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1. 发明申请

US20060269197A1 Bidirectional optical module and light transmitting apparatus 审中-公开
标题翻译：双向光模块和发光装置
公开(公告)号：US20060269197A1
公开(公告)日：2006-11-30
申请号：US10547768
申请日：2004-03-05
申请人： Hitoshi Uno , Hiroaki Asano , Hironori Souda , Syougo Horinouchi , Toshinori Kai , Toshihiro Koga , Masaharu Fukakusa
发明人： Hitoshi Uno , Hiroaki Asano , Hironori Souda , Syougo Horinouchi , Toshinori Kai , Toshihiro Koga , Masaharu Fukakusa
IPC分类号： G02B6/36
CPC分类号： G02B6/4246 , G02B6/4214 , H01L2224/48091 , H01L2224/48463 , H01L2224/73265 , H01L2924/3025 , H01S5/02252 , H01S5/02284 , H01S5/02292 , H01L2924/00014 , H01L2924/00
摘要： In a bidirectional optical module, a technique for attaining a miniaturization and a lower cost of a bidirectional optical module in which one optical fiber propagation path can be bused in two ways is disclosed. According to this technique, a molded product 12 is made of a transparent material, and a beam splitter layer 121 is inclined and embedded. A sub carrier 15 has a stage portion constituting an upper stage and a lower stage and is mounted on a flat top plane of a carrier 19. A semiconductor laser 14 is mounted on the upper stage of the sub-carrier, and a light receiving device 13 is mounted at a lower position of the molded product on the lower stage, and a side of the molded product is mounted on the side, and the respective planes are consequently bonded.
摘要翻译：在双向光模块中，公开了一种用于实现双向光模块的小型化和低成本的技术，其中一个光纤传播路径可以以两种方式被布置。根据该技术，模制品12由透明材料制成，并且分束器层121倾斜并嵌入。副载体15具有构成上段和下段的载物台部分，并且安装在载体19的平坦顶平面上。半导体激光器14安装在副载体的上层上，并且光接收装置 13被安装在下阶段的模制品的下部位置，并且模制品的侧面安装在侧面上，并且因此粘合各个平面。

2. 发明申请

US20050248822A1 Optical transmission/reception module 审中-公开
标题翻译：光传输/接收模块
公开(公告)号：US20050248822A1
公开(公告)日：2005-11-10
申请号：US10525507
申请日：2003-08-26
申请人： Hitomaro Tohgoh , Hiroaki Asano , Hitoshi Uno , Masaki Kobayashi , Nobutaka Itabashi , Nobuyuki Akiya
发明人： Hitomaro Tohgoh , Hiroaki Asano , Hitoshi Uno , Masaki Kobayashi , Nobutaka Itabashi , Nobuyuki Akiya
IPC分类号： G02B6/42 , G03H1/00
CPC分类号： G02B6/421 , G02B6/4214 , G02B6/4246
摘要： A small-sized optical transceiver module, wherein any stress attributable to the differences in coefficient of thermal expansion between a transmission section optical system, a receiving section optical system, and the components which integrate and fix them and the like is not applied therebetween, and which is not influenced by any stress at the time of attachment/detachment of the optical connector is disclosed. The optical transceiver module is one wherein the transmission section optical system 1 which comprises a laser diode and an optical fiber or an optical waveguide optically connected to the laser diode and of which the electric input terminal of the laser diode is a flexible cable, a receiving section optical system 2 which comprises a photo diode and an optical fiber or an optical waveguide optically connected to the photo diode and of which the electric output terminal of the photo diode is a flexible cable, and an optical I/O optical receptacle 3 are optically connected, mechanically integrated and fixed, and the two flexible cables are spatially spaced out and disposed.
摘要翻译：一种小尺寸的光收发模块，其中不会在其间施加归因于传输部分光学系统，接收部分光学系统和其组合和固定它们的部件之间的热膨胀系数差异的任何应力，公开了在光连接器的附接/拆卸时不受任何应力的影响。光收发器模块是其中传输部分光学系统1包括激光二极管和光纤或光学波导，光学连接到激光二极管，激光二极管的电输入端是柔性电缆，接收器包括光电二极管和光纤或与光电二极管光学连接的光波导，其光电二极管的电输出端为柔性电缆，光学I / O光插座3为光学连接，机械一体化和固定，并且两个柔性电缆在空间上间隔开并布置。

3. 发明授权

US4758566A 2-(1-piperazinyl)-4-substituted phenylquinoline derivatives, processes for the preparation thereof, and pharmaceutical composition containing the same 失效
标题翻译： 2-（1-哌嗪基）-4-取代苯基喹啉衍生物，其制备方法和含有它们的药物组合物
公开(公告)号：US4758566A
公开(公告)日：1988-07-19
申请号：US893311
申请日：1986-07-28
申请人： Hitoshi Uno , Katsuhiko Hino , Toshiaki Kadokawa , Katsuyoshi Kawashima
发明人： Hitoshi Uno , Katsuhiko Hino , Toshiaki Kadokawa , Katsuyoshi Kawashima
IPC分类号： A61K31/47 , A61P1/04 , C07D215/38 , A61K31/495 , C07D401/02
CPC分类号： C07D215/38
摘要： Compounds of the formula: ##STR1## wherein R.sub.1 represents fluorine atom at the para position, chlorine atom at the para position, methyl group at the para position or trifluoromethyl group at the para or meta position; and R.sub.2 represents hydrogen atom, methyl group, ethyl group, 2-hydroxyethyl group or 3-hydroxypropyl group, provided that R.sub.2 represents ethyl group, 2-hydroxyethyl group or 3-hydroxypropyl group when R.sub.1 represents fluorine atom at the para position, methyl group at the para position or trifluoromethyl group at the para position, and a pharmaceutically acceptable salt therof, process for the preparation thereof, and pharmaceutical composition containing the same. The compounds and pharmaceutically acceptable salts thereof show excellent cytoprotective effect and useful for prophylaxis and treatment of peptic ulcer and inflammatory gastrointestinal diseases.
摘要翻译： PCT No.PCT / JP85 / 00654 Sec。 371日期1986年7月28日第 102（e）日期1986年7月28日PCT提交1985年11月27日PCT公布。公开号WO86 / 03198 日期：1986年6月5日。下式的化合物：其中R1表示对位的氟原子，对位的氯原子，对位的甲基或对位或间位的三氟甲基; R2表示氢原子，甲基，乙基，2-羟乙基或3-羟丙基，条件是当R1表示对位的氟原子时，R2表示乙基，2-羟基乙基或3-羟丙基，甲基在对位或在对位的三氟甲基，和其药学上可接受的盐，其制备方法和含有它们的药物组合物。所述化合物及其药学上可接受的盐显示出优异的细胞保护作用并且可用于预防和治疗消化性溃疡和炎性胃肠道疾病。

4. 发明授权

US4677107A Anti-peptic ulcer agent 失效
标题翻译：抗消化性溃疡剂
公开(公告)号：US4677107A
公开(公告)日：1987-06-30
申请号：US784215
申请日：1985-10-04
申请人： Toshiaki Kadokawa , Katsuyoshi Kawashima , Hitoshi Uno , Katsuhiko Hino
发明人： Toshiaki Kadokawa , Katsuyoshi Kawashima , Hitoshi Uno , Katsuhiko Hino
IPC分类号： A61K31/47 , C07D215/38 , A61K31/495
CPC分类号： C07D215/38 , A61K31/47 , Y10S514/926 , Y10S514/927
摘要： Use of a compound of the formula: ##STR1## wherein R is hydrogen atom or ethyl group, or a pharmaceutically acceptable salt thereof for prophylaxis and/or treatment of peptic ulcer, and a method for prophylaxis and/or treatment of peptic ulcer disease which comprises administering an effective amount of the above-mentioned compound to warm blooded aninal, especially human. Said active compounds have excellent pharmacological activities such as inhibition of ulceration and inhibition of gastric secretion, and hence, are useful as an anti-peptic ulcer agent.
摘要翻译：下式化合物：其中R是氢原子或乙基的化合物或其药学上可接受的盐用于消化性溃疡的预防和/或治疗，以及预防和/或治疗消化性溃疡疾病的方法，其中包括将有效量的上述化合物给予温血的阴性，特别是人。所述活性化合物具有优异的药理活性，例如抑制溃疡和抑制胃分泌，因此可用作抗消化性溃疡剂。

5. 发明授权

US4528299A 1-(2,3-Dimethyl-4-methoxyphenyl)-2-methyl-3-(1-pyrrolidinyl)-1-propanone and anti-spastic use thereof 失效
标题翻译： 1-（2,3-二甲基-4-甲氧基苯基）-2-甲基-3-（1-吡咯烷基）-1-丙酮及其抗痉挛性用途
公开(公告)号：US4528299A
公开(公告)日：1985-07-09
申请号：US530096
申请日：1983-09-07
申请人： Hitoshi Uno , Tadahiko Karasawa , Tatsuya Kon , Tsugutaka Ito
发明人： Hitoshi Uno , Tadahiko Karasawa , Tatsuya Kon , Tsugutaka Ito
IPC分类号： C07D295/10 , A61K31/40 , A61P25/00 , A61P25/08 , C07D295/108 , C07D207/04
CPC分类号： C07D295/108
摘要： 1-(2,3-Dimethyl-4-methoxyphenyl)-2-methyl-3-(1-pyrrolidinyl)-1-propanone and its pharmaceutically acceptable acid addition salts, which are useful as centrally acting muscle relaxants in the treatment of spasticity in mammals including humans, process for the preparation thereof, and pharmaceutical composition containing said compound as an active ingredient.
摘要翻译： 1-（2,3-二甲基-4-甲氧基苯基）-2-甲基-3-（1-吡咯烷基）-1-丙酮及其药学上可接受的酸加成盐，其用作中枢作用的肌肉松弛剂用于治疗痉挛状态在包括人的哺乳动物中，其制备方法和含有所述化合物作为活性成分的药物组合物。

6. 发明授权

US4649144A Antibacterial 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8- naphthyridine-3-carboxylic acid derivatives 失效
标题翻译：抗菌7-（3-氨基-1-吡咯烷基）-1-环丙基-6-氟-1,4-二氢-4-氧代-1,8-二氮杂萘-3-羧酸衍生物
公开(公告)号：US4649144A
公开(公告)日：1987-03-10
申请号：US632853
申请日：1984-07-20
申请人： Jun-ichi Matsumoto , Teruyuki Miyamoto , Hitoshi Uno , Shinichi Nakamura
发明人： Jun-ichi Matsumoto , Teruyuki Miyamoto , Hitoshi Uno , Shinichi Nakamura
IPC分类号： C07D487/04 , A61K31/435 , A61K31/4375 , A61P31/04 , C07D207/12 , C07D207/14 , C07D213/61 , C07D213/78 , C07D213/80 , C07D213/85 , C07D401/04 , C07D471/04
CPC分类号： C07D213/78 , C07D207/12 , C07D207/14 , C07D213/61 , C07D213/80 , C07D213/85 , C07D401/04 , C07D471/04
摘要： The present invention relates to a 1,8-naphthyridine derivative of the formula ##STR1## wherein R.sub.1, R.sub.2 and R.sub.3 are the same or different and each hydrogen or lower alkyl having 1 to 5 carbon atoms; and esters thereof and salts thereof and processes for preparation thereof. These compounds show excellent antibacterial activity and are useful antibacterial agents.
摘要翻译：本发明涉及下式的1,8-萘啶衍生物，其中R 1，R 2和R 3相同或不同，每个氢或具有1至5个碳原子的低级烷基; 及其酯及其盐及其制备方法。这些化合物显示出优异的抗菌活性，并且是有用的抗菌剂。

7. 发明授权

US4356186A Acetic acid derivatives and composition containing the same 失效
标题翻译：乙酸衍生物及含有其的组合物
公开(公告)号：US4356186A
公开(公告)日：1982-10-26
申请号：US246114
申请日：1981-03-20
申请人： Hitoshi Uno , Mikio Kurokawa , Hideo Nakamura
发明人： Hitoshi Uno , Mikio Kurokawa , Hideo Nakamura
IPC分类号： A61K31/34 , A61K31/38 , A61P29/00 , C07D313/12 , C07D337/12 , C07D337/14 , C07D405/06 , C07D409/06 , A61K31/335
CPC分类号： C07C323/00 , C07D313/12 , C07D337/12 , Y10S514/825 , Y10S514/916
摘要： Novel acetic acid derivatives of the formula: ##STR1## wherein X is oxygen or sulfur; R.sub.1 is hydrogen or a lower alkyl; R.sub.2 is hydroxy, an alkoxy, an alkenyloxy, a cycloalkyloxy, an aryloxy, a substituted aryloxy, an aryl-lower alkoxy, a substituted aryl-lower alkoxy, an aryl-lower alkenyloxy, a substituted aryl-lower alkenyloxy, an .omega.-disubstituted amino-lower alkoxy, a lower alkoxycrbonyl-lower alkoxy, a lower alkoxy-lower alkoxy, a hydroxy-lower alkoxy-lower alkoxy, an acyl-lower alkoxy, or a group ##STR2## wherein R.sub.3 is hydrogen, hydroxy, a lower alkyl, an aryl-lower alkyl, a hydroxy-lower alkyl, or a carboxy-lower alkyl, R.sub.4 is hydrogen, a lower alkyl or a hydroxy-lower alkyl, or the R.sub.3 and R.sub.4 may combine together with the nitrogen atom to which they are joined to form a heterocyclic group; and the group --CH(R.sub.1)COR.sub.2 is joined to the carbon atom at 2- or 3-position, and pharmaceutically acceptable salts thereof, processes for their preparation, and pharmaceutical compositions containing these compounds. They have excellent anti-inflammatory, analgesic and antipyretic activities with weak ulcerogenicity in the gastrointestinal tract and toxicity.
摘要翻译：下式的新型乙酸衍生物：其中X是氧或硫; R1是氢或低级烷基; R2是羟基，烷氧基，烯氧基，环烷氧基，芳氧基，取代的芳氧基，芳基 - 低级烷氧基，取代的芳基 - 低级烷氧基，芳基 - 低级烯氧基，取代的芳基 - 低级烯氧基，ω-二取代氨基 - 低级烷氧基，低级烷氧基羰基 - 低级烷氧基，低级烷氧基 - 低级烷氧基，羟基 - 低级烷氧基 - 低级烷氧基，酰基 - 低级烷氧基或基团，其中R3是氢，羟基，低级烷基，芳基 - 低级烷基，羟基 - 低级烷基或羧基 - 低级烷基，R 4是氢，低级烷基或羟基 - 低级烷基，或者R 3和R 4可以与它们所在的氮原子结合在一起连接形成杂环基; 并且基团-CH（R 1）COR 2与2-或3-位的碳原子及其药学上可接受的盐连接，其制备方法和含有这些化合物的药物组合物。它们具有优良的抗炎，止痛和解热活性，肠胃道溃疡性弱，毒性低。

8. 发明授权

US4237135A 2-(4-Ethyl-1-piperazinyl)-4-phenylquinoline, process for preparation thereof, and composition thereof 失效
标题翻译： 2-（4-乙基-1-哌嗪基）-4-苯基喹啉，其制备方法及其组合
公开(公告)号：US4237135A
公开(公告)日：1980-12-02
申请号：US022779
申请日：1979-03-22
申请人： Hitoshi Uno , Yasutaka Nagai , Tadahiko Karasawa , Kiyoshi Furukawa
发明人： Hitoshi Uno , Yasutaka Nagai , Tadahiko Karasawa , Kiyoshi Furukawa
IPC分类号： A61K31/38 , A61K31/495 , A61P25/24 , A61P25/26 , C07D215/38 , C07D401/04
CPC分类号： C07D215/38
摘要： 2-(4-Ethyl-1-piperazinyl)-4-phenylquinoline and its pharmaceutically acceptable acid addition salts, which are useful as antidepressant agents in the treatment of depression or depressive state in mammals including humans, and processes for the preparation thereof.
摘要翻译： 2-（4-乙基-1-哌嗪基）-4-苯基喹啉及其药学上可接受的酸加成盐，其可用作抗抑郁药用于治疗包括人在内的哺乳动物的抑郁或抑郁状态及其制备方法。

9. 发明授权

US3948928A 3-Substituted-1,2-benzisoxazoles and pharmaceutically acceptable acid addition salts thereof 失效
标题翻译： 3-取代的1,2-苯并异恶唑及其药学上可接受的酸加成盐
公开(公告)号：US3948928A
公开(公告)日：1976-04-06
申请号：US340195
申请日：1973-03-12
申请人： Haruki Nishimura , Masanao Shimizu , Hitoshi Uno , Tetsuo Hirooka , Yoshinobu Masuda , Mikio Kurokawa
发明人： Haruki Nishimura , Masanao Shimizu , Hitoshi Uno , Tetsuo Hirooka , Yoshinobu Masuda , Mikio Kurokawa
IPC分类号： A61K31/42 , C07D261/20
CPC分类号： A61K31/42 , C07D261/20
摘要： 3-Substituted-1,2-benzisoxazole derivative of the following formula: ##SPC1##Wherein R.sub.1 is hydrogen, hydroxy, nitro, alkyl, alkoxy, halogen or amino; R.sub.2 is hydroxyamino, amino, hydrazino, mono- or di- alkyl substituted amino, aralkylamino, acyloxyamino, morpholino, piperazine which is unsubstituted or substituted with alkyl, aralkyl or aryl at 4 position, or pyrrolidino, or R.sub.2 may combine with imino group and form together with the adjacent carbon atom a heterocyclic ring such as imidazoline or tetrahydropyrimidine; and n is an integer of 0 to 3, and its pharmaceutically acceptable acid addition salt, and preparation thereof. The present compounds show valuable pharmacological properties, such as anti-reserpine activity, central nervous depressing activity, anti-hypertensive activity and l-dopa potentiating activity.
摘要翻译： 3-取代的1,2-苯并异恶唑衍生物：

10. 发明授权

US5955918A Burst mode digital data amplifier circuit unit and amplifier circuit 失效
标题翻译：突发模式数字数字放大器电路单元和放大电路
公开(公告)号：US5955918A
公开(公告)日：1999-09-21
申请号：US997895
申请日：1997-12-24
申请人： Hitoshi Uno
发明人： Hitoshi Uno
IPC分类号： H03G11/00 , H03F3/08 , H03F3/45 , H03F1/02
CPC分类号： H03F3/087
摘要： An amplifier circuit unit is composed of an offset compensation circuit for equalizing and issuing a DC potential in data input period of one input signal of differential input signals, and a DC potential in data input period of other input signal, and an amplitude limiting amplifier circuit for receiving a differential output signal from this offset compensation circuit as an input signal, and issuing to a differential output terminal as a differential output signal kept in a constant output signal amplitude while amplifying in a linear region. This amplifier circuit unit is connected in cascade in plural stages as required, and is applied to an amplifier circuit of an optical receiving circuit and others.
摘要翻译：放大器电路单元由偏移补偿电路构成，用于在差分输入信号的一个输入信号的数据输入周期中平衡并发出DC电位，并且在其他输入信号的数据输入周期中的DC电位和限幅放大器电路用于接收来自该偏移补偿电路的差分输出信号作为输入信号，并且在线性区域放大的同时，向差分输出端子发出作为保持在恒定输出信号幅度的差分输出信号。该放大器电路单元根据需要以多级级联连接，并被应用于光接收电路等的放大电路。

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