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    • 8. 发明申请
    • Substituted tricyclic heterocycles as serotonin receptor agonists and antagonists
    • 取代的三环杂环作为血清素受体激动剂和拮抗剂
    • US20070049613A1
    • 2007-03-01
    • US11509354
    • 2006-08-24
    • Wenting ChenTaekyu Lee
    • Wenting ChenTaekyu Lee
    • A61K31/473C07D221/06
    • C07D221/16
    • The present application describes compounds, including all pharmaceutically acceptable salts, prodrugs, solvates and stereoisomers thereof, according to Formula I, pharmaceutical compositions, comprising at least one compound according to Formula I and optionally at least one additional therapeutic agent and methods of treating various diseases, conditions and disorders associated with modulation of serotonin receptors such as, for example: metabolic diseases, which includes but is not limited to obesity, diabetes, diabetic complications, atherosclerosis, impared glucose tolerance and dyslipidemia; central nervous system diseases which includes but is not limited to, anxiety, depression, obsessive compulsive disorder, panic disorder, psychosis, schizophrenia, sleep disorder, sexual disorder and social phobias; cephalic pain; migraine; and gastrointestinal disorders using compounds according to Formula I
    • 本申请描述了根据式I的化合物,包括其所有药学上可接受的盐,前药,溶剂合物和立体异构体,药物组合物,其包含至少一种根据式I的化合物和任选的至少一种另外的治疗剂以及治疗各种疾病的方法 与调节血清素受体相关的病症和紊乱,例如:代谢疾病,其包括但不限于肥胖,糖尿病,糖尿病并发症,动脉粥样硬化,葡萄糖耐量异常和血脂异常; 包括但不限于焦虑,抑郁,强迫症,惊恐障碍,精神病,精神分裂症,睡眠障碍,性障碍和社交恐惧症的中枢神经系统疾病; 头痛 偏头痛 和使用根据式I的化合物的胃肠道疾病
    • 9. 发明授权
    • Substituted pyridoindoles as serotonin agonists and antagonists
    • 取代的吡啶并吲哚作为血清素激动剂和拮抗剂
    • US06699852B2
    • 2004-03-02
    • US10026611
    • 2001-12-19
    • Albert RobichaudJohn M. FevigIan S. MitchellTaekyu LeeWenting ChenJoseph Cacciola
    • Albert RobichaudJohn M. FevigIan S. MitchellTaekyu LeeWenting ChenJoseph Cacciola
    • A61K3133
    • C07D471/16C07D498/16C07D513/16
    • The present invention is directed to certain novel compounds represented by structural Formula (I) or pharmaceutically acceptable salt forms thereof, wherein R1, R5, R6, R7, R8, R9, X, b, k, and n, and the dashed lines are described herein. The invention is also concerned with pharmaceutical formulations comprising these novel compounds as active ingredients and the use of the novel compounds and their formulations in the treatment of certain disorders. The compounds of this invention are serotonin agonists and antagonists and are useful in the control or prevention of central nervous system disorders including obesity, anxiety, depression, psychosis, schizophrenia, sleep disorders, sexual disorders, migraine, conditions associated with cephalic pain, social phobias, and gastrointestinal disorders such as dysfunction of the gastrointestinal tract motility.
    • 本发明涉及由结构式(I)表示的某些新化合物或其药学上可接受的盐形式,其中R 1,R 5,R 6,R 7,R 8,R <9>,X,b,k和n,这里描述虚线。 本发明还涉及包含这些新化合物作为活性成分的药物制剂,以及新型化合物及其制剂在治疗某些疾病中的用途。 本发明的化合物是血清素激动剂和拮抗剂,可用于控制或预防中枢神经系统疾病,包括肥胖症,焦虑症,抑郁症,精神病,精神分裂症,睡眠障碍,性障碍,偏头痛,与头痛相关的病症,社交恐怖症 ,以及胃肠道疾病如胃肠道运动功能障碍。