http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-0301000-A2

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filingDate 2001-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c74f052c8a428a8d9db920ad69afd8b2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e4fa44086b35689836a8de868f5d9043
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd5a9fe02ad54c98561c67eead50292b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_97384ca26795e55b34ddb734a8969dc3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9f233c0395ff49b858e2d038b5bcda02
publicationDate 2003-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0301000-A2
titleOfInvention 2-Aminotiazoline derivatives, process for their preparation, pharmaceutical compositions containing the compounds and their use as inhibitors of NO synthase
abstract The present invention relates to 2-aminothiazoline derivatives of the formula (I) and pharmaceutically acceptable salts thereof, wherein R 1 is hydrogen or alkyl and R 2 is alkyl, -alk-NH 2, -CH 2 -R 3, -CH 2 -S-R 4 or nitro-substituted phenyl. or -NH-C (= NH) CH3, or R1 is alkyl and R2 is hydrogen, R3 is -cycloalkyl, pyridyl, pyridyl-N-oxide, thienyl, thiazolyl, imidazolyl, pyrazinyl, triazolyl, phenyl or phenyl substituted with nitro, hydroxy or carboxyl, R4 is pyridyl or pyridyl N-oxide, alk is alkylene. The present invention also relates to the preparation of such compounds, pharmaceutical compositions containing them and their use as NO synthase inhibitors. HE
priorityDate 2000-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419583539
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448110213
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419488510
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422162602
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426248706
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP18061
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449323691
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422160078
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394983
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID162224370
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453445542
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86584426
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO02367
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447708632
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451096393
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1551329
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7311736
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538190
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9813130
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69698379
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID4326903
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449109238
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414771689
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69885572
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID100533274
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ40302
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410049330
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID62412
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID547786
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9GRJ1
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO61309
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424640622
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413740589
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414770747
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424640216
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID430942954
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69885129
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413989248
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID75687

Total number of triples: 656.