N-aminoalkyl amide inhibitors of protein kinase C
AssigneesSphinx Pharmaceuticals Corporation, Duke University
InventorsRobert M. Bell, Robert J. Fogelsong, Jeffrey B. Nichols
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AssigneesSphinx Pharmaceuticals Corporation, Duke University
InventorsRobert M. Bell, Robert J. Fogelsong, Jeffrey B. Nichols
Estimating the term…
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.
A method of inhibiting protein kinase C which comprises contacting protein kinase C with an inhibitory amount of a compound having the formula ##STR27## wherein R.sub.1 is C.sub.8 through C.sub.15 alkyl;
A method of inhibiting protein kinase C which comprises contacting protein kinase C with an inhibitory amount of a compound having the formula ##STR28## wherein R.sub.1 is C.sub.1 through C.sub.3 alkyl;
Dependencies are inferred from the claim text.