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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C335-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-32
filingDate 1993-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1994-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a091eb67637413066b64009f0c983d9d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a4fa5f79d2cae4b4278edb48212bc81
publicationDate 1994-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5364881-A
titleOfInvention S-alkyl-isothioureido-amino acids and use thereof
abstract Inhibitors of nitric oxide formation from arginine useful for treating hypotension, inflammation, stroke and to restore vascular contractile sensitivity to the effects of α 1 -adrenergic agonists are physiologically active compounds including N.sup.δ -substituted ornithine or N.sup.ε -substituted lysine moieties or monoalkyl carbon-substituted N.sup.δ -substituted ornithine or N.sup.ε -substituted lysine moieties, having the formula ##STR1## wherein R is (CH 2 ) y CH 3 or H, R' is CH 2 or C(H)(CH 2 ) y CH 3 , and R" is CH 2 or C(H)(CH 2 ) y CH 3 , with y ranging from 0 to 5, and x is 0 or 1 and wherein none or only one of R, R' and R" provides an alkyl substituent on ornithine or lysine moiety, and wherein Q is alkyl having 1 to 5 carbon atoms, and physiologically acceptable acid addition salts thereof.
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