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    • 81. 发明授权
    • Preheating control apparatus for diesel engines
    • 柴油机预热控制装置
    • US4962300A
    • 1990-10-09
    • US239608
    • 1981-03-02
    • Kiyoshi Watanabe
    • Kiyoshi Watanabe
    • F02B3/06F02P19/02
    • F02P19/025F02B3/06
    • A preheating control apparatus for diesel engines of the present invention is provided wherein the voltage developed across a sensing resistor connected in series with a glow plug, which voltage is indicative of the temperature of the glow plug, is amplified by an amplifier. The amplified voltage is compared with a predetermined reference voltage to control the preheating current through the glow plug so that the temperature of the glow plug can be precisely controlled without increasing the resistance value of the sensing resistor. Further, a protection circuit may be provided to end the preheating current to the glow plug in response to an abnormal change in the voltage applied to the glow plug.
    • 提供了本发明的柴油发动机的预热控制装置,其中跨越与电热塞串联的感测电阻器产生的电压被放大器放大,该电热塞指示电热塞的温度。 将放大的电压与预定的参考电压进行比较,以控制通过电热塞的预热电流,使得可以精确地控制电热塞的温度而不增加感测电阻器的电阻值。 此外,可以提供保护电路以响应于施加到电热塞的电压的异常变化而将预热电流结束到电热塞。
    • 85. 发明授权
    • Method for producing optically active glycol derivatives
    • 光学活性二醇衍生物的制备方法
    • US4745066A
    • 1988-05-17
    • US846766
    • 1986-04-01
    • Shigeki HamaguchiTakehisa OhashiKiyoshi Watanabe
    • Shigeki HamaguchiTakehisa OhashiKiyoshi Watanabe
    • C07B31/00C07C67/00C07C301/00C07C303/22C07C309/72C12P11/00C12P41/00C12R1/01C12R1/38C12R1/66C12R1/785C12R1/845
    • C12P41/004C07C309/00C12P11/00
    • A method for producing optically active glycol derivatives by biochemical resolution which comprises contacting a racemic ester of the general formula 1 ##STR1## (wherein R.sub.1 is an aliphatic hydrocarbon group of 1 to 16 carbon atoms, R.sub.2 is an aliphatic hydrocarbon group of 1 to 8 carbon atoms, and R.sub.3 is an aromatic hydrocarbon group such as phenyl, tolyl or naphtyl) with a microorganism- or animal organ-derived enzyme having stereoselective hydrolytic activity to asymmetrically hydrolyze said racemic ester of general formula 1 to produce an optically active alcohol of general formula 2* ##STR2## (wherein R.sub.1 and R.sub.3 have the same meanings as defined above) and an unreacted ester of the general formula 1* ##STR3## (wherein R.sub.1, R.sub.2 and R.sub.3 have the same meanings as defined hereinbefore), separating the optically active compounds from each other, hydrolyzing said ester of general formula 1* to give an optically active glycol derivative which is antipodal to the alcohol of general formula 2* and, then, isolating the same optically active glycol derivative. The invention provides a method for producing optically active glycol derivatives, which is expedient, does not require costly reagents and is suited to commercial scale production.
    • 一种通过生物化学拆分制备光学活性二醇衍生物的方法,其包括使通式1的外消旋酯1(其中R 1是1至16个碳原子的脂族烃基,R 2是1的脂族烃基, 8个碳原子,并且R 3是芳族烃基如苯基,甲苯基或萘基)与具有立体选择性水解活性的微生物或动物器官衍生的酶不对称地水解所述通式1的外消旋酯以产生光学活性的醇 通式2 * 2 *(其中R 1和R 3具有与上述相同的含义)和通式1 *未反应的酯*(其中R 1,R 2和R 3具有与定义相同的含义) 将光学活性化合物彼此分离,水解所述通式1 *的酯,得到对通式为醇的对映体的光学活性二醇衍生物 2 *,然后分离相同的光学活性二醇衍生物。 本发明提供了一种制备光学活性二醇衍生物的方法,这是有利的,不需要昂贵的试剂并且适于商业规模生产。
    • 88. 发明授权
    • Stable composition of S-adenosyl-L-methionine
    • S-腺苷-L-甲硫氨酸的稳定组成
    • US4369177A
    • 1983-01-18
    • US208842
    • 1980-11-20
    • Yuichi KozakiShingo HataHajime KawaharadaKiyoshi Watanabe
    • Yuichi KozakiShingo HataHajime KawaharadaKiyoshi Watanabe
    • C07H19/16A61K31/70
    • C07H19/16Y10S514/97Y10S514/973
    • A stable composition of S-adenosyl-L-methionine is disclosed which includes a salt of S-adenosyl-L-methionine and a pharmaceutically acceptable, water-soluble salt of a bivalent or trivalent metal. The salt of S-adenosyl-L-methionine is, for example, a salt of S-adenosyl-L-methionine with hydrochloric acid, sulfuric acid, p-toluenesulfonic acid, phosphoric acid, formic acid, acetic acid, citric acid, tartaric acid, or maleic acid; or a double salt of S-adenosyl-L-methionine with the foregoing acids. The salt of a bivalent or trivalent metal is, for example, calcium chloride, ferric chloride, magnesium chloride, or magnesium sulfate. A process for preparing the composition is also disclosed. The composition is suitable for preparing pharmaceutical preparations of S-adenosyl-L-methionine.
    • 公开了S-腺苷-L-甲硫氨酸的稳定组合物,其包括S-腺苷-L-甲硫氨酸的盐和二价或三价金属的药学上可接受的水溶性盐。 S-腺苷-L-甲硫氨酸的盐例如是S-腺苷-L-甲硫氨酸与盐酸,硫酸,对甲苯磺酸,磷酸,甲酸,乙酸,柠檬酸,酒石酸的盐 酸或马来酸; 或S-腺苷-L-甲硫氨酸与上述酸的双重盐。 二价或三价金属的盐是例如氯化钙,氯化铁,氯化镁或硫酸镁。 还公开了制备该组合物的方法。 该组合物适用于制备S-腺苷-L-甲硫氨酸的药物制剂。
    • 90. 发明授权
    • Sheet stacking apparatus and image forming apparatus
    • 片材堆垛装置和成像装置
    • US08651480B2
    • 2014-02-18
    • US13545247
    • 2012-07-10
    • Kiyoshi WatanabeHideki KushidaToshiyuki Iwata
    • Kiyoshi WatanabeHideki KushidaToshiyuki Iwata
    • B65H31/36
    • B65H31/10B65H31/26B65H31/34B65H31/38B65H2301/42192B65H2404/1114B65H2404/7414B65H2404/742B65H2801/27G03G15/6552
    • A finisher 100 includes a pair of bundle discharge rollers 130, a lower stack tray 137, and a width-direction aligning portion 200. The width-direction aligning portion includes a pair of aligning members 1 and a driving motor. The aligning member includes a pair of first aligning members 91 that is rotatably supported while being movable in the sheet width direction orthogonal to the discharge direction and a pair of second aligning members 92. The driving motor rotates the pair of first aligning members and moves the pair of first aligning members in the width direction. When the pair of first aligning members rotates and one of the pair of second aligning members abuts on the sheet, the pair of second aligning members forms opposite surfaces in which the sheet can be aligned in the width direction, and the pair of first aligning members align the sheet by the opposite surfaces.
    • 整理器100包括一对排纸辊130,下堆叠托盘137和宽度方向对准部分200.宽度方向对准部分包括一对对准构件1和驱动电机。 对准构件包括一对第一对准构件91,该一对第一对准构件91可在与放电方向正交的片材宽度方向上可移动地可旋转地支撑,以及一对第二对准构件92.驱动电机使一对第一对准构件旋转, 一对第一对准构件在宽度方向上。 当一对第一对准构件旋转并且一对第二对准构件中的一个抵接在片材上时,一对第二对准构件形成相对的表面,在该表面中片材可以在宽度方向上对齐,并且一对第一对准构件 将纸张对准表面。