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filingDate 1998-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_05f8affe840cbe77f385346566f5efc1
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publicationDate 1998-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2286385-A1
titleOfInvention Quinoline derivatives, having in particular antiviral properties, preparation and biological applications thereof
abstract The quinoline derivatives correspond to formula (I) in which: Ra, Rb and Rc, identical or different, represent one or more substituents, themselves same or different, occupying any position on the rings, this or these substituents being chosen from a group - (CH2) n -Y or -CH = CH-Y, where Y is halogen, -OH, -OR, -COH, -COR, -COOH, -COOR, -COH, -COR, -CONH2, -CON (Rx, Ry) -CH = NOH, -CO-CH = NOH, -NH2, -N (Rx, Ry), -NO2, -PO (OR) 2 -SH2, -SR, -SO2R, -SO2NHR, CN, or Z (Rc), where R is an alkyl of 1 to 8 carbon, or aryl or heterocyclic, Rx and Ry, identical or different, are alkyl from 1 to 5 carbon, Z an aryl or heterocycle and n is zero or an integer from 1 to 5, Rb which may also represent hydrogen, and when Y is -COOH or -COOR in Rc, Z, if it represents an aryl, has at least 3 substituents or the quinoline nucleus is trisubstituted, X is an ethylenic double bond; a group - (CH2) n-, where n is an integer from 1 to 5: or a group -CH (Rd) -CH (Re), Rd and Re, identical or different, representing a hydrogen, halogen, hydroxy or epoxy; or a group - (CH2) n ', -OC (O) - (CH2) m-, - (CH2) n, -C (O) -O- (CH2) m-, -(CH2) n, -O- (CH2) m-, - (CH2) n, -N (Q) - (CH2) m-, or - (CH2) n, -S (O) t- (CH2) m -, where n = 1 to 8, m = 0 to 8, t = 0.1 or 2, and Q = H, aryl or alkyl, as well as the salts pharmaceutically acceptable of these derivatives, their diastereoisomeric forms and their enantiomeric forms. Application as effect drugs HIV anti-integrase inhibitor.
priorityDate 1997-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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