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POLYPEPTIDE RENIN INHIBITORS CONTAINING STATINE OR DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

机译:含有他汀类或衍生物的多肽肾素抑制剂和含有它们的药物组合物

摘要

Polypeptides of formula (I) and their salts are new. R-W-W'-NH-CHR2-CHR3-CH2-COR1 (I) W = Phe, His, Leu, Tyr, 1-naphthyl-Ala or 2-phenylmethyl 2-phenylmethylpropionylene; W' = Phe, His, Leu, Tyr or Nle; when W = Phe and W' = His, then the peptide link between W and W' may be replaced by -CH(1-4C)Alkyl-NH-; R = H, amino-protecting acyl of molecular wt. up to 500, or Pro or pGlu both amino protected; R2 = H, 1-6C alkyl, Ph, 4-7C cycloalkyl, Ph-(1-3C)alkyl or 5-10C cycloalkylalkyl; R3 = OH, NH2, NHR9, NHCOR9, OR9 or OCOR9; R9 = 1-4C alkyl; R1 = A-E-B; a gp. of formula (II); NH2; 1-4C alkoxy; 5-benzylipiperazin-1-yl; 1,2,3,4-tetrahydroquinolin-1-yl or -2-yl; 1,2,3,4-tetrahydro-3-aminocarbonyl isoquinolin-2-yl or the corresp. 3-methoxycarbonyl gp.; 1,2,3,4,5,6,7,8-decahydro-3-methoxycarbonyl isoquinolin-2-yl; 2-methoxycarbonylpyrrolidin -1-yl; 2-aminocarbonylpyrrolindin-1-yl; 4-phenylmethylpiperidin-1-yl; Pro-B; or Lys-B; -X-NH-CHZ-(CH2)n-Q-CHZ1-(CH2)m-Y (II) A = Lys or Pro or when R3 = NH2, Ile; E = Phe, Gly, Ala, Val, Leu, Ile, Lys, Orn, Arg, Asp opt. gamma-esterified or Glu opt. delta-esterified; B = OR4, NR4R5, glutamic acid (-OR4)2, glutamic acid (-OR4)(-NR4R5) or glutamic acid (-NR4R5)2; R4, R5 = H, 1-4C alkyl, Ph-(1-3C)alkyl or 5-10C cycloalkylalkyl; X = absent or Ala, Ile, Lys, Pro, Orn, Arg, N-(1-4C alkyl)- or N,N-(di-(1-4C) alkyl)-Lys or -Orn; Z, Z1 = H, 1-6C alkyl, 4-7C cycloalkyl, 5-10C cycloalkylalkyl or Ph-(1-3C)alkyl; n, m = 0-6; Q = CH2, CH=CH, O, NH, CH(OH) or CO; Y = Me, Ph, COOR6, CONR6R7, NH2, benzyloxycarbonylamino, CO-glutamic acid (-OR6)2, CO-glutamic acid (OR6)(NR6R7) or CO-glutamic acid (-NR6R7); R6, R7 = H, 1-4C alkyl, Ph-(1-3C)alkyl or 5-10C cycloalkylalkyl.
机译:式(I)的多肽及其盐是新的。 R-W-W'-NH-CHR2-CHR3-CH2-COR1(I)W = Phe,His,Leu,Tyr,1-萘基-Ala或2-苯基甲基2-苯基甲基亚丙基; W'= Phe,His,Leu,Tyr或Nle;当W = Phe且W′= His时,则W与W′之间的肽键可以被-CH(1-4C)烷基-NH-取代; R = H,分子重量的氨基保护酰基。最多500个,或Pro或pGlu均受氨基保护; R2 = H,1-6C烷基,Ph,4-7C环烷基,Ph-(1-3C)烷基或5-10C环烷基烷基; R3 = OH,NH2,NHR9,NHCOR9,OR9或OCOR9; R9 = 1-4C烷基; R1 = A-E-B; gp。式(II); NH2; 1-4C烷氧基; 5-苄基哌嗪-1-基; 1,2,3,4-四氢喹啉-1-基或-2-基; 1,2,3,4-四氢-3-氨基羰基异喹啉-2-基或相应的。 3-甲氧基羰基; 1,2,3,4,5,6,7,8-十氢-3-甲氧基羰基异喹啉-2-基; 2-甲氧基羰基吡咯烷-1-基; 2-氨基羰基吡咯啉-1-基; 4-苯基甲基哌啶-1-基;概率;或Lys-B; -X-NH-CHZ-(CH 2)n -Q-CHZ 1-(CH 2)m -Y(II)A = Lys或Pro或当R3 = NH2时,Ile; E = Phe,Gly,Ala,Val,Leu,Ile,Lys,Orn,Arg,Asp opt。 γ酯化或Glu opt。酯化B = OR4,NR4R5,谷氨酸(-OR4)2,谷氨酸(-OR4)(-NR4R5)或谷氨酸(-NR4R5)2; R4,R5 = H,1-4C烷基,Ph-(1-3C)烷基或5-10C环烷基烷基; X =不存在或Ala,Ile,Lys,Pro,Orn,Arg,N-(1-4C烷基)-或N,N-(二-(1-4C)烷基)-Lys或-Orn; Z,Z1 = H,1-6C烷基,4-7C环烷基,5-10C环烷基烷基或Ph-(1-3C)烷基; n,m = 0-6; Q = CH 2,CH = CH,O,NH,CH(OH)或CO; Y = Me,Ph,COOR6,CONR6R7,NH2,苄氧羰基氨基,CO-谷氨酸(-OR6)2,CO-谷氨酸(OR6)(NR6R7)或CO-谷氨酸(-NR6R7); R6,R7 = H,1-4C烷基,Ph-(1-3C)烷基或5-10C环烷基烷基。

著录项

  • 公开/公告号IL74572A

    专利类型

  • 公开/公告日1989-09-28

    原文格式PDF

  • 申请/专利权人 PFIZER INC.;

    申请/专利号IL19850074572

  • 发明设计人

    申请日1985-03-12

  • 分类号C07K5/06;A61K37/64;

  • 国家 IL

  • 入库时间 2022-08-22 06:39:04

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