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36 条记录 (耗时 0.033 秒)

    Method and system for preventing copying of information from previews of webpages
    6.
    发明授权
    Method and system for preventing copying of information from previews of webpages 有权
    防止从网页预览中复制信息的方法和系统

    公开(公告)号：US08677509B2

    公开(公告)日：2014-03-18

    申请号：US13243750

    申请日：2011-09-23

    申请人： Suyoung Kim ,  Tae Ho Lee

    发明人： Suyoung Kim ,  Tae Ho Lee

    IPC分类号： H04L29/06 ,  G06F21/00

    CPC分类号： H04L63/10 ,  G06F17/3089 ,  G06F21/10 ,  G06F2221/2119

    摘要： A touch screen device may include: a touch panel receiving a touch signal; a noise measurement unit measuring a noise value input to the touch panel; a determination unit determining whether or not the measured noise value exceeds a threshold; and a control unit controlling an operation mode to be maintained or switched according to a determination result of the determination unit.

    摘要翻译： 触摸屏设备可以包括：触摸面板，其接收触摸信号; 测量输入到触摸面板的噪声值的噪声测量单元; 确定单元，确定所测量的噪声值是否超过阈值; 以及控制单元，根据确定单元的确定结果控制要保持或切换的操作模式。

    NOVEL OXAZOLIDINONE DERIVATIVES
    7.
    发明申请
    NOVEL OXAZOLIDINONE DERIVATIVES 有权
    新型氧杂环丁酮衍生物

    公开(公告)号：US20090192197A1

    公开(公告)日：2009-07-30

    申请号：US12211655

    申请日：2008-09-16

    申请人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    发明人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    IPC分类号： A61K31/4439 ,  C07D413/14 ,  A61P3/04

    CPC分类号： A61K31/4439 ,  A61K31/675 ,  C07D263/32 ,  C07D413/14 ,  C07D417/10 ,  C07D417/14 ,  C07F9/653 ,  C07F9/65583

    摘要： The present invention relates to novel derivatives of oxazolidinone, a method thereof and pharmaceutical compositions comprising the derivatives for use in an antibiotic. The oxazolidinone derivatives of the present invention show inhibitory activity against a broad spectrum of bacteria and lower toxicity. The prodrugs, prepared by reacting the compound having hydroxyl group with amino acid or phosphate, have an excellent efficiency on solubility thereof against water. Further, the derivatives of the present invention may exert potent antibacterial activity versus various human and animal pathogens, including Gram-positive bacteria such as Staphylococi, Enterococci and Streptococi, anaerobic microorganisms such as Bacteroides and Clostridia, and acid-resistant microorganisms such as Mycobacterium tuberculosis and Mycobacterium avium. Accordingly, the compositions comprising the oxazolidinone are used in an antibiotic.

    摘要翻译： 本发明涉及恶唑烷酮的新衍生物，其方法和药物组合物，其包含用于抗生素的衍生物。 本发明的恶唑烷酮衍生物显示出对广谱细菌的抑制活性和较低的毒性。 通过使具有羟基的化合物与氨基酸或磷酸酯反应制备的前药在对水的溶解性方面具有优异的效果。 此外，本发明的衍生物可以相对于各种人和动物病原体，包括葡萄球菌，肠球菌和链球菌等革兰阳性菌，拟杆菌和梭菌等厌氧菌，耐结核菌如结核分枝杆菌 和鸟分枝杆菌。 因此，包含恶唑烷酮的组合​​物用于抗生素中。

    DNA encoding tumor necrosis factor stimulated gene 6 (TSG-6)
    8.
    发明授权
    DNA encoding tumor necrosis factor stimulated gene 6 (TSG-6) 失效
    DNA编码肿瘤坏死因子刺激基因6（TSG-6）

    公开(公告)号：US5846763A

    公开(公告)日：1998-12-08

    申请号：US242097

    申请日：1994-05-13

    申请人： Tae Ho Lee ,  Hans-Georg Wisniewski ,  Jan Vilcek

    发明人： Tae Ho Lee ,  Hans-Georg Wisniewski ,  Jan Vilcek

    IPC分类号： C07K14/47 ,  C12N1/21 ,  C12N5/10 ,  C12N15/12

    CPC分类号： C07K14/4718

    摘要： TSG-6 protein and functional derivatives thereof, DNA coding therefor, expression vehicles, such as a plasmids, and host cells transformed or transfected with the DNA molecule, and methods for producing the protein and the DNA are provided, as well as antibodies specific for the TSG-6 protein; a method for detecting the presence of TSG-6 protein in a biological sample; a method for detecting the presence of nucleic acid encoding a normal or mutant TSG-6 protein; a method for measuring induction of expression of TSG-6 in a cell using either nucleic acid hybridization or immunoassay; a method for identifying a compound capable of inducing the expression of TSG-6 in a cell; and a method for measuring the ability of a cell to respond to TNF.

    摘要翻译： TSG-6蛋白及其功能衍生物，编码DNA，表达载体如质粒和用DNA分子转化或转染的宿主细胞，以及产生蛋白质和DNA的方法，以及针对 TSG-6蛋白; 用于检测生物样品中TSG-6蛋白的存在的方法; 用于检测编码正常或突变型TSG-6蛋白的核酸的存在的方法; 使用核酸杂交或免疫测定来测量细胞中TSG-6的表达诱导的方法; 用于鉴定能够诱导细胞中TSG-6表达的化合物的方法; 以及测定细胞对TNF反应能力的方法。

    METHOD FOR DIRECT TRANSACTION OF METAL SCRAPS THROUGH ENLARGED COLLECTION QUANTITIES
    9.
    发明申请
    METHOD FOR DIRECT TRANSACTION OF METAL SCRAPS THROUGH ENLARGED COLLECTION QUANTITIES 审中-公开

    公开(公告)号：US20180285955A1

    公开(公告)日：2018-10-04

    申请号：US15518367

    申请日：2016-08-01

    申请人： Tae Ho Lee ,  JOALOGIS CO., LTD.

    发明人： Tae Ho Lee

    IPC分类号： G06Q30/06 ,  G06Q50/28

    摘要： There is provided a method for direct transaction of metal scrap through enlarged collection quantities that can increase profitability by enabling to calculate a conversion price in which a weight value on a weight basis and on timing basis of scraps formed in a large quantity is reflected while making small quantities secured by scrap dealers to a large quantity by collecting, to transmit the conversion price to each dealer, to determine a sale intention, to sell the scraps to several kinds of buyers, and to sell the scraps to a dealer, a middle merchant, and a large merchant with a highest price and that can enhance productivity while minimizing a management cost by providing a large quantity of scraps to steel companies.

    Oxazolidinone derivatives
    10.
    发明授权
    Oxazolidinone derivatives 有权
    恶唑烷酮衍生物

    公开(公告)号：US08420676B2

    公开(公告)日：2013-04-16

    申请号：US12211655

    申请日：2008-09-16

    申请人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    发明人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    IPC分类号： A61K31/4439 ,  C07D413/14

    CPC分类号： A61K31/4439 ,  A61K31/675 ,  C07D263/32 ,  C07D413/14 ,  C07D417/10 ,  C07D417/14 ,  C07F9/653 ,  C07F9/65583

    摘要： The present invention relates to novel derivatives of oxazolidinone, a method thereof and pharmaceutical compositions comprising the derivatives for use in an antibiotic. The oxazolidinone derivatives of the present invention show inhibitory activity against a broad spectrum of bacteria and lower toxicity. The prodrugs, prepared by reacting the compound having hydroxyl group with amino acid or phosphate, have an excellent efficiency on solubility thereof against water. Further, the derivatives of the present invention may exert potent antibacterial activity versus various human and animal pathogens, including Gram-positive bacteria such as, Staphylococci, Enterococci and Streptococci anaerobic microorganisms such as Bacteroides and Clostridia, and acid-resistant microorganisms such as Mycobacterium tuberculosis and Mycobacterium avium. Accordingly, the compositions comprising the oxazolidinone are used in an antibiotic.

    摘要翻译： 本发明涉及恶唑烷酮的新衍生物，其方法和药物组合物，其包含用于抗生素的衍生物。 本发明的恶唑烷酮衍生物显示出对广谱细菌的抑制活性和较低的毒性。 通过使具有羟基的化合物与氨基酸或磷酸酯反应制备的前药在对水的溶解性方面具有优异的效果。 此外，本发明的衍生物相对于各种人和动物病原体，包括革兰氏阳性菌如葡萄球菌，肠球菌和链球菌厌氧微生物如拟杆菌和梭菌，以及耐酸微生物如结核分枝杆菌 和鸟分枝杆菌。 因此，包含恶唑烷酮的组合​​物用于抗生素中。