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filingDate 1998-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2001-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20010023695-A
titleOfInvention Substituted Oxindole Derivatives as Protein Tyrosine Kinase and as Protein Serine/Threonine Kinase Inhibitors
abstract A pharmaceutical formulation comprising a compound of formula (I), for treatment, in particular a compound of formula (I) for use in the treatment of diseases mediated by CDK2 activity, such as alopecia due to cancer chemotherapy or radiotherapy.n n n <Formula I>n n n n n n n n Wheren n n X is N, CH, CCF 3 , or C (C 1-12 aliphatic);n n n R 4 is sulfonic acid, C 1-12 aliphatic-sulfonyl, sulfonyl-C 1-12 aliphatic, C 1-12 aliphatic-sulfonyl-C 1-6 aliphatic, C 1-6 aliphatic-amino, R 7 -sul Ponyl, R 7 -sulfonyl-C 1-12 aliphatic, R 7 -aminosulfonyl, R 7 -aminosulfonyl-C 1-12 aliphatic, R 7 -sulfonylamino, R 7 -sulfonylamino-C 1 -12 aliphatic, amino, sulfonyl, amino, di -C 1-12 aliphatic amino, di -C 1-12 aliphatic aminocarbonyl, di -C 1-12 aliphatic aminosulfonyl, di -C 1-12 aliphatic amino, di -C 1-12 aliphatic aminocarbonyl, di-C 1-12 aliphatic aminosulfonyl-C 1-12 aliphatic, (R 8 ) 1-3 -arylamino, (R 3 ) 1-3 -arylsulfonyl, (R 8 ) 1-3 -aryl-aminosulfonyl, (R 8 ) 1-3 -aryl-sulfonylamino, Het-amino, Het-sulfonyl, Het-aminosulfonyl, aminoiminoamino, or aminoimino Aminosulfonyl;n n n R 5 is hydrogen;n n n Or R 4 and R 5 are optionally linked to form a fused ring.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015137668-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015034169-A1
priorityDate 1997-09-05-04:00^^<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: 1088.