; 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: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
公开/公告号RU2235094C2
专利类型
公开/公告日2004-08-27
原文格式PDF
申请/专利权人
申请/专利号RU20000114195
发明设计人 LOKHREJ BRADZH BKHUSHAN (IN);LOKHREJ VIDIA BKHUSHAN (IN);BADZHI ASHOK CHANNAVEERAPPA (IN);KALCHAR SHIVARAMAJJA (IN);RAMANUDZHAM RADZHAGOPALAN (IN);CHAKRABARTI RANDZHAN (IN);
申请日1998-01-23
分类号C07D279/22;C07D279/26;C07D265/38;C07D307/81;C07D417/06;C07D413/06;C07C69/734;C07C59/64;A61K31/54;A61K31/535;A61P5/00;
国家 RU
入库时间 2022-08-21 22:44:54