首页> 外国专利> DERIVATIVES OF 4-(2-AMINO-1-HYDROXIETHYL)PHENOL AS β2-ADRENERGIC RECEPTOR ANTAGONISTS

DERIVATIVES OF 4-(2-AMINO-1-HYDROXIETHYL)PHENOL AS β2-ADRENERGIC RECEPTOR ANTAGONISTS

机译:4-(2-氨基-1-羟乙基)苯酚作为β2-肾上腺素受体拮抗剂的衍生物

摘要

FIELD: medicine, pharmaceutics.;SUBSTANCE: invention relates to a compound of formula I where: R1 represents a group selected from among -CH2OH, -NH(CO)H while R2 represents a hydrogen atom or R1, together with R2, forms group -NH-C(O)-CH=CH- where the nitrogen atom is bonded to the carbon atom in the phenyl ring whereto R1 is bonded, the carbon atom bonded to the carbon atom in the phenyl ring whereto R2 is bonded; R3a and R3b are independently selected from the group consisting of hydrogen atoms and C1-4alkyl groups; X and Y are independently selected from the group consisting of an ordinary bond and an oxygen atom; n, m and q (each) independently have a value selected from among 0, 1, 2 and 3; p has a value selected from among 1, 2 and 3; R4 and R5 are independently selected from the group consisting of hydrogen atoms, a halogen atoms, C1-4alcoxy, -CONH2, -NHCONH2, -SR7, -SO2R7 where R7 represents C3-4cycloalkyl; R6 is selected from the group consisting of hydrogen atoms, a halogen atoms, C1-4 alkyl and C1-4alcoxy or its pharmaceutically acceptable salt or a stereoisomer thereof. Additionally, the invention relates to a pharmaceutical composition based on the compound with formula I and to a method for β2-adrenergic receptor activity modulation.;EFFECT: produced are new 4-(2-amino-1-hydroxiethyl) phenol derivatives possessing the activity of β2-adrenergic receptor antagonists.;22 cl, 32 ex
机译:技术领域:本发明涉及式I的化合物,其中:R 1 代表选自-CH 2 OH,-NH(CO)的基团)H,而R 2 代表氢原子或R 1 与R 2 一起形成-NH-C(O)-CH基= CH-,其中氮原子键合至与R 1 相连的苯环中的碳原子,碳原子键合至与R 2 是键合的; R 3a 和R 3b 独立地选自氢原子和C 1-4 烷基。 X和Y独立地选自普通键和氧原子; n,m和q(每个)独立地具有选自0、1、2和3的值; p具有从1、2和3中选择的值; R 4 和R 5 独立地选自氢原子,卤素原子,C 1-4 烷氧基,-CONH < Sub> 2 ,-NHCONH 2 ,-SR 7 ,-SO 2 R 7 其中R 7 代表C 3-4 环烷基; R 6 选自氢原子,卤素原子,C 1-4 烷基和C 1-4 烷氧基或其基团。药学上可接受的盐或其立体异构体。另外,本发明涉及基于式的化合物的药物组合物,并且涉及效果:产生具有β2-肾上腺素能受体拮抗剂活性的新的4-(2-氨基-1-羟乙基)苯酚衍生物。; 22 cl,32 ex

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