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filingDate 2002-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7ce385c359d2dcbcd41f7a3cb0379e6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d5680dc39257b5e523f2681afe28fb6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_866558167361172435abe3f7dd01e4f1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_437252d383e59fb2014bba852be5a994
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33cc2a5a00440dc570f6d4439ffff5b7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_335ad2509abd01707dbb1ef43e144f16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8deb04e9ae780fe7cddbea7a3851173a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c0d2e10c2568314491692e2ec393af36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0e38e9b9a0e4ecd283107e112959cab
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publicationDate 2003-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200306178-A
titleOfInvention Chemical compounds
abstract The invention relates to compounds of formula (I): wherein: R1 represents a group selected from: each of which optionally contain a further heteroatom N, Z represents an optional substituent halogen, -CH2NH2, -NRaRb or -CN, Z' represents an optional substituent halogen, -CH2NH2, or -CN, alk represents alkylene or alkenylene, T represents S, O or NH; R2 represents hydrogen, -C1-3alkylCONRaRb, -C1-3alkylCO2C1-4alkyl, -C1-3alkylmorpholino, -CO2C1-4alkyl, or -C1-3alkylCO2H; X represents phenyl or a 5 or 6 membered aromatic or non-aromatic heterocyclic group containing at least one heteroatom selected from O, N or S, each of which is optionally substituted by 0-2 groups selected from: halogen, -CN, -C1-4alkyl, -C2-4alkenyl, -CF3, -NRaRb ,-NO2, -N(C1-4alkyl)(CHO), -NHCOC1-4alkyl, -NHSO2Rc, C0-4alkylORd, -C(O)Rc, -C(O)NRaRb, -S(O)nRc, and-S(O)2NRaRb; Y represents (i) a substituent selected from hydrogen, halogen, -CN, -C1-4alkyl, -C2-4alkenyl, -CF3, -NRaRb,-NO2,-N(C1-4alkyl)(CHO), -NHCOC1-4alkyl, -NHSO2Rc, C0-4alkylORd, -C(O)Rc, -C(O)NRaRb,-S(O)nRc, or -S(O)2NRaRb, or (ii) phenyl or a 5 or 6 membered aromatic or non-aromatic heterocyclic group containing at least one heteroatom selected from O, N or S, each of which is optionally substituted by 0-2 groups selected from: halogen, -CN, -C1-4alkyl, -CF3, -(CH2)nNRaRb, -(CH2)nN+RaRbCH2CONH2, C0-4alkylORd, -C(O)Rc, - C(O)NRaRb, -S(O)nRc, -S(O)2NRaRb,=O, oxide to a ring N, -CHO, -NO2, and -N(Ra)(SO2Rc); Ra and Rb independently represent hydrogen, -C1-6alkyl, or together with the N atom to which they are bonded form a 5-, 6- or 7- membered heterocyclic ring optionally containing an additional heteroatom selected from O, N or S, optionally substituted by C1-4alkyl, and optionally the S heteroatom is substituted by O i.e. represents S(O)n; Rc represents -C1-6alkyl; Rd represents hydrogen or -C1-6alkyl; n represents 0-2; and pharmaceutically acceptable derivatives thereof. The invention also relates to processes for the preparation of compounds of formula (I), pharmaceutical compositions containing compounds of formula (I) and to the use of compounds of formula (I) in medicine, particularly in the amelioration of a clinical condition for which a Factor Xa inhibitor is indicated.
priorityDate 2001-12-21-04:00^^<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: 478.