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Substituted diphenylsulfides as serotonin uptake inhibitors

机译:取代二苯硫醚5-羟色胺再摄取抑制剂

摘要

A class of halogen-substituted diphenylsulfide compounds are disclosed. In formula (I), n and m are the same or different and are each 0, 1, 2 or 3; R and R1 are the same or different and are each hydrogen or straight or branched C1-6 alkyl; R2 and R4 are the same or different and are each hydrogen or C1-4 alkyl; R3 and R5 are the same or different and are each hydrogen, halo (e.g. fluoro, bromo, iodo, chloro), trifluoromethyl, C1-4 alkyl, C1-4 alkylthio, nitro or NR6R7 wherein R6 and R7 are the same or different and are hydrogen or C1-3 alkyl; provided that both R3 and R5 are not hydrogen and further provided that when n and m are 0, R2 and R4 are hydrogen and R5 is halo and is in the 5 position of the phenyl ring (A'), then R3 cannot be hydrogen; or a pharmaceutically acceptable ester, salt or other physiologically functional derivative thereof, which produce a large selective inhibition of serotonin uptake in brain. Such compounds are useful in the treatment or prevention of a range of depressive conditions as well as anxiety, obsessive compulsive disorders and alcoholism.
机译:公开了一类卤素取代的二苯硫醚化合物。式(I)中,n和m相同或不同,分别为0、1、2或3。 R和R 1相同或不同,分别为氢或直链或支链的C 1-6烷基; R 2和R 4相同或不同,分别为氢或C 1-4烷基。 R 3和R 5相同或不同,并且各自为氢,卤素(例如氟,溴,碘,氯),三氟甲基,C 1-4烷基,C 1-4烷硫基,硝基或NR 6 R <7>其中R 6和R 7相同或不同,且为氢或C 1-3烷基;前提是R 3和R 5都不是氢,并且还提供当n和m为0时,R 2和R 4是氢并且R 5是卤素并且在5位在苯环(A’)的R 3上,R 3不能为氢;或其药学上可接受的酯,盐或其他生理功能性衍生物,它们可选择性地抑制大脑中血清素的摄取。此类化合物可用于治疗或预防一系列抑郁症以及焦虑症,强迫症和酒精中毒。

著录项

  • 公开/公告号AU3091792A

    专利类型

  • 公开/公告日1993-07-19

    原文格式PDF

  • 申请/专利权人 THE WELLCOME FOUNDATION LIMITED;

    申请/专利号AU19920030917

  • 发明设计人 LAWRENCE EDWARD BRIEADDY;

    申请日1992-12-10

  • 分类号C07C323/32;A61K31/135;

  • 国家 AU

  • 入库时间 2022-08-22 05:07:53

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