发明名称 BENZO-[F]-QUINOLINONES, METHOD OF INHIBITION, METHOD OF SYNTHESIS OF BENZO-[F]-QUINOLINONES, METHOD OF RACEMATES SPLITTING AND DI-P-TOLUOYL-(D)- OR (L)-TARTARIC ACID SALT
摘要 FIELD: organic chemistry, medicine. SUBSTANCE: invention relates to benzo-[a] -quinolinone of the formula (I) <EMI ID=0.384 HE=36 WI=42 TI=CHI> where R is H, alkyl or phenalkyl; Z and Z' - are H, alkyl or one of Z and Z' with R forms a bond carbon-carbon Y is H or methyl or with SSS forms a band carbon-carbon; R is H or forms a bond carbon-carbon with one of Y or R ; R is H or C<SB>1-4</SB> alkyl; R is H or R forms a bond carbon-carbon; R is H or with R forms a bond carbon-carbon; R is H or with one of Z or Z' forms a bond carbon-carbon; n = 1 or 2; X is H, halogen, NO<SB>2</SB>, cyano-group, CF<SB>3</SB>, C<SB>1-6</SB>-alkyl, alkoxy-, carboxy-, alkoxycarbonyl-, amino-, amido-group or a group -A-O-R where A is C<SB>1-6</SB>-alkylene, C<SB>2-6</SB>-alkenyl or C<SB>2-6</SB>-alkynylene; R - halogen, hydroxy, alkylamido-group or its pharmaceutically acceptable salt. Compounds of the formula (I) are selective steroid inhibitors of 5alpha--reductase showing strong effect and can be used for treatment of patients with prostate benignity tumors, alopecia, acnes and seborrhea in males. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 19 cl, 1 tbl, 69 ex
申请公布号 RU2126386(C1) 申请公布日期 1999.02.20
申请号 SU19925052860 申请日期 1992.08.20
申请人 EHLI LILLI EHND KOMPANI 发明人 DZHEJMS EHDMUND ODIA;KENNET STIVEN KHERCH;CHARL'Z DEHVID DZHONS;DEHVID EHRNST LOKHORN;LORETTA EHMS MAKKUAJD
分类号 A61K31/47;A61K31/435;A61K31/473;A61P13/08;A61P17/00;A61P17/08;A61P17/10;A61P17/14;A61P35/00;A61P43/00;C07C45/00;C07C45/51;C07C45/56;C07C49/697;C07C49/737;C07C49/747;C07C49/755;C07C205/45;C07C229/46;C07D211/00;C07D221/06;C07D221/10;C12N9/99 主分类号 A61K31/47
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