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filingDate 1990-02-09^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-04-16^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1ff7879d67aaff2e09f90ff9e8abaa3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_400a069edc9b21d1671432e9f31cacd1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f002608f45c28d7a34b4eabf38366dd8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e67e9c8471d98ef297cc7cdccc7ea2c7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1b1a5357ea402f078c71ed560f6b9cf
publicationDate 2002-04-16^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2009690-C
titleOfInvention Phenylhydrazones, the manufacture thereof and therapeutic and cosmetic compositions prepared therefrom
abstract A Phenylhydrazone of formula I: in which R1, R2, and R3 are independently of one another hydrogen, halogen, C1-C4-alkyl, hydroxyl, C1-C4-alkoxy or acetoxy, R4 is hydrogen, hydroxyl, tert.-butyl, C1-C6-alkoxy or C2-C6-alkoxyalkyl, R5 is hydrogen or C1-C4-alkyl, or R4 and R5 together form a ring which is -C(CH3)2-A-C(CH3)2-(where A is -CH2CH2-, -CH(CH3)-, -CH2C(O)-or-CH2CHOH-) or is -(CH2)3C(CH3)2-, -OCH2CH2C(CH3)2-, -C(CH3)2CH(CH3)CH2C(CH3)2- or -NHC(O)CH2C(CH3)2-, where R4 and R5 together form a ring of the type specified or R4 is branched C4-C6-alkoxy or branched C4-C6-alkoxyalkyl when R1, R2 and R3 are each hydrogen, R6 is hydrogen, methyl, ethyl or cyclopropyl, m and n are different and denote 0 or 1, X is hydrogen, nitro, methoxy or nitrile, a sulfonic acid radical or -CONR7 OR7, -CO2R7, -PO(OR8)2, -S(O)n R8 where n is 0,1 or 2, -SO2-NR9R10 or -CONR9R10, where R7 is hydrogen, C1-C3-alkyl or phenyl, which may or may not be substituted by one or two amino, C1-C4-acylamino, C1-C4-alkyl or C1-C4-alkoxy groups, R8 is C1-C3-alkyl and R9 and R10 are independently of each other hydrogen or C1-C4-alkyl or together form a piperidine, piperazine, morpholine or thiomorpholine ring, where R4 and R5 together form a ring of the type specified or R3 and R5 are each isopropyl, isobutyl or tert.-butyl, when X is hydrogen, methoxy, nitrile or nitro or when X is carboxyl and R1 and R2 is hydroxyl, and R4 is not hydroxyl when m is 0, and their physiologically tolerated salts.
priorityDate 1989-02-10^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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