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filingDate 1993-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ea5723db948fd82402846da55e439f5
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publicationDate 1993-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05286916-A
titleOfInvention NO synthase and cyclooxygenase inhibitory compounds, their production method and pharmaceutical composition
abstract (57) [Summary] (Modified) [Structure] General formula AB [wherein A represents a cyclooxygenase inhibitor having a usable acid functional group, and the cyclooxygenase inhibitor is represented by the general formula RCOOH (where COOH is Represents a possible acid functional group, and R represents a suitable residue of the cyclooxygenase inhibitor). B is the following formula: (In the formula, R 1 represents a hydrogen atom, a methyl group or an ethyl group, R 2 represents a hydrogen atom or a nitro group, R 3 represents an amino group, a methylamino group, an ethylamino group, a hydrazino group, a methyl group or an ethyl group. Represents a group; provided that when AB is a salt and R 2 represents a hydrogen atom, R 3 represents an L form of an arginine analog represented by the formula). A compound, which may be a salt or an amide, a process for producing the same, and a pharmaceutical composition containing the compound. [Effect] The above compound has L-arginine / nitric oxide inhibitory action and cyclooxygenase inhibitory action, and is useful for treating heart and cerebrovascular disorders, inflammation, immunodeficiency and the like.
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