N-aminoalkyl amide inhibitors of protein kinase C
    7.
    发明授权
    N-aminoalkyl amide inhibitors of protein kinase C 失效
    蛋白激酶C的N-氨基烷基酰胺抑制剂

    公开(公告)号:US5270310A

    公开(公告)日:1993-12-14

    申请号:US807084

    申请日:1991-12-13

    摘要: The present invention provides methods for inhibiting protein kinase C which comprise contacting protein kinase C with an inhibitory amount of a compound having the formula ##STR1## wherein R.sub.1 is C.sub.8 through C.sub.15 alkyl; R.sub.2 is H, C.sub.1 through C.sub.10 alkyl, or benzyl; R.sub.3 is N-heterocyclic, N-alkylheterocyclic, quaternized N-heterocyclic, NR.sub.4 R.sub.5 or N.sup.+ R.sub.4 R.sub.5 R.sub.6 X.sup.- ; R.sub.4, R.sub.5 and R.sub.6 are independently C.sub.1 through C.sub.10 alkyl; n is 2, 3, 4, or 5; and X is an anion. The invention also provides novel compounds having the formula ##STR2## wherein R.sub.1 is C.sub.8 through C.sub.15 alkyl; R.sub.2 is H, C.sub.1 through C.sub.10 alkyl, or benzyl; R.sub.3 is N-heterocyclic, N-alkylheterocyclic or quaternized N-heterocyclic; and n is 2, 3, 4, or 5.

    摘要翻译: 本发明提供了抑制蛋白激酶C的方法,其包括使蛋白激酶C与抑制量的具有下式的化合物接触:其中R 1为C 8至C 15烷基; R2是H,C1-C10烷基或苄基; R3是N-杂环,N-烷基杂环,季铵化的N-杂环,NR4R5或N + R4R5R6X-; R4,R5和R6独立地为C1至C10烷基; n为2,3,4或5; X为阴离子。 本发明还提供具有式“IMAGE”的新化合物,其中R 1为C 8至C 15烷基; R2是H,C1-C10烷基或苄基; R3是N-杂环,N-烷基杂环或季铵化的N-杂环; n为2,3,4或5。