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1. 发明授权

US07984791B2 Oil discharge structure of baffle plate 有权
标题翻译：挡板排油结构
公开(公告)号：US07984791B2
公开(公告)日：2011-07-26
申请号：US11223351
申请日：2005-09-09
申请人： Hiromi Taguchi , Hitoshi Suzuki , Katsuyoshi Nakajima
发明人： Hiromi Taguchi , Hitoshi Suzuki , Katsuyoshi Nakajima
IPC分类号： F16H57/04
CPC分类号： F16H57/0483 , F16H57/0423 , Y10T74/19991 , Y10T74/2188
摘要： An oil discharge structure of a baffle plate for discharging oil from a space of a gear side to a space of a transmission side with a space-saving design is provided. A slit is formed in a side face plate facing a final gear of a case side baffle plate to discharge the oil from an oil volume X in the circumference of the final gear to an oil volume Y stored in a clearance between the case side baffle plate and the transmission case, and in a clearance between the housing side baffle plate and the housing. This provides a compact structure that is not larger in a radial direction of the final gear and discharges the oil in the oil volume X.
摘要翻译：提供了一种用于将节气门设计从齿轮侧的空间排出到传动侧的空间的挡板的排油结构。在面向壳体侧挡板的最终齿轮的侧面板上形成狭缝，以将油从最终齿轮的圆周中的油量X排出到储存在壳体侧挡板之间的间隙中的油量Y 和变速器壳体，以及壳体侧挡板和壳体之间的间隙。这提供了在最终齿轮的径向方向上不大并且排出油体积X中的油的紧凑结构。

2. 发明申请

US20060048600A1 Oil discharge structure of baffle plate 有权
标题翻译：挡板排油结构
公开(公告)号：US20060048600A1
公开(公告)日：2006-03-09
申请号：US11223351
申请日：2005-09-09
申请人： Hiromi Taguchi , Hitoshi Suzuki , Katsuyoshi Nakajima
发明人： Hiromi Taguchi , Hitoshi Suzuki , Katsuyoshi Nakajima
IPC分类号： F16H57/02
CPC分类号： F16H57/0483 , F16H57/0423 , Y10T74/19991 , Y10T74/2188
摘要： An oil discharge structure of a baffle plate for discharging oil from a space of a gear side to a space of a transmission side with a space-saving design is provided. A slit is formed in a side face plate facing a final gear of a case side baffle plate to discharge the oil from an oil volume X in the circumference of the final gear to an oil volume Y stored in a clearance between the case side baffle plate and the transmission case, and in a clearance between the housing side baffle plate and the housing. This provides a compact structure that is not larger in a radial direction of the final gear and discharges the oil in the oil volume X.
摘要翻译：提供了一种用于将节气门设计从齿轮侧的空间排出到传动侧的空间的挡板的排油结构。在面向壳体侧挡板的最终齿轮的侧面板上形成狭缝，以将油从最终齿轮的圆周中的油量X排出到储存在壳体侧挡板之间的间隙中的油量Y 和变速器壳体，以及壳体侧挡板和壳体之间的间隙。这提供了在最终齿轮的径向方向上不大并且排出油体积X中的油的紧凑结构。

3. 发明申请

US20130029964A1 [5, 6] HETEROCYCLIC COMPOUND 审中-公开
标题翻译： [5,6]杂环化合物
公开(公告)号：US20130029964A1
公开(公告)日：2013-01-31
申请号：US13595608
申请日：2012-08-27
申请人： Kazumasa Aoki , Satoshi Matsui , Kenji Yoshikawa , Hiroki Shimizu , Junko Sasaki , Katsuyoshi Nakajima , Osamu Kanno , Kiyoshi Oizumi
发明人： Kazumasa Aoki , Satoshi Matsui , Kenji Yoshikawa , Hiroki Shimizu , Junko Sasaki , Katsuyoshi Nakajima , Osamu Kanno , Kiyoshi Oizumi
IPC分类号： A61K31/4184 , C07D471/04 , A61K31/437 , C07D235/14 , C07D401/10 , C07D413/10 , A61K31/5377 , C07D405/12 , C07D491/056 , A61K31/4188 , C07D403/10 , A61K31/496 , A61K31/506 , A61K31/454 , A61K31/4439 , A61P19/08 , A61P19/10 , C07D235/12
CPC分类号： C07D235/06 , A61K31/4184 , A61K31/4188 , A61K31/437 , A61K31/4439 , A61K31/454 , A61K31/496 , A61K31/506 , A61K31/5377 , C07D401/04 , C07D403/04 , C07D405/12 , C07D405/14 , C07D417/04 , C07D471/04 , C07D491/056
摘要： An object of the present invention is to provide a novel low molecular weight compound exhibiting an osteogenesis-promoting action. This object is achieved by a compound having the general formula (I) or a pharmacologically acceptable salt thereof. In the general formula (I), R1 and R2 represent hydrogen atoms, and the like; R3 represents a hydrogen atom, and the like; X, Y, and Z represent nitrogen atoms, and the like; A represents a phenylene group, and the like; n represents 1 or 2, and the like; and V and W represent oxygen atoms, and the like.
摘要翻译：本发明的目的是提供一种表现出成骨促进作用的新型低分子量化合物。该目的通过具有通式（I）的化合物或其药理学上可接受的盐来实现。在通式（I）中，R 1和R 2表示氢原子等; R3表示氢原子等; X，Y和Z表示氮原子等; A表示亚苯基等; n表示1或2，等等; V和W表示氧原子等。

4. 发明授权

US6159967A Heterocyclic compounds having tachykinin receptor antagonist activity their preparation and their use 失效
标题翻译：具有速激肽受体拮抗剂活性的杂环化合物的制备及其用途
公开(公告)号：US6159967A
公开(公告)日：2000-12-12
申请号：US758421
申请日：1996-12-02
申请人： Takahide Nishi , Koki Ishibashi , Katsuyoshi Nakajima , Tetsuya Fukazawa , Hitoshi Kurata , Takeshi Yamaguchi , Kazuhiro Ito
发明人： Takahide Nishi , Koki Ishibashi , Katsuyoshi Nakajima , Tetsuya Fukazawa , Hitoshi Kurata , Takeshi Yamaguchi , Kazuhiro Ito
IPC分类号： A61K31/44 , A61K31/4523 , A61K31/4709 , A61K31/495 , A61K31/535 , A61K31/5377 , A61K31/55 , A61K31/553 , A61P17/00 , A61P19/00 , A61P25/00 , C07D263/04 , C07D413/06 , C07D413/14 , C07D417/06 , C07D471/10 , C07D487/10 , C07D491/10 , C07D495/10 , C07D498/10 , C07D265/00 , C07D265/30 , C07D295/00
CPC分类号： C07D263/04 , C07D413/06 , C07D413/14 , C07D471/10 , C07D491/10 , C07D495/10
摘要： Compounds of the formula and quaternary ammonium ions thereof, wherein R.sup.1 and R.sup.2 are the same or different and are carbocyclic aryl or aromatic heterocyclic; A is methylene, carbonyl or sulfonyl; B is a single bond, C.sub.1 -C.sub.4 alkylene or C.sub.2 -C.sub.4, alkenylene; D is oxygen; E is C.sub.2 alkylene; G is C.sub.1 -C.sub.4 alkylene or C.sub.2 -C.sub.4 alkenylene; and L is --C(R.sup.4)(R.sup.5), wherein R.sup.4 and R.sup.5 together with the carbon atom to which they are attached represent a C.sub.5 -C.sub.10 cycloalkyl or a C.sub.5 -C.sub.10 heterocyclic. Especially preferred are compounds wherein L represents ##STR1## wherein J is a C.sub.1 -C.sub.6 alkylene; Ar is a ring carbocyclic or aromatic heterocyclic and S*.fwdarw.O is a sulfoxide in which the sulfur atom is in the 5-configuration. The compounds have tachykinin receptor antagonist activity and exhibit an activity against both the NK.sub.1 and NK.sub.2 receptors.
摘要翻译：式及其季铵离子的化合物，其中R 1和R 2相同或不同，为碳环芳基或芳族杂环; A是亚甲基，羰基或磺酰基; B是单键，C 1 -C 4亚烷基或C 2 -C 4亚烯基; D是氧; E为C2亚烷基; G是C 1 -C 4亚烷基或C 2 -C 4亚烯基; 并且L是-C（R 4）（R 5），其中R 4和R 5与它们所连接的碳原子一起代表C5-C10环烷基或C5-C10杂环。特别优选的是其中L表示其中J为C1-C6亚烷基的化合物; Ar是环碳环或芳族杂环，并且S * - > O是其中硫原子为5构型的亚砜。该化合物具有速激肽受体拮抗剂活性，并表现出对NK1和NK2受体的活性。

5. 发明申请

US20110269746A1 CYCLIC COMPOUND HAVING HETERO ATOM 失效
标题翻译：具有异位原子的环状化合物
公开(公告)号：US20110269746A1
公开(公告)日：2011-11-03
申请号：US13182777
申请日：2011-07-14
申请人： Osamu Kanno , Katsuyoshi Nakajima , Kazumasa Aoki , Ryoichi Tanaka , Shimpei Hirano , Kiyoshi Oizumi , Daigo Asano
发明人： Osamu Kanno , Katsuyoshi Nakajima , Kazumasa Aoki , Ryoichi Tanaka , Shimpei Hirano , Kiyoshi Oizumi , Daigo Asano
IPC分类号： A61K31/55 , A61K31/5377 , A61K31/496 , A61K31/4375 , A61K31/4725 , A61P19/00 , C07D413/14 , C07D413/04 , C07D471/04 , A61P19/10 , C07D405/14 , C07D401/14 , A61K31/5513 , C07D401/04
CPC分类号： C07D217/22 , C07D217/24 , C07D401/04 , C07D401/12 , C07D405/14 , C07D413/04 , C07D413/12 , C07D417/12 , C07D471/04
摘要： Compounds exhibiting an osteogenesis-promoting action having the general formula (I) or a pharmacologically acceptable salt thereof: wherein A is selected from among a 3- to 10-membered heterocyclyl group, B is selected from among an amino group, and X is selected from N and CH.
摘要翻译：表现出具有通式（I）的成骨促进作用的化合物或其药理学上可接受的盐：其中A选自3-至10-元杂环基，B选自氨基，X选自来自N和CH。

6. 发明授权

US06511975B1 Spiropiperidine derivatives 失效
标题翻译：螺哌啶衍生物
公开(公告)号：US06511975B1
公开(公告)日：2003-01-28
申请号：US09616092
申请日：2000-07-13
申请人： Takahide Nishi , Takeshi Yamaguchi , Yukiko Iio , Toshiyasu Takemoto , Katsuyoshi Nakajima
发明人： Takahide Nishi , Takeshi Yamaguchi , Yukiko Iio , Toshiyasu Takemoto , Katsuyoshi Nakajima
IPC分类号： C07D41306
CPC分类号： C07D413/06
摘要： A compound of the formula (I) wherein R1 and R2 is a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group. A is CH2, CO or SO2. B is a single bond, alkylene or alkenylene. D is O or S. E is alkylene or alkenylene. wherein G is a substituted or unsubstituted cycloalkene ring, or a substituted cycloalkane ring. Ar is a substituted or unsubstituted aryl ring, or a substituted or unsubstituted heteroaryl ring. R3 is alkyl. n is 1-3. The invention includes a pharmacologically acceptable salt, ester or other derivative of a compound of the formula (I). The invention also provides pharmaceutical compositions and methods of treating specified diseases utilizing a compound of formula (I).
摘要翻译：式（I）的化合物，其中R 1和R 2是取代或未取代的芳基，或取代或未取代的杂芳基。 A是CH 2，CO或SO 2。 B是单键，亚烷基或亚烯基。 D是O或S.E是亚烷基或亚烯基，其中G是取代或未取代的环烯烃环或取代的环烷烃环。 Ar是取代或未取代的芳基环，或取代或未取代的杂芳基环。 R3是烷基。 n为1-3。本发明包括式（I）化合物的药学上可接受的盐，酯或其它衍生物。本发明还提供了利用式（I）化合物治疗特定疾病的药物组合物和方法。

7. 发明授权

US06448247B1 Method for treating an inflammatory disease 失效
标题翻译：治疗炎性疾病的方法
公开(公告)号：US06448247B1
公开(公告)日：2002-09-10
申请号：US09533061
申请日：2000-03-22
申请人： Takahide Nishi , Koki Ishibashi , Katsuyoshi Nakajima , Tetsuya Fukazawa , Hitoshi Kurata , Takeshi Yamaguchi , Kazuhiro Ito
发明人： Takahide Nishi , Koki Ishibashi , Katsuyoshi Nakajima , Tetsuya Fukazawa , Hitoshi Kurata , Takeshi Yamaguchi , Kazuhiro Ito
IPC分类号： A61K315375
CPC分类号： C07D263/04 , C07D413/06 , C07D413/14 , C07D471/10 , C07D491/10 , C07D495/10
摘要： Compounds of the formula and quaternary ammonium ions thereof, wherein R1 and R2 are the same or different and are carbocyclic aryl or aromatic heterocyclic; A is methylene, carbonyl or sulfonyl; B is a single bond, C1-C4 alkylene or C2-C4 alkenylene; D is oxygen or sulfur; E is C2-C6 alkylene, C1-C6 haloalkylene, C3-C6 cycloalkane-1,1-diyl or C3-C6-cycloalkane-1,1-diylmethyl; G is C1-C4 alkylene or C2-C4 alkenylene; and L is —NR3 or —C(R4)(R5), wherein R3 is a carbocyclic aryl or an aromatic heterocyclic; R4 is hydrogen, carbocyclic aryl or aromatic heterocyclic; R5 is —COR6, C1-C6 alkyl, C1-C6 alkoxy, amino, or acylamino, wherein R6 is C1-C6 alkyl or C1-C6 alkoxy, or R4 and R5 together with the carbon atom to which they are attached represent a C5-C10 cycloalkyl or a C5-C10 heterocyclic. The compounds have tachykinin receptor antagonist activity and exhibit an activity against both the NK1 and NK2 receptors.
摘要翻译：其中式和季铵离子的化合物，其中R 1和R 2相同或不同，为碳环芳基或芳族杂环; A是亚甲基，羰基或磺酰基; B是单键，C1-C4亚烷基或C2-C4亚烯基; D是氧或硫; E为C2-C6亚烷基，C1-C6卤代亚烷基，C3-C6环烷烃-1,1-二基或C3-C6-环烷烃-1,1-二基甲基; G是C 1 -C 4亚烷基或C 2 -C 4亚烯基; 并且L是-NR 3或-C（R 4）（R 5），其中R 3是碳环芳基或芳族杂环; R4是氢，碳环芳基或芳族杂环; R 5是-COR 6，C 1 -C 6烷基，C 1 -C 6烷氧基，氨基或酰氨基，其中R 6是C 1 -C 6烷基或C 1 -C 6烷氧基，或者R 4和R 5与它们所连接的碳原子一起代表C5 -C 10环烷基或C 5 -C 10杂环。该化合物具有速激肽受体拮抗剂活性，并表现出对NK1和NK2受体的活性。

8. 发明申请

US20120040936A1 CYCLIC COMPOUND HAVING SUBSTITUTED PHENYL GROUP 失效
标题翻译：具有取代的苯基的环化合物
公开(公告)号：US20120040936A1
公开(公告)日：2012-02-16
申请号：US13253792
申请日：2011-10-05
申请人： Osamu Kanno , Katsuyoshi Nakajima , Kazumasa Aoki , Ryoichi Tanaka , Shimpei Hirano , Kiyoshi Oizumi , Satoru Naito
发明人： Osamu Kanno , Katsuyoshi Nakajima , Kazumasa Aoki , Ryoichi Tanaka , Shimpei Hirano , Kiyoshi Oizumi , Satoru Naito
IPC分类号： A61K31/675 , A61K31/496 , A61K31/4375 , A61K31/4725 , A61K31/472 , A61P19/08 , C07D401/12 , C07F9/06 , C07D471/04 , C07D401/10 , C07D217/04 , A61P19/10 , A61K31/5377 , C07D413/12
CPC分类号： C07D217/14 , C07D217/16 , C07D401/04 , C07D401/10 , C07D405/12 , C07D417/04 , C07D471/04
摘要： Low molecular weight compound exhibiting an osteogenesis-promoting action having the general formula (I) or a pharmacologically acceptable salt thereof:
摘要翻译：表现出具有通式（I）的成骨促进作用的低分子量化合物或其药理学上可接受的盐：

9. 发明授权

US6166721A Mouse as computer input device having additional mechanism for controlling additional function such as scrolling 失效
标题翻译：鼠标作为具有用于控制诸如滚动的附加功能的附加机构的计算机输入设备
公开(公告)号：US6166721A
公开(公告)日：2000-12-26
申请号：US122521
申请日：1998-07-24
申请人： Kouichi Kuroiwa , Katsuyoshi Nakajima , Hiroshi Fujikake
发明人： Kouichi Kuroiwa , Katsuyoshi Nakajima , Hiroshi Fujikake
IPC分类号： G06F3/0354 , G09G5/08
CPC分类号： G06F3/03543 , G06F2203/0333
摘要： In a mouse having two click switches with buttons, a motion detector and an additional control switch mechanism for a function of scrolling are provided. The additional control switch mechanism includes a first, a second, and a third switch for producing an up-scroll signal, a down-scroll signal, and a scroll mode selection signal, respectively when being actuated. A single actuator rod having a top push button is disposed to be able to incline opposite directions to selectively actuate the first and second switches and to be pushed down to actuate the third switch. The top push button is disposed between the click switch buttons. Alternatively, the third switch with a push button thereof is disposed at a sidewall of the mouse. In another arrangement, the third switch and the push button thereof are disposed between the two click switch mechanisms, and the first switch a push button thereof and the second switch with a push button thereof are disposed in a sidewall of the mouse.
摘要翻译：在具有按钮的两个点击开关的鼠标中，提供了用于滚动功能的运动检测器和附加控制开关机构。附加的控制开关机构包括分别在被致动时产生上滚信号，下滚信号和滚动模式选择信号的第一开关，第二开关和第三开关。具有顶部按钮的单个致动器杆被设置成能够倾斜相反的方向以选择性地致动第一和第二开关并被向下推动以致动第三开关。顶部按钮设置在点击开关按钮之间。或者，具有按钮的第三开关设置在鼠标的侧壁。在另一种布置中，第三开关及其按钮设置在两个点击开关机构之间，并且第一开关及其按钮及其按钮的第二开关设置在鼠标的侧壁中。

10. 发明授权

US08685981B2 Cyclic compound having hetero atom 失效
标题翻译：具有杂原子的环状化合物
公开(公告)号：US08685981B2
公开(公告)日：2014-04-01
申请号：US13182777
申请日：2011-07-14
申请人： Osamu Kanno , Katsuyoshi Nakajima , Kazumasa Aoki , Ryoichi Tanaka , Shimpei Hirano , Kiyoshi Oizumi , Daigo Asano
发明人： Osamu Kanno , Katsuyoshi Nakajima , Kazumasa Aoki , Ryoichi Tanaka , Shimpei Hirano , Kiyoshi Oizumi , Daigo Asano
IPC分类号： A61K31/497
CPC分类号： C07D217/22 , C07D217/24 , C07D401/04 , C07D401/12 , C07D405/14 , C07D413/04 , C07D413/12 , C07D417/12 , C07D471/04
摘要： Compounds exhibiting an osteogenesis-promoting action having the general formula (I) or a pharmacologically acceptable salt thereof: wherein A is selected from among a 3- to 10-membered heterocyclyl group, B is selected from among an amino group, and X is selected from N and CH.
摘要翻译：表现出具有通式（I）的成骨促进作用的化合物或其药理学上可接受的盐：其中A选自3-至10-元杂环基，B选自氨基，X选自来自N和CH。

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