首页> 外国专利> Compounds for the treatment of Sexual Dysfunction of mu opioid receptor Selective antagonist. Use. Pharmaceutical composition

Compounds for the treatment of Sexual Dysfunction of mu opioid receptor Selective antagonist. Use. Pharmaceutical composition

机译:用于治疗μ阿片受体选择性拮抗剂性功能障碍的化合物。采用。药物成分

摘要

Procedures for the treatment of Female Sexual Dysfunction with an antagonist Selective for the mu opioid receptors. It also describes Combination Treatments with other classes of agents.Claim 1: Use of a selective antagonist of mu opioid receptors is characterized in that in the preparation of a Medicament for the Prevention and / or treatment of Female Sexual Dysfunction (DSF). Claim 1: Use according to claim 17, wherein the compound is Mesylate Exo - N - {3 - [6 - (ethyl - 2 - hydroxy - 3 - methyl - 2 - indan) - 3 - aza Bicyclo [3.1.Hex - il - 6 0]}] - phenyl - methanesulfonamide.Claim 1: use an antagonist Selective for the mu opioid receptors together with an Auxiliary Agent wherein is selected from one or more of: (i) compounds that modulate the action of natriuretic factors.In particular the atrial natriuretic factor; (ii) compounds that inhibit angiotensin converting Enzyme; (iii) no synthase Substrates; (iv) cholesterol lowering agents; (V) modulators of the estrogen Receptors and estrogen agonists / antagonists of estrogen and / or INH; (VI) Ibidores of phosphodiesterase (PDE); (vii) vasoactive intestinal Protein (IVP), Mimetic of IVP,Analogue of IVP, a receptor agonist of IVP or Fragment of IVP or a combination of an antagonist of adrenoceptors with PIV; (viii) agonist, antagonist of the serotonin receptor modulators or agents; (IX) replacement of testosterone or testosterone implants; X) Selective Androgen receptor modulators of estrogen, XI);Estrogens and medroxyprogesterone or medroxyprogesterone acetate (MPA) (i.e., in the form of Combination) or estrogen and hormone replacement treatment agent of methyltestosterone; (XII) or progesterone, progesterone agonist modulators such as gestodine, ethinyl estradiol, ethynodiol, Etonogesterol Implant, dihidrogesterona, progesterone, totelle sekvens,Norethynodrel or progesterone Creams or gels such as muprogest, natragest and FEM - gest; XIII) modulators of conveyors for noradrenaline.Dopamine and serotonin and / or; (XIV) agonists or modulators of the oxytocin / vasopressin receptor agonists); 15th or 16th Melanocortin Receptor modulators; inhibitors of monoamine Transport); (XVII) dopamine agonists (in particular Selective agents Selective D2, D3,Selective D2 and D4 selective); XVIII) Alpha adrenergic Receptor Antagonists (also known as Alpha adrenoceptor blockers, Alpha blockers, or Receptor Blockers)Anti diabetic agents; XIX and XX) receptor modulators (NPY agonists and / or antagonists) in the preparation of a Medicament for the Prevention and / or treatment of Female Sexual Dysfunction.Claim 1: a Pharmaceutical composition which comprises a selective antagonist of mu opioid Receptors and one or more Auxiliary agents selected from: (i) compounds that modulate the action of natriuretic factors.In particular the atrial natriuretic factor; (ii) compounds that inhibit angiotensin converting Enzyme; (iii) no synthase Substrates; (iv) cholesterol lowering agents; (V) modulators of the estrogen Receptors and estrogen agonists / antagonists of estrogen and / or INH; (VI) Ibidores of phosphodiesterase (PDE); VII (IVP), vasoactive intestinal Protein Mimetic of IVP,Analogue of IVP, a receptor agonist of IVP or Fragment of IVP or a combination of an antagonist of adrenoceptors with PIV; viii) agonists, antagonists and modulators of serotonin receptors; (IX) replacement agents of testosterone or testosterone implants; X Selective Androgen receptor modulators); (XI) estrogenEstrogens and medroxyprogesterone or medroxyprogesterone acetate (MPA) (i.e., in the form of Combination) or estrogen and hormone replacement Treatment agents of methyltestosterone; (XII) or progesterone, progesterone agonist modulators such as gestodine, ethinyl estradiol, ethynodiol, Etonogesterol Implant, dihidrogesterona, progesterone, totelle sekvens,Norethynodrel or progesterone Creams or gels such as muprogest, natragest and FEM - gest; XIII) modulators of conveyors for noradrenaline.Dopamine and serotonin and / or; (XIV) agonists or modulators of the oxytocin / vasopressin receptor agonists); 15th or 16th Melanocortin Receptor modulators; inhibitors of monoamine Transport); (XVII) dopamine agonists (in particular Selective agents Selective D2, D3,Selective D2 and D4 selective); XVIII) Alpha adrenergic Receptor Antagonists (also known as Alpha adrenoceptor blockers, Alpha blockers or Receptor Blockers), anti diabetic agents; XIX) and (XX) modulators of NPY Receptor agonists and / or antagonist ( As).Claim 21: A Selective antagonist of mu opioid receptors because is characterized for use in the Prevention and / or treatment of Female Sexual Dysfunction (DSF).
机译:用对阿片类阿片受体有选择性的拮抗剂治疗女性性功能障碍的程序。权利要求1:μ阿片样物质受体选择性拮抗剂的用途,其特征在于在制备预防和/或治疗女性性功能障碍(DSF)的药物中。权利要求1:根据权利要求17的用途,其中所述化合物是甲磺酸酯Exo -N-{3-[6--乙基-2-羟基-3-甲基-2-茚满]-3-氮杂双环[3.1.Hex-il -6 0]}]-苯基-甲磺酰胺。声明1:与mu阿片受体结合使用的拮抗剂与辅助剂一起使用,其中辅助剂选自以下一种或多种:(i)调节利钠因子作用的化合物。特别是心房利钠因子; (ii)抑制血管紧张素转化酶的化合物; (iii)没有合酶底物; (iv)降胆固醇剂; (V)雌激素和雌激素和/或INH拮抗剂的雌激素受体和雌激素激动剂的调节剂; (VI)磷酸二酯酶(PDE)的同上异构体; (vii)血管活性肠蛋白(IVP),IVP的模拟物,IVP的类似物,IVP的受体激动剂或IVP的片段或肾上腺素受体拮抗剂与PIV的组合; (viii)激动剂,5-羟色胺受体调节剂或试剂的拮抗剂; (IX)更换睾丸激素或睾丸激素植入物; X)雌激素的选择性雄激素受体调节剂,XI);雌激素和甲羟孕酮或乙酸甲羟孕酮(MPA)(即,以组合形式)或雌激素和甲基睾丸激素的替代治疗剂; (XII)或黄体酮,黄体酮激动剂调节剂,如孕激素,炔雌醇,乙二醇,乙内酯植入物,双甲状腺酮,黄体酮,妥托酮,去甲肾上腺素或黄体酮乳膏或凝胶剂,例如孕酮,鼻孕酮和FEM- XIII)去甲肾上腺素输送机的调节剂。多巴胺和5-羟色胺和/或; (XIV)催产素/血管加压素受体激动剂的激动剂或调节剂);第15或第16个Melanocortin受体调节剂;单胺运输抑制剂); (XVII)多巴胺激动剂(特别是对选择性D2,D3,选择性D2和D4具有选择性的选择性试剂); XVIII)α肾上腺素能受体拮抗剂(也称为Alpha肾上腺素能受体阻滞剂,Alpha阻滞剂或受体阻滞剂)。 XIX和XX)受体调节剂(NPY激动剂和/或拮抗剂)在制备预防和/或治疗女性性功能障碍的药物中。权利要求1:药物组合物,其包含mu阿片受体的选择性拮抗剂和一种或多种选自以下的辅助剂:(i)调节利钠因子作用的化合物。特别是心钠素; (ii)抑制血管紧张素转化酶的化合物; (iii)没有合酶底物; (iv)降胆固醇剂; (V)雌激素和雌激素和/或INH拮抗剂的雌激素受体和雌激素激动剂的调节剂; (VI)磷酸二酯酶(PDE)的同上异构体; VII(IVP),IVP的血管活性肠蛋白模拟物,IVP的类似物,IVP的受体激动剂或IVP的片段或肾上腺素受体与PIV的拮抗剂的组合; viii)5-羟色胺受体的激动剂,拮抗剂和调节剂; (IX)睾丸激素或睾丸激素植入物的替代剂; X选择性雄激素受体调节剂); (XI)雌激素雌激素和甲羟孕酮或乙酸甲羟孕酮(MPA)(即组合形式)或雌激素和激素替代物甲基睾丸激素的治疗​​剂; (XII)或黄体酮,黄体酮激动剂调节剂,如孕激素,炔雌醇,乙二醇,乙内酯植入物,双甲状腺酮,黄体酮,妥托酮,去甲肾上腺素或黄体酮乳膏或凝胶剂,例如孕酮,鼻孕酮和FEM- XIII)去甲肾上腺素输送机的调节剂。多巴胺和5-羟色胺和/或; (XIV)催产素/血管加压素受体激动剂的激动剂或调节剂);第15或第16黑色素皮质激素受体调节剂;单胺运输抑制剂); (XVII)多巴胺激动剂(特别是对选择性D2,D3,选择性D2和D4具有选择性的选择性试剂); XVIII)α肾上腺素能受体拮抗剂(也称为Alpha肾上腺素受体阻滞剂,Alpha阻滞剂或受体阻滞剂),抗糖尿病药; XIX)和(XX)NPY受体激动剂和/或拮抗剂(As)的调节剂。权利要求21:mu阿片类药物受体的选择性拮抗剂,因为其特征是用于预防和/或治疗女性性功能障碍(DSF) 。

著录项

  • 公开/公告号AR064368A1

    专利类型

  • 公开/公告日2009-04-01

    原文格式PDF

  • 申请/专利权人 PFIZER LIMITED;

    申请/专利号AR2007P105640

  • 申请日2007-12-14

  • 分类号A61K31/635;A61K31/403;A61K31/57;A61K31/565;A61K9/08;A61K9/32;A61P15/00;

  • 国家 AR

  • 入库时间 2022-08-21 19:28:40

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