIEL A;BEHNKE MARK L;TIBBITTS THOMAS T;GROGAN MICHAEL J;PELUSO STEPHANE;LEBLANC YVES;GRENIER LOUIS;EVANS CATHERINE A;LIU TAO
分类号 C07D261/02;A61K31/42;A61P29/00 主分类号 C07D261/02
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