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Composition used for treating diseases associated with dysfunction of cystic fibrosis transmembrane conductance regulator channels comprises compound that forms zwitterion at physiological pH

机译:用于治疗与囊性纤维化的功能障碍有关的疾病的组合物跨膜电导调节剂通道包含在生理pH下形成两性离子的化合物

摘要

Composition comprises a compound (I) that forms a zwitterion (II) at physiological pH. Composition comprises a compound (I) that forms a zwitterion of formula (II) at physiological pH. [Image] Independent claims are also included for: (1) zwitterionic 4,5-dihydroxy-3,4,5,6-tetrahydropyrimidine-6-carboxylic acid derivatives of formula (IA), produced by reacting an amidine of formula H 2N-CR 1=NR 2with a glyoxal compound of formula R 3-CO-CHO and R 4-CO-CHO, provided that the amidine is not 2-aminopyridine, adenine, adenosine, 2'-deoxyadenosine, 9-propyladenine, cytosine, polyadenylic acid, arginine or their derivatives when methylglyoxal is used; (2) zwitterionic pyrimidine derivatives of formula (IB), and (3) preparation of (IB). [Image] R 1-R 4optionally substituted cyclic or acyclic carbon chain optionally containing heteroatoms, and Z : O or S. ACTIVITY : Antidiarrheic; Respiratory-Gen.; Antiasthmatic. MECHANISM OF ACTION : Cystic fibrosis transmembrane conductance regulator (CFTR) channel modulator. In a test, the adduct of 2'-deoxyadenosine and methylglyoxal exhibited an IC 50value of 70.8 pM against forskoline-induced activation of CFTR receptor in transfected Chinese hamster ovary cells.
机译:组合物包含在生理pH下形成两性离子(II)的化合物(I)。组合物包含在生理pH下形成式(II)的两性离子的化合物(I)。 [图像]还包括以下方面的独立权利要求:(1)通过使式H 2N的react反应制备的式(IA)的两性离子的4,5-二羟基-3,4,5,6-四氢嘧啶-6-羧酸衍生物-CR 1 = NR 2与式R 3-CO-CHO和R 4-CO-CHO的乙二醛化合物,条件是the不是2-氨基吡啶,腺嘌呤,腺苷,2'-脱氧腺苷,9-丙基腺嘌呤,胞嘧啶,当使用甲基乙二醛时,聚腺苷酸,精氨酸或其衍生物; (2)式(IB)的两性离子嘧啶衍生物,和(3)(IB)的制备。 [图像] R 1-R 4任选取代的环状或无环碳链,任选包含杂原子,Z:O或S。呼吸器;抗哮喘。作用机理:囊性纤维化跨膜电导调节剂(CFTR)通道调节剂。在一项测试中,针对福斯科林诱导的中国仓鼠卵巢细胞中CFTR受体的激活,2'-脱氧腺苷和甲基乙二醛的加合物显示出IC 50值为70.8 pM。

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