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filingDate 1989-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46562b79a8b790c5fa47db5287e0a476
publicationDate 1991-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5059712-A
titleOfInvention Isolating aminoarginine and use to block nitric oxide formation in body
abstract Pharmaceutically pure physiologically active N G -aminoarginine (i.e., the L or D,L form) or pharmaceutically acceptable salt thereof is administered in a nitric oxide synthesis inhibiting amount to a subject in need of such inhibition (e.g. a subject with low blood pressure or needing immunosuppressive effect) or is added to a medium containing isolated organs, intact cells, cell homogenates or tissue homogenates in an amount sufficient to inhibit nitric oxide formation to elucide or control the biosynthesis, metabolism or physiological role of nitric oxide. n N G -amino-L-arginine is prepared and isolated as a pharmaceutically pure compound by reducing N G -nitro-L-arginine, converting L-arginine by-product to L-ornithine with arginase and separating N G -amino-L-arginine from the L-ornithine. N G -amino-D,L-arginine is prepared in similar fashion starting with N G -nitro-D,L-arginine.
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