![]() Method for preparation n-/(4- [(indolo
专利摘要:
An indoloquinoline system compound represented by the following formula (1): A benzo(b)acridine system compound represented by the following formula (2): A benzo(c)acridine system compound represented by the following formula (3): Processes for preparing the above compounds and carcinostatic composition containing at least one of the above compounds. 公开号:SU1706390A3 申请号:SU894613720 申请日:1989-03-09 公开日:1992-01-15 发明作者:Ямато Масатоси 申请人:Мект Корпорейшн (Фирма); IPC主号:
专利说明:
The concentration of the compound capable of causing 50% growth inhibition (ED50) compared with the control is determined. The compound is considered effective at less than L μg / ml. The test results for the cancer-static effect are given in Table 1. 1 In Table 3, comparisons of known compounds are given.
权利要求:
Claims (1) [1] EN50 2 CH 3 available in that the indolo (3,2-b) -Y-chloroquinoline of the formula 40 is reacted with 2-methoxy-4-methylsulfamidoplaniline of the formula εΗ 3 50 2 ΝΗ- <δ -ΝΗ 2 main 3 in the presence of concentrated hydrochloric acid.
类似技术:
公开号 | 公开日 | 专利标题 SU1706390A3|1992-01-15|Method for preparation n-/| chinoline - 10-yl)amino]-3-methoxyphenyl) amide hydrochloride JPH01207288A|1989-08-21|Indole derivative JPS59108785A|1984-06-23|5-oxime derivative of milbemycins JPS63211266A|1988-09-02|Intermediate for dihydropyridine derivative JPH0348648A|1991-03-01|Pharmaceutical acting as anti-arteriosclerotic and novel di-t-butyl hydroxyphenyl derivative JPH03118377A|1991-05-20|1,3-dihydro-1-|-2h-indol-2-one and its production JPS625962A|1987-01-12|Desmosine derivative and reagent for preparation of artificial antigen JPH01146885A|1989-06-08|Phosphorylating reagent and its use JPH02204475A|1990-08-14|Enzyme-inhibiting amino acid derivative and production thereof IE881788L|1988-12-15|Cycloalkylamides of |-1-alkyl-6-|¹ergolines JPH023665A|1990-01-09|Renin-inhibiting amino acid derivative JPH01261388A|1989-10-18|Substituted quinoline derivative MY104829A|1994-06-30|3-phenyl-5, 6-dihydrobenz [c]acridine-7-carboxylic acids and related compounds as cancer chemotherapeutic agents. JPH02152963A|1990-06-12|4-phenyl-4-| amido) piperidine derivative and pharmaceutical composition containing the same JPH02300184A|1990-12-12|Indole derivative KR930006003A|1993-04-20|Imidazolylmethyl-pyridine compounds JPH02138263A|1990-05-28|Imidazole derivative, production thereof and anti-ulcer agent containing the same derivative JPH0217176A|1990-01-22|Compound having analgesic action, its production and analgesic containing the compound JPS574977A|1982-01-11|2-guanidinothiazole derivative JPH02134320A|1990-05-23|Pharmaceutical composition EP0666263A4|1995-09-06| JPH04198160A|1992-07-17|New carbodiimide derivative and its production KR890003725A|1989-04-17|Amine derivatives and salts thereof, preparation methods thereof and ulcers containing the same JPS6422898A|1989-01-25|2-alanyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivative JPS5233640A|1977-03-14|Process for preparation of benzenedicarboxylic acid amides
同族专利:
公开号 | 公开日 DK116289A|1989-09-11| IL89510A|1992-08-18| NO167861B|1991-09-09| FI891061A0|1989-03-06| JPH01228965A|1989-09-12| BR8901100A|1989-10-31| AU3112089A|1989-09-14| AU618991B2|1992-01-16| IL89510D0|1989-09-10| FI891061A|1989-09-11| HUT50818A|1990-03-28| NO891024D0|1989-03-09| US5128345A|1992-07-07| EP0332190A2|1989-09-13| NZ228275A|1990-12-21| ZA891758B|1989-11-29| KR890014536A|1989-10-24| NO167861C|1991-12-18| EP0332190A3|1991-04-24| CN1036763A|1989-11-01| DK116289D0|1989-03-10| HU203225B|1991-06-28| NO891024L|1989-09-11|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 JPS63101369A|1986-10-17|1988-05-06|Mect Corp|Indenoquinoline compound, production thereof and anti-cancer drug comprising said compound as active ingredient| JPH02256667A|1988-12-27|1990-10-17|Masatoshi Yamato|Condensed quinoline-based compound and production thereof|JPH02256667A|1988-12-27|1990-10-17|Masatoshi Yamato|Condensed quinoline-based compound and production thereof| WO2005054236A1|2003-11-20|2005-06-16|Crystax Pharmaceuticals S.L.|Substituted quinolines for the treatment of cancer| CN103497211B|2013-10-15|2016-07-20|中国海洋大学|Indoloquinoline derivant and its preparation method and application| CN103614134B|2013-11-08|2014-11-05|吉林奥来德光电材料股份有限公司|Organic electroluminescent material and preparation method thereof| CN104860945B|2014-02-25|2016-08-24|北京大学|Condense acridine derivatives and pharmaceutical composition, preparation method and application| CN103951694A|2014-04-14|2014-07-30|上海大学|Acridine or benzacridine derivative and synthesis method thereof| CN105669551B|2015-12-02|2018-04-17|广西中医药大学|7 benzoacridines are to fluorobenzoyl amido thiocarbamide and its preparation method and application| CN105418501B|2015-12-02|2018-04-17|广西中医药大学|7 pairs of anisidino- benzo [c] acridine hydrochlorides and its preparation method and application| CN105481769B|2015-12-02|2018-07-10|广西中医药大学|A kind of benzoacridine derivatives and its preparation method and application| CN105399671B|2015-12-02|2018-04-17|广西中医药大学|7 p-totuidine base benzo [c] acridine hydrochlorides and its preparation method and application|
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申请号 | 申请日 | 专利标题 JP63056883A|JPH01228965A|1988-03-10|1988-03-10|Condensed quinoline and condensed acridine, their production and anticancer agent containing said compounds| 相关专利
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