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1. 发明申请

US20100152443A1 PYRAZOLE DERIVATIVE, INTERMEDIATE THEREFOR, PROCESSES FOR PRODUCING THESE, AND HERBICIDE CONTAINING THESE AS ACTIVE INGREDIENT 审中-公开
标题翻译：吡唑衍生物，其中间体，其制备方法和包含这些作为活性成分的除草剂
公开(公告)号：US20100152443A1
公开(公告)日：2010-06-17
申请号：US12713421
申请日：2010-02-26
申请人： Kenji Hirai , Atsushi Uchida , Atsuko Watanabe , Taeko Abe , Takuya Ueda , Hiroshi Sakurai
发明人： Kenji Hirai , Atsushi Uchida , Atsuko Watanabe , Taeko Abe , Takuya Ueda , Hiroshi Sakurai
IPC分类号： C07D413/12 , C07D231/18 , C07D401/12 , C07D405/12
CPC分类号： A01N47/38 , C07D231/20
摘要： The present invention provides a pyrazole derivative of the general formula (1), which has an excellent efficacy as an active component for a herbicide, an intermediate for the production thereof, processes for the production thereof, and a herbicide containing the derivative as an active ingredient.
摘要翻译：本发明提供通式（1）的吡唑衍生物，其作为除草剂的活性成分，其制备中间体，其制备方法和含有该衍生物作为活性成分的除草剂具有优异的功效成分。

2. 发明申请

US20090043119A1 TANTALUM COMPOUND, METHOD FOR PRODUCING SAME, TANTALUM-CONTAINING THIN FILM AND METHOD FOR FORMING SAME 有权
标题翻译：钛化合物，其制造方法，含有薄膜的薄膜及其形成方法
公开(公告)号：US20090043119A1
公开(公告)日：2009-02-12
申请号：US11815386
申请日：2006-01-25
申请人： Kenichi Sekimoto , Ken-ichi Tada , Mayumi Takamori , Tetsu Yamakawa , Taishi Furukawa , Noriaki Oshima
发明人： Kenichi Sekimoto , Ken-ichi Tada , Mayumi Takamori , Tetsu Yamakawa , Taishi Furukawa , Noriaki Oshima
IPC分类号： C07F9/00
CPC分类号： C23C16/18 , C07F17/00
摘要： Objects of the present invention are to provide a novel tantalum compound which enables to selectively form a tantalum-containing thin film free of halogen and the like, and various tantalum-containing thin films which contain the desired element, and a method for producing the same, and further provide a method for stably forming a tantalum-containing thin film which contains the desired element.The present invention relates to a tantalum compound represented by the following formula (1) (In the formula, R1 represents a straight-chain alkyl group having from 2 to 6 carbon atoms), or a tantalum compound represented by the general formula (2) (In the formula, R2 represents a straight-chain alkyl group having from 2 to 6 carbon atoms), and a method for producing the same.The present invention further relates to form a tantalum-containing thin film by using a tantalum compound represented by the following general formula (6) (In the formula, j, k, m and n is an integer of from 1 to satisfying j+k=5 and m+n=5, and R3 to R6 represent a hydrogen atom, an alkyl group having from 1 to 6 carbon atoms, and the like) as a raw material.
摘要翻译：本发明的目的是提供一种新颖的钽化合物，其能够选择性地形成不含卤素等的含钽薄膜，以及含有所需元素的各种含钽薄膜及其制造方法并且还提供了一种稳定地形成含有所需元素的含钽薄膜的方法。本发明涉及由下式（1）表示的钽化合物（式中，R1表示碳原子数2〜6的直链烷基）或通式（2）表示的钽化合物，（式中，R 2表示碳原子数2〜6的直链烷基）及其制造方法。本发明还涉及通过使用由以下通式（6）表示的钽化合物形成含钽薄膜（在式中，j，k，m和n是从1到满足j + k的整数 = 5，m + n = 5，R3〜R6表示氢原子，碳原子数1〜6的烷基等）作为原料。

3. 发明申请

US20090018345A1 PYRAZOLE-1-CARBOXYLATE DERIVATIVES, PROCESS FOR THE PRODUCTION THEREOF AND PROCESS FOR THE PRODUCTION OF PYRAZOLE DERIVATIVES 失效
标题翻译：吡咯-1-羧酸衍生物，其生产方法及其制备方法制备吡唑衍生物
公开(公告)号：US20090018345A1
公开(公告)日：2009-01-15
申请号：US11915016
申请日：2006-05-22
申请人： Atsushi Uchida , Wakako Yokota , Kenji Hirai , Tomoyuki Yano
发明人： Atsushi Uchida , Wakako Yokota , Kenji Hirai , Tomoyuki Yano
IPC分类号： C07D231/20
CPC分类号： C07D231/20
摘要： Disclosed are pyrazole-1-carboxylate derivatives of the general formula (1), (wherein symbols are as defined in the specification), a process for the production thereof and processes for producing herbicidally active 3-aryloxypyrazole-1-carboxamide derivatives from the above compound and an intermediate therefor. According to this invention, there can be industrially advantageously produced 3-aryloxypyrazole-1-carboxamide derivatives that does not cause chemical damage on crops but exhibits excellent herbicidal activity against weeds that impair the growth of such crops.
摘要翻译：公开了通式（1）的吡唑-1-羧酸酯衍生物（其中符号如说明书中所定义），其制备方法和从上述产生除草活性3-芳氧基吡唑-1-甲酰胺衍生物的方法化合物及其中间体。根据本发明，可以在工业上有利地生产不对作物造成化学损害的3-芳氧基吡唑-1-甲酰胺衍生物，但是对于损害这些作物生长的杂草显示出优异的除草活性。

4. 发明授权

US07470808B2 Method for producing fluorine-containing acrylate 有权
标题翻译：含氟丙烯酸酯的制造方法
公开(公告)号：US07470808B2
公开(公告)日：2008-12-30
申请号：US10550387
申请日：2004-03-24
申请人： Takamasa Fuchikami , Noriko Wakasa , Kenji Tokuhisa , Hideyuki Mimura , Shoji Arai
发明人： Takamasa Fuchikami , Noriko Wakasa , Kenji Tokuhisa , Hideyuki Mimura , Shoji Arai
IPC分类号： C07C69/63 , C07C67/36 , C07C69/66
CPC分类号： C07C67/36 , C07C2601/14 , C07C2601/18 , C07C2603/74 , C07C69/653
摘要： A process for producing a fluorine-containing acrylic acid ester represented by CH2═C(Rf)(COOR) characterized in that 1-bromo-1-perfluoroalkylethene represented by CH2═CBr—Rf, or 1,2-dibromo-1-perfluoroalkylethane represented by CH2CBr—CHBr—Rf is allowed to react with an alcohol represented by ROH in the presence of a palladium catalyst, carbon monoxide, and two or more kinds of bases. The fluorine-containing acrylic acid ester is a useful compound having wide applications in materials for pharmaceuticals and functional polymers.
摘要翻译：一种由CH2-C（Rf）（COOR）表示的含氟丙烯酸酯的制备方法，其特征在于由CH2-CBr-Rf表示的1-溴-1-全氟烷基烯或1,2-二溴-1-全氟烷基乙烷由二氯甲烷CH 2 Cl-Rf表示的化合物与钯催化剂，一氧化碳和两种或更多种碱的存在下与ROH表示的醇进行反应。含氟丙烯酸酯是广泛用于药物和功能聚合物的材料的有用化合物。

5. 发明申请

US20020106777A1 Human PEC-60-like protein and DNA encoding this protein 审中-公开
标题翻译：人类PEC-60样蛋白和编码该蛋白的DNA
公开(公告)号：US20020106777A1
公开(公告)日：2002-08-08
申请号：US09941309
申请日：2001-08-28
申请人： Sagami Chemical Research Center
发明人： Seishi Kato , Tomoko Yamaguchi , Shingo Sekine , Kouju Kamata
IPC分类号： C12N009/24 , C12N009/64 , C07H021/04
CPC分类号： C07K14/575 , A61K38/00 , C07K2319/00
摘要： The present invention provides a human PEC-60-like protein, a gastrointestinal hormone excreted by a stomach tissue and a cDNA encoding this protein. The protein and the gene of the present invention can provide a protein containing the amino acid sequence represented by Sequence No. 1 and a t DNA encoding said protein exemplified as a cDNA containing the base sequence represented by Sequence No. 1. as well as a human cDNA encoding a human PEC-60-like protein and said protein by the expression of this human cDNA recombinant.
摘要翻译：本发明提供人类PEC-60样蛋白质，由胃组织排出的胃肠激素和编码该蛋白质的cDNA。本发明的蛋白质和基因可以提供含有序列号1所示的氨基酸序列的蛋白质和编码所述蛋白质的DNA，该DNA作为含有序列号1所示的碱基序列的cDNA，以及人通过该人cDNA重组体的表达，编码人类PEC-60样蛋白质的cDNA和所述蛋白质。

6. 发明授权

US6090946A Process for the preparation of 3-(substituted phenyl)-5-alkylidene-1,3-oxazolidine-2,4-dione derivatives 失效
标题翻译： 3-（取代苯基）-5-亚烷基-1,3-恶唑烷-2,4-二酮衍生物的制备方法
公开(公告)号：US6090946A
公开(公告)日：2000-07-18
申请号：US894655
申请日：1997-12-15
申请人： Kenji Hirai , Katsuyuki Masuda , Tomoyuki Yano , Ryuta Ohno , Tomoko Matsukawa , Kiyomi Imai , Natsuko Okano , Tomoko Yoshii , Takehito Mouri
发明人： Kenji Hirai , Katsuyuki Masuda , Tomoyuki Yano , Ryuta Ohno , Tomoko Matsukawa , Kiyomi Imai , Natsuko Okano , Tomoko Yoshii , Takehito Mouri
IPC分类号： C07C67/31 , C07D263/44
CPC分类号： C07D263/44 , C07C67/31
摘要： The present invention provides an industrial process for efficiently preparing a 3-(substituted phenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione derivative having a potent herbicidal activity without using phosgene or the like. The present invention relates to a process for preparing a 3-(substituted phenyl)-5-alkylidene-1,3-oxazolidine-2,4-dione derivative represented by general formula (III), which comprises reaction of an N-(substituted phenyl)carbamate represented by general formula (I) with a 2-hydroxy-3-alkenoate represented by-general formula (II) or with a 3-alkoxy-2-hydroxyalkanoate represented by general formula (IV): ##STR1## (wherein Ar is a substituted phenyl group, R.sup.1 is an alkyl group having a carbon number of from 1 to 6, R.sup.2 and R.sup.3 are independently hydrogen atoms or alkyl groups having carbon numbers of from 1 to 12, and R.sup.4 and R.sup.5 are independently alkyl groups having carbon numbers of from 1 to 6).
摘要翻译： PCT No.PCT / JP96 / 00430 Sec。 371 1997年12月15日第 102（e）日期1997年12月15日PCT提交1996年2月26日PCT公布。公开号WO96 / 26930 PCT。日本1996年9月6日本发明提供了一种不使用光气等有效制备具有强效除草活性的3-（取代苯基）-5-异亚丙基-1,3-恶唑烷-2,4-二酮衍生物的工业方法。本发明涉及一种制备由通式（III）表示的3-（取代苯基）-5-亚烷基-1,3-恶唑烷-2,4-二酮衍生物的方法，该方法包括N-（取代的苯基）氨基甲酸酯与由通式（II）表示的2-羟基-3-烯酸酯或由通式（IV）表示的3-烷氧基-2-羟基链烷酸酯反应：（其中Ar为取代的苯基，R1是碳数为1至6的烷基，R2和R3独立地为氢原子或碳数为1至12的烷基，R4和R5独立地为碳数为从1到6）。

7. 发明授权

US6051424A Human cDNAs and proteins encoded thereby 失效
标题翻译：人类cDNA和由此编码的蛋白质
公开(公告)号：US6051424A
公开(公告)日：2000-04-18
申请号：US390207
申请日：1995-02-16
申请人： Seishi Kato , Suwan Oh , Shingo Sekine , Namsoon Kim , Takae Kato , Akiyo Iwahori
发明人： Seishi Kato , Suwan Oh , Shingo Sekine , Namsoon Kim , Takae Kato , Akiyo Iwahori
IPC分类号： C07K14/47 , C12N9/10 , C12N9/14 , C12N15/12 , C07H21/00 , C12N15/63
CPC分类号： C12N9/1007 , C07K14/47 , C12N9/14
摘要： Isolated cDNAs derived from mRNAs expressed in human cells are provided, as are DNAs and RNAs comprising their nucleotide sequences, and vectors for expressing the cDNAs. The cDNAs encode proteins which have functions similar to known proteins.
摘要翻译：提供了源自人细胞中表达的mRNA的分离的cDNA，以及包含其核苷酸序列的DNA和RNA以及用于表达cDNA的载体。 cDNA编码具有与已知蛋白质相似功能的蛋白质。

8. 发明授权

US5683898A Gene coding for eicosapentaenoic acid synthesizing enzymes and process for production of eicosapentaenoic acid 失效
标题翻译：二十碳五烯酸合成酶的基因编码和二十碳五烯酸的生产方法
公开(公告)号：US5683898A
公开(公告)日：1997-11-04
申请号：US375709
申请日：1995-01-20
申请人： Kazunaga Yazawa , Akiko Yamada , Seishi Kato , Kiyosi Kondo
发明人： Kazunaga Yazawa , Akiko Yamada , Seishi Kato , Kiyosi Kondo
IPC分类号： C12N1/21 , C12N9/00 , C12P7/64 , C07H19/00 , C12N1/20 , C12N15/00
CPC分类号： C12N9/93 , C12P7/6427 , C12P7/6472
摘要： There is provided an advantageous process for production of EPA by a gene recombinant technique wherein genes coding for biosynthesis enzymes for eicosapentaenoic acid (EPA) useful as pharmaceuticals, agrochemicals, foods, feeds or the like is obtained from microorganisms. EPA is produced by obtaining genes coding for eicosapentaenoic acid (EPA) biosynthesis enzymes, constructing a plasmid by joining the genes to a vector, transforming E. coli with the plasmid, and culturing the transformed E. coli.
摘要翻译：提供了通过基因重组技术生产EPA的有利方法，其中可从微生物获得编码二十碳五烯酸（EPA）的生物合成酶的基因，其用作药物，农业化学品，食品，饲料等。 EPA通过获得编码二十碳五烯酸（EPA）生物合成酶的基因产生，通过将基因连接到载体构建质粒，用质粒转化大肠杆菌，并培养转化的大肠杆菌。

9. 发明授权

US5629430A Trifluoromethylpyrroloindolecarboxylic acid ester and process for production thereof 失效
标题翻译：三氟甲基吡咯烷羧酸酯及其制备方法
公开(公告)号：US5629430A
公开(公告)日：1997-05-13
申请号：US381981
申请日：1995-06-14
申请人： Shiro Terashima , Yasumichi Fukuda , Yasuo Oomori
发明人： Shiro Terashima , Yasumichi Fukuda , Yasuo Oomori
IPC分类号： A61K31/40 , A61P31/04 , A61P35/00 , C07D487/04 , C07D487/10 , C07D519/00
CPC分类号： C07D487/04 , C07D487/10 , Y02P20/55
摘要： Trifluoromethylpyrroloindolecarboxylic acid ester derivatives, and optical isomers and pharmaceutically acceptable salts thereof are provided which are represented by the general formula (1): ##STR1## or the general formula (2): ##STR2## The compounds are antineoplastic agents which are selective to cancer cells, effective also to solid cancer, and less toxic.
摘要翻译： PCT No.PCT / JP93 / 01159 Sec。 371 1995年6月14日第 102（e）1995年6月14日PCT PCT 1993年8月19日PCT公布。第WO94 / 04535号公报日期：1994年3月3日提供三氟甲基吡咯并吲哚羧酸酯衍生物及其光学异构体及其药学上可接受的盐，它们由通式（1）表示：或通式（2）：该化合物是抗肿瘤剂其对癌细胞是选择性的，对实体癌也有效，毒性较小。

10. 发明授权

US5624826A Cloning vector plasmid vector-primer derived therefrom and preparation method of the same 失效
标题翻译：来源于其的克隆载体质粒载体引物及其制备方法
公开(公告)号：US5624826A
公开(公告)日：1997-04-29
申请号：US466111
申请日：1995-06-06
申请人： Seishi Kato , Takashi Aoki , Yuri Umezawa
发明人： Seishi Kato , Takashi Aoki , Yuri Umezawa
IPC分类号： C12N15/00 , C07K14/525 , C12N15/09 , C12N15/10 , C12N15/70 , C12N15/85 , C12N15/64
CPC分类号： C12N15/1096 , C07K14/525 , C12N15/85 , C12N2800/108
摘要： Disclosed is a cloning vector plasmid suitable for preparing cDNA banks. The cloning vector plasmid of the present invention comprises, in the order mentioned from upstream to downstream region unless otherwise specified, a promoter PR1 acting in mammalian cells; an unique restriction enzyme site RE1 rarely existing in eukaryotic DNA and a promoter PR2 of RNA polymerase; an unique restriction enzyme site RE2 generating 3'-protruding dG tail; an unique arbitrary restriction enzyme site RE3; an unique arbitrary restriction enzyme site RE4 generating 3'-protruding terminus; an unique restriction enzyme site RE5 rarely existing in eukaryotic DNA and a promoter PR3 of RNA polymerase; and at least one kind of arbitrary restriction enzyme site RE6 generating 3'-protruding terminus existing at the arbitrary position before the restriction site RE1; and further, at arbitrary positions other than the above-described restriction enzyme sites and promoters, an origin OR1 for replication in mammalian cells, an origin OR2 for replication of a single-stranded phage, an origin OR3 for replication in E. coli, and a selective marker.
摘要翻译：公开了适用于制备cDNA库的克隆载体质粒。除非另有说明，本发明的克隆载体质粒以上游至下游区域的顺序包含在哺乳动物细胞中起作用的启动子PR1; 在真核DNA中很少存在的独特的限制酶位点RE1和RNA聚合酶的启动子PR2; 独特的限制酶位点RE2产生3'突出的dG尾巴; 独特的任意限制酶位点RE3; 独特的任意限制酶位点RE4产生3'突出的末端; 在真核DNA中很少存在一个独特的限制酶位点RE5和RNA聚合酶的启动子PR3; 以及存在于限制性位点RE1前的任意位置的产生3'突出末端的至少一种任意限制酶位点RE6; 此外，在除了上述限制酶位点和启动子之外的任意位置，用于在哺乳动物细胞中复制的起始OR1，用于复制单链噬菌体的起点OR2，用于在大肠杆菌中复制的起始OR3，以及选择性标记。

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