where R1, R2, R3, R4, R5, R6, R7 may be hydrogens, halogen atoms, (C1-C4)-alkyl groups, nitro groups; "n" can be 1-3, and their physiologically acceptable salts which are inhibitors of zinc-dependent metalloproteinases (MMP-2 and MMP-9). Also a method for preparation of compounds of formula (1) and a method for treating by remodelling of the left ventricle of the heart in the peracute phase of myocardial infarction using compounds of the formula (1) are provided.;EFFECT: increased efficiency of treatment.;4 cl, 3 dwg, 2 tbl, 3 ex"/> INHIBITORS OF ZINC-DEPENDENT METALLOPROTEINASES (MMP-2 AND MMP-9) IN NUMBER OF BENZOILAMINO (PHENYLSULFONYL)-SUBSTITUTED CYCLIC AMINO ACIDS AS POTENTIAL PHARMACEUTICALS THAT PREVENT POSTINFARCT REMODELLING OF LEFT VENTRICLE
首页> 外国专利> INHIBITORS OF ZINC-DEPENDENT METALLOPROTEINASES (MMP-2 AND MMP-9) IN NUMBER OF BENZOILAMINO (PHENYLSULFONYL)-SUBSTITUTED CYCLIC AMINO ACIDS AS POTENTIAL PHARMACEUTICALS THAT PREVENT POSTINFARCT REMODELLING OF LEFT VENTRICLE

INHIBITORS OF ZINC-DEPENDENT METALLOPROTEINASES (MMP-2 AND MMP-9) IN NUMBER OF BENZOILAMINO (PHENYLSULFONYL)-SUBSTITUTED CYCLIC AMINO ACIDS AS POTENTIAL PHARMACEUTICALS THAT PREVENT POSTINFARCT REMODELLING OF LEFT VENTRICLE

机译:锌依赖性金属蛋白酶(MMP-2和MMP-9)在苯甲酰氨基(苯磺酰基)取代的环氨基酸中作为抑制剂的潜力,可预防左后室重塑

摘要

FIELD: biotechnology.;SUBSTANCE: benzoilamino (phenylsulfonyl)-substituted cyclic amino acids of the general formula where R1, R2, R3, R4, R5, R6, R7 may be hydrogens, halogen atoms, (C1-C4)-alkyl groups, nitro groups; "n" can be 1-3, and their physiologically acceptable salts which are inhibitors of zinc-dependent metalloproteinases (MMP-2 and MMP-9). Also a method for preparation of compounds of formula (1) and a method for treating by remodelling of the left ventricle of the heart in the peracute phase of myocardial infarction using compounds of the formula (1) are provided.;EFFECT: increased efficiency of treatment.;4 cl, 3 dwg, 2 tbl, 3 ex
机译:领域:生物技术。;物质:通式为<图像文件=“ 00000029.JPG” he =“ 89” imgContent =“ undefined” imgFormat =“ JPEG” wi =“ 151” /的苯甲酰氨基(苯磺酰基)取代的环状氨基酸>其中R 1 ,R 2 ,R 3 ,R 4 ,R 5 ,R 6 ,R 7 可以是氢,卤素原子,(C 1 -C 4 )-烷基,硝基; “ n”可以是1-3,以及它们的生理学上可接受的盐,它们是锌依赖性金属蛋白酶(MMP-2和MMP-9)的抑制剂。还提供了使用式(1)的化合物制备式(1)的化合物的方法和通过在心肌梗塞的急性期重塑心脏的左心室来治疗的方法。处理。; 4 cl,3 dwg,2 tbl,3 ex

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