http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1930308-A1

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filingDate 1998-05-19^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba742fc724b2067e6a208c98ebd2635a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83852dc2a1c1624c80f965fdf2bd3115
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13fd00f1cd1690d0f5c1b722bc67bf3b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_64e8e2372d2432ca7176ebf84b94e1e8
publicationDate 2008-06-11^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1930308-A1
titleOfInvention Pharmaceutical agents for the treatment of cerebral amyloidosis
abstract The invention relates to a compound of the following general formula (III):n nwherein: nR 1 and R 2 each are one or more independent substituents selected from the group consisting of hydrogen, C1-C5 alkyl, C2-C5 alkenyl, C3-C5 cycloalkyl, C1-C5 alkoxy, C2-C5 alkynyl, halogen, C1-C5 haloalkyl, alkylamino, phenyl, nitro and carboxyl; nR 3 is selected from the group consisting of amino, C1-C5 substituted amino and CH 2 ; nn and m are independently an integer of from 0-5; n nor a pharmaceutically acceptable salt of such compound; na compound of the following general formula (IV):n nwherein: nR 1 and R 2 each are one or more independent substituents selected from the group consisting of hydrogen, C1-C5 alkyl, C2-C5 alkenyl, C3-C5 cycloalkyl, C1-C5 alkoxy, C2-C5 alkynyl, halogen, C1-C5 haloalkyl, alkylamino, phenyl, nitro and ca rboxyl; nR 3 and R 4 each are independent and selected from the group consisting of hydrogen and C1-C5 alkyl; nn is an integer of from 1 to 5; n nor a pharmaceutically acceptable salt of such compound; na compound of the following general formula (V):n nwherein: nR 1 and R 2 each are one or more independent substituents selected from the group consisting of hydrogen, C1-C5 alkyl, C2-C5 alkenyl, C3-C5 cycloalkyl, C1-C5 alkoxy, C2-C5 alkynyl, halogen, C1-C5 haloalkyl, alkylamino, phenyl, nitro and carboxyl; nR 3 is selected from hydrogen and C1-C5 alkyl; nR 4 is selected from hydrogen and C1-C5 alkyl; nn is an integer of from 1 to 5 inclusive; nor a pharmaceutically acceptable salt of such compound; and na compound of the following general formula (VI):n nwherein: nR 1 and R 2 each are one or more independent substituents selected from the group consisting of hydrogen, C1-C5 alkyl, C2-C5 alkenyl, C3-C5 cycloalkyl, C1-C5 alkoxy, C2-C5 alkynyl, halogen, C1-C5 haloalkyl, alkylamino, phenyl, nitro and carboxyl; nR3 and R4 each are independent and selected from hydrogen and C1-C5 alkyl; nn is an integer of from 1 to 5 inclusive; nor a pharmaceutically acceptable salt of such compound. n Also compositions comprising the compounds III-VI as well as uses of said compounds.
priorityDate 1997-05-19^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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