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11. 发明申请

US20070173498A1 Melanin concentrating hormone antagonist 审中-公开
标题翻译：黑色素浓缩激素拮抗剂
公开(公告)号：US20070173498A1
公开(公告)日：2007-07-26
申请号：US11224744
申请日：2005-09-12
申请人： Kaneyoshi Kato , Jun Terauchi , Masaaki Mori , Nobuhiro Suzuki , Yukio Shimomura , Shiro Takekawa , Yuji Ishihara
发明人： Kaneyoshi Kato , Jun Terauchi , Masaaki Mori , Nobuhiro Suzuki , Yukio Shimomura , Shiro Takekawa , Yuji Ishihara
IPC分类号： A61K31/538 , A61K31/4706 , A61K31/40 , A61K31/165 , A61K31/353
CPC分类号： C07D207/277 , C07C217/74 , C07C219/28 , C07C233/29 , C07C233/44 , C07C233/80 , C07C235/42 , C07C235/50 , C07C235/56 , C07C235/64 , C07C235/84 , C07C237/40 , C07C271/28 , C07C275/42 , C07C311/21 , C07C2602/10 , C07C2602/12 , C07D209/18 , C07D209/22 , C07D209/42 , C07D211/16 , C07D211/18 , C07D211/22 , C07D211/26 , C07D211/32 , C07D211/52 , C07D211/62 , C07D211/70 , C07D213/56 , C07D213/81 , C07D213/82 , C07D215/14 , C07D215/38 , C07D233/24 , C07D239/28 , C07D239/30 , C07D261/18 , C07D263/14 , C07D263/34 , C07D265/28 , C07D271/06 , C07D295/096 , C07D295/13 , C07D295/185 , C07D307/68 , C07D307/81 , C07D311/58 , C07D317/60 , C07D319/20 , C07D333/24 , C07D333/28 , C07D333/38 , C07D335/16 , C07D405/04 , C07D405/12 , C07D413/04 , C07D413/12 , C07D493/04
摘要： A melanin-concentrating hormone antagonist which comprises a compound of the formula: wherein Ar1 is a cyclic group which may have substituents; X is a spacer having a main chain of 1 to 6 atoms; Y is a bond or a spacer having a main chain of 1 to 6 atoms; Ar is a monocyclic aromatic ring which may be condensed with a 4 to 8 membered non-aromatic ring, and may have further substituents; R1 and R2 are independently hydrogen atom or a hydrocarbon group which may have substituents; R1 and R2, together with the adjacent nitrogen atom, may form a nitrogen-containing hetero ring which may have substituents; R2 may form a spiro ring together with Ar; or R2, together with the adjacent nitrogen atom and Y, may form a nitrogen-containing hetero ring which may have substituents; or a salt thereof; which is useful as an agent for preventing or treating obesity, etc.
摘要翻译：一种黑色素浓缩激素拮抗剂，其包含下式化合物：其中Ar 1是可以具有取代基的环状基团; X是具有1至6个原子的主链的间隔物; Y是具有1至6个原子的主链的键或间隔基; Ar是可以与4至8元非芳族环稠合的单环芳环，并且可以具有其它取代基; R 1和R 2独立地是氢原子或可以具有取代基的烃基; R 1和R 2与相邻的氮原子一起可以形成可以具有取代基的含氮杂环; R 2可以与Ar一起形成螺环; 或R 2连同相邻的氮原子和Y可以形成可具有取代基的含氮杂环; 或其盐; 其可用作预防或治疗肥胖症等的药剂。

12. 发明授权

US07183415B2 Quinoline compound 失效
标题翻译：喹啉化合物
公开(公告)号：US07183415B2
公开(公告)日：2007-02-27
申请号：US10493427
申请日：2002-10-24
申请人： Yuji Ishihara , Makoto Kamata , Shiro Takekawa , Nobuhiro Suzuki , Koki Kato
发明人： Yuji Ishihara , Makoto Kamata , Shiro Takekawa , Nobuhiro Suzuki , Koki Kato
IPC分类号： C07D215/38 , C07D215/14
CPC分类号： C07D401/06 , A61K31/47 , A61K31/4709 , A61K31/496 , A61K31/5377 , A61K31/55 , C07D215/38 , C07D401/12 , C07D405/12 , C07D409/12 , C07D471/04
摘要： A compound, which has a melanin-concentrating hormone antagonistic action and useful as an agent for preventing or treating obesity, and which is represented by the formula: wherein Ar is a cyclic group optionally having substituent(s); X is a bond or a spacer having a main chain of 1 to 6 atoms; R1 and R2 are the same or different and each is a hydrogen atom or a hydrocarbon group optionally having substituent(s), or R1 and R2 may form, together with the adjacent nitrogen atom, a nitrogen-containing heterocycle optionally having substituent(s); Y is a divalent hydrocarbon group optionally having substituent(s) (except CO); R3 is a hydrogen atom or a hydrocarbon group optionally having substituent(s); and ring A and ring B may further have substituents, and when ring B further has a substituent, the substituent may be linked to R1 to form a ring, or a salt thereof, or a prodrug thereof, is provided.
摘要翻译：一种化合物，其具有黑色素浓集激素拮抗作用并且可用作预防或治疗肥胖症的药剂，并且其由下式表示：其中Ar是任选具有取代基的环状基团; X是具有1至6个原子的主链的键或间隔基; R 1和R 2相同或不同，各自为氢原子或任选具有取代基的烃基，或R 1〜 >和R 2可以与相邻的氮原子一起形成任选具有取代基的含氮杂环; Y是任选具有取代基（CO除外）的二价烃基; R 3是氢原子或任选具有取代基的烃基; 并且环A和环B可以进一步具有取代基，并且当环B还具有取代基时，取代基可以与R 1连接形成环，或其盐或其前药，被提供。

13. 发明申请

US20050222174A1 Thienopyrimidines, process for preparing the same and use thereof 有权
标题翻译：噻吩并嘧啶，其制备方法及其用途
公开(公告)号：US20050222174A1
公开(公告)日：2005-10-06
申请号：US10502903
申请日：2003-01-29
申请人： Shuichi Furuya , Takashi Imada , Takenori Hitaka , Kazuhiro Miwa , Masami Kusaka , Nobuhiro Suzuki
发明人： Shuichi Furuya , Takashi Imada , Takenori Hitaka , Kazuhiro Miwa , Masami Kusaka , Nobuhiro Suzuki
IPC分类号： A61P5/08 , A61P5/24 , A61P13/08 , A61P15/00 , A61P15/08 , A61P17/10 , A61P17/14 , A61P25/28 , A61P35/00 , A61P35/04 , A61P43/00 , C07D495/04 , A61K31/519 , C07D498/02
CPC分类号： C07D495/04
摘要： The present invention provides a thienopyrimidine compound, represented by the formula [wherein, R1 is C1-4 alkyl, R2 is (1) phenyl optionally having a substituent such as amino, mono C1-4 alkylamino and di C1-4 alkylamino, or (2) a heterocyclic group optionally having a substituent such as amino, mono C1-4 alkylamino and di C1-4 alkylamino and the like, R3 is a hydrogen atom or C1-4 alkyl, R4 is C1-4 alkyl optionally having a substituent such as C1-4 alkoxy-carbonyl, carboxyl, mono C1-4 alkylamino and N—C1-4 alkyl-N—C7-10 aralkylamino and the like] or a salt thereof, which has antagonistic action for gonadotropin-releasing hormone.
摘要翻译：本发明提供由式[其中R 1为C 1-4烷基，R 2为（1）表示的噻吩并嘧啶化合物为（1 ）任选具有取代基的苯基，例如氨基，单C 1-4烷基氨基和二-C 1-4烷基氨基，或（2）任选具有取代基的杂环基作为氨基，单C 1-4烷基氨基和二C 1-4烷基氨基等，R 3是氢原子或C < C 1-4烷基，R 4是任选具有取代基的C 1-4烷基，例如C 1-4烷基，烷氧基羰基，羧基，单C 1-4烷基氨基和NC 1-4烷基-NC 7-10芳烷基氨基等]或其盐对促性腺激素释放激素具有拮抗作用。

14. 发明申请

US20050009313A1 Manufacturing method for semiconductor device 审中-公开
标题翻译：半导体器件的制造方法
公开(公告)号：US20050009313A1
公开(公告)日：2005-01-13
申请号：US10861337
申请日：2004-06-04
申请人： Nobuhiro Suzuki , Kenji Imai
发明人： Nobuhiro Suzuki , Kenji Imai
IPC分类号： H01L23/52 , H01L21/00 , H01L21/301 , H01L21/3205 , H01L21/44 , H01L21/46 , H01L21/70 , H01L21/768 , H01L21/78 , H01L23/12 , H01L23/31 , H01L23/485
CPC分类号： H01L24/10 , H01L21/76898 , H01L23/3114 , H01L24/13 , H01L2224/05001 , H01L2224/05008 , H01L2224/05024 , H01L2224/05124 , H01L2224/05139 , H01L2224/05144 , H01L2224/05147 , H01L2224/05155 , H01L2224/05166 , H01L2224/05181 , H01L2224/05184 , H01L2224/05548 , H01L2224/05569 , H01L2224/05624 , H01L2224/05639 , H01L2224/05644 , H01L2224/05647 , H01L2224/05655 , H01L2224/05666 , H01L2224/05681 , H01L2224/05684 , H01L2224/13 , H01L2224/13099 , H01L2924/01004 , H01L2924/01006 , H01L2924/01013 , H01L2924/01022 , H01L2924/01023 , H01L2924/01029 , H01L2924/01033 , H01L2924/01047 , H01L2924/01073 , H01L2924/01074 , H01L2924/01079 , H01L2924/014 , H01L2924/09701 , H01L2924/10329 , H01L2924/14 , H01L2924/00 , H01L2924/00014
摘要： An internal wire is formed via an oxide film on the front surface of a semiconductor substrate so as to extend toward the boundary relative to an adjacent integrated circuit region. An upper supporting base is fixedly formed on the front surface of the semiconductor substrate by means of a resin layer of epoxy adhesive or the like, and a lower supporting base is fixedly formed on the back surface of the semiconductor substrate by means of a resin layer of epoxy adhesive or the like, whereby a laminated body is formed. The resin layer and the internal wire are partially removed, leaving a portion of the laminated body, to thereby form an inverted-V shaped groove (a cut-off groove) where a part of the internal wire is exposed to the outside. Thereafter, the resulting cut-off groove is exposed to plasma atmosphere to thereby dissolve, and thus remove, any remaining resin fragments attached to the exposed end portion of the internal wire.
摘要翻译：通过半导体衬底的前表面上的氧化膜形成内部线，以便相对于相邻的集成电路区域向边界延伸。通过环氧树脂粘合剂等的树脂层在半导体基板的前表面上固定地形成上支撑基座，并且通过树脂层固定地形成在半导体基板的背面上的下支撑基底的环氧树脂粘合剂等，由此形成层压体。部分地除去树脂层和内部线，留下层叠体的一部分，从而形成内部线的一部分暴露于外部的倒V形槽（切断槽）。此后，将所得到的切断槽暴露于等离子体气氛中，从而溶解，从而除去附着在内部导线的露出端部的剩余树脂碎片。

15. 发明授权

US06661030B2 Semiconductor light emitting device including a fluorescent material 有权
公开(公告)号：US06661030B2
公开(公告)日：2003-12-09
申请号：US10002467
申请日：2001-10-23
申请人： Satoshi Komoto , Koichi Nitta , Nobuhiro Suzuki , Kuniaki Konno , Hideto Sugawara , Chisato Furukawa
发明人： Satoshi Komoto , Koichi Nitta , Nobuhiro Suzuki , Kuniaki Konno , Hideto Sugawara , Chisato Furukawa
IPC分类号： H01L3300
CPC分类号： H01L33/508 , F21Y2101/00 , H01L33/40 , H01L33/507 , H01L2224/32245 , H01L2224/48091 , H01L2224/48247 , H01L2224/48257 , H01L2224/48465 , H01L2224/49107 , H01L2224/73265 , H01L2224/8592 , H01L2924/181 , H01L2924/00014 , H01L2924/00 , H01L2924/00012
摘要： A light emitting device or image display includes a fluorescent material as a wavelength converter for converting a wavelength into another. The fluorescent material is disposed in a predetermined positional relation, to prevent external leakage of primary light and to extract secondary light made by wavelength-converting the primary light with a very high efficiency. By using a semiconductor light emitting element for ultraviolet emission and combining it with a fluorescent material or any other appropriate material having a wavelength converting function, various kinds of applications, such as illuminator, having a remarkably long-life light source can be made. The semiconductor light emitting element preferably has a emission wavelength near 330 nm, and preferably uses BGaN in its light emitting layer.

16. 外观设计

USD452983S1 Baseball glove 失效
标题翻译：棒球手套
公开(公告)号：USD452983S1
公开(公告)日：2002-01-15
申请号：US29126905
申请日：2000-07-26
申请人： Soichi Fujimoto , Shigeki Kuroda , Nobuhiro Suzuki
设计人： Soichi Fujimoto , Shigeki Kuroda , Nobuhiro Suzuki

17. 发明授权

US06329388B2 Thienopyridine compounds, their production and use 失效
标题翻译：噻吩并吡啶化合物，其生产和使用
公开(公告)号：US06329388B2
公开(公告)日：2001-12-11
申请号：US09736641
申请日：2000-12-14
申请人： Shuichi Furuya , Nobuo Choh , Nobuhiro Suzuki , Takashi Imada
发明人： Shuichi Furuya , Nobuo Choh , Nobuhiro Suzuki , Takashi Imada
IPC分类号： A61K31435
CPC分类号： C07D495/04
摘要： The compounds of the present invention possess excellent gonadotropin-releasing hormone antagonizing activity, and is useful for preventing or treating sex hormone-dependent diseases, e.g., sex hormone-dependent cancers (e.g., prostatic cancer, uterine cancer, breast cancer, pituitary tumor), prostatic hypertrophy, hysteromyoma, endometriosis, precocious puberty, amenorrhea syndrome, multilocular ovary syndrome, pimples etc, or as a pregnancy regulator (e.g., contraceptive), infertility remedy or menstruation regulator.
摘要翻译：本发明的化合物具有优异的促性腺激素释放激素拮抗活性，并且可用于预防或治疗性激素依赖性疾病，例如性激素依赖性癌症（例如前列腺癌，子宫癌，乳腺癌，垂体瘤），前列腺肥大，子宫肌瘤，子宫内膜异位症，早熟青春期，闭经综合征，多腔卵巢综合征，丘疹等，或作为妊娠调节剂（如避孕药），不育补救或月经调节剂。

18. 发明授权

US06297379B1 Thienopyrimidine compounds, their production and use 失效
标题翻译：噻吩并嘧啶化合物，其生产和使用
公开(公告)号：US06297379B1
公开(公告)日：2001-10-02
申请号：US09530495
申请日：2000-04-26
申请人： Shuichi Furuya , Nobuhiro Suzuki , Nobuo Choh , Yoshi Nara
发明人： Shuichi Furuya , Nobuhiro Suzuki , Nobuo Choh , Yoshi Nara
IPC分类号： C07D49504
CPC分类号： C07D495/04
摘要： A compound of formula (I) wherein R1 and R2 each is hydrogen, hydroxy, C1-4 alkoxy, C1-4 alkoxy-carbonyl or C1-4 alkyl which may be substituted; R3 is hydrogen, halogen, hydroxy or C1-4 alkoxy which may be substituted; or adjacent two R3 may form C1-4 alkylenedioxy; R4 is hydrogen or C1-4 alkyl; R6 is C1-4 alkyl which may be substituted or a group of the formula (A) wherein R5 is hydrogen of R4 and R5 may form heterocycle; and n is 0-5, or a salt thereof, has an excellent GnRH-antagonizing activity, and is useful for preventing or treating sex hormone-dependent diseases.
摘要翻译：其中R 1和R 2各自为氢，羟基，C 1-4烷氧基，C 1-4烷氧基 - 羰基或可被取代的C 1-4烷基的式（I）化合物; R3是氢，卤素，羟基或可被取代的C1-4烷氧基; 或相邻的两个R 3可以形成C 1-4亚烷基二氧基; R4是氢或C1-4烷基; R 6是可以被取代的C 1-4烷基或式（A）的基团，其中R 5是氢的R 4和R 5可以形成杂环; n为0-5或其盐具有优异的GnRH拮抗活性，可用于预防或治疗性激素依赖性疾病。

19. 发明授权

US06262267B1 Thienopyridine compound 失效
标题翻译：噻吩并吡啶化合物
公开(公告)号：US06262267B1
公开(公告)日：2001-07-17
申请号：US09402206
申请日：1999-09-30
申请人： Shuichi Furuya , Nobuo Choh , Nobuhiro Suzuki , Takashi Imada
发明人： Shuichi Furuya , Nobuo Choh , Nobuhiro Suzuki , Takashi Imada
IPC分类号： C07D47104
CPC分类号： C07D495/04
摘要： The compound of the present invention possesses excellent gonadotropin-releasing hormone antagonizing activity, and is useful for preventing or treating sex hormone-dependent diseases, e,g., sex hormone-dependent cancers (e.g., prostatic cancer, uterine cancer, breast cancer, pituitary tumor), prostatic hypertrophy, hysteromyoma, endometriosis, precocious puberty, amenorrhea sydrome, multilocular ovary sydrome, pimples etc, or as a pregnancy regulator (e.g., contraceptive), infertility remedy or menstruation regulator.
摘要翻译：本发明的化合物具有优异的促性腺激素释放激素拮抗活性，并且可用于预防或治疗性激素依赖性疾病，例如性激素依赖性癌症（例如，前列腺癌，子宫癌，乳腺癌，垂体肿瘤），前列腺肥大，子宫肌瘤，子宫内膜异位症，早熟青春期，闭经症状，多腔卵巢综合征，丘疹等，或作为妊娠调节者（如避孕药），不育补救或月经调节剂。

20. 发明授权

US5210725A Tray loading apparatus for disc players 失效
标题翻译：托盘装载装置
公开(公告)号：US5210725A
公开(公告)日：1993-05-11
申请号：US817077
申请日：1992-01-06
申请人： Masao Kase , Ryo Matsuura , Nobuhiro Suzuki
发明人： Masao Kase , Ryo Matsuura , Nobuhiro Suzuki
IPC分类号： G11B15/675 , G11B17/04 , G11B19/12
CPC分类号： G11B17/0565 , G11B15/675 , G11B19/12
摘要： A control circuit of a tray loading apparatus determines, according to a disc size and a tray moving direction, a time during which to control the motor at a constant speed. When the specified time has elapsed after the motor was started, the control circuit produces a pulse-width modulated output to slowly lower the motor speed, eliminating impact noise when the tray strikes a stopper. This motor deceleration time is measured. When the measured deceleration time disagrees with a preset or previously detected target deceleration time, the difference is either added to or subtracted from a constant-speed motor operation time and the resultant value is taken as the next target time for constant-speed motor operation. In this way, by changing the time during which the motor is driven at a constant speed, any variations in the tray moving speed as might occur from varying loads on the motor are absorbed to keep the motor deceleration time and decelerating speed unchanged, thus making the tray motion smooth.
摘要翻译：托盘装载装置的控制电路根据盘尺寸和托盘移动方向确定以恒定速度控制马达的时间。当电机启动后经过指定时间后，控制电路产生脉冲宽度调制输出，以缓慢降低电机转速，消除托盘撞击停止时的冲击噪音。测量该电机减速时间。当所测量的减速时间与预设或先前检测到的目标减速时间不一致时，将该差加到或从一个恒定速度的马达运行时间中减去，并将该结果值作为恒速马达操作的下一个目标时间。以这种方式，通过改变电机以恒定速度驱动的时间，吸收马达上的负载变化所引起的托盘运动速度的任何变化，以保持马达减速时间和减速速度不变，从而使托盘运动顺畅。

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