; wherein R1, R2, R3 and R4 can be similar or different and represent hydrogen atom, hydroxy-group, (C1-C3)-alkyl; cycle A condensed with cycle comprising X and nitrogen atom (N) represents 6-membered aromatic cyclic structure comprising carbon atoms; X represents a heteroatom taken among oxygen and sulfur atoms; Ar represents bivalent phenylene, naphthylene or benzofuranyl; R5 represents hydrogen atom; R6 represents hydrogen atom; or R6 forms a bond in common with R5; R7 represents hydrogen atom or optionally substituted linear or branched (C1-C16)-alkyl; R8 represents hydrogen atom or optionally substituted or branched (C1-C16)-alkyl; Y represents oxygen atom or NR10 wherein R10 represents hydrogen atom, phenyl, hydroxy-(C1-C16)-alkyl; n is a whole number in the range 1-4; m = 0 or 1, or its pharmaceutically acceptable salts or pharmaceutically acceptable solvates. Also, invention describes intermediate compounds, methods for their preparing, methods for preparing compounds of the formula (I), pharmaceutical composition based on compounds of the formula (I), methods for treatment and prophylaxis of diseases based on new compounds. Invention provides preparing new compounds eliciting useful biological properties.;EFFECT: improved preparing method, valuable medicinal properties of compounds.;31 cl, 23 ex"/> BETA-ARYL-ALPHA-HYDROXY-SUBSTITUTED ALKYLCARBOXYLIC ACIDS, METHODS FOR THEIR PREPARING, INTERMEDIATE COMPOUNDS, METHODS FOR THEIR PREPARING, PHARMACEUTICAL COMPOSITION, METHODS FOR TREATMENT OR PROPHYLAXIS OF DISEASES BASED ON NEW COMPOUNDS
首页> 外国专利> BETA-ARYL-ALPHA-HYDROXY-SUBSTITUTED ALKYLCARBOXYLIC ACIDS, METHODS FOR THEIR PREPARING, INTERMEDIATE COMPOUNDS, METHODS FOR THEIR PREPARING, PHARMACEUTICAL COMPOSITION, METHODS FOR TREATMENT OR PROPHYLAXIS OF DISEASES BASED ON NEW COMPOUNDS

BETA-ARYL-ALPHA-HYDROXY-SUBSTITUTED ALKYLCARBOXYLIC ACIDS, METHODS FOR THEIR PREPARING, INTERMEDIATE COMPOUNDS, METHODS FOR THEIR PREPARING, PHARMACEUTICAL COMPOSITION, METHODS FOR TREATMENT OR PROPHYLAXIS OF DISEASES BASED ON NEW COMPOUNDS

机译:β-芳基-α-羟基取代的烷基羧酸,其制备方法,中间体化合物,其制备方法,药物成分,基于新化合物的疾病的治疗或预防方法

摘要

FIELD: organic chemistry, medicine, pharmacy.;SUBSTANCE: invention relates to new compounds that can be used in medicine as hypolipidemic or anti-hyperglycaemic agents. Invention describes -aryl--hydroxy-substituted alkylcarboxylic acids of the formula (I):; ; wherein R1, R2, R3 and R4 can be similar or different and represent hydrogen atom, hydroxy-group, (C1-C3)-alkyl; cycle A condensed with cycle comprising X and nitrogen atom (N) represents 6-membered aromatic cyclic structure comprising carbon atoms; X represents a heteroatom taken among oxygen and sulfur atoms; Ar represents bivalent phenylene, naphthylene or benzofuranyl; R5 represents hydrogen atom; R6 represents hydrogen atom; or R6 forms a bond in common with R5; R7 represents hydrogen atom or optionally substituted linear or branched (C1-C16)-alkyl; R8 represents hydrogen atom or optionally substituted or branched (C1-C16)-alkyl; Y represents oxygen atom or NR10 wherein R10 represents hydrogen atom, phenyl, hydroxy-(C1-C16)-alkyl; n is a whole number in the range 1-4; m = 0 or 1, or its pharmaceutically acceptable salts or pharmaceutically acceptable solvates. Also, invention describes intermediate compounds, methods for their preparing, methods for preparing compounds of the formula (I), pharmaceutical composition based on compounds of the formula (I), methods for treatment and prophylaxis of diseases based on new compounds. Invention provides preparing new compounds eliciting useful biological properties.;EFFECT: improved preparing method, valuable medicinal properties of compounds.;31 cl, 23 ex
机译:技术领域:本发明涉及可以在医学上用作降血脂药或抗高血糖药的新化合物。本发明描述了式(I)的-芳基-羟基取代的烷基羧酸: ;其中R 1 ,R 2 ,R 3 和R 4 可以相同或不同,并且代表氢原子,羟基,(C 1 -C 3 )-烷基;环与X和氮原子(N)稠合的环表示包含碳原子的6元芳族环状结构。 X代表氧原子和硫原子之间的杂原子; Ar表示二价亚苯基,亚萘基或苯并呋喃基; R 5 代表氢原子; R 6 代表氢原子;或R 6 与R 5 共同形成一个键; R 7 代表氢原子或任选取代的直链或支链(C 1 -C 16 )-烷基; R 8 代表氢原子或任选取代或支链的(C 1 -C 16 )-烷基; Y代表氧原子或NR 10 ,其中R 10 代表氢原子,苯基,羟基-(C 1 -C 16 )-烷基; n是1-4范围内的整数; m = 0或1,或其可药用盐或可药用溶剂化物。此外,本发明还描述了中间体化合物,其制备方法,制备式(I)化合物的方法,基于式(I)化合物的药物组合物,基于新化合物的治疗和预防疾病的方法。发明提供了制备具有有用生物学特性的新化合物。效果:改进的制备方法,该化合物的有价值的医学特性。31 cl,23 ex

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