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公开(公告)号:US5903200A
公开(公告)日:1999-05-11
申请号:US787103
申请日:1997-01-22
申请人: Takanori Ogawa , Masao Fukuda
发明人: Takanori Ogawa , Masao Fukuda
CPC分类号: H01H50/042 , H01H2050/367 , H01H50/021
摘要: An electromagnetic relay in which an iron core 2 is fixed to a yoke 3, and one end of the yoke 3 is fixed by press-fitting to a base 4. The base 4 is formed with a yoke-receiving groove 4b into which tongue pieces 3e, 3e at one end of the yoke 3 are press-fitted, and a cutout groove 4c into which a head portion 2c of the iron core 2 is received. The yoke 3 is formed with a seal projection 3f disposed by insertion in an opening end of a cutout groove 4c of the base 4. This construction of the electromagnetic relay eliminates poor operation by preventing metal chips produced during assembly from adhering to electrical contacts of the relay.
摘要翻译: 一种电磁继电器,其中铁芯2固定到磁轭3,并且磁轭3的一端通过压配固定在基座4上。基座4形成有轭接收槽4b,舌片 3e,3e在轭3的一端被压配合,以及切口槽4c,铁芯2的头部2c被容纳在该切口槽4c中。 轭3形成有通过插入基座4的切口槽4c的开口端而设置的密封突起3f。电磁继电器的这种结构通过防止组装期间产生的金属屑粘附到 中继。
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公开(公告)号:US06310210B1
公开(公告)日:2001-10-30
申请号:US09530828
申请日:2000-05-03
申请人: Takanori Ogawa , Takashi Yaegashi , Seigo Sawada , Tomio Furuta
发明人: Takanori Ogawa , Takashi Yaegashi , Seigo Sawada , Tomio Furuta
IPC分类号: C07D47104
CPC分类号: C07D471/14
摘要: The present invention relates to new camptothecin derivatives shown by the below formula, which are water-soluble and excellent in an anti-tumor activity, and to salts thereof. In the formula, R1 represents a hydrogen atom or an alkyl group with 1-6 carbon atoms, R2 represents identically or differently 0-4 alkyl groups with 1-6 carbon atoms, a halogen atom, an alkoxyl or hydroxyl group, R3 represents a lower alkylamino, di-lower alkylamino, arylamino, cyclicamino or lower alkoxyl group, and salts thereof.
摘要翻译: 本发明涉及由下式表示的新的喜树碱衍生物,它是水溶性的,抗肿瘤活性优异的盐及其盐。式中R1表示氢原子或1-6位烷基 碳原子,R2表示相同或不同的具有1-6个碳原子的0-4个烷基,卤素原子,烷氧基或羟基,R3表示低级烷基氨基,二低级烷基氨基,芳基氨基,环氨基或低级烷氧基, 的盐。
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公开(公告)号:USD652842S1
公开(公告)日:2012-01-24
申请号:US29355871
申请日:2010-02-16
申请人: Tomoko Obama , Takanori Ogawa , Tomoko Nakagawa
设计人: Tomoko Obama , Takanori Ogawa , Tomoko Nakagawa
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公开(公告)号:US06268381B1
公开(公告)日:2001-07-31
申请号:US09581908
申请日:2000-06-19
申请人: Hideaki Shimizu , Atsuhiro Abe , Takanori Ogawa , Hiroshi Nagata , Seigo Sawada
发明人: Hideaki Shimizu , Atsuhiro Abe , Takanori Ogawa , Hiroshi Nagata , Seigo Sawada
IPC分类号: A61K31445
CPC分类号: C07D405/12 , C07D305/14 , C07D405/14 , C07D407/12
摘要: The present invention relates to taxane derivatives each represented by the following formula (1): [wherein, A1 represents a group (in which R1 represents H or a (substituted) alkyl group) or a group (in which R2 represents an amino group, a mono- or di-alkylamino group, a piperidino group, a pyrrolidino group or a morpholino group), X represents H, an alkoxycarbonyl group or a benzoyl group, Y represents H or a trialkylsilyl group, A2 represents a furyl group, an alkylfuryl group, an alkyl group or a fluorophenyl group, Ac represents an acetyl group, and Bz represents a benzoyl group] or salts thereof; and drugs containing the same as an active ingredient. These compounds have excellent water solubility and antitumor activity.
摘要翻译: 本发明涉及各种由下式(1)表示的紫杉烷衍生物:[其中,A1表示基团(其中R1表示H或(取代的(alkyl))烷基)或基团(其中R2表示氨基, 一或二烷基氨基,哌啶子基,吡咯烷子基或吗啉代基),X表示H,烷氧基羰基或苯甲酰基,Y表示H或三烷基甲硅烷基,A2表示呋喃基,烷基 基团,烷基或氟苯基,Ac表示乙酰基,Bz表示苯甲酰基]或其盐; 和含有相同活性成分的药物。这些化合物具有优异的水溶性和抗肿瘤活性。
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公开(公告)号:US06743918B2
公开(公告)日:2004-06-01
申请号:US10239113
申请日:2002-11-25
申请人: Takashi Yaegashi , Takanori Ogawa , Seigo Sawada
发明人: Takashi Yaegashi , Takanori Ogawa , Seigo Sawada
IPC分类号: C07D49112
CPC分类号: C07D491/22 , A61K31/475
摘要: Problem: A large scale production of camptothecin, which is a starting compound of irinotecan hydrochloride and various camptothecin derivatives, at a low cost and with ease. Solution: A process for preparing camptothecin, characterized in that it comprises the following steps (a) and (b); (a) the step to hydrolyze 9-methoxycamptothecin or a natural material containing 9-methoxycamptothecin; (b) the step to convert 9-hydroxycamptothecin obtained in the step (a) into camptothecin by 9-O—perfluoro-lower-alkylsulfonylation or 9-O—phenyltetrazolylation, followed by hydrogenolysis.
摘要翻译: 问题:大量生产喜树碱,它是伊立替康盐酸盐和各种喜树碱衍生物的起始化合物,成本低,易于使用。溶液:一种制备喜树碱的方法,其特征在于它包括以下步骤(a)和 (b);(a)水解9-甲氧基喜树碱或含有9-甲氧基喜树碱的天然物质的步骤;(b)将步骤(a)中得到的9-羟基喜树碱通过9-O-全氟低级 - 烷基磺酰化或9-O-苯基四唑化,然后氢解。
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公开(公告)号:US6136808A
公开(公告)日:2000-10-24
申请号:US508092
申请日:2000-03-16
申请人: Atsuhiro Abe , Hideaki Shimizu , Seigo Sawada , Takanori Ogawa , Hiroshi Nagata
发明人: Atsuhiro Abe , Hideaki Shimizu , Seigo Sawada , Takanori Ogawa , Hiroshi Nagata
IPC分类号: A61K31/337 , A61K31/443 , A61K31/445 , A61K31/495 , A61K31/496 , A61P35/00 , C07D305/14 , C07D405/12 , C07D401/00 , C07D405/00 , C07D409/00
CPC分类号: C07D405/12 , A61K31/337 , A61K31/496 , C07D305/14
摘要: This invention relates to a taxane derivative represented by the following formula (1): ##STR1## (wherein A represents a substituted piperazino or piperidino group, X represents an alkyl, pyridyl, thienyl, furyl, cycloalkyloxy or the like and Y represents H or trialkylsilyl) and also to a drug containing the same.This compound has high solubility in water and also has excellent antitumor activities.
摘要翻译: PCT No.PCT / JP98 / 04180 Sec。 371日期2000年3月16日 102(e)日期2000年3月16日PCT提交1998年9月17日PCT公布。 公开号WO99 / 14209 1999年3月25日本发明涉及下述式(1)所示的紫杉烷衍生物:其中,A表示取代的哌嗪子基或哌啶子基,X表示烷基,吡啶基,噻吩基,呋喃基,环烷基氧基等,Y表示 H或三烷基甲硅烷基),以及含有它们的药物。 该化合物在水中的溶解度高,抗肿瘤活性也优异。
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公开(公告)号:US07378555B2
公开(公告)日:2008-05-27
申请号:US11517621
申请日:2006-09-08
IPC分类号: C07C209/36
CPC分类号: C07D213/64 , C07C205/22 , C07C205/37 , C07C205/44 , C07C205/45 , C07C225/22 , C07D491/04 , C07D491/14 , Y02P20/55
摘要: The present invention is to prepare efficiently 2′-amino-5′-hydroxypropiophenone corresponding to the AB-ring part of camptothecin (CPT) skeleton and a tricyclic ketone corresponding to the CDE-ring part in order to provide efficiently CPT by the total synthesis, which is a starting material for irinotecan hydrochloride and various kinds of camptothecin derivatives, and to provide stably CPT and its derivatives.
摘要翻译: 本发明是为了有效地制备对应于喜树碱(CPT)骨架的AB-环部分的2'-氨基-5'-羟基苯丙酮和对应于CDE-环部分的三环酮,以便通过全合成提供高效的CPT ,其为盐酸伊立替康和各种喜树碱衍生物的起始原料,并提供稳定的CPT及其衍生物。
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公开(公告)号:US20070010674A1
公开(公告)日:2007-01-11
申请号:US11517621
申请日:2006-09-08
IPC分类号: C07D471/14
CPC分类号: C07D213/64 , C07C205/22 , C07C205/37 , C07C205/44 , C07C205/45 , C07C225/22 , C07D491/04 , C07D491/14 , Y02P20/55
摘要: The present invention is to prepare efficiently 2′-amino-5′-hydroxypropiophenone corresponding to the AB-ring part of camptothecin (CPT) skeleton and a tricyclic ketone corresponding to the CDE-ring part in order to provide efficiently CPT by the total synthesis, which is a starting material for irinotecan hydrochloride and various kinds of camptothecin derivatives, and to provide stably CPT and its derivatives.
摘要翻译: 本发明是为了有效地制备对应于喜树碱(CPT)骨架的AB-环部分的2'-氨基-5'-羟基苯丙酮和对应于CDE-环部分的三环酮,以便通过全合成提供有效的CPT ,其为盐酸伊立替康和各种喜树碱衍生物的起始原料,并提供稳定的CPT及其衍生物。
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公开(公告)号:US07126000B2
公开(公告)日:2006-10-24
申请号:US10467987
申请日:2002-02-21
IPC分类号: C07D491/052
CPC分类号: C07D213/64 , C07C205/22 , C07C205/37 , C07C205/44 , C07C205/45 , C07C225/22 , C07D491/04 , C07D491/14 , Y02P20/55
摘要: The present invention is to prepare efficiently 2′-amino-5′-hydroxypropiophenone corresponding to the AB-ring part of camptothecin (CPT) skeleton and a tricyclic ketone corresponding to the CDE-ring part in order to provide efficiently CPT by the total synthesis, which is a starting material for irinotecan hydrochloride and various kinds of camptothecin derivatives, and to provide stably CPT and its derivatives.
摘要翻译: 本发明是为了有效地制备对应于喜树碱(CPT)骨架的AB-环部分的2'-氨基-5'-羟基苯丙酮和对应于CDE-环部分的三环酮,以便通过全合成提供有效的CPT ,其为盐酸伊立替康和各种喜树碱衍生物的起始原料,并提供稳定的CPT及其衍生物。
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