首页> 外国专利> USE OF 10-(3R)-1-AZABICYCLO2.2.2OCT-3-YLMETHYL-10H-PHENOTHIAZINE FOR THE PREPARATION OF A DURG HAVING A SELECTIVE INHIBITION OF MUSCARINIC M1, M2 AND M3 RECEPTORS

USE OF 10-(3R)-1-AZABICYCLO2.2.2OCT-3-YLMETHYL-10H-PHENOTHIAZINE FOR THE PREPARATION OF A DURG HAVING A SELECTIVE INHIBITION OF MUSCARINIC M1, M2 AND M3 RECEPTORS

机译:使用10-[(3R)-1-氮杂双环[2.2.2] OCT-3-甲基] -10H-苯并噻嗪制备选择性抑制肌肉M1,M2和M3受体的药物

摘要

Use of 10-[(3R)-1-azabicyclo[2.2.2]oct-3-ylmethyl]-10H-phenothiazine (I) and its salts for the manufacture of a medicament to prevent or treat disorders, diseases and/or pathologies by selectively inhibiting of muscarinic M1 receptor, muscarinic M2 receptor and muscarinic M3 receptor, is claimed. ACTIVITY : Uropathic; Antibacterial; Fungicide. MECHANISM OF ACTION : Muscarinic M1 receptor inhibitor; Muscarinic M2 receptor inhibitor; Muscarinic M3 receptor inhibitor. The effect of (I) to inhibit the muscarinic M1 receptor was tested in Chinese hamster ovary cells using in vitro assay. The results showed that (I) exhibited an IC 5 0 value of 1.6 nM.
机译:10-[(3R)-1-氮杂双环[2.2.2]辛-3-基甲基] -10H-吩噻嗪(I)及其盐在制备用于预防或治疗疾病,疾病和/或病理的药物中的用途通过选择性抑制毒蕈碱M1受体,要求毒蕈碱M2受体和毒蕈碱M3受体。活动:空灵;抗菌;杀菌剂。作用机理:毒蕈碱型M1受体抑制剂;毒蕈碱型M2受体抑制剂;毒蕈碱M3受体抑制剂。使用体外测定法在中国仓鼠卵巢细胞中测试了(I)抑制毒蕈碱性M1受体的作用。结果显示(I)显示出1.6 nM的IC 5 0值。

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