http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2252531-A1

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filingDate 1997-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4fd5cacf5c99db67f696c07d554db8d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20b50004a26f30bc7d46ca406506a68a
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publicationDate 1997-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2252531-A1
titleOfInvention Quinoline carboxamides as tnf inhibitors and as pde-iv inhibitors
abstract A compound of general formula (i), wherein X is CO or CS; R is H, halogen or alkyl; R1 represents OH, alkoxy optionally substituted with one or more halogens, or thioalkyl; R2, R3 and R4 are the same or different and are each H, R7, OR11, COR7, C(=NOR7)R7, alkyl-C(=NOR7)R7, halogen CF3, alkyl-C(=NOH)R7, C(=NOH)R7, CN, CO2H, CO2R11, CONH2, CONHR7, CON(R7)2, NR9R10 or CONR12R13 where NR12R13 is a heterocyclic ring optionally substituted with one or more R15; R5 represents H, arylalkyl, heteroarylalkyl, heterocycloalkyl, S(O)mR11 or alkyl optionally substituted with one or more substituents chosen from hydroxy, alkoxy, CO2R8, SO2NR12R13, CONR12R13, CN, carbonyl oxygen, NR9R10, COR11 and S(O)nR11; R6 represents aryl, heteroaryl, heterocyclo, arylalkyl, heteroarylalkyl or heterocycloalkyl; in R5 and/or R6, the aryl/heteroaryl/heterocyclo portion is optionally substituted with one or more substituents alkyl-R14 or R14. The compounds can be used to treat disease states, for example disease states associated with proteins that mediate cellular activity, for example by inhibiting tumour necrosis factor and/or by inhibiting phosphodiesterase IV.
priorityDate 1996-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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