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1. 发明申请

US20120249441A1 TOUCH PANEL AND METHOD OF MANUFACTURING A TOUCH PANEL 有权
标题翻译：触控面板和制造触控面板的方法
公开(公告)号：US20120249441A1
公开(公告)日：2012-10-04
申请号：US13311556
申请日：2011-12-06
申请人： YUH-WEN LEE , Ching-Shan Lin , Lichun yang , Fang Fang
发明人： YUH-WEN LEE , Ching-Shan Lin , Lichun yang , Fang Fang
IPC分类号： G06F3/041 , B05D5/00
CPC分类号： G06F3/044 , G06F2203/04103
摘要： The present invention discloses a touch panel and a method of manufacturing a touch panel, to reduce the visibility of the transparent etching line of the transparent electrodes on the touch panel. The touch panel comprises a plurality of transparent electrode disposed distantly on the transparent conductive layer and the passivation layer of a transparent substrate, where the passivation layer covering the transparent conductive layer, to make the refractive index of the passivation layer and the transparent electrodes match with each other. Oxide with high refractive index added in the passivation material is filled in the etched area of the transparent conductive layer, so that the optical refractive index of the etched area and ITO area on transparent conductive layer become closer, and the difference in refractive index curve between ITO area and etched area is reduced, therefore, the effect of making the transparent electrode pattern is achieved.
摘要翻译：本发明公开了触摸面板和制造触摸面板的方法，以降低触摸面板上的透明电极的透明蚀刻线的可视性。触摸面板包括多个透明电极，其设置在透明导电层上的透明电极和透明衬底的钝化层，其中钝化层覆盖透明导电层，以使钝化层和透明电极的折射率与彼此。在钝化材料中加入高折射率的氧化物被填充在透明导电层的蚀刻区域中，使得透明导电层上的蚀刻区域和ITO区域的光学折射率变得更接近，并且折射率之间的折射率差 ITO区域和蚀刻面积减少，因此，实现了形成透明电极图案的效果。

2. 发明授权

US09933896B2 Touch panel and method of manufacturing a touch panel 有权
公开(公告)号：US09933896B2
公开(公告)日：2018-04-03
申请号：US13311556
申请日：2011-12-06
申请人： Yuh-Wen Lee , Ching-Shan Lin , Lichun Yang , Fang Fang
发明人： Yuh-Wen Lee , Ching-Shan Lin , Lichun Yang , Fang Fang
IPC分类号： G06F3/044
CPC分类号： G06F3/044 , G06F2203/04103
摘要： The present invention discloses a touch panel and a method of manufacturing a touch panel, to reduce the visibility of the transparent etching line of the transparent electrodes on the touch panel. The touch panel comprises a plurality of transparent electrode disposed distantly on the transparent conductive layer and the passivation layer of a transparent substrate, where the passivation layer covering the transparent conductive layer, to make the refractive index of the passivation layer and the transparent electrodes match with each other. Oxide with high refractive index added in the passivation material is filled in the etched area of the transparent conductive layer, so that the optical refractive index of the etched area and ITO area on transparent conductive layer become closer, and the difference in refractive index curve between ITO area and etched area is reduced, therefore, the effect of making the transparent electrode pattern is achieved.

3. 发明授权

US09284330B2 1,4-dihydro-naphthyridine derivative and pharmaceutical composition and use thereof 有权
标题翻译： 1,4-二氢 - 萘啶衍生物及其药物组合物及其用途
公开(公告)号：US09284330B2
公开(公告)日：2016-03-15
申请号：US14362735
申请日：2012-12-07
申请人： Rong Chen , Lin Feng , Zhengping Zhang , Fang Fang , Qingli Dong , Fulong Li , Lei Wang , Yao Hua , Shibao Yang , Peng Wang
发明人： Rong Chen , Lin Feng , Zhengping Zhang , Fang Fang , Qingli Dong , Fulong Li , Lei Wang , Yao Hua , Shibao Yang , Peng Wang
IPC分类号： C07D495/14 , C07D471/14 , C07D471/04 , C07D471/12 , C07D491/14
CPC分类号： C07D495/14 , C07D471/04 , C07D471/12 , C07D471/14 , C07D491/14
摘要： Disclosed are 1,4-dihydro-naphthyridine derivatives and pharmaceutical composition and uses thereof. The 1,4-dihydro-naphthyridine derivatives are a compound capable of inhibiting acetylcholinesterase activity and preventing extracellular calcium from flowing into a cell via a calcium channel, i.e., having a dual-activity, which are of potential importance as a pharmaceutical and can be used to prepare the drugs for treating cardiovascular diseases, cerebrovascular diseases and dementia.
摘要翻译：公开了1,4-二氢 - 萘啶衍生物及其药物组合物及其用途。 1,4-二氢 - 萘啶衍生物是能够抑制乙酰胆碱酯酶活性并防止细胞外钙通过钙通道流入细胞的化合物，即具有作为药物具有潜在重要性的双重活性，可以是用于制备治疗心血管疾病，脑血管疾病和痴呆症的药物。

4. 发明授权

US08729303B2 2,2′,6,6′-tetrasubstituted aminophosphine ligand and its synthesis method 有权
标题翻译： 2,2'，6,6'-四取代氨基膦配体及其合成方法
公开(公告)号：US08729303B2
公开(公告)日：2014-05-20
申请号：US12377000
申请日：2007-08-10
申请人： Wanbin Zhang , Fang Xie , Fang Fang
发明人： Wanbin Zhang , Fang Xie , Fang Fang
IPC分类号： C07F9/02
CPC分类号： C07F9/46
摘要： The present invention relates to a 2,2′,6,6′-tetrasubstituted aminophosphine ligand and its synthesis method. The structure of the ligand is shown as below. Its synthesis method comprises: Step (1) coupling 2,6-dinitrochlorobenzene as the starting material to obtain 2,2′,6,6′-tetranitrobiphenyl; Step (2): hydrogenating the 2,2′,6,6′-tetranitrobiphenyl with Pd/C to obtain 2,2′,6,6′-tetraminobiphenyl; Step (3): reacting the 2,2′,6,6′-tetraminobiphenyl with a phosphine halide to obtain the 2,2′,6,6′-tetrasubstituted aminophosphine ligand. The ligand of the present invention is an achiral compound, and its preparation method is simple. The ligand can be converted to a chiral bimetallic catalyst with single configuration eventually through introduction of external chirality. Moreover, the ligand can be used in various asymmetric reaction catalyzed by metals with high reactivity and stereoselectivity.
摘要翻译：本发明涉及2,2'，6,6'-四取代氨基膦配体及其合成方法。配体的结构如下所示。其合成方法包括：步骤（1）以2,6-二硝基氯苯为原料，得到2,2'，6,6'-四硝基联苯; 步骤（2）：用Pd / C氢化2,2'，6,6'-四硝基二苯并得到2,2'，6,6'-四氨基联苯; 步骤（3）：使2,2'，6,6'-四磺酰联苯与卤化膦反应，得到2,2'，6,6'-四取代氨基膦配体。本发明的配体是非手性化合物，其制备方法简单。最终可以通过引入外部手性将配体转化为具有单一配置的手性双金属催化剂。此外，配体可用于由具有高反应性和立体选择性的金属催化的各种不对称反应中。

5. 发明申请

US20130156703A1 Methods, Compounds, and Compositions For Treatment and Prophylaxis in the Respiratory Tract 审中-公开
公开(公告)号：US20130156703A1
公开(公告)日：2013-06-20
申请号：US13769095
申请日：2013-02-15
申请人： Fang Fang , David Wurtman , Ron Moss , Michael Malakhov
发明人： Fang Fang , David Wurtman , Ron Moss , Michael Malakhov
IPC分类号： A61K38/47
CPC分类号： A61K38/47 , A61K9/0014 , A61K9/0019 , A61K9/0043 , A61K9/0053 , A61K9/0073 , A61K9/06 , A61K31/05 , A61K31/198 , A61K31/4172 , A61K31/7016 , A61K33/06 , A61K33/14 , A61K38/1808 , A61K45/06 , A61K47/02 , A61K47/22 , A61K47/26 , A61K47/32 , A61K47/34 , A61K49/0008 , C07K14/485 , C07K2319/00 , C12N9/2402 , C12N9/2477 , C12Q1/34 , C12Y302/01018 , G01N2500/00 , G01N2800/122 , A61K2300/00
摘要： The present invention provides a method of reducing the quanitity of mucus in the respiratory tract of a subject with elevated levels of mucus in said respiratory tract. The method includes administering to the subject a compound or composition containing a therapeutically effective amount of a fusion protein comprising a sialidase or an active portion thereof and an anchoring domain. The therapeutically effective amount comprises an amount of the fusion protein that results in a reduction of the quanitity of mucus in the respiratory tract after administration of the compound or composition when compared to the quantity of mucus present prior to administration of the compound or composition.

6. 发明授权

US07696324B2 Humanized antibodies 失效
标题翻译：人源化抗体
公开(公告)号：US07696324B2
公开(公告)日：2010-04-13
申请号：US11519322
申请日：2006-09-11
申请人： Fang Fang , Lori Kohlstaedt , John Reno
发明人： Fang Fang , Lori Kohlstaedt , John Reno
IPC分类号： C07K16/28 , C12P21/08
CPC分类号： C07K16/2896 , A61K2039/505 , C07K16/2821 , C07K2317/24 , C07K2317/622 , C07K2317/92 , C07K2319/00 , Y02A50/412
摘要： Humanized antibodies that bind ICAM-1 are provided. Antibodies include those selected from: SEQ ID NO:1 and 3 (HumA); SEQ ID NO:5 and 7 (HumB); SEQ ID NO:9 and 11 (HumC); SEQ ID NO:13 and 15 (HumD); SEQ ID NO:17 and 19 (HumE); SEQ ID NO:21 and 23 (HumF); SEQ ID NO:25 and 27 (HumG); SEQ ID NO:29 and 31 (HumH); and SEQ ID NO:33 and 35 (HumI). Subsequences of the humanized antibodies capable of binding an ICAM-1 epitope are also provided. Methods of inhibiting pathogen infection (e.g., HRV) of a cell employing humanized antibodies capable of binding an ICAM-1 epitope are further provided.
摘要翻译：提供了结合ICAM-1的人源化抗体。抗体包括选自：SEQ ID NO：1和3（HumA）的那些; SEQ ID NO：5和7（HumB）; SEQ ID NO：9和11（HumC）; SEQ ID NO：13和15（HumD）; SEQ ID NO：17和19（HumE）; SEQ ID NO：21和23（HumF）; SEQ ID NO：25和27（HumG）; SEQ ID NO：29和31（HumH）; 和SEQ ID NO：33和35（HumI）。还提供了能够结合ICAM-1表位的人源化抗体的子序列。还提供了使用能够结合ICAM-1表位的人源化抗体抑制细胞病原体感染（例如HRV）的方法。

7. 发明申请

US20070190163A1 Technology for preparation of macromolecular microspheres 审中-公开
标题翻译：高分子微球的制备技术
公开(公告)号：US20070190163A1
公开(公告)日：2007-08-16
申请号：US11657812
申请日：2007-01-24
申请人： Michael Malaknov , Fang Fang
发明人： Michael Malaknov , Fang Fang
IPC分类号： C07K1/02 , A61K9/16
CPC分类号： A61K9/1682 , A61K9/0073 , A61K9/14 , A61K9/1617 , A61K9/1647 , A61K9/19 , A61K38/18 , A61K38/47 , A61K38/57 , C12Y302/01018 , Y02A50/385 , Y02A50/387 , Y02A50/393 , Y02A50/401 , Y02A50/402 , Y02A50/411 , Y02A50/469 , Y02A50/47 , Y02A50/471 , Y02A50/478 , Y02A50/48 , Y02A50/483 , Y02A50/491 , Y10T428/2982
摘要： Microspheres are produced by contacting an aqueous solution of a protein or other macromolecule with an organic solvent and a counterion, and chilling the solution. The microspheres are useful for preparing pharmaceuticals of defined dimensions.
摘要翻译：通过使蛋白质或其他高分子的水溶液与有机溶剂和抗衡离子接触并冷却溶液来制备微球体。微球可用于制备具有限定尺寸的药物。

8. 外观设计

USD1021275S1 Dog crate 有权
公开(公告)号：USD1021275S1
公开(公告)日：2024-04-02
申请号：US29919483
申请日：2023-12-05
申请人： Zhihui Zheng , Zihan Geng , Fang Fang
设计人： Zhihui Zheng , Zihan Geng , Fang Fang
摘要： FIG. 1 is a front, top, and left perspective view of a dog crate showing my new design;
FIG. 2 is a front elevational view thereof;
FIG. 3 is a rear elevational view thereof;
FIG. 4 is a left side elevational view thereof;
FIG. 5 is a right side elevational view thereof;
FIG. 6 is a top plan view thereof;
FIG. 7 is a bottom plan view thereof; and,
FIG. 8 is a rear, bottom, and right perspective view thereof.
The broken lines shown in the drawings represent portions of the dog crate that form no part of the claimed design.

9. 发明授权

US10085470B2 Method for improving the quality of soy sauce using Bacillus amyloliquefaciens 有权
公开(公告)号：US10085470B2
公开(公告)日：2018-10-02
申请号：US15204991
申请日：2016-07-07
申请人： Fang Fang , Jiran Zhang , Xifei Yang , Chuanwang Hu , Jian Chen , Guocheng Du
发明人： Fang Fang , Jiran Zhang , Xifei Yang , Chuanwang Hu , Jian Chen , Guocheng Du
IPC分类号： A23L5/20 , A23L27/50 , A23L23/00 , C12N1/20 , C12R1/07
摘要： The present invention provides a method for improving the quality of soy sauce using Bacillus amyloliquefaciens, which relates to the field of microbiology and food technology. The method comprises inoculating Bacillus amyloliquefaciens BBE JY06 during soy sauce fermentation. With Bacillus amyloliquefaciens addition during soy sauce fermentation, the aroma and tastes of soy sauce is improved and the ethyl carbamate content in soy sauce is decreased as well.

10. 外观设计

USD827313S1 Fabric swatch 有权
公开(公告)号：USD827313S1
公开(公告)日：2018-09-04
申请号：US29641258
申请日：2018-03-20
申请人： Edward Eng , Fang Fang
设计人： Edward Eng , Fang Fang

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