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filingDate 1998-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b89f45c31b347921b8fad68e27bb6dd0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_464da7eeef26a484eb225ac473777a37
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95ae7eb2c6ec00e9b8943d6bc8cb1078
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72b431f9a5d3debc51b15730c2d3b986
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_020d2a3308ac79895479fdf3d2cd17c5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9677447ba0741fe8ee34b4d43a1edd62
publicationDate 2004-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1486486-A2
titleOfInvention Substituted B-thiocarboxylic acids
abstract This invention relates to compounds of general formula (I) :n nwherein n   R 1 and R 3 may be the same or different and each independently represents a groupn-L 1 -R 5 [where L 1 is a direct bond, a straight or branched C 1-6 alkylene chain, a straight ornbranched C 2-6 alkenylene chain, a straight or branched C 2-6 alkynylene chain or a straight ornbranched C 1-6 alkylene chain containing an oxygen or sulfur atom, a phenylene, imino (-NH-) ornalkylimino linkage, or a sulfinyl or sulfonyl group, in which each of the alkylene, alkenylene andnalkynylene chains may be optionally substituted, the substituents chosen from alkoxy, aryl,ncarboxy, cyano, cycloalkyl, halogen, heteroaryl, hydroxyl, or oxo; and R 5 represents hydrogen,naryl, aroyl, carboxy or an acid bioisostere, cyano, cycloalkyl, cycloalkenyl, heterocycloalkyl,nheteroaryl, arylalkoxycarbonyl, -NH-C(=O)-NH 2 , -C=N-O-C(=O)-NH 2 , -C(=O)-NY 1 Y 2 ,n-NY 1 SO 2 aryl, -NHR 6 , -SR 6 , or -OR 6 ]; n   R 2 and R 4 may be the same or different and are each independently hydrogen or alkyl;nor n   R 2 and R 4 together form a bond; or R 1 and R 2 , or R 1 and R 3 , or R 3 and R 4 togethernwith the carbon atom(s) to which they are attached form a 3 to 8 membered cycloalkyl orncycloalkenyl ring, optionally substituted by alkyl, arylalkyl, or heteroarylalkyl, and which maynoptionally contain a heteroatom selected from O, S or NR 6 ; or R 1 and R 3 together with thencarbon atoms to which they are attached form a heteroaryl ring; n   Y represents tetrazolyl, 3,5-dioxo-1,2,4-oxadiazolidinyl, 3-hydroxyisoxazolyl or 3-hydroxy-1-methylpyrazolyl; n   A 1 represents a direct bond, a straight or branched C 1-4 alkylene chain or a NR 6 group; n   Ar is a group chosen from :n nandn nand n   n is 0, 1 or 2; n   and N-oxides thereof, and their prodrugs, pharmaceutically acceptable salts, and solvatesn(e.g. hydrates), thereof. n Such compounds inhibit the production or physiological effects of TNF and inhibit cyclic AMPnphosphodiesterase. The invention is also directed to pharmaceutical compositions comprisingncompounds of formula (I), their pharmaceutical use and methods for their preparation.
priorityDate 1997-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 886.