http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5093330-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_79751aeaa9923745648e5ae7d9c35782
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D498-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-22
filingDate 1991-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b57a841b305dc67e161d38c4e81f90b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b7803254c38908e1f8838ff90630877e
publicationDate 1992-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5093330-A
titleOfInvention Staurosporine derivatives substituted at methylamino nitrogen
abstract N-substituted derivatives of staurosporine of the general formula [Stau]-N(CH3)-R(I) in which [Stau] represents a residue of the partial formula <IMAGE> and R represents a hydrocarbyl radical Ro or an acyl radical Ac, which radicals preferably have a maximum of 30 carbon atoms, and salts of compounds of the formula I having salt-forming properties, are distinguished as selective inhibitors of proteinkinase C. They are manufactured by conventional alkylation or acylation, respectively, of staurosporine.
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Total number of triples: 814.