embedded image ;wherein Z is a template-fixed chain of 8 α-amino acid residues which, depending on their positions in the chain (counted starting from the N-terminal amino acid), are Gly or Pro or of certain types which, as the remaining symbols in the above formula, are defined in the description and the claims, and salts thereof, have agonizing or antagonizing activity against urotensin II or show inhibition of the STAT6/NCoA-1 interaction and can be used for preventing or treating diseases or disorders related to urotensin II, STAT6 and NCoA-1.;These β-hairpin peptidomimetics can be manufactured by a process which is based on a mixed solid- and solution phase synthetic strategy."/> TEMPLATE-FIXED BETA-HAIRPIN PEPTIDOMIMETICS THAT ARE LIGANDS FOR G-PROTEIN-COUPLED RECEPTORS (GPCRS) AND ARE MODULATORS OF TRANSCRIPTION FACTORS AND COACTIVATORS
首页> 外国专利> TEMPLATE-FIXED BETA-HAIRPIN PEPTIDOMIMETICS THAT ARE LIGANDS FOR G-PROTEIN-COUPLED RECEPTORS (GPCRS) AND ARE MODULATORS OF TRANSCRIPTION FACTORS AND COACTIVATORS

TEMPLATE-FIXED BETA-HAIRPIN PEPTIDOMIMETICS THAT ARE LIGANDS FOR G-PROTEIN-COUPLED RECEPTORS (GPCRS) AND ARE MODULATORS OF TRANSCRIPTION FACTORS AND COACTIVATORS

机译:固定G-蛋白偶联受体(GPCR)的模板固定的BETA-Hairpin肽假拟物,并且是转录因子和激活剂的调节剂

摘要

Template-fixed β-hairpin peptidomimetics of the general formula; embedded image ;wherein Z is a template-fixed chain of 8 α-amino acid residues which, depending on their positions in the chain (counted starting from the N-terminal amino acid), are Gly or Pro or of certain types which, as the remaining symbols in the above formula, are defined in the description and the claims, and salts thereof, have agonizing or antagonizing activity against urotensin II or show inhibition of the STAT6/NCoA-1 interaction and can be used for preventing or treating diseases or disorders related to urotensin II, STAT6 and NCoA-1.;These β-hairpin peptidomimetics can be manufactured by a process which is based on a mixed solid- and solution phase synthetic strategy.
机译:通式固定模板的β-发夹肽模拟物; “嵌入式图像” ;其中Z是8个α-氨基酸残基的模板固定链,取决于它们在链中的位置(从N-末端氨基酸开始计算),是Gly或Pro或某些类型,作为剩余的上式中的符号,在说明书和权利要求书中定义的及其盐,具有对尿紧张素II的激动或拮抗活性或显示出对STAT6 / NCoA-1相互作用的抑制作用,并可用于预防或治疗与疾病有关的疾病或病症这些β-发夹肽模拟物可以通过基于固相和溶液相混合合成策略的方法制备。

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