专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

11. 发明申请

US20050099197A1 Dynamic burn-in apparatus and adapter card for dynamic burn-in apparatus 失效
标题翻译：动态老化装置和动态老化装置适配卡
公开(公告)号：US20050099197A1
公开(公告)日：2005-05-12
申请号：US10945839
申请日：2004-09-21
申请人： Yoshihiro Maesaki , Hiroshi Teshigawara , Sadao Ishihara , Yukio Tabuchi
发明人： Yoshihiro Maesaki , Hiroshi Teshigawara , Sadao Ishihara , Yukio Tabuchi
IPC分类号： G01R31/26 , G01R31/02 , G01R31/28 , G01R31/30
CPC分类号： G01R31/2879 , G01R31/2863
摘要： An adapter card is provided which comprises: a clock signal converting circuit (1) which converts a clock signal, output from a signal generator contained in a burn-in apparatus, into a higher-frequency clock signal; and a plurality of delay circuits (2) for causing each burn-in signal output from the signal generator to synchronize with the clock signal, wherein a connector (4) of the adapter (10) is connected between a burn-in card and a connector mounted in a burn-in chamber, to burn in a semiconductor device mounted on the burn-in card. Alternatively, the input connector (4) of the adapter card (10) is connected to a connector mounted, for example, on the rear side of a back board of the burn-in apparatus; then, the output of the signal generator is fed into the adapter card via its connector (4), and the output of the adapter card (10) is supplied to the semiconductor device mounted on the burn-in card to burn in the semiconductor device.
摘要翻译：提供了一种适配器卡，包括：时钟信号转换电路（1），其将从老化装置中包含的信号发生器输出的时钟信号转换成高频时钟信号; 以及用于使从所述信号发生器输出的每个老化信号与所述时钟信号同步的多个延迟电路（2），其中所述适配器（10）的连接器（4）连接在老化卡和连接器安装在老化室中，在安装在老化卡上的半导体器件中燃烧。或者，适配器卡（10）的输入连接器（4）连接到例如安装在老化装置的背板的后侧的连接器; 然后，信号发生器的输出通过其连接器（4）馈送到适配器卡中，并且适配器卡（10）的输出被提供给安装在老化卡上的半导体器件，以在半导体器件中燃烧。

12. 发明授权

US06591576B1 Structural member having closed sections, and apparatus and method for producing the structural member 失效
标题翻译：具有闭合部分的结构构件，以及用于制造结构构件的装置和方法
公开(公告)号：US06591576B1
公开(公告)日：2003-07-15
申请号：US09666143
申请日：2000-09-20
申请人： Masataka Iida , Masahiko Takeuchi , Sadao Ishihara , Takanori Matsukura , Takayuki Furuhata
发明人： Masataka Iida , Masahiko Takeuchi , Sadao Ishihara , Takanori Matsukura , Takayuki Furuhata
IPC分类号： E04C330
CPC分类号： B21D47/01 , B60R19/18 , B60R2019/1813 , E04C2003/0456
摘要： A structural member having a closed section, and an apparatus and a method for producing the same are provided to decrease production costs and secure the dimensional accuracy by a simple construction. The apparatus produces a structural member provided with a channel-shaped sectional portion and closed sectional portions adjacent thereto by bending a work and includes a press mold formed of a punch and a die oppositely installed and used for press-forming so that both side edges of the work are caused to overlap on the bottom wall of the channel-shaped sectional portion, and a fall-down prevention means which prevents both side edges opposed to each other of the work to be press-formed in the press mold from falling down and guides both side edges so that the end faces thereof are brought into contact with each other. Since the die applies a compression force to the work due to the end faces of the work brought into contact with the fall-down prevention means being pressed to each other, a curved portion having a residual compression stress between the longitudinal outer side wall and the vertical outer side wall is formed.
摘要翻译：提供具有封闭部分的结构件，以及用于制造该装置及其制造方法以降低生产成本并通过简单的结构确保尺寸精度。该装置通过弯曲工件产生具有通道形截面部分和与其相邻的封闭截面部分的结构部件，并且包括由冲压件和模具形成的冲压模具，所述冲模和模具相反地安装并用于压制成形，使得两侧边缘导致工件在通道形截面部分的底壁上重叠，并且防止下降的装置防止工件相对的两个侧边缘在压模中压制成坠落，并且引导两个侧边缘使得其端面彼此接触。由于模具由于与防倒下装置相接触的工件的端面相互挤压而对工件施加压缩力，所以在纵向外侧壁和纵向外侧壁之间具有残余压缩应力的弯曲部分形成垂直外侧壁。

13. 发明授权

US5880147A Amide derivatives having ACAT inhibitory activity, their preparation and their therapeutic and prohylactic use 失效
标题翻译：具有ACAT抑制活性的酰胺衍生物，其制备及其治疗和预防用途
公开(公告)号：US5880147A
公开(公告)日：1999-03-09
申请号：US715589
申请日：1996-09-18
申请人： Akira Yoshida , Kozo Oda , Takashi Kasai , Kousei Shimada , Hiroshi Kogen , Ichiro Hayakawa , Sadao Ishihara , Teiichiro Koga , Eiichi Kitazawa , Taro Tokui
发明人： Akira Yoshida , Kozo Oda , Takashi Kasai , Kousei Shimada , Hiroshi Kogen , Ichiro Hayakawa , Sadao Ishihara , Teiichiro Koga , Eiichi Kitazawa , Taro Tokui
IPC分类号： C07C275/28 , A61K31/16 , A61K31/17 , A61K31/18 , A61K31/275 , A61K31/40 , A61K31/445 , A61K31/535 , A61P9/10 , C07C233/08 , C07C235/38 , C07C237/22 , C07C237/42 , C07C237/52 , C07C251/48 , C07C255/01 , C07C255/44 , C07C255/49 , C07C255/57 , C07C255/60 , C07C259/10 , C07C271/12 , C07C271/20 , C07C271/64 , C07C275/24 , C07C275/32 , C07C275/34 , C07C275/38 , C07C275/40 , C07C275/42 , C07C311/04 , C07C311/29 , C07C311/32 , C07C311/37 , C07C311/46 , C07C317/18 , C07C317/46 , C07C323/62 , C07D207/02 , C07D211/04 , C07D213/56 , C07D213/75 , C07D213/81 , C07D213/82 , C07D213/88 , C07D231/12 , C07D231/40 , C07D233/54 , C07D239/28 , C07D239/42 , C07D241/20 , C07D241/24 , C07D265/28 , C07D277/30 , C07D277/46 , C07D295/192 , C07D295/215 , C07D317/58 , C07D317/60 , C07D405/12 , C07D521/00 , A61K31/335 , A61K31/165 , C07C233/05 , C07D319/16
CPC分类号： C07D213/75 , C07C235/38 , C07C237/22 , C07C237/42 , C07C237/52 , C07C251/48 , C07C255/44 , C07C255/57 , C07C255/60 , C07C259/10 , C07C271/12 , C07C271/20 , C07C271/64 , C07C275/24 , C07C275/40 , C07C275/42 , C07C311/04 , C07C311/29 , C07C311/46 , C07C317/18 , C07C317/46 , C07C323/62 , C07D213/56 , C07D213/81 , C07D213/82 , C07D213/88 , C07D231/12 , C07D231/40 , C07D233/56 , C07D233/64 , C07D239/28 , C07D239/42 , C07D241/20 , C07D241/24 , C07D249/08 , C07D277/30 , C07D277/46 , C07D295/192 , C07D295/215 , C07D317/58 , C07D317/60 , C07D405/12
摘要： Compounds of formula (I): ##STR1## wherein: R.sup.1 is alkyl; R.sup.2a, R.sup.2b, R.sup.2c and R.sup.2d are the same or different and each is hydrogen, optionally substituted alkyl, --(C.dbd.O)--B.sup.1 (wherein B.sup.1 is hydrogen or alkyl), nitro, --NR.sup.c R.sup.d (wherein R.sup.c is hydrogen or alkyl and Rd is alkyl), hydroxy, protected hydroxy group, alkoxy, cyano, alkylthio, alkylsulfinyl, alkylsulfonyl or halogen;R.sup.3 is alkyl; R.sup.4 is a group of the formula (II) ##STR2## wherein A.sup.1 is a single bond, alkylene or alkenylene; R.sup.5a and R.sup.5b are the same or different and each is hydrogen, alkyl or --A.sup.4 R.sup.5.sub.c wherein A is a single bond, alkylene or alkenylene and R.sup.5.sub.c is alkoxy; and n is 0, and pharmaceutically acceptable salts thereof. Such compounds have valuable inhibitory activity against acyl-CoA (cholesterol acyl transferase).
摘要翻译：式（I）的化合物：其中：R 1是烷基; R2a，R2b，R2c和R2d相同或不同，各自为氢，任选取代的烷基， - （C = O）-B1（其中B1为氢或烷基），硝基，-NRcRd（其中Rc为氢或烷基， Rd是烷基），羟基，保护的羟基，烷氧基，氰基，烷硫基，烷基亚磺酰基，烷基磺酰基或卤素; R3是烷基; R4是式（Ⅱ）的基团，其中A1是单键，亚烷基或亚烯基; R5a和R5b相同或不同，各自为氢，烷基或-A4R5c，其中A为单键，亚烷基或亚烯基，R5c为烷氧基; 和n为0，及其药学上可接受的盐。这些化合物对酰基辅酶A（胆固醇酰基转移酶）具有有价值的抑制活性。

14. 发明授权

US5356918A Oxazolidinone compounds and method of using the same as a vasodilator 失效
标题翻译：恶唑烷酮化合物及其用作血管扩张剂的方法
公开(公告)号：US5356918A
公开(公告)日：1994-10-18
申请号：US162675
申请日：1993-12-06
申请人： Sadao Ishihara , Fujio Saito , Takao Yoshioka , Hiroyuki Koike , Shigeki Miyake , Hiroshi Mizuno
发明人： Sadao Ishihara , Fujio Saito , Takao Yoshioka , Hiroyuki Koike , Shigeki Miyake , Hiroshi Mizuno
IPC分类号： A61K31/42 , A61K31/421 , A61K31/422 , A61K31/425 , A61K31/426 , A61K31/427 , A61K31/44 , A61P9/00 , A61P9/08 , A61P9/10 , C07D263/20 , C07D263/24 , C07D277/14 , C07D413/04 , C07D417/04
CPC分类号： C07D417/04 , C07D263/20 , C07D277/14
摘要： Compounds of formula (I): ##STR1## wherein W represents an oxygen atom and X represents a group of formula --N(R.sup.1)--; R.sup.1 is hydrogen, alkyl or aralkyl; R.sub.2 and R.sup.3 are each hydrogen, alkyl, aralkyl, aryl or aromatic heterocyclic; R.sup.4 is hydrogen, alkyl or aralkyl; and A is alkylene which is optionally substituted by carboxy; and pharmaceutically acceptable salts and esters thereof, have a valuable vasodilatory activity.
摘要翻译：式（I）化合物：其中W表示氧原子，X表示式-N（R1） - 基团; R1是氢，烷基或芳烷基; R2和R3各自为氢，烷基，芳烷基，芳基或芳族杂环; R4是氢，烷基或芳烷基; 并且A是任选被羧基取代的亚烷基; 及其药学上可接受的盐和酯具有有价值的血管舒张活性。

15. 发明授权

US4157222A Document hold-down cover for use in copying apparatus 失效
标题翻译：用于复印设备的文档压盖
公开(公告)号：US4157222A
公开(公告)日：1979-06-05
申请号：US897212
申请日：1978-04-17
申请人： Sadao Ishihara
发明人： Sadao Ishihara
IPC分类号： G03B27/62
CPC分类号： G03B27/6228
摘要： A document hold-down device in a copying apparatus includes a rectangular relatively stiff plate and a relatively stiff anchoring bar spaced from and parallel to the plate rear edge, the bar and plate being sandwiched between flexible synthetic resin sheets which envelope the bar and plate and are bonded to each other along their coinciding borders and preferrably along a hinge defining line intermediate the proximate edges of the sheet and bar. Fastening members releasably anchor the bar to the apparatus proximate the document support plate. Advantageously, to accommodate thick documents, a second bar is disposed between the anchoring bar and plate and enveloped between the flexible sheets which are bonded to each other along hinge lines along opposite sides of the second bar. A resilient sponge sheet may underlie the plate to accommodate uneven documents. A handle is provided at the plate outer edge and a device is provided for alternatively swinging the hold-down device toward open and closed positions or to retain it in an intermediate position.
摘要翻译：复印装置中的原稿压紧装置包括矩形相对刚性的板和与板后边缘间隔开并平行的相对刚性的固定杆，该杆和板夹在包围杆和板的柔性合成树脂片之间，沿着它们的重合边界彼此结合，并且优选地沿着在片材和条的近边缘之间的铰链限定线。紧固构件将杆可释放地锚定到靠近文件支撑板的装置。有利地，为了容纳厚的文件，第二条杆设置在锚定杆和板之间并且包围在沿着第二杆的相对侧的铰接线彼此结合的柔性片之间。弹性海绵片可以在板的下面以容纳不均匀的文件。手柄设置在板外缘处，并且设置有用于将压紧装置朝向打开和关闭位置交替摆动或将其保持在中间位置的装置。

16. 发明授权

US5925658A Optically active thiazolidinone derivative 失效
标题翻译：光学活性噻唑烷酮衍生物
公开(公告)号：US5925658A
公开(公告)日：1999-07-20
申请号：US923745
申请日：1997-09-02
申请人： Sadao Ishihara , Fujio Saito , Yasuo Ohhata , Shigeki Miyake , Ryosuke Yorikane , Norio Fukuda
发明人： Sadao Ishihara , Fujio Saito , Yasuo Ohhata , Shigeki Miyake , Ryosuke Yorikane , Norio Fukuda
IPC分类号： C07D277/14 , A61K31/425
CPC分类号： C07D277/14
摘要： An optically active thiazolidinone derivative having the general formula: ##STR1## wherein: R.sup.1 represents a hydrogen atom, a C.sub.1 -C.sub.4 alkyl group, a phenyl group, a substituted phenyl group (said substituent represents C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy or halogen), a phenyl-C.sub.1 -C.sub.2 alkyl group or a substituted phenyl-C.sub.3 -C.sub.2 alkyl group (the substituent of said phenyl represents C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy or halogen); R.sup.2 represents a C.sub.1 -C.sub.6 alkyl group; and n represents 1 or 2!.EffectThe optically active thiazolidinone derivative of the present invention has excellent anti-angina pectoris action and is useful as a preventive agent or a therapeutic agent for angina pectoris.
摘要翻译：具有以下通式的光学活性噻唑烷酮衍生物：其中：R1表示氢原子，C1-C4烷基，苯基，取代苯基（所述取代基表示C1-C4烷基，C1-C4烷氧基或卤素），苯基-C 1 -C 2烷基或取代的苯基-C 3 -C 2烷基（所述苯基的取代基代表C1-C4烷基，C1-C4烷氧基或卤素）; R2表示C1-C6烷基; n表示1或2]。效果本发明的光学活性噻唑烷酮衍生物具有优异的抗心绞痛作用，可用作心绞痛的预防剂或治疗剂。

17. 发明授权

US5614550A Amide and urea derivatives having anti-hypercholesteremic activity, their preparation and their therapeutic uses 失效
标题翻译：具有抗高血胆固醇活性的酰胺和尿素衍生物及其制备方法及其治疗用途
公开(公告)号：US5614550A
公开(公告)日：1997-03-25
申请号：US607821
申请日：1996-02-27
申请人： Akira Yoshida , Koza Oda , Sadao Ishihara , Fujio Saito , Hiroyuki Koike , Teiichiro Koga , Eiichi Kitazawa , Hiroshi Kogen , Ichiro Hayakawa
发明人： Akira Yoshida , Koza Oda , Sadao Ishihara , Fujio Saito , Hiroyuki Koike , Teiichiro Koga , Eiichi Kitazawa , Hiroshi Kogen , Ichiro Hayakawa
IPC分类号： A61K31/165 , A61K31/00 , A61K31/16 , A61K31/167 , A61K31/17 , A61K31/215 , A61K31/235 , A61K31/265 , A61K31/335 , A61K31/35 , A61K31/352 , A61K31/41 , A61K31/415 , A61K31/535 , A61P3/06 , A61P9/10 , A61P43/00 , C07C233/07 , C07C233/11 , C07C233/25 , C07C233/26 , C07C235/38 , C07C235/48 , C07C237/06 , C07C237/40 , C07C275/18 , C07C275/28 , C07C275/34 , C07C323/39 , C07D233/12 , C07D233/56 , C07D233/58 , C07D233/60 , C07D235/08 , C07D235/12 , C07D311/82 , C07D311/90 , C07D313/12 , C07D405/12 , C07D413/12 , C07D521/00 , C07F9/09 , C12N9/99 , A61K31/24 , C07C235/00 , C07C237/00 , C07D313/00
CPC分类号： C07D231/12 , C07C233/25 , C07C233/26 , C07C235/48 , C07D233/56 , C07D249/08 , C07D311/90 , C07D313/12 , C07D405/12
摘要： Compounds of formula (I) are provided: ##STR1## wherein: R.sup.1 represents an alkyl group; or a group of formula (II), (III), (IV) or (V): ##STR2## and wherein the groups R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are hydrogen or various organic groups; and pharmaceutically acceptable salts thereof; as well as methods for the preparation of such compounds and their use in the treatment and prophylaxis of hypercholesteremia and arteriosclerosis.
摘要翻译：提供式（I）化合物：其中：R 1表示烷基; （II），（III），（IV）或（V）的基团：其中基团R 2 ，R3，R4和R5是氢或各种有机基团; 及其药学上可接受的盐; 以及制备这些化合物的方法及其在治疗和预防高胆固醇血症和动脉硬化中的用途。

18. 发明授权

US5491167A Hexahydronaphthalene ester derivatives, their preparation and their therapeutic uses 失效
标题翻译：六氢萘酯衍生物，其制备及其治疗用途
公开(公告)号：US5491167A
公开(公告)日：1996-02-13
申请号：US189040
申请日：1994-01-31
申请人： Sadao Ishihara , Hiroshi Kogen , Teiichiro Koga , Eiichi Kitazawa , Nobufusa Serizawa
发明人： Sadao Ishihara , Hiroshi Kogen , Teiichiro Koga , Eiichi Kitazawa , Nobufusa Serizawa
IPC分类号： A61K31/19 , A61K31/015 , A61K31/121 , A61K31/215 , A61K31/22 , A61K31/275 , A61K31/365 , A61K31/366 , A61P3/06 , A61P9/00 , C07C67/08 , C07C69/03 , C07C69/708 , C07C69/712 , C07C69/73 , C07C69/734 , C07C69/736 , C07C205/34 , C07C205/35 , C07C217/84 , C07C255/54 , C07D309/30 , C07F7/18 , C12P7/40 , C12P7/62 , C12P17/06 , C12R1/465 , A61K31/75 , C07C69/013
CPC分类号： C07F7/1856 , C07C69/736 , C07D309/30 , C12P7/62 , Y02P20/55
摘要： Compounds of formula (I): ##STR1## and their salts and esters have the ability to inhibit the synthesis of cholesterol, and can thus be used for the treatment and prophylaxis of hypercholesterolemia and of various cardiac disorders.
摘要翻译：式（I）化合物：其中（I）及其盐和酯具有抑制胆固醇合成的能力，因此可用于治疗和预防高胆固醇血症和各种心脏疾病。

19. 发明授权

US5451688A Hexahydronaphthalene ester derivatives, their preparation and their therapeutic uses 失效
标题翻译：六氢萘酯衍生物，其制备及其治疗用途
公开(公告)号：US5451688A
公开(公告)日：1995-09-19
申请号：US174661
申请日：1993-12-28
申请人： Hiroshi Kogen , Sadao Ishihara , Teiichiro Koga , Eiichi Kitazawa , Nobufusa Serizawa , Kiyoshi Hamano
发明人： Hiroshi Kogen , Sadao Ishihara , Teiichiro Koga , Eiichi Kitazawa , Nobufusa Serizawa , Kiyoshi Hamano
IPC分类号： A61K31/22 , A61K31/35 , A61K31/365 , A61K31/366 , A61P3/06 , C07C69/03 , C07C69/24 , C07C69/33 , C07C69/67 , C07C69/675 , C07C69/732 , C07C69/734 , C07D309/30 , C12N9/02 , C12P7/62 , C12P17/06 , C12R1/01 , C12R1/465 , C12R1/785 , C07C69/74
CPC分类号： C07C69/33 , C07C69/675 , C07C69/732 , C07D309/30 , C12N9/0093 , C12P17/06 , C12P7/62 , Y02P20/55
摘要： Compounds of formula (I): ##STR1## [wherein R.sup.1 represents a group of formula (II) or (III): ##STR2## R.sup.2 is alkyl, alkenyl or alkynyl; R.sup.3 and R.sup.4 are each hydrogen, alkyl, alkenyl or alkynyl; R.sup.5 is hydrogen or a carboxy-protecting group; R.sup.a is hydrogen or a group of formula and --OR.sup.6 ; R.sup.6, R.sup.6a and R.sup.6b are each hydrogen, a hydroxy-protecting group, alkyl, alkanesulfonyl, halogenated alkanesulfonyl or arylsulfonyl] and their salts and esters have the ability to inhibit the synthesis of cholesterol, and can thus be used for the treatment and prophylaxis of hypercholesterolemia and of various cardiac disorders.
摘要翻译：式（I）化合物：其中R 1表示式（II）或（III）的基团：烯基或炔基; R3和R4各自为氢，烷基，烯基或炔基; R5是氢或羧基保护基; R a是氢或式-OR 6基团; R6，R6a和R6b各自为氢，羟基保护基，烷基，烷基磺酰基，卤代烷磺酰基或芳基磺酰基），其盐和酯具有抑制胆固醇合成的能力，因此可用于治疗和预防高胆固醇血症和各种心脏疾病。

20. 发明授权

US5298516A Thiazolidone compounds and method of using the same as a vasodilator 失效
标题翻译：噻唑烷酮化合物及其作为血管扩张剂使用的方法
公开(公告)号：US5298516A
公开(公告)日：1994-03-29
申请号：US856491
申请日：1992-03-24
申请人： Sadao Ishihara , Fujio Saito , Takao Yoshioka , Hiroyuki Koike , Shigeki Miyake , Hiroshi Mizuno
发明人： Sadao Ishihara , Fujio Saito , Takao Yoshioka , Hiroyuki Koike , Shigeki Miyake , Hiroshi Mizuno
IPC分类号： A61K31/42 , A61K31/421 , A61K31/422 , A61K31/425 , A61K31/426 , A61K31/427 , A61K31/44 , A61P9/00 , A61P9/08 , A61P9/10 , C07D263/20 , C07D263/24 , C07D277/14 , C07D413/04 , C07D417/04 , C07D77/14
CPC分类号： C07D417/04 , C07D263/20 , C07D277/14
摘要： Compounds of formula (I): ##STR1## wherein W represents a sulfur atom and X represents a group of formula --N(R.sup.1)--, or W represents a group of formula --N(R.sup.1)-- and X represents a sulfur atom; R.sup.1 is hydrogen, alkyl or aralkyl; R.sup.2 and R.sup.3 are each hydrogen, alkyl, aralkyl, aryl or aromatic heterocyclic; R.sup.4 is hydrogen, alkyl or aralkyl; and A is alkylene which is optionally substituted by carboxy; and pharmaceutically acceptable salts and esters thereof, have a valuable vasodilatory activity.
摘要翻译：式（I）化合物：（*化学结构*）（I）其中W表示硫原子，X表示式-N（R1） - 基团，或W表示式-N（R1） - 的基团，和 X表示硫原子; R1是氢，烷基或芳烷基; R2和R3各自为氢，烷基，芳烷基，芳基或芳族杂环; R4是氢，烷基或芳烷基; 并且A是任选被羧基取代的亚烷基; 及其药学上可接受的盐和酯具有有价值的血管舒张活性。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式