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filingDate 1999-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36700e103de1dcae3c964eb702a5c088
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_125673220fc5406c78406ae7c0b8fd2c
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_920177f67a2df2e5561d8b076d8cd860
publicationDate 1999-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-9900804-A2
titleOfInvention Use of Phenoxyacetic Acid and Phenoxymethyl Tetrazole Derivatives with Tumor Effect to Produce Pharmaceutical Compounds and New Compounds
abstract The present invention relates to compounds of the general formula (I) in which the -O-C (R 1) (R 2) - (CH 2) p -A can be attached to the trace, meta or para position; A is carboxyl, C 1 -C 4 alkoxycarbonyl or cyanide or R (G) wherein R 'is hydrogen or C 1 -C 4 alkyl; or A- (CH 2) p -C (R 1) (R 2) - menthol is phenyl, benzyl or indolylmethyl, which may be substituted by R 4; p is 0.1 or 2; R 1 and R 2 independently of one another are hydrogen or C 1-8 -alkyl, or R 1 and R 2 together with the carbon to which they are attached form a C 3-7 -cyclic alkylpyrrolid; R 4 is O-2 chloro, bromo, iodo, fluoro, linear or branched C 1-8 alkyl, hydroxy, C 1-4 alkoxy and / or 1-4 carbon acyl; or the Horn (H) in the general Formula (I) represents naphthyl, which may be substituted by R 4; n is 1-4; m is 0 or 1; B is a straight or branched C 1-10 alkyl piperidine, -CO-C (R 3) -CH-R, -CH = C (R 3) -CO-Ar, -CO-CH (R 3) -CH 2 -R or -CO -CH (R3) -CH2-NR5R6; or -CO-CH (R 3) -CO-Ar when m is 1; R is a hydrogen hydrogen atom, -Ar or -CO-Ar; R3 is hydrogen or C 1-8 alkylpiperidine; R5 and R6 are each independently C1-C4 alkylpiperidine, or R5 and R6 together with the nitrogen atom to which it is attached are piperidine, piperazine, (C1-C8 alkyl) piperazine, monomeric or thiopyrene; Ar is phenyl substituent which may be unsubstituted or may be substituted with one to three chlorine, bromine, iodine, fluorine, straight or branched C 1 -C 8 alkyl, hydroxy, C 1 -C 4 alkoxy and / or C 1 -C 4 acyl substituents. Use of their stereoisomerizing acids or salts thereof with pharmaceutically acceptable acids or bases for the preparation of a medicament having MDM2 antagonist activity. The invention further relates to the novel compounds of general formula (I) and to pharmaceutical compositions containing them. (I) (G) (H) ŕ
priorityDate 1998-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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