[EN] BICYCLIC HETEROCYCLE DERIVATIVES AS HISTAMINE H3 RECEPTOR ANTAGONISTS<br/>[FR] DÉRIVÉS D'HÉTÉROCYCLES BICYCLIQUES UTILISÉS EN TANT QU'ANTAGONISTES DE RÉCEPTEUR D'HISTAMINE H3
申请人:SCHERING CORP
公开号:WO2010011657A1
公开(公告)日:2010-01-28
The present invention relates to novel bicyclic heterocycle derivatives, pharmaceutical compositions comprising the bicyclic heterocycle derivatives and the use of these compounds for treating or preventing allergy, an allergy-induced airway response, congestion, a cardiovascular disease, an inflammatory disease, a gastrointestinal disorder, a neurological disorder, a metabolic disorder, obesity or an obesity-related disorder, diabetes, a diabetic complication, impaired glucose tolerance or impaired fasting glucose. R1 is: I, Ia, Ib ou Ic. R2 is alkyl, alkenyl, aryl, cycloalkyl. heterocycloalkyl or heteroaryl, any of which can be optionally substituted with R3; Y is -C(O)-, -S-, -S(O)-, -S(O)2-, -CH2- or -O-, such that if Y is -O- or -S-, then M is other than N and R1 is (Ib);
本发明涉及新型双环杂环衍生物,包括含有这些双环杂环衍生物的制药组合物,以及这些化合物用于治疗或预防过敏、过敏引起的气道反应、充血、心血管疾病、炎症性疾病、消化系统紊乱、神经系统紊乱、代谢性疾病、肥胖或肥胖相关疾病、糖尿病、糖尿病并发症、糖耐量受损或空腹血糖受损的用途。其中R1为:I、Ia、Ib或Ic。R2为烷基、烯基、芳基、环烷基、杂环烷基或杂环芳基,其中任何一种都可以选择性地被R3取代。Y为-C(O)-、-S-、-S(O)-、-S(O)2-、-CH2-或-O-,如果Y为-O-或-S-,则M不同于N且R1为(Ib)。