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59 条记录 (耗时 0.028 秒)

    Method for producing oil and fat composition with reduced trans-fatty acid content and processed oil and fat product containing the oil and fat composition
    1.
    发明申请
    Method for producing oil and fat composition with reduced trans-fatty acid content and processed oil and fat product containing the oil and fat composition 审中-公开
    生产具有降低的反式脂肪酸含量的油脂组合物的方法，含有油脂组合物的加工油脂产品

    公开(公告)号：US20070231446A1

    公开(公告)日：2007-10-04

    申请号：US11806222

    申请日：2007-05-30

    申请人： Takeshi Nagasawa ,  Akira Akahane ,  Kaori Muroga ,  Masahiro Arikai

    发明人： Takeshi Nagasawa ,  Akira Akahane ,  Kaori Muroga ,  Masahiro Arikai

    IPC分类号： A23D9/00

    CPC分类号： C12P7/6454 ,  A23D9/00 ,  C11C3/10

    摘要： A method for producing an oil and fat composition includes the steps of (a) mixing an oil and fat (A) wherein fatty acids with 14 or less carbon atoms are contained in an amount of 50 to 100% by mass of the entire constituent fatty acids of the triglycerides with an oil and fat (B) wherein fatty acids with 16 to 24 carbon atoms are contained in an amount of 80 to 100% by mass of the entire constituent fatty acids of the triglycerides to obtain an oil and fat mixture; (b) subjecting the oil and fat mixture to random transesterification using an enzyme having no positional specificity, and (c) obtaining an oil and fat composition free from trans-fatty acid.

    摘要翻译： 油脂组合物的制造方法包括以下步骤：（a）将含有14个以下碳原子的脂肪酸的油脂（A）以50〜100质量％ 甘油三酸酯与油脂（B）的酸，其中含有16至24个碳原子的脂肪酸的量为甘油三酯的全部构成脂肪酸的80至100质量％，以获得油脂混合物; （b）使用不具有位置特异性的酶对油脂混合物进行无规酯交换反应，和（c）获得不含反式脂肪酸的油脂组合物。

    Method of quantitative assay for 1,5-anhydroglucitol
    4.
    发明授权
    Method of quantitative assay for 1,5-anhydroglucitol 失效
    1,5-脱水葡萄糖醇的定量测定方法

    公开(公告)号：US06268166B1

    公开(公告)日：2001-07-31

    申请号：US08230440

    申请日：1994-04-19

    申请人： Ryo Kojima ,  Yoshiro Sato ,  Takeshi Nagasawa

    发明人： Ryo Kojima ,  Yoshiro Sato ,  Takeshi Nagasawa

    IPC分类号： C12Q126

    CPC分类号： C12Q1/26 ,  C12P7/02

    摘要： There is provided an enzymatic method of rapid quantitative assay for 1,5-anhydroglucitol which is also applicable to an automated analysis device. The enzymatic method of quantitative assay for 1,5-anhydroglucitol is characterized by using a pyranose oxidase derived from Basidiomycetous fungi No. 52 as a pyranose oxidase. According to the assaying method of the present invention, assay for 1,5-anhydroglucitol in a specimen can be performed using an automated analysis device, results in rapid assay and improved accuracy.

    摘要翻译： 提供了用于1,5-脱水葡萄糖醇的快速定量测定法的酶法，其也适用于自动化分析装置。 1,5-脱水葡萄糖醇的定量测定法的特征在于使用源自Basidiomycetous真菌No.52的吡喃糖氧化酶作为吡喃糖氧化酶。 根据本发明的测定方法，可以使用自动分析装置进行样品中1,5-脱水葡萄糖醇的测定，结果快速测定并提高精度。

    L-argininal acetal derivatives and a process for production thereof
    6.
    发明授权
    L-argininal acetal derivatives and a process for production thereof 失效
    L-精氨酸缩醛衍生物及其制备方法

    公开(公告)号：US5416238A

    公开(公告)日：1995-05-16

    申请号：US755527

    申请日：1991-09-05

    申请人： Yoshihito Abe ,  Akio Hashimoto ,  Takeshi Nagasawa ,  Katsumasa Kuroiwa

    发明人： Yoshihito Abe ,  Akio Hashimoto ,  Takeshi Nagasawa ,  Katsumasa Kuroiwa

    IPC分类号： C07C279/12 ,  B01J31/02 ,  C07B61/00 ,  C07C277/08 ,  C07C279/24 ,  C07C209/78

    CPC分类号： C07C279/12 ,  C07C279/24 ,  Y02P20/55

    摘要： Novel N.sup.G -protected or unprotected-L-argininal-dibutyl acetals (I) can be prepared from L-argininal derivatives (III) merely by reacting in an azeotropic solvent in the presence of p-toluenesulfonic acid. In the products (I), L-form amounts to more than 99%, without further optical resolution. The L-argininal acetals (I) are useful as starting materials for preparing peptidyl-L-argininal derivatives which can provide protease inhibitors or ligands used for affinity chromatography of various proteases.

    摘要翻译： 只有通过在对甲苯磺酸存在下在共沸溶剂中反应，可以由L-精氨酸衍生物（III）制备新的NG-保护的或未受保护的L-精氨酸 - 二丁基缩醛（I）。 在产品（I）中，L型大于99％，无需进一步的光学拆分。 L-精氨酸缩醛（I）可用作制备肽基-L-精氨酸衍生物的起始原料，其可以提供蛋白酶抑制剂或用于各种蛋白酶亲和层析的配体。

    Facsimile apparatus
    8.
    发明授权
    Facsimile apparatus 失效
    传真机

    公开(公告)号：US4667252A

    公开(公告)日：1987-05-19

    申请号：US861989

    申请日：1986-05-12

    申请人： Takuji Nakamura ,  Toshinori Otsuki ,  Takeshi Nagasawa ,  Yoshihiro Ikemoto

    发明人： Takuji Nakamura ,  Toshinori Otsuki ,  Takeshi Nagasawa ,  Yoshihiro Ikemoto

    IPC分类号： H04N1/00 ,  H04N1/10 ,  H04N1/22

    CPC分类号： H04N1/00519

    摘要： A facsimile apparatus using a continuous length of recording paper with its first surface for recording and its second surface for transmitting scripts. Received facsimile signals are recorded on the first surface through a recording section, and scripts which are to be transmitted are written on the second surface and read through a reading section. This arrangement needs only one paper feeding passage and enables the paper to be efficiently used, since the non-recording surface of the paper can be used as a surface on which scripts are written.

    摘要翻译： 一种使用连续长度的记录纸及其第一表面用于记录的传真装置，其第二表面用于发送脚本。 接收的传真信号通过记录部分被记录在第一表面上，并且要发送的脚本被写在第二表面上并通过阅读部分读取。 这种布置仅需要一个给纸通道，并且能够有效地使用纸张，因为纸张的非记录表面可以用作写入脚本的表面。

    Process for acylation of amino, imino and hydroxyl groups using pyrimidine derivatives
    10.
    发明授权
    Process for acylation of amino, imino and hydroxyl groups using pyrimidine derivatives 失效
    使用嘧啶衍生物酰化氨基，亚氨基和羟基的方法

    公开(公告)号：US3960829A

    公开(公告)日：1976-06-01

    申请号：US509221

    申请日：1974-09-25

    申请人： Takeshi Nagasawa ,  Katumasa Kuroiwa ,  Kouichi Narita

    发明人： Takeshi Nagasawa ,  Katumasa Kuroiwa ,  Kouichi Narita

    IPC分类号： C07K1/08 ,  C07C103/52 ,  C07C69/00 ,  C07C125/00

    CPC分类号： C07K1/086 ,  C07K1/084

    摘要： Pyrimidine derivatives represented by the formula, ##SPC1##Wherein R.sub.1 and R.sub.2 are individually a hydrogen atom or a methyl group, and R.sub.3 is a group formed by removing the carboxyl group from a carboxylic acid, are quite useful in acylating compounds having amino and/or imino and/or hydroxyl groups. The pyrimidine derivatives can easily be prepared by reacting a 2-mercapto-4- and/or 6-methyl-substituted or unsubstituted pyrimidine with a carboxylic acid or a reactive derivative thereof in an inert solvent.

    摘要翻译： 由式WHEREIN R1和R2表示的嘧啶衍生物分别为氢原子或甲基，R3为通过从羧酸除去羧基而形成的基团，在酰化具有氨基和/或亚氨基的化合物和 /或羟基。 嘧啶衍生物可以容易地通过使2-巯基-4-和/或6-甲基取代或未取代的嘧啶与羧酸或其活性衍生物在惰性溶剂中反应来制备。