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1. 发明申请

US20070192434A1 Network system, terminal, and gateway 有权
标题翻译：网络系统，终端和网关
公开(公告)号：US20070192434A1
公开(公告)日：2007-08-16
申请号：US11451126
申请日：2006-06-12
申请人： Takeshi Kodama , Tetsumei Tsuruoka , Naoki Oguchi
发明人： Takeshi Kodama , Tetsumei Tsuruoka , Naoki Oguchi
IPC分类号： G06F15/16
CPC分类号： H04L29/12377 , H04L29/125 , H04L29/12547 , H04L61/2517 , H04L61/2564 , H04L61/2582
摘要： A virtual interface having a global address of a physical interface on an Internet side of a gateway is provided in a terminal. An application unit of the terminal transmits a packet to the Internet using the virtual interface. The packet is transferred to the gateway through a downlink transfer path. The gateway transmits the packet from the physical interface on the Internet side to the Internet.
摘要翻译：具有在网关的因特网侧的物理接口的全局地址的虚拟接口被提供在终端中。终端的应用单元使用虚拟接口将分组发送到因特网。分组通过下行链路传输路径传送到网关。网关将数据包从Internet侧的物理接口传输到Internet。

2. 发明授权

US08670451B2 Network system, terminal, and gateway 有权
标题翻译：网络系统，终端和网关
公开(公告)号：US08670451B2
公开(公告)日：2014-03-11
申请号：US11451126
申请日：2006-06-12
申请人： Takeshi Kodama , Tetsumei Tsuruoka , Naoki Oguchi
发明人： Takeshi Kodama , Tetsumei Tsuruoka , Naoki Oguchi
IPC分类号： H04L12/28
CPC分类号： H04L29/12377 , H04L29/125 , H04L29/12547 , H04L61/2517 , H04L61/2564 , H04L61/2582
摘要： A virtual interface having a global address of a physical interface on an Internet side of a gateway is provided in a terminal. An application unit of the terminal transmits a packet to the Internet using the virtual interface. The packet is transferred to the gateway through a downlink transfer path. The gateway transmits the packet from the physical interface on the Internet side to the Internet.
摘要翻译：具有在网关的因特网侧的物理接口的全局地址的虚拟接口被提供在终端中。终端的应用单元使用虚拟接口将分组发送到因特网。分组通过下行链路传输路径传送到网关。网关将数据包从Internet侧的物理接口传输到Internet。

3. 发明申请

US20120238274A1 WIRELESS COMMUNICATION APPARATUS AND CONTROL METHOD 有权
标题翻译：无线通信设备和控制方法
公开(公告)号：US20120238274A1
公开(公告)日：2012-09-20
申请号：US13420758
申请日：2012-03-15
申请人： Takeshi Kodama , Tetsumei Tsuruoka
发明人： Takeshi Kodama , Tetsumei Tsuruoka
IPC分类号： H04W36/30
CPC分类号： H04W36/0083
摘要： A wireless communication apparatus including a wireless communication interface configured to receive radio waves, and a processor configured to measure radio-wave qualities of the radio waves from a plurality of base stations in a periodic measurement period, to divide one measurement period out of the periodic measurement period, and to measure radio-wave qualities of the corresponding measurement-target base stations, to determine a base station to be excluded from the measurement-target base stations in a next measurement period in the periodic measurement period on the basis of the radio-wave qualities, and to allocate the measurement time period that has been allocated to the base station to be excluded in a measurement period to a measurement-target base station in the next measurement period.
摘要翻译：一种无线通信装置，包括被配置为接收无线电波的无线通信接口，以及处理器，被配置为在周期性测量周期内测量来自多个基站的无线电波的无线电波质量，以将一个测量周期除以周期性测量周期，并且测量相应的测量目标基站的无线电波质量，基于无线电在周期性测量周期中确定在测量目标基站中的下一个测量周期中排除的基站波质量，并且在下一测量周期中将在测量周期中被分配给要被排除的基站的测量时间段分配给测量目标基站。

4. 发明授权

US09094879B2 Handover method of wireless communication system, and wireless base station and wireless terminal of the same system 有权
标题翻译：无线通信系统的切换方式，以及同一系统的无线基站和无线终端
公开(公告)号：US09094879B2
公开(公告)日：2015-07-28
申请号：US12476480
申请日：2009-06-02
申请人： Takeshi Kodama , Tetsumei Tsuruoka
发明人： Takeshi Kodama , Tetsumei Tsuruoka
IPC分类号： H04W80/04 , H04W36/00 , H04W28/22
CPC分类号： H04W36/0083 , H04W28/22
摘要： To prevent throughput reduction during handover, the wireless communication system includes a wireless terminal and a plurality of wireless base stations communicating wirelessly with the wireless terminal and performs control to lower the speed at which the wireless terminal communicates with a communication party upon time-out of a timer value generated in accordance with the time required for transmission/reception of a signal between the wireless terminal and a communication party, wherein the wireless base station performs the control to lower the speed of the communication with the wireless terminal so as to increase the timer value when the wireless base station decides execution of the handover of the communication with the wireless terminal to another wireless base station autonomously or in response to a request from the wireless terminal, and subsequently, executes the handover.
摘要翻译：为了防止切换期间的吞吐量降低，无线通信系统包括无线终端和与无线终端进行无线通信的多个无线基站，并且执行控制以降低无线终端在超时时与通信方通信的速度根据无线终端和通信方之间的信号的发送/接收所需的时间生成的定时器值，其中无线基站进行控制以降低与无线终端的通信速度，从而增加当无线基站自主地决定执行与无线终端的通信切换到另一无线基站时的响应时间，或者响应于来自无线终端的请求，执行切换。

5. 发明授权

US09042885B2 Wireless communication apparatus and scan control method 有权
标题翻译：无线通信装置和扫描控制方法
公开(公告)号：US09042885B2
公开(公告)日：2015-05-26
申请号：US13420758
申请日：2012-03-15
申请人： Takeshi Kodama , Tetsumei Tsuruoka
发明人： Takeshi Kodama , Tetsumei Tsuruoka
IPC分类号： H04W4/00 , H04W36/00
CPC分类号： H04W36/0083
摘要： A wireless communication apparatus including a wireless communication interface configured to receive radio waves, and a processor configured to measure radio-wave qualities of the radio waves from a plurality of base stations in a periodic measurement period, to divide one measurement period out of the periodic measurement period, and to measure radio-wave qualities of the corresponding measurement-target base stations, to determine a base station to be excluded from the measurement-target base stations in a next measurement period in the periodic measurement period on the basis of the radio-wave qualities, and to allocate the measurement time period that has been allocated to the base station to be excluded in a measurement period to a measurement-target base station in the next measurement period.
摘要翻译：一种无线通信装置，包括被配置为接收无线电波的无线通信接口，以及处理器，被配置为在周期性测量周期内测量来自多个基站的无线电波的无线电波质量，以将一个测量周期除以周期性测量周期，并且测量相应的测量目标基站的无线电波质量，基于无线电在周期性测量周期中确定在测量目标基站中的下一个测量周期中排除的基站波质量，并且在下一测量周期中将在测量周期中被分配给要被排除的基站的测量时间段分配给测量目标基站。

6. 发明申请

US20090239541A1 Handover Method Of Wireless Communication System, And Wireless Base Station And Wireless Terminal Of The Same System 有权
标题翻译：无线通信系统，无线基站和同一系统的无线终端切换方法
公开(公告)号：US20090239541A1
公开(公告)日：2009-09-24
申请号：US12476480
申请日：2009-06-02
申请人： Takeshi Kodama , Tetsumei Tsuruoka
发明人： Takeshi Kodama , Tetsumei Tsuruoka
IPC分类号： H04W36/38
CPC分类号： H04W36/0083 , H04W28/22
摘要： To prevent throughput reduction during handover, the wireless communication system includes a wireless terminal and a plurality of wireless base stations communicating wirelessly with the wireless terminal and performs control to lower the speed at which the wireless terminal communicates with a communication party upon time-out of a timer value generated in accordance with the time required for transmission/reception of a signal between the wireless terminal and a communication party, wherein the wireless base station performs the control to lower the speed of the communication with the wireless terminal so as to increase the timer value when the wireless base station decides execution of the handover of the communication with the wireless terminal to another wireless base station autonomously or in response to a request from the wireless terminal, and subsequently, executes the handover.
摘要翻译：为了防止切换期间的吞吐量降低，无线通信系统包括无线终端和与无线终端进行无线通信的多个无线基站，并且执行控制以降低无线终端在超时时与通信方通信的速度根据无线终端和通信方之间的信号的发送/接收所需的时间生成的定时器值，其中无线基站进行控制以降低与无线终端的通信速度，从而增加当无线基站自主地决定执行与无线终端的通信切换到另一无线基站时的响应时间，或者响应于来自无线终端的请求，执行切换。

7. 发明授权

US08188277B2 Aromatic compounds for suppressing the generation of collagen 失效
标题翻译：抑制胶原蛋白产生的芳香族化合物
公开(公告)号：US08188277B2
公开(公告)日：2012-05-29
申请号：US11659689
申请日：2005-08-03
申请人： Tae Fukushima , Shuji Matsumura , Noriaki Takemura , Hideaki Satou , Nobuaki Ito , Takuya Shitsuta , Hironori Tsutsui , Michinori Tanaka , Keizo Kan , Hitoshi Nagao , Kenji Watanabe , Kuninori Tai , Takashi Nakagawa , Hideki Takasu , Makoto Sakamoto , Keisuke Miyajima , Satoshi Yamada , Yutaka Kojima , Koichi Yasumura , Naoto Ohi , Mitsuhiro Okuno , Kazuhisa Sugiyama , Kunihiko Kiyono , Takashi Suzuki , Seiji Akamatsu , Takeshi Kodama , Yasuo Yanagihara , Takumi Sumida
发明人： Tae Fukushima , Shuji Matsumura , Noriaki Takemura , Hideaki Satou , Nobuaki Ito , Takuya Shitsuta , Hironori Tsutsui , Michinori Tanaka , Keizo Kan , Hitoshi Nagao , Kenji Watanabe , Kuninori Tai , Takashi Nakagawa , Hideki Takasu , Makoto Sakamoto , Keisuke Miyajima , Satoshi Yamada , Yutaka Kojima , Koichi Yasumura , Naoto Ohi , Mitsuhiro Okuno , Kazuhisa Sugiyama , Kunihiko Kiyono , Takashi Suzuki , Seiji Akamatsu , Takeshi Kodama , Yasuo Yanagihara , Takumi Sumida
IPC分类号： C07D241/36 , C07D413/12 , C07D403/12 , C07D221/02 , C07D401/12 , C07D213/62 , A61K31/535 , A61K31/497 , A61K31/445
CPC分类号： C07C229/18 , C07C205/38 , C07C217/90 , C07C233/45 , C07C233/75 , C07C271/58 , C07C275/34 , C07C2601/02 , C07C2601/08 , C07C2601/14 , C07C2601/18 , C07D211/46 , C07D211/58 , C07D211/62 , C07D211/70 , C07D213/75 , C07D239/42 , C07D241/20 , C07D295/185 , C07D295/192 , C07D317/58 , C07D401/12 , C07D401/14 , C07D405/12 , C07D405/14 , C07D409/12 , C07D409/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14
摘要： The present invention provides a novel compound, which has an excellent effect of suppressing the generation of collagen and less side effects, with being excellent in terms of safety. The compound of the present invention is represented by the following general formula (1): [wherein X1 represents a nitrogen atom or a group —CH═; R1 represents a group —Z—R6, wherein Z represents a group —CO—, a group —CH(OH)—, or the like, and R6 represents a 5- to 15-membered monocyclic, dicyclic, or tricyclic, saturated or unsaturated heterocyclic group having 1 to 4 nitrogen atoms, oxygen atoms, or sulfur atoms; R2 represents a hydrogen atom, a halogen atom or a lower alkylene group; Y represents a group —O—, a group —CO—, a group —CH(OH)—, a lower alkylene group, or the like; and A represents a group or the like, wherein R3 represents a hydrogen atom, a lower alkoxy group, or the like, p represents 1 or 2, and R4 represents an imidazolyl lower alkyl group or the like.
摘要翻译：本发明提供了一种新颖的化合物，其具有优异的抑制胶原产生的效果和较少的副作用。本发明的化合物由以下通式（1）表示：[其中X 1表示氮原子或-CH =; R1表示基团-Z-R6，其中Z表示基团-CO-，基团-CH（OH） - 等，R6表示5至15元单环，双环或三环饱和或具有1-4个氮原子的不饱和杂环基，氧原子或硫原子; R2表示氢原子，卤素原子或低级亚烷基; Y表示基团-O-，基团-CO-，基团-CH（OH） - ，低级亚烷基基团等; A表示基团等，其中R3表示氢原子，低级烷氧基等，p表示1或2，R4表示咪唑基低级烷基等。

8. 发明申请

US20100210661A1 STAT3/5 ACTIVATION INHIBITOR 失效
标题翻译： STAT3 / 5激活抑制剂
公开(公告)号：US20100210661A1
公开(公告)日：2010-08-19
申请号：US12311500
申请日：2007-10-02
申请人： Kazuo Sekiguchi , Takashi Suzuki , Yutaka Ohbuchi , Mitsuhiro Okuno , Naoto Ohi , Kenji Ohnishi , Masaaki Motoyama , Kenji Yoshida , Takeshi Kodama , Kazuhisa Sugiyama , Seiji Akamatsu , Kunihiko Kiyono , Yasuo Yanagihara , Takashi Watanabe , Kazuhiko Hayashi , Hideo Tanaka , Takumi Sumida
发明人： Kazuo Sekiguchi , Takashi Suzuki , Yutaka Ohbuchi , Mitsuhiro Okuno , Naoto Ohi , Kenji Ohnishi , Masaaki Motoyama , Kenji Yoshida , Takeshi Kodama , Kazuhisa Sugiyama , Seiji Akamatsu , Kunihiko Kiyono , Yasuo Yanagihara , Takashi Watanabe , Kazuhiko Hayashi , Hideo Tanaka , Takumi Sumida
IPC分类号： A61K31/496 , C07D401/14 , C07D405/10 , A61P3/04 , A61P25/28 , A61P3/10
CPC分类号： C07D401/12 , C07D213/38 , C07D401/04 , C07D405/12 , C07D405/14
摘要： An object of the present invention is to provide a STAT3/5 activation inhibitor. The present invention provides a STAT3/5 activation inhibitor containing an aromatic compound represented by the general formula or a salt thereof as an active ingredient: wherein X1 represents a nitrogen atom or a group —CH═, R1 represents a group —Z—R6, in which Z represents a group —CO—, a group —CH(OH)— or the like, R6 represents a 5- to 15-membered monocyclic, dicyclic or tricyclic saturated or unsaturated heterocyclic group having 1 to 4 nitrogen atoms, oxygen atoms or sulfur atoms, R2 represents a hydrogen atom or a halogen atom, Y represents a group —O—, a group —CO—, a group —CH(OH)— or a lower alkylene group, and A represents a group wherein R3 represents a hydrogen atom, a lower alkoxy group or the like, p represents 1 or 2, R4 represents an imidazolyl lower alkyl group or the like.
摘要翻译：本发明的目的是提供一种STAT3 / 5激活抑制剂。本发明提供含有通式所示的芳香族化合物或其盐作为活性成分的STAT3 / 5活化抑制剂，其中，X1表示氮原子或-CH =，R1表示-Z-R6基，其中Z表示-CO-基团，-CH（OH） - 基等，R6表示具有1-4个氮原子的5至15元单环，二环或三环饱和或不饱和杂环基，氧原子或硫原子，R 2表示氢原子或卤素原子，Y表示基团-O-，基团-CO-，基团-CH（OH） - 或低级亚烷基，A表示其中R 3表示氢原子，低级烷氧基等，p表示1或2，R4表示咪唑基低级烷基等。

9. 发明申请

US20070270422A1 Aromatic Compounds 失效
标题翻译：芳香族化合物
公开(公告)号：US20070270422A1
公开(公告)日：2007-11-22
申请号：US11659689
申请日：2005-08-03
申请人： Tae Fukushima , Shuji Matsumura , Noriaki Takemura , Hideaki Satou , Nobuaki Ito , Takuya Shitsuta , Hironori Tsutsui , Michinori Tanaka , Keizo Kan , Hitoshi Nagao , Kenji Watanabe , Kuninori Tai , Takashi Nakagawa , Hideki Takasu , Makoto Sakamoto , Keisuke Miyajima , Satoshi Yamada , Yutaka Kojima , Koichi Yasumura , Naoto Ohi , Mitsuhiro Okuno , Kazuhisa Sugiyama , Kunihiko Kiyono , Takashi Suzuki , Seiji Akamatsu , Takeshi Kodama , Yasuo Yanagihara , Takumi Sumida
发明人： Tae Fukushima , Shuji Matsumura , Noriaki Takemura , Hideaki Satou , Nobuaki Ito , Takuya Shitsuta , Hironori Tsutsui , Michinori Tanaka , Keizo Kan , Hitoshi Nagao , Kenji Watanabe , Kuninori Tai , Takashi Nakagawa , Hideki Takasu , Makoto Sakamoto , Keisuke Miyajima , Satoshi Yamada , Yutaka Kojima , Koichi Yasumura , Naoto Ohi , Mitsuhiro Okuno , Kazuhisa Sugiyama , Kunihiko Kiyono , Takashi Suzuki , Seiji Akamatsu , Takeshi Kodama , Yasuo Yanagihara , Takumi Sumida
IPC分类号： C07D401/14 , A61K31/165 , A61K31/167 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/4523 , A61K31/495 , A61K31/496 , A61K31/5375 , A61K31/5377 , A61P11/00 , C07C233/00 , C07C233/92 , C07D211/00 , C07D211/40 , C07D211/56 , C07D241/04 , C07D413/14 , C07D413/02 , C07D241/36
CPC分类号： C07C229/18 , C07C205/38 , C07C217/90 , C07C233/45 , C07C233/75 , C07C271/58 , C07C275/34 , C07C2601/02 , C07C2601/08 , C07C2601/14 , C07C2601/18 , C07D211/46 , C07D211/58 , C07D211/62 , C07D211/70 , C07D213/75 , C07D239/42 , C07D241/20 , C07D295/185 , C07D295/192 , C07D317/58 , C07D401/12 , C07D401/14 , C07D405/12 , C07D405/14 , C07D409/12 , C07D409/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14
摘要： The present invention provides a novel compound, which has an excellent effect of suppressing the generation of collagen and less side effects, with being excellent in terms of safety. The compound of the present invention is represented by the following general formula (1): [wherein X1 represents a nitrogen atom or a group —CH═; R1 represents a group -Z-R6, wherein Z represents a group —CO—, a group —CH(OH)—, or the like, and R6 represents a 5- to 15-membered monocyclic, dicyclic, or tricyclic, saturated or unsaturated heterocyclic group having 1 to 4 nitrogen atoms, oxygen atoms, or sulfur atoms; R2 represents a hydrogen atom, a halogen atom or a lower alkylene group; Y represents a group —O—, a group —CO—, a group —CH(OH)—, a lower alkylene group, or the like; and A represents a group or the like, wherein R3 represents a hydrogen atom, a lower alkoxy group, or the like, p represents 1 or 2, and R4 represents an imidazolyl lower alkyl group or the like.
摘要翻译：本发明提供了一种新颖的化合物，其具有优异的抑制胶原产生的效果和较少的副作用。本发明的化合物由以下通式（1）表示：[其中X 1表示氮原子或基团-CH-; R 1表示基团-ZR 6，其中Z表示-CO-基团，-CH（OH） - 基等基团，R“ 6表示具有1至4个氮原子，氧原子或硫原子的5至15元单环，二环或三环饱和或不饱和杂环基; R 2表示氢原子，卤素原子或低级亚烷基; Y表示基团-O-，基团-CO-，基团-CH（OH） - ，低级亚烷基基团等; A表示基团等，其中R 3表示氢原子，低级烷氧基等，p表示1或2，R 4表示咪唑基低级烷基等。

10. 发明授权

US08236826B2 Diarylether derivatives as antitumor agents 失效
标题翻译：二元醚衍生物作为抗肿瘤剂
公开(公告)号：US08236826B2
公开(公告)日：2012-08-07
申请号：US12095930
申请日：2006-12-04
申请人： Hironori Matsuyama , Kenji Ohnishi , Takashi Nakagawa , Hideki Takasu , Makoto Sakamoto , Kumi Higuchi , Keisuke Miyajima , Satoshi Yamada , Masaaki Motoyama , Yutaka Kojima , Koichi Yasumura , Takeshi Kodama , Shun Otsuji , Keizo Kan , Takumi Sumida
发明人： Hironori Matsuyama , Kenji Ohnishi , Takashi Nakagawa , Hideki Takasu , Makoto Sakamoto , Kumi Higuchi , Keisuke Miyajima , Satoshi Yamada , Masaaki Motoyama , Yutaka Kojima , Koichi Yasumura , Takeshi Kodama , Shun Otsuji , Keizo Kan , Takumi Sumida
IPC分类号： A61K31/44
CPC分类号： A61K31/496 , A61K31/495
摘要： An object of the present invention is to provide a medicinal drug much improved in anti tumor activity and excellent in safety. According to the present invention, there is provided a medicinal drug containing a compound represented by the following general formula (1) or a salt thereof as an active ingredient: [Formula 1] wherein X1 represents a nitrogen atom or a group —CH═, R1 represents a group —Z—R6, in which Z represents a group —CO—, a group —CH(OH)— or the like, R6 represents a 5- to 15-membered monocyclic, dicyclic or tricyclic saturated or unsaturated heterocyclic group having 1 to 4 nitrogen atoms, oxygen atoms or sulfur atoms, R2 represents a hydrogen atom or a halogen atom, Y represents a group —O—, a group —CO—, a group —CH(OH)— or a lower alkylene group, and A represents [Formula 2] wherein R3 represents a hydrogen atom, a lower alkoxy group or the like, p represents 1 or 2, R4 represents an imidazolyl lower alkyl group or the like.
摘要翻译：本发明的目的在于提供一种抗肿瘤活性大大提高的安全性药物。根据本发明，提供了含有下述通式（1）表示的化合物或其盐作为有效成分的药物：[式1]其中X1表示氮原子或基团-CH =， R1表示基团-Z-R6，其中Z表示基团-CO-，基团-CH（OH） - 等，R6表示5至15元单环，二环或三环饱和或不饱和杂环基具有1至4个氮原子，氧原子或硫原子，R 2表示氢原子或卤素原子，Y表示基团-O-，基团-CO-，基团-CH（OH） - 或低级亚烷基 A表示[式2]其中R3表示氢原子，低级烷氧基等，p表示1或2，R4表示咪唑基低级烷基等。

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