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1. 发明授权

US4542578A Method of manufacturing photovoltaic device 失效
标题翻译：制造光伏器件的方法
公开(公告)号：US4542578A
公开(公告)日：1985-09-24
申请号：US589886
申请日：1984-03-15
申请人： Masaru Yamano , Isao Nagaoka , Yukinori Kuwano , Hiroshi Kawada , Souichi Sakai
发明人： Masaru Yamano , Isao Nagaoka , Yukinori Kuwano , Hiroshi Kawada , Souichi Sakai
IPC分类号： H01L31/042 , H01L27/142 , H01L31/0392 , H01L31/04 , H01L31/18
CPC分类号： H01L31/03921 , H01L31/046 , H01L31/0463 , Y02E10/50
摘要： Mutually spaced apart TCO film portions are formed on a glass substrate. An amorphous silicon film of PIN junction type is formed to cover these TCO film portions, and an aluminum film is formed thereon. The aluminum film in the vicinity of the gap between adjacent TCO film portions is removed by means of a laser beam, and the amorphous silicon film is removed by reactive plasma etching using the aluminum film as a mask to thereby expose portions of the TCO film. An aluminum-titanium film is formed over the aluminum film and the exposed portions of the TCO film. The aluminum-titanium film is separated by means of a laser beam to form a plurality of photoelectric converting regions. The photoelectric converting regions thus formed on the glass substrate are connected in series.
摘要翻译：相互间隔开的TCO膜部分形成在玻璃基板上。形成PIN结型非晶硅膜以覆盖这些TCO膜部分，并在其上形成铝膜。通过激光束去除相邻的TCO膜部分之间的间隙附近的铝膜，通过使用铝膜作为掩模的反应等离子体蚀刻来去除非晶硅膜，从而暴露部分TCO膜。在铝膜上和TCO膜的暴露部分上形成铝钛膜。铝 - 钛膜通过激光束分离以形成多个光电转换区域。由此形成在玻璃基板上的光电转换区域串联连接。

2. 发明授权

US4049170A Device for pulling up and paying out an oil boom 失效
标题翻译：用于拉起和支付油柱的装置
公开(公告)号：US4049170A
公开(公告)日：1977-09-20
申请号：US679613
申请日：1976-04-23
申请人： Hiroshi Kawakami , Isao Nagaoka , Yukio Tsukagawa
发明人： Hiroshi Kawakami , Isao Nagaoka , Yukio Tsukagawa
IPC分类号： E02B15/04 , E02B15/10 , B65H17/34
CPC分类号： E02B15/08
摘要： A device for pulling up and paying out an oil boom comprises a structural frame, a pair of end pulleys horizontally journaled on the frame, an endless belt engaged with the end pulleys and having a plurality of engaging projections for oil boom and a pusher member for slightly urging the oil boom against the endless belt, the pusher member being resiliently supported by a supporting member with a proper distance held between the bottom portion of the pusher member and the upper surface of the endless belt.
摘要翻译：用于拉出并支付油斗的装置包括结构框架，在框架上水平地轴颈的一对端滑轮，与端滑轮接合的环形带，并且具有用于油斗的多个接合突起和用于稍微推动油臂抵靠环形带，推动器构件被支撑构件弹性地支撑，并且在推动构件的底部与环形带的上表面之间保持适当的距离。

3. 发明授权

US07452856B2 Antibacterial peptide 有权
标题翻译：抗菌肽
公开(公告)号：US07452856B2
公开(公告)日：2008-11-18
申请号：US11093875
申请日：2005-03-29
申请人： Isao Nagaoka , Daiju Okuda , Shin Yomogida , Hiroshi Tamura
发明人： Isao Nagaoka , Daiju Okuda , Shin Yomogida , Hiroshi Tamura
IPC分类号： A61K38/00 , C07K17/00
CPC分类号： C07K14/4723
摘要： The present invention provides a novel peptide based on CAP11 as well as provides an antibacterial agent, an LPS-cell-binding inhibitor, and a drug such as a bacterial-infection-treating agent or an endotoxin-shock suppressant, each containing the peptide as an active ingredient. The peptide has the following amino acid sequence (SEQ ID NO: 1): X01 X02 X03 X03 X04 X02 X03 X03 X05 X04 X03 X04 X02 X01 X03 X02 X05 X03 (wherein X01 represents a cationic amino acid residue or a polar uncharged amino acid residue, X02 represents a non-polar amino acid residue, X03 represents a cationic amino acid residue, X04 represents a non-polar amino acid residue or a cationic amino acid residue, and X05 represents a non-polar amino acid residue or a polar uncharged amino acid residue). Each of the antibacterial agent, lipopolysaccharide-cell-binding inhibitor, and drug (e.g., bacterial-infection-treating agent or endotoxin-shock suppressant) contains the peptide as an active ingredient. The present invention also provides for a peptide comprised of a sequence of cationic and non-polar or polar uncharged amino acids forming an α-helix wherein the amino acids are arranged along the α-helix such that when represented as a helical wheel, there is a substantial bi-lateral symmetry between cationic versus non-polar or polar uncharged amino acids.
摘要翻译：本发明提供了一种基于CAP11的新型肽，并且提供了抗细菌剂，LPS-细胞结合抑制剂和细菌感染处理剂或内毒素 - 休克抑制剂等药物，每种含有肽作为活性成分。肽具有以下氨基酸序列（SEQ ID NO：1）：X01 X02 X03 X03 X04 X02 X03 X03 X05 X04 X03 X04 X02 X01 X03 X02 X05 X03（其中X01表示阳离子性氨基酸残基或极性不带电荷的氨基酸残基 X02表示非极性氨基酸残基，X03表示阳离子性氨基酸残基，X04表示非极性氨基酸残基或阳离子性氨基酸残基，X05表示非极性氨基酸残基或极性不带电氨基酸残基）。各抗菌剂，脂多糖 - 细胞结合抑制剂和药物（例如细菌感染处理剂或内毒素 - 休克抑制剂）均含有作为有效成分的肽。本发明还提供了由阳离子和非极性或极性不带电荷的氨基酸序列组成的肽，其形成α-螺旋，其中氨基酸沿着α-螺旋排列，使得当以螺旋轮表示时，存在阳离子与非极性或极性不带电氨基酸之间的实质双侧对称性。

4. 发明申请

US20090149632A1 Antibacterial peptide 有权
标题翻译：抗菌肽
公开(公告)号：US20090149632A1
公开(公告)日：2009-06-11
申请号：US12148094
申请日：2008-04-16
申请人： Isao Nagaoka , Daiju Okuda , Shin Yomogida , Hiroshi Tamura
发明人： Isao Nagaoka , Daiju Okuda , Shin Yomogida , Hiroshi Tamura
IPC分类号： C07K7/00 , C07K1/00
CPC分类号： C07K14/4723
摘要： The present invention provides a novel peptide based on CAP11 as well as provides an antibacterial agent, an LPS-cell-binding inhibitor, and a drug such as a bacterial-infection-treating agent or an endotoxin-shock suppressant, each containing the peptide as an active ingredient. The peptide has the following amino acid sequence (SEQ ID NO: 1): X01 X02 X03 X03 X04 X02 X03 X03 X05 X04 X03 X04 X02 X01 X03 X02 X05 X03 (wherein X01 represents a cationic amino acid residue or a polar uncharged amino acid residue, X02 represents a non-polar amino acid residue, X03 represents a cationic amino acid residue, X04 represents a non-polar amino acid residue or a cationic amino acid residue, and X05 represents a non-polar amino acid residue or a polar uncharged amino acid residue). Each of the antibacterial agent, lipopolysaccharide-cell-binding inhibitor, and drug (e.g., bacterial-infection-treating agent or endotoxin-shock suppressant) contains the peptide as an active ingredient. The present invention also provides for a peptide comprised of a sequence of cationic and non-polar or polar uncharged amino acids forming an α-helix wherein the amino acids are arranged along the α-helix such that when represented as a helical wheel, there is a substantial bi-lateral symmetry between cationic versus non-polar or polar uncharged amino acids.
摘要翻译：本发明提供了一种基于CAP11的新型肽，并且提供了抗细菌剂，LPS-细胞结合抑制剂和细菌感染处理剂或内毒素 - 休克抑制剂等药物，每种含有肽作为活性成分。肽具有以下氨基酸序列（SEQ ID NO：1）：X01 X02 X03 X03 X04 X02 X03 X03 X05 X04 X03 X04 X02 X01 X03 X02 X05 X03（其中X01表示阳离子性氨基酸残基或极性不带电荷的氨基酸残基 X02表示非极性氨基酸残基，X03表示阳离子性氨基酸残基，X04表示非极性氨基酸残基或阳离子性氨基酸残基，X05表示非极性氨基酸残基或极性不带电氨基酸残基）。各抗菌剂，脂多糖 - 细胞结合抑制剂和药物（例如细菌感染处理剂或内毒素 - 休克抑制剂）均含有作为有效成分的肽。本发明还提供了由阳离子和非极性或极性不带电荷的氨基酸序列组成的肽，其形成α-螺旋，其中氨基酸沿着α-螺旋排列，使得当以螺旋轮表示时，存在阳离子与非极性或极性不带电氨基酸之间的实质双侧对称性。

5. 发明授权

US3931136A Catalytic production of a high molecular weight cis-1,4-polyisoprene 失效
标题翻译：催化生产高分子量顺式-1,4-聚异戊二烯
公开(公告)号：US3931136A
公开(公告)日：1976-01-06
申请号：US472632
申请日：1974-05-23
申请人： Kan Mori , Hiroharu Ikeda , Isao Nagaoka , Tooru Shibata , Sigeo Kawatani , Tatsuhiko Kikuchi
发明人： Kan Mori , Hiroharu Ikeda , Isao Nagaoka , Tooru Shibata , Sigeo Kawatani , Tatsuhiko Kikuchi
IPC分类号： C08F136/08 , C08D1/14 , C08D3/12
CPC分类号： C08F136/08
摘要： High molecular weight cis-1,4-polyisoprene is produced by contacting isoprene with a catalyst formed by admixing (A) a titanium tetrachloride, (B) a trihydrocarbylaluminum and (C) a beta-diketone. The activity of this ternary catalyst is not adversely affected by such impurities as cyclopentadiene that are contained in the feed stock isoprene.
摘要翻译：通过使异戊二烯与（A）四氯化钛，（B）三烃基铝和（C）β-二酮混合形成的催化剂接触来制备高分子量顺式-1,4-聚异戊二烯。这种三元催化剂的活性不受包含在原料异戊二烯中的杂环如环戊二烯的不利影响。

6. 发明授权

US4082817A Process for producing maleic anhydride adduct of high molecular weight 1,2-polybutadiene 失效
标题翻译：生产高分子量1,2-聚丁二烯的马来酸酐的方法
公开(公告)号：US4082817A
公开(公告)日：1978-04-04
申请号：US671147
申请日：1976-03-29
申请人： Fumitake Imaizumi , Isao Nagaoka , Mitsuo Kurokawa , Koei Komatsu
发明人： Fumitake Imaizumi , Isao Nagaoka , Mitsuo Kurokawa , Koei Komatsu
IPC分类号： C08C19/28 , C08F8/46
CPC分类号： C08C19/28 , Y10S525/914
摘要： A process for producing a maleic anhydride adduct of high molecular weight 1,2-polybutadiene by contacting with heat maleic anhydride with high molecular weight 1,2-polybutadiene in the absence of a radical initiator in a halogenated aromatic hydrocarbon solvent. The adduct obtained by this process has a high molecular weight of more than 10,000 and is quite free from gel. Said process enables the addition of maleic anhydride in any desired proportion.

7. 发明授权

US4075096A Suction device for an oil separation tank 失效
标题翻译：油分离罐吸油装置
公开(公告)号：US4075096A
公开(公告)日：1978-02-21
申请号：US723865
申请日：1976-09-16
申请人： Hiroshi Kawakami , Yukio Tsukagawa , Isao Nagaoka
发明人： Hiroshi Kawakami , Yukio Tsukagawa , Isao Nagaoka
IPC分类号： C02F1/40 , B01D17/02 , B04B5/12 , E02B15/04 , E02B15/10 , B01D21/24
CPC分类号： B01D17/0214 , E02B15/107 , Y10S210/923
摘要： A suction device for an oil separation tank mounted on a floating body comprises a liquid piping structure for transporting floating oil from the oil separation tank into a storage tank and a vacuum piping structure for always retaining floating oil in the oil separation tank at a suction state, and may automatically control an intermittent suction operation.
摘要翻译：用于安装在浮体上的油分离罐的抽吸装置包括用于将浮油从油分离罐输送到储罐中的液体管道结构和用于在吸入状态下始终将浮油保持在油分离罐中的真空管道结构，并且可以自动控制间歇抽吸操作。

8. 发明授权

US08242082B2 Antibacterial peptide 有权
标题翻译：抗菌肽
公开(公告)号：US08242082B2
公开(公告)日：2012-08-14
申请号：US12148094
申请日：2008-04-16
申请人： Isao Nagaoka , Daiju Okuda , Shin Yomogida , Hiroshi Tamura
发明人： Isao Nagaoka , Daiju Okuda , Shin Yomogida , Hiroshi Tamura
IPC分类号： A61K38/10
CPC分类号： C07K14/4723
摘要： The present invention provides a novel peptide based on CAP11 as well as provides an antibacterial agent, an LPS-cell-binding inhibitor, and a drug such as a bacterial-infection-treating agent or an endotoxin-shock suppressant, each containing the peptide as an active ingredient. The peptide has the following amino acid sequence (SEQ ID NO: 1): X01 X02 X03 X03 X04 X02 X03 X03 X05 X04 X03 X04 X02 X01 X03 X02 X05 X03 (wherein X01 represents a cationic amino acid residue or a polar uncharged amino acid residue, X02 represents a non-polar amino acid residue, X03 represents a cationic amino acid residue, X04 represents a non-polar amino acid residue or a cationic amino acid residue, and X05 represents a non-polar amino acid residue or a polar uncharged amino acid residue). Each of the antibacterial agent, lipopolysaccharide-cell-binding inhibitor, and drug (e.g., bacterial-infection-treating agent or endotoxin-shock suppressant) contains the peptide as an active ingredient. The present invention also provides for a peptide comprised of a sequence of cationic and non-polar or polar uncharged amino acids forming an α-helix wherein the amino acids are arranged along the α-helix such that when represented as a helical wheel, there is a substantial bi-lateral symmetry between cationic versus non-polar or polar uncharged amino acids.
摘要翻译：本发明提供了一种基于CAP11的新型肽，并且提供了抗细菌剂，LPS-细胞结合抑制剂和细菌感染处理剂或内毒素 - 休克抑制剂等药物，每种含有肽作为活性成分。肽具有以下氨基酸序列（SEQ ID NO：1）：X01 X02 X03 X03 X04 X02 X03 X03 X05 X04 X03 X04 X02 X01 X03 X02 X05 X03（其中X01表示阳离子性氨基酸残基或极性不带电荷的氨基酸残基 X02表示非极性氨基酸残基，X03表示阳离子性氨基酸残基，X04表示非极性氨基酸残基或阳离子性氨基酸残基，X05表示非极性氨基酸残基或极性不带电氨基酸残基）。各抗菌剂，脂多糖 - 细胞结合抑制剂和药物（例如细菌感染处理剂或内毒素 - 休克抑制剂）均含有作为有效成分的肽。本发明还提供了由阳离子和非极性或极性不带电荷的氨基酸序列组成的肽，其形成α-螺旋，其中氨基酸沿α螺旋排列，使得当以螺旋轮表示时，存在阳离子与非极性或极性不带电氨基酸之间的实质双侧对称性。

9. 发明申请

US20060009374A1 Antibacterial peptide 有权
公开(公告)号：US20060009374A1
公开(公告)日：2006-01-12
申请号：US11093875
申请日：2005-03-29
申请人： Isao Nagaoka , Daiju Okuda , Shin Yomogida , Hiroshi Tamura
发明人： Isao Nagaoka , Daiju Okuda , Shin Yomogida , Hiroshi Tamura
IPC分类号： A61K38/16 , C07K14/195
CPC分类号： C07K14/4723
摘要： The present invention provides a novel peptide based on CAP11 as well as provides an antibacterial agent, an LPS-cell-binding inhibitor, and a drug such as a bacterial-infection-treating agent or an endotoxin-shock suppressant, each containing the peptide as an active ingredient. The peptide has the following amino acid sequence (SEQ ID NO: 1): X01 X02 X03 X03 X04 X02 X03 X03 X05 X04 X03 X04 X02 X01 X03 X02 X05 X03 (wherein X01 represents a cationic amino acid residue or a polar uncharged amino acid residue, X02 represents a non-polar amino acid residue, X03 represents a cationic amino acid residue, X04 represents a non-polar amino acid residue or a cationic amino acid residue, and X05 represents a non-polar amino acid residue or a polar uncharged amino acid residue). Each of the antibacterial agent, lipopolysaccharide-cell-binding inhibitor, and drug (e.g., bacterial-infection-treating agent or endotoxin-shock suppressant) contains the peptide as an active ingredient. The present invention also provides for a peptide comprised of a sequence of cationic and non-polar or polar uncharged amino acids forming an α-helix wherein the amino acids are arranged along the α-helix such that when represented as a helical wheel, there is a substantial bi-lateral symmetry between cationic versus non-polar or polar uncharged amino acids.

10. 发明授权

US06627621B2 Neutrophil function inhibitors 有权
公开(公告)号：US06627621B2
公开(公告)日：2003-09-30
申请号：US09906771
申请日：2001-07-18
申请人： Isao Nagaoka , Koji Sakamoto
发明人： Isao Nagaoka , Koji Sakamoto
IPC分类号： A61K3170
CPC分类号： A61K31/7008 , A23L2/52 , A23L33/17
摘要： Glucosamine salts are effective for the inhibition of neutrophil functions, and hence, are useful for the prevention and/or treatment of diseases, caused as a result of an excessive extracellular release of active oxygen and antibiotic proteins by neutrophils, such as respiratory disease syndrome and adult respiratory disease syndrome. Use of glucosamine salts can, therefore, provide neutrophil function inhibitors, preventives and/or remedies for diseases caused as a result of an excessive extracellular release of active oxygen and antibiotic proteins by neutrophils, and also methods for the prevention and/or treatment of such diseases.

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