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    • 1. 发明公开
    • Functionalized peptidyl aminodiols and -triols
    • 功能性磷酸二肽和 -
    • EP0230266A3
    • 1990-01-17
    • EP87100422.2
    • 1987-01-15
    • ABBOTT LABORATORIES
    • Rosenberg, Saul HowardPlattner, Jacob JohnLuly, Jay Richard
    • C07K5/06C07K5/02C07K5/08C07D233/64A61K31/415A61K37/02A61K37/64
    • C07D233/64A61K38/00C07K5/0227C07K5/06043C07K5/06078C07K5/0806
    • The invention relates to renin inhibiting compounds of the formula
      wherein A is hydrogen; loweralkyl; arylalkyl; OR₈ or SR₈ wherein R₈ is hydrogen, loweralkyl or aminoalkyl; NR₉R₁₀ wherein R₉ and R₁₀ are independently selected from hydrogen, loweralkyl, aminoalkyl, cyanoalkyl and hydroxyalkyl;
      wherein B is NH, alkylamino, S, O, CH₂ or CHOH and R₁₁ is loweralkyl, cycloalkyl, aryl, arylalkyl, alkoxy, alkenyloxy, hydroxyalkoxy, dihydroxyalkoxy, arylalkoxy, arylalkoxyalkyl, amino, alkylamino, dialkylamino, (hydroxyalkyl)(alkyl)amino, (dihydroxy­alkyl)(alkyl)amino, carboxylic acid-substituted alkyl, alkoxycarbonylalkyl, aminoalkyl, N-protected aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, (N-protected)­ alkyl)aminoalkyl, (heterocyclic)alkyl or a substituted or unsubstituted heterocyclic; R₁ is loweralkyl, cycloalkylmethyl, benzyl, α-methylbenzyl, α, α-di­methylbenzyl, 4-methoxybenzyl, halobenzyl, (1-naphthyl)­methyl, (2-naphthyl)methyl, (4-imidazoyl)methyl, phenethyl, phenoxy, thiophenoxy or anilino; provided if R₁ is phenoxy, thiophenoxy or anilino, B is CH₂ or CHOH or A is hydrogen; R₃ is loweralkyl, benzyl or heterocyclic ring-substituted methyl; R₄ is lower­alkyl, cycloalkyl- methyl or benzyl; R₂, R₅ and R₆ are independently hydrogen or loweralkyl; X is O, NH or S; R₇ is hydrogen, loweralkyl, alkanoyl, alkylsulfonyl.
      wherein R₁₂ and R₁₃ are independently hydrogen or loweralkyl, n is 0-2 and R₁₄ is substituted or unsubstituted penyl or heterocyclic; or XR₇ together are loweralkylsulfonyl, N₃ or Cl, and pharmaceutically acceptable salts thereof.
    • 6. 发明公开
    • Peptidylaminodiols
    • EP0229667A2
    • 1987-07-22
    • EP87100424.8
    • 1987-01-15
    • ABBOTT LABORATORIES
    • Luly, Jay RichardKempf, Dale JohnPlattner, Jacob John
    • C07K5/06C07K5/08C07K5/02C07D233/64C07C237/12A61K31/415A61K37/02A61K37/64A61K31/16
    • C07D233/64A61K38/00C07K5/0202C07K5/0227C07K5/06026C07K5/06043C07K5/0606C07K5/06078C07K5/0806C07K5/0808C07K5/0821C07K5/0823Y02P20/55
    • A renin inhibiting compound of the formula:
      wherein A is a substituent; W is C=O or CHOH; U is CH₂ or NR₂, provided that when W is CHOH then U is CH₂; R₁ is loweralkyl, cycloalkylmethyl, benzyl, 4-methoxybenzyl, halobenzyl, (1-naphthyl)methyl, (2-naphthyl)methyl, (4-imidazoyl)methyl, α, α -dimethylbenzyl, 1-benzyloxyethyl, phenethyl, phenoxy, thiophenoxy or anilino; R₂ is hydrogen or loweralkyl; R₃ is loweralkyl, [(alkoxy)alkoxy]alkyl, (thioalkoxy)alkyl, lowerakenyl, benzyl or heterocyclic ring substituted methyl; R₄ is loweralkyl, cycloalkylmethyl or benzyl; R₅ is vinyl, formyl, hydroxymethyl or hydrogen; R₇ is hydrogen or loweralkyl; R₈ and R₉ are independently selected from OH and NH₂; and R₆ is hydrogen, loweralkyl, vinyl or arylalkyl; provided that when R₅ and R₇ are both hydrogen and R₈ and R₉ are OH, the carbon bearing R₅ is of the "R" configuration and the carbon bearing R₆ is of the "S" configuration; or pharmaceutically acceptable salts or esters thereof. Also disclosed are renin inhibiting compositions, a method of treating hypertension, methods of making the renin inhibiting compounds and intermediates useful in making the renin inhibiting compounds.
    • 一种下式的肾素抑制化合物:其中A是取代基; W是C = O或CHOH; U是CH 2或NR 2,条件是当W是CHOH时,则U是CH 2; (1-萘基)甲基,(2-萘基)甲基,(4-咪唑基)甲基,α,α-二甲基苄基,1-苄氧基乙基,苯乙基,苯氧基,硫代苯氧基(低级烷基) 或苯胺基; R 2是氢或低级烷基; R 3是低级烷基,[(烷氧基)烷氧基]烷基,(硫代烷氧基)烷基,低级链烯基,苄基或杂环取代的甲基; R 4是低级烷基,环烷基甲基或苄基; R 5是乙烯基,甲酰基,羟甲基或氢; R 7是氢或低级烷基; R 7和R 7独立地选自OH和NH 2; 和R 6是氢,低级烷基,乙烯基或芳基烷基; 条件是当R 5和R 7都是氢而R 7和R 7是OH时,带有R 5的碳是“R”构型,带有R 6的碳是“S”构型; 或其药学上可接受的盐或酯。 还公开了肾素抑制组合物,治疗高血压的方法,制备肾素抑制化合物和中间体用于制备肾素抑制化合物的方法。
    • 9. 发明公开
    • Functionalized peptidyl aminodiols and -triols
    • 磷脂酰胺和三聚氰胺。
    • EP0230266A2
    • 1987-07-29
    • EP87100422.2
    • 1987-01-15
    • ABBOTT LABORATORIES
    • Rosenberg, Saul HowardPlattner, Jacob JohnLuly, Jay Richard
    • C07K5/06C07K5/02C07K5/08C07D233/64A61K31/415A61K37/02A61K37/64
    • C07D233/64A61K38/00C07K5/0227C07K5/06043C07K5/06078C07K5/0806
    • The invention relates to renin inhibiting compounds of the formula
      wherein A is hydrogen; loweralkyl; arylalkyl; OR₈ or SR₈ wherein R₈ is hydrogen, loweralkyl or aminoalkyl; NR₉R₁₀ wherein R₉ and R₁₀ are independently selected from hydrogen, loweralkyl, aminoalkyl, cyanoalkyl and hydroxyalkyl;
      wherein B is NH, alkylamino, S, O, CH₂ or CHOH and R₁₁ is loweralkyl, cycloalkyl, aryl, arylalkyl, alkoxy, alkenyloxy, hydroxyalkoxy, dihydroxyalkoxy, arylalkoxy, arylalkoxyalkyl, amino, alkylamino, dialkylamino, (hydroxyalkyl)(alkyl)amino, (dihydroxy­alkyl)(alkyl)amino, carboxylic acid-substituted alkyl, alkoxycarbonylalkyl, aminoalkyl, N-protected aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, (N-protected)­ alkyl)aminoalkyl, (heterocyclic)alkyl or a substituted or unsubstituted heterocyclic; R₁ is loweralkyl, cycloalkylmethyl, benzyl, α-methylbenzyl, α, α-di­methylbenzyl, 4-methoxybenzyl, halobenzyl, (1-naphthyl)­methyl, (2-naphthyl)methyl, (4-imidazoyl)methyl, phenethyl, phenoxy, thiophenoxy or anilino; provided if R₁ is phenoxy, thiophenoxy or anilino, B is CH₂ or CHOH or A is hydrogen; R₃ is loweralkyl, benzyl or heterocyclic ring-substituted methyl; R₄ is lower­alkyl, cycloalkyl- methyl or benzyl; R₂, R₅ and R₆ are independently hydrogen or loweralkyl; X is O, NH or S; R₇ is hydrogen, loweralkyl, alkanoyl, alkylsulfonyl.
      wherein R₁₂ and R₁₃ are independently hydrogen or loweralkyl, n is 0-2 and R₁₄ is substituted or unsubstituted penyl or heterocyclic; or XR₇ together are loweralkylsulfonyl, N₃ or Cl, and pharmaceutically acceptable salts thereof.
    • 本发明涉及式:CHEM的肾素抑制化合物,其中A是氢; 低级烷基; 芳; OR8或SR8,其中R8是氢,低级烷基或氨基烷基; NR 9 R 10,其中R 9和R 10独立地选自氢,低级烷基,氨基烷基,氰基烷基和羟烷基; 其中B是NH,烷基氨基,S,O,CH 2或CHOH,R 11是低级烷基,环烷基,芳基,芳基烷基,烷氧基,烯氧基,羟基烷氧基,二羟基烷氧基,芳基烷氧基,芳基烷氧基烷基,氨基,烷基氨基,二烷基氨基,(羟基烷基) 烷基)氨基,(二羟基烷基)(烷基)氨基,羧酸取代的烷基,烷氧基羰基烷基,氨基烷基,N-保护的氨基烷基,烷基氨基烷基,二烷基氨基烷基,(N-保护的)烷基)氨基烷基,(杂环)烷基或取代或未取代的杂环 ; R1是低级烷基,环烷基甲基,苄基,α-甲基苄基,α,α-二甲基苄基,4-甲氧基苄基,卤代苄基,(1-萘基)甲基,(2-萘基)甲基,(4-咪唑基)甲基,苯乙基,苯氧基, 或anilino; 如果R1是苯氧基,硫代苯氧基或苯胺基,B是CH 2或CHOH或A是氢; R3是低级烷基,苄基或杂环环取代的甲基; R4是低级烷基,环烷基 - 甲基或苄基; R2,R5和R6独立地是氢或低级烷基; X是O,NH或S; R 7是氢,低级烷基,烷酰基,烷基磺酰基。 其中R 12和R 13独立地为氢或低级烷基,n为0-2,R 14为取代或未取代的吡啶基或杂环基; 或XR7一起是低级烷基磺酰基,N 3或Cl,及其药学上可接受的盐。