in which (i) aa1 is Adi and aa4 is Glu or (ii) each of aa1 and aa4 is Adi, L is sulfur, sulfoxide, oxygen or methylene, which compound (and its conjugates) bind to an SH2 domain in a protein comprising an SH2 domain, is non-phosphorylated, is redox-stable in vivo, is characterized by an IC50 in vivo of less than about 4.0 μM with respect to the SH2 domain in Grb2, and, upon binding to the SH2 domain of Grb2, has a turn conformation. A conjugate comprising a compound as described above and a carrier agent, a composition comprising (i) a compound or a conjugate as described above and (ii) a carrier, a method of inhibiting binding of an SH2 domain in a protein comprising an SH2 domain to a target protein in an animal, wherein the SH2 domain is contacted with a target protein-binding inhibiting effective amount of a compound or a conjugate as described above, and a method of synthesizing such conjugates."/> REDOX-STABLE, NON-PHOSPHORYLATED CYCLIC PEPTIDE INHIBITORS OF SH2 DOMAIN BINDING TO TARGET PROTEIN, CONJUGATES, THEREOF, COMPOSITIONS AND METHODS OF SYNTHESIS AND USE
首页> 外国专利> REDOX-STABLE, NON-PHOSPHORYLATED CYCLIC PEPTIDE INHIBITORS OF SH2 DOMAIN BINDING TO TARGET PROTEIN, CONJUGATES, THEREOF, COMPOSITIONS AND METHODS OF SYNTHESIS AND USE

REDOX-STABLE, NON-PHOSPHORYLATED CYCLIC PEPTIDE INHIBITORS OF SH2 DOMAIN BINDING TO TARGET PROTEIN, CONJUGATES, THEREOF, COMPOSITIONS AND METHODS OF SYNTHESIS AND USE

机译:氧化还原稳定的非磷酸化的SH2域环肽抑制剂与目标蛋白,结合物,其缀合物,组成,合成方法及用途

摘要

A compound of formula: in which (i) aa1 is Adi and aa4 is Glu or (ii) each of aa1 and aa4 is Adi, L is sulfur, sulfoxide, oxygen or methylene, which compound (and its conjugates) bind to an SH2 domain in a protein comprising an SH2 domain, is non-phosphorylated, is redox-stable in vivo, is characterized by an IC50 in vivo of less than about 4.0 μM with respect to the SH2 domain in Grb2, and, upon binding to the SH2 domain of Grb2, has a turn conformation. A conjugate comprising a compound as described above and a carrier agent, a composition comprising (i) a compound or a conjugate as described above and (ii) a carrier, a method of inhibiting binding of an SH2 domain in a protein comprising an SH2 domain to a target protein in an animal, wherein the SH2 domain is contacted with a target protein-binding inhibiting effective amount of a compound or a conjugate as described above, and a method of synthesizing such conjugates.
机译:式的化合物: <图像文件=“ US20080031812A1-20080207-C00001.GIF” he =“ 13.72mm” imgContent =“ chem” imgFormat =“ GIF” wi =“ 70.70mm” /> < /化学>其中(i)aa 1 是Adi,而aa 4 是Glu或(ii)aa 1 和aa 4 < / Sup>是Adi,L是硫,亚砜,氧或亚甲基,该化合物(及其结合物)结合到包含SH2结构域的蛋白质中的SH2结构域上,未被磷酸化,在体内氧化还原稳定,其特征在于相对于Grb2中的SH2结构域,通过体内IC 50 小于约4.0μM,并且在结合至Grb2的SH2结构域时具有转向构象。包含如上所述的化合物和载体的缀合物,包含(i)如上所述的化合物或缀合物和(ii)载体的组合物,抑制包含SH2结构域的蛋白质中的SH2结构域结合的方法如上所述,将SH2结构域与动物中的靶蛋白结合,其中将SH2结构域与抑制靶蛋白结合的有效量的化合物或缀合物接触,以及合成此类缀合物的方法。

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