SUBSTITUTED OXADIAZOLE COMPOUNDS AND THEIR USE AS OPIOID RECEPTOR LIGANDS
    82.
    发明申请
    SUBSTITUTED OXADIAZOLE COMPOUNDS AND THEIR USE AS OPIOID RECEPTOR LIGANDS 有权
    取代的奥沙利多化合物及其作为阿片受体配体的用途

    公开(公告)号:US20090005427A1

    公开(公告)日:2009-01-01

    申请号:US12143550

    申请日:2008-06-20

    摘要: Substituted oxadiazole compounds corresponding to formula I: in which X denotes CH, CH2, CH═CH, CH2CH2, CH2CH═CH or CH2CH2CH2; R1 denotes aryl or heteroaryl, in each case unsubstituted or mono- or polysubstituted; or a C1-3 alkyl group-linked aryl or heteroaryl group, in each case unsubstituted or mono- or polysubstituted; R2 denotes aryl or heteroaryl, in each case unsubstituted or mono- or polysubstituted; a C1-3 alkyl chain-attached aryl group, in each case unsubstituted or mono- or polysubstituted; and R3 and R4 independently denote H; C1-6 alkyl, in each case saturated or unsaturated, branched or unbranched, wherein R3 and R4 do not simultaneously mean H; or R3 and R4 together denote CH2CH2OCH2CH2, or (CH2)3-6. The compounds have an affinity for the μ-opioid receptor and may take the form of the racemate; enantiomers, diastereomers, mixtures of enantiomers or diastereomers, an individual enantiomer or diastereomer, a free base, or a salt with a physiologically acceptable acid.

    摘要翻译: 对应于式I的取代的恶二唑化合物:其中X表示CH,CH 2,CH-CH,CH 2 CH 2,CH 2 CH-CH或CH 2 CH 2 CH 2; R 1表示芳基或杂芳基,在每种情况下是未取代的或单取代或多取代的; 或者C 1-3烷基连接的芳基或杂芳基,在各种情况下是未取代的或单取代或多取代的; R 2表示芳基或杂芳基,在各种情况下为未取代或单取代或多取代; 在各种情况下为未取代或单取代或多取代的C 1-3烷基链连接的芳基; R3和R4独立地表示H; C 1-6烷基,各自为饱和或不饱和的,支链或非支链的,其中R3和R4不同时表示H; 或者R 3和R 4一起表示CH 2 CH 2 OCH 2 CH 2或(CH 2)3-6。 这些化合物对μ-阿片受体具有亲和力,并且可以采取外消旋体的形式; 对映体,非对映异构体,对映异构体或非对映异构体的混合物,单独的对映异构体或非对映体,游离碱或与生理上可接受的酸的盐。

    Substituted 5-aminomethyl-1H-pyrrole-2-carboxylic acid amides
    83.
    发明申请
    Substituted 5-aminomethyl-1H-pyrrole-2-carboxylic acid amides 失效
    取代的5-氨基甲基-1H-吡咯-2-羧酸酰胺

    公开(公告)号:US20070135494A1

    公开(公告)日:2007-06-14

    申请号:US11600827

    申请日:2006-11-17

    CPC分类号: C07D207/34

    摘要: Substituted 5-aminomethyl-1H-pyrrole-2-carboxylic acid amides, a process for the production thereof, pharmaceutical preparations containing these compounds and the use of these compounds in pharmaceutical preparations for treatment or inhibition of withdrawal symptoms, memory disorders, neurodegenerative diseases, epilepsy, cardiovascular disorders, water retention, intestinal motility disorders, urinary incontinence, anorexia, tinnitus, pruritus, depression, sexual dysfunction, airways diseases, food intake disorders, or type II (non-insulin-dependent) diabetes, or for anxiolysis, diuresis, suppression of the urinary reflex, reducing the addictive potential of opioids, modulating locomotor activity, influencing the cardiovascular system, or regulating electrolyte balance.

    摘要翻译: 取代的5-氨基甲基-1H-吡咯-2-羧酸酰胺,其制备方法,含有这些化合物的药物制剂以及这些化合物在药物制剂中用于治疗或抑制戒断症状,​​记忆障碍,神经变性疾病, 癫痫,心血管疾病,保水,肠蠕动障碍,尿失禁,厌食症,耳鸣,瘙痒,抑郁症,性功能障碍,气道疾病,食物摄取障碍或II型(非胰岛素依赖型)糖尿病,或用于焦虑症,利尿 抑制尿反射,降低阿片类药物的上瘾潜力,调节运动活性,影响心血管系统或调节电解质平衡。