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1. 发明申请

US20100160335A1 PYRIDAZINONE DERIVATIVE AND PDE INHIBITOR CONTAINING THE SAME AS ACTIVE INGREDIENT 审中-公开
标题翻译：含有相同活性成分的吡咯烷酮衍生物和PDE抑制剂
公开(公告)号：US20100160335A1
公开(公告)日：2010-06-24
申请号：US12452172
申请日：2008-06-18
申请人： Yasushi Kohno , Koji Ochiai , Satoshi Takita , Akihiko Kojima , Tomohiko Eiraku , Tetsuya Kishi
发明人： Yasushi Kohno , Koji Ochiai , Satoshi Takita , Akihiko Kojima , Tomohiko Eiraku , Tetsuya Kishi
IPC分类号： A61K31/50 , A61K31/501 , C07D403/00
CPC分类号： C07D413/14 , C07D401/14 , C07D403/14 , C07D405/14 , C07D409/14 , C07D417/14 , C07D471/04
摘要： It is to provide a novel pyridazinone derivative represented by the following general formula (1), which is useful as a pharmaceutical and has a phosphodiesterase inhibitory action: wherein R1 represents H or C1-6 alkyl, each of R2 and R3 represents H, X, C1-6 alkoxy, Z represents O or S, and A represents AA or BB, wherein AA represents: and BB represents: wherein R4 represents H or C1-6 alkyl, and each of R5 and R6 represents C1-6 alkyl.
摘要翻译：提供由以下通式（1）表示的新的哒嗪酮衍生物，其可用作药物并具有磷酸二酯酶抑制作用：其中R1表示H或C1-6烷基，R2和R3各自表示H，X C 1-6烷氧基，Z表示O或S，A表示AA或BB，其中AA表示：BB表示：其中R4表示H或C1-6烷基，R5和R6各自表示C1-6烷基。

2. 发明申请

US20100130738A1 PYRAZOLONE DERIVATIVE AND PDE INHIBITOR CONTAINING THE SAME AS ACTIVE INGREDIENT 审中-公开
标题翻译：含有该活性成分的吡唑啉酮衍生物和PDE抑制剂
公开(公告)号：US20100130738A1
公开(公告)日：2010-05-27
申请号：US12452173
申请日：2008-06-18
申请人： Yasushi Kohno , Koji Ochiai , Satoshi Takita , Tetsuya Kishi
发明人： Yasushi Kohno , Koji Ochiai , Satoshi Takita , Tetsuya Kishi
IPC分类号： C07D401/14 , C07D471/04 , C07D417/14 , C07D403/14 , C07D407/10
CPC分类号： C07D401/14 , C07D403/14 , C07D405/14 , C07D409/14 , C07D417/14 , C07D471/04
摘要： It is to provide a novel pyrazolone derivative represented by the following general formula (1), which is useful as a pharmaceutical and has a phosphodiesterase inhibitory action: wherein R1,R2: C1-6 alkyl; R3,R4: H, X, C1-6 alkoxy; Z:O, S; A:AA, BB, wherein AA represents wherein BB represents wherein R5: H, C1-6 alkyl; R6,R7: C1-6 alkyl.
摘要翻译：提供由以下通式（1）表示的新型吡唑啉酮衍生物，其可用作药物并具有磷酸二酯酶抑制作用：其中R1，R2：C1-6烷基; R3，R4：H，X，C1-6烷氧基; Z：O，S; A：AA，BB，其中AA表示其中BB表示其中R5：H，C1-6烷基; R6，R7：C1-6烷基。

3. 发明申请

US20090318385A1 Pyrazolopyride derivative and phosphodiesterase ( pde) inhibitors containing the same as active ingredient 审中-公开
标题翻译：吡唑并吡啶衍生物和含有与活性成分相同的磷酸二酯酶（pde）抑制剂
公开(公告)号：US20090318385A1
公开(公告)日：2009-12-24
申请号：US12310736
申请日：2007-09-05
申请人： Yasushi Kohno , Satoshi Takita , Akihiko Kojima , Tetsuya Kishi
发明人： Yasushi Kohno , Satoshi Takita , Akihiko Kojima , Tetsuya Kishi
IPC分类号： A61K31/695 , C07D471/04 , A61K31/437 , C07F7/02
CPC分类号： C07D471/04
摘要： A novel pyrazolopyridine derivative is provided which is useful as a pharmaceutical drug having phosphodiesterase inhibitory activity.The pyrazolopyridine derivative is represented by the following general formula (1): [wherein R1 is a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, or the like, R2 is an optionally substituted alkyl group having 1 to 6 carbon atoms or the like, R5 and R6 are independently a hydrogen atom or a halogen atom, R13 is a hydrogen atom or a halogen atom, n is 0 or 1, is a single or double bond, R3 is a hydrogen atom, a hydroxyl group, or the like, and R4 is a hydrogen atom, a phenyl group, or the like] or a pharmaceutically acceptable salt thereof, and a hydrate thereof.
摘要翻译：提供一种新颖的吡唑并吡啶衍生物，其可用作具有磷酸二酯酶抑制活性的药物。吡唑并吡啶衍生物由以下通式（1）表示：[其中R 1是氢原子，任选取代的具有1至6个碳原子的烷基等，R 2是任选取代的具有1至6个碳的烷基原子等，R 5和R 6独立地为氢原子或卤素原子，R 13为氢原子或卤素原子，n为0或1，为单键或双键，R 3为氢原子，羟基等，R 4为氢原子，苯基等]或其药学上可接受的盐及其水合物。

4. 发明申请

US20110178041A1 HETEROCYCLIC BIARYL DERIVATIVE AND PDE INHIBITOR COMPRISING SAME AS ACTIVE INGREDIENT 审中-公开
标题翻译：含有作为活性成分的异源二异氰酸酯衍生物和PDE抑制剂
公开(公告)号：US20110178041A1
公开(公告)日：2011-07-21
申请号：US13121099
申请日：2009-09-24
申请人： Yasushi Kohno , Tatsunobu Sumiya , Satoshi Takita , Akihiko Kojima
发明人： Yasushi Kohno , Tatsunobu Sumiya , Satoshi Takita , Akihiko Kojima
IPC分类号： A61K31/437 , C07D471/04 , C07F5/02 , A61K31/69 , A61P11/00 , A61P19/02 , A61P25/00 , A61P25/28 , A61P25/16 , A61P25/24 , A61P25/18 , A61P3/00 , A61P3/04 , A61P29/00 , A61P11/06 , A61P11/02
CPC分类号： C07D215/26 , C07D401/04 , C07D405/04 , C07D409/04 , C07D413/04 , C07D417/04 , C07D471/04
摘要： Novel heterocyclic biaryl derivatives were disclosed which are useful as pharmaceutical agents and which exhibit a phosphodiesterase-inhibitory action.The heterocyclic biaryl derivatives are represented by the following general formula (1): wherein the Heterocycle 1 and the Heterocycle 2 are directly bonded together.
摘要翻译：公开了可用作药剂并且表现出磷酸二酯酶抑制作用的新型杂环联芳基衍生物。杂环联芳基衍生物由以下通式（1）表示：其中杂环1和杂环2直接键合在一起。

5. 发明申请

US20110224250A1 ISOQUINOLINE DERIVATIVE, AND PDE INHIBITOR COMPRISING SAME AS ACTIVE INGREDIENT 审中-公开
标题翻译：异喹啉衍生物和含有相同活性成分的PDE抑制剂
公开(公告)号：US20110224250A1
公开(公告)日：2011-09-15
申请号：US13123274
申请日：2009-10-08
申请人： Yasushi Kohno , Satoshi Takita , Akihiko Kojima
发明人： Yasushi Kohno , Satoshi Takita , Akihiko Kojima
IPC分类号： A61K31/437 , C07D471/04 , C07D401/10 , A61K31/4725 , A61P9/00 , A61P9/04 , A61P9/12 , A61P11/06 , A61P11/00 , A61P25/28 , A61P29/00 , A61P19/02 , A61P19/10 , A61P25/00 , A61P25/16 , A61P25/24 , A61P25/18 , A61P3/04 , A61P3/00 , A61P1/16
CPC分类号： C07D401/04 , C07D471/04
摘要： The present invention provides a novel isoquinoline derivative which is useful as a pharmaceutical agent having a phosphodiesterase inhibitory activity.The isoquinoline derivative of the present invention is represented by the following general formula (1):
摘要翻译：本发明提供了可用作具有磷酸二酯酶抑制活性的药剂的新型异喹啉衍生物。本发明的异喹啉衍生物由以下通式（1）表示：

6. 发明申请

US20100056791A1 Pyrazolopyridine carboxamide derivative and phosphodiesterase (pde) inhibitor containing the same 审中-公开
标题翻译：吡唑并吡啶甲酰胺衍生物和含有它们的磷酸二酯酶（pde）抑制剂
公开(公告)号：US20100056791A1
公开(公告)日：2010-03-04
申请号：US12310562
申请日：2007-08-30
申请人： Yasushi Kohno , Koji Ochiai , Akihiko Kojima
发明人： Yasushi Kohno , Koji Ochiai , Akihiko Kojima
IPC分类号： C07D471/02
CPC分类号： C07D471/04
摘要： A novel pyrazolopyridine carboxamide derivative is provided that is useful as a pharmaceutical drug having phosphodiesterase inhibitory activity.The pyrazolopyridine carboxamide derivative is represented by the following general formula (1): (Example: 2-ethyl-7-methoxypyrazolo[1,5-a]pyridine-4-carboxylic acid (3,5-dichloropyridin-4-yl)amide).
摘要翻译：提供一种新颖的吡唑并吡啶羧酰胺衍生物，其可用作具有磷酸二酯酶抑制活性的药物。吡唑并吡啶羧酰胺衍生物由以下通式（1）表示：（实施例：2-乙基-7-甲氧基吡唑并[1,5-a]吡啶-4-甲酸（3,5-二氯吡啶-4-基）酰胺）。

7. 发明授权

US08695409B2 Air flow rate measuring apparatus 有权
标题翻译：空气流量测量仪
公开(公告)号：US08695409B2
公开(公告)日：2014-04-15
申请号：US13596385
申请日：2012-08-28
申请人： Yasushi Kohno , Takao Ban , Hidehito Tsujii
发明人： Yasushi Kohno , Takao Ban , Hidehito Tsujii
IPC分类号： G01M15/04
CPC分类号： G01F1/6842 , G01F1/698 , G01F1/6983 , G01F5/00
摘要： An air flow rate measuring apparatus includes a heater and a control circuit. The heater heats a part of an intake air sucked into an engine. The control circuit controls an energization of the heater. The heater has a measuring-mode temperature when a flow rate of the intake air is measured. The control circuit has a heat cleaner which temporarily raises a temperature of the heater higher than the measuring-mode temperature when an energization of the air flow rate measuring apparatus is started.
摘要翻译：空气流量测量装置包括加热器和控制电路。加热器加热吸入发动机的进气的一部分。控制电路控制加热器的通电。当测量进气的流量时，加热器具有测量模式温度。控制电路具有在开始空气流量测量装置通电时临时使加热器的温度高于测量模式温度的热清洁器。

8. 发明申请

US20130317065A1 INDOLE DERIVATIVE AND PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF 有权
标题翻译：包含衍生物和药理学上可接受的盐
公开(公告)号：US20130317065A1
公开(公告)日：2013-11-28
申请号：US13980604
申请日：2012-01-24
申请人： Kazuya Tatani , Atsushi Kondo , Tatsuhiro Kondo , Naohiro Kawamura , Shigeki Seto , Yasushi Kohno
发明人： Kazuya Tatani , Atsushi Kondo , Tatsuhiro Kondo , Naohiro Kawamura , Shigeki Seto , Yasushi Kohno
IPC分类号： A61K31/4439 , C07D401/14 , C07D413/14 , C07D405/06 , C07D417/06 , A61K31/506 , A61K31/444 , A61K31/427 , A61K31/41 , A61K31/4245 , C07D401/06 , C07D405/14 , C07D409/14 , A61K31/404
CPC分类号： A61K31/4245 , A61K31/404 , A61K31/41 , A61K31/427 , A61K31/4439 , A61K31/444 , A61K31/506 , A61K45/06 , C07D209/18 , C07D401/06 , C07D401/14 , C07D403/10 , C07D405/06 , C07D405/14 , C07D409/14 , C07D413/14 , C07D417/06 , C07D419/14 , A61K2300/00
摘要： The present invention provides a compound represented by the general formula (I) of the present invention, which has EP1 receptor antagonism: wherein A represents a benzene ring, a pyridine ring, or the like; Y1 represents a C1-6 alkylene group or the like; Y2 represents a single bond or the like; Z represents —C(═O)—NHSO2R6, an acidic 5-membered hetero ring group, or the like; R1 represents a hydrogen atom or the like; R2 represents a phenyl group, a 5-membered aromatic heterocyclic group, or the like; R3 represents a halogen atom, a C1-6 alkoxy group, or the like; R4 represents a hydrogen atom, a halogen atom, or the like; R5 represents a hydrogen atom or the like; and R6 represents a C1-6 alkyl group or the like], or a pharmaceutically acceptable salt thereof. Furthermore, the compound (I) of the present invention can be used as an agent for treating or preventing LUTS, in particular, various symptoms of OABs.
摘要翻译：本发明提供了具有EP1受体拮抗作用的本发明通式（I）表示的化合物：其中A表示苯环，吡啶环等; Y1表示C1-6亚烷基等; Y2表示单键等; Z表示-C（= O）-NHSO 2 R 6，酸性5元杂环基等; R1表示氢原子等; R 2表示苯基，5元芳族杂环基等; R3表示卤素原子，C1-6烷氧基等; R 4表示氢原子，卤素原子等; R5表示氢原子等; R6表示C1-6烷基等〕或其药学上可接受的盐。此外，本发明的化合物（I）可以用作治疗或预防LUTS，特别是OAB的各种症状的药剂。

9. 发明授权

US07703320B2 Flow measuring device having resistors arranged in nesting arrangement 失效
标题翻译：具有布置成嵌套布置的电阻的流量测量装置
公开(公告)号：US07703320B2
公开(公告)日：2010-04-27
申请号：US12120517
申请日：2008-05-14
申请人： Junzo Yamaguchi , Yasushi Kohno
发明人： Junzo Yamaguchi , Yasushi Kohno
IPC分类号： G01F1/68
CPC分类号： G01F1/692
摘要： According to a flow measuring device, first ranges formed by a first plurality of resistors form a single continuous value range on a flow direction coordinate axis. Thus, the first plurality of resistors is limited from being thermally insulated from one another in the flow direction, and thereby detectivity is improved. Also, second ranges formed by a second plurality of resistors form an other single continuous value range on a longitudinal direction coordinate axis. The other continuous value range includes a position that corresponds to a half length of a heating element in a longitudinal direction. As a result, detection difference is obtained at the position, at which a temperature is most optimally detected, and thereby detectivity is further improved.
摘要翻译：根据流量测量装置，由第一多个电阻器形成的第一范围在流动方向坐标轴上形成单个连续值范围。因此，第一多个电阻器被限制为在流动方向上彼此热绝缘，从而提高了检测性。此外，由第二多个电阻器形成的第二范围在纵向坐标轴上形成另一个单个连续值范围。另一连续值范围包括对应于加热元件在纵向上的半长度的位置。结果，在最佳检测温度的位置处获得检测差异，从而进一步提高检测性。

10. 发明申请

US20080275008A1 Aminophosphonic acid derivative, salt thereof, and modulator of sip receptor 有权
标题翻译：氨基膦酸衍生物，其盐和sip受体的调节剂
公开(公告)号：US20080275008A1
公开(公告)日：2008-11-06
申请号：US12213187
申请日：2008-06-16
申请人： Yasushi Kohno , Kiyoaki Tanaka , Kazuhiko Kuriyama , Wataru Hori
发明人： Yasushi Kohno , Kiyoaki Tanaka , Kazuhiko Kuriyama , Wataru Hori
IPC分类号： A61K31/662
CPC分类号： C07C47/575 , C07C45/71 , C07F7/1804 , C07F9/3826 , C07F9/3882 , C07F9/4015 , C07F9/4056 , C07F9/653
摘要： Aminophosphonic acid derivatives (e.g., 2-amino-5-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-methylpentylphosphonate monoester) are represented by the following general formula (1): and act as effective S1P receptor modulators while posing less side effects.
摘要翻译：氨基膦酸衍生物（例如2-氨基-5- [4-（3-苄氧基苯硫基）-2-氯苯基] -2-甲基戊基膦酸酯单酯）由以下通式（1）表示：作为有效的S1P受体调节剂，减少副作用。

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