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filingDate 1998-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9dc421021cf1db66ae1b9622ffa5e7db
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ed0215c88f52405946d4ad8f7717056
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_832f8bfa05666c14cdcb6495b178f0b2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c40fcf2927a37b84ff696f09fa1b199
publicationDate 1999-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-306998-A3
titleOfInvention Sulfonamide substituted chromanes, a process for their preparation, their use as medicaments, and pharmaceutical compositions containing them
abstract Sulfonamide-substituted chromane derivatives (I) are new. Sulfonamide-substituted chromane derivatives of formula (I), and salts of (I), are new: R<1>, R<2> = H, CF3, C2F5, C3F7, 1-6C alkyl, or optionally substituted phenyl; or R<1> +R<2> = a 2-10C alkylene chain; R<3> = R<10>-VCnH2n-NR<11> or R<10>-CnH2n; V = CnH2n in which one CH2 group may be replaced by O, CO, S, SO, SO2 or N(R<12>a); R<10> = H, Me, Cy, CF3, C2F5 or C3F7; R<11> = H or; or R1<0> + R<11> = a bond, provided that n is not less than 3; n = 0-10; R<4> = R<13>-CrH2r-Z-CqH2q; q, r = 0-8; Z = eg. CO-NH<14> or OCO-NR<14>; R<14> = eg. H or 1-3C alkyl; R<5>, R<6>, R<7>, R<8> = H, F, Cl, Br, I, 1-5C alkyl, 3-8C cycloalkyl, CN, CF3, C2F5, C3F7, N3, NO2, Y-CsH2s-R<18> or optionally substituted phenyl; Y = eg. O, CO, CO-O, O-CO, S, SO or SO2; s = 0-6; R<18> = eg. H, CF3C2F5, C3F7, COOH, 1-piperidyl, 1-pyrrolidinyl, 4-morpholinyl, pyridyl, thienyl, imidazolyl, quinolyl, isoquinolyl or phenyl; R<9> = eg. H, OH, 1-3C alkoxy; B' = H; or R<9> + B' = a bond
priorityDate 1997-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 454.