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filingDate 1999-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2004-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-3564543-B2
titleOfInvention Furopyridine antibacterial agent
abstract This invention provides a compound of formula (I): <CHEM> or pharmaceutically acceptable salts thereof, wherein X<1> and X<2> are C or N, respectively; R<1> and R<2> are independently phenyl optionally substituted with a hydroxy group with proviso that X<1> and X<2> are not simultaneously C or N, when X<1> is N, R<1> is absent, and when X<2> is N, R<2> is absent; R<3> is methyl or hydroxymethyl; R<4> is formyl, hydroxymethyl or hydroxy C3-6 alkenyl; R<5> is hydroxy, C3-6 alkenyl or hydroxy C3-6 alkenyl; or R<4> and R<5>, together with the carbon atoms in the furopyridine ring to which they are attached, may form the following ring (to be fused with the furopyridine ring): <CHEM> with the proviso that when R<3> is methyl and R<5> is 2-buten-2-yl, X<2> is not N. These compounds and pharmaceutical compositions containing such compounds are useful for treating infectious diseases caused by bacteria.
priorityDate 1998-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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