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    • 44. 发明申请
    • High Efficient and High Power Plane Centric Gear Unit
    • 高效高功率平面中心减速器
    • US20130059693A1
    • 2013-03-07
    • US13603449
    • 2012-09-05
    • ZUPENG FANGDAN FANGFANG FANGYAFENG ZHAO
    • ZUPENG FANGDAN FANGFANG FANGYAFENG ZHAO
    • F16H1/32
    • F16H1/32
    • A plane centric gear unit has a circumferentially floating ring gear 1. Both ends of the ring gear 1 are respectively fixed with cloth boards 3 equipped with hollow shaft sleeves 4; the reaction forces of the ring gear 1 and external gear 2 are equal and in opposite directions, and act on inner ring bearings 7 of the hollow shaft sleeves 4 on the same straight line; the outer ring bearings 8 of the hollow shaft sleeves 4 are unloaded, therefore the sum of the bearing reaction forces is reduced, the total transmission efficiency and power reaches above 97% and tens of thousands KW grade, the noises are lower, the gear surface contact pressure is about 1/10 of the external mesh pair, the gear surface contact life is increased by 1000 times than the external mesh pair, and the total weight is reduced by 2˜3 times.
    • 平面中心减速器具有周向浮动的环形齿轮1.齿圈1的两端分别固定有装有中空轴套4的布板3; 环形齿轮1和外齿轮2的反作用力相等且相反方向,并且作用在同一直线上的中空轴套4的内圈轴承7上; 空心轴套4的外圈​​轴承8被卸载,因此轴承反作用力的总和减小,总传动效率和功率达到97%以上,几万KW级,噪声较低,齿轮面 接触压力约为外啮合对的1/10,齿轮表面接触寿命比外啮合对增加1000倍,总重量减少2〜3倍。
    • 47. 发明授权
    • Broad spectrum anti-viral therapeutics and prophylaxis
    • 广谱抗病毒治疗和预防
    • US08084036B2
    • 2011-12-27
    • US10718986
    • 2003-11-21
    • Mang YuFang FangMichael Malakhov
    • Mang YuFang FangMichael Malakhov
    • A61K39/00C12N9/36
    • B82Y5/00A61K38/47A61K38/57
    • The present invention provides new compositions and methods for preventing and treating pathogen infection. In particular, the present invention provides compounds having an anchoring domain that anchors the compound to the surface of a target cell, and a therapeutic domain that can act extracellularly to prevent infection of the target cell by a pathogen, such as a virus. Preferred target cells are epithelial cells. The invention provides compositions and methods for preventing viral diseases, such as influenza, using compounds having anchoring domains that can bind target cells linked to enzymatic activities that can act extracellularly to interfere with viral infection of target cells. The invention also provides compositions and methods for preventing viral diseases such as influenza using compounds having anchoring domains that can bind target cells linked to protease inhibitors that can act extracellularly to interfere with viral infection of target cells.
    • 本发明提供了用于预防和治疗病原体感染的新的组合物和方法。 特别地,本发明提供具有将化合物锚定在靶细胞表面的锚定结构域的化合物,以及可以在细胞外作用以防止病原体如病毒感染靶细胞的治疗结构域。 优选的靶细胞是上皮细胞。 本发明提供了用于预防病毒性疾病(例如流行性感冒)的组合物和方法,使用具有锚定结构域的化合物,所述化合物具有可结合与细胞外作用以干扰靶细胞的病毒感染的酶活性连接的靶细胞。 本发明还提供了用于使用具有锚定结构域的化合物来预防病毒性疾病例如流感的组合物和方法,所述化合物具有可以结合与蛋白酶抑制剂连接的靶细胞,其可以在细胞外作用以干扰靶细胞的病毒感染。
    • 49. 发明申请
    • 2, 2', 6, 6'- TETRASUBSTITUTED AMINOPHOSPHINE LIGAND AND ITS SYNTHESIS METHOD
    • 2,2',6,6'-四唑基氨基磷酰胺配体及其合成方法
    • US20100217040A1
    • 2010-08-26
    • US12377000
    • 2007-08-10
    • Wanbin ZhangFang XieFang Fang
    • Wanbin ZhangFang XieFang Fang
    • C07F9/50
    • C07F9/46
    • 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.
    • 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。
    • 50. 发明授权
    • Avian hepatitis E virus, vaccines and methods of protecting against avian hepatitis-splenomegaly syndrome and mammalian hepatitis E
    • 禽类戊型肝炎病毒,疫苗和防止禽流感 - 脾肿大综合征和哺乳动物性肝炎的方法
    • US07582303B2
    • 2009-09-01
    • US11184574
    • 2005-07-19
    • Xiang-Jin MengGholamreza HaqshenasFang-Fang Huang
    • Xiang-Jin MengGholamreza HaqshenasFang-Fang Huang
    • A61K39/29C12Q1/70C12Q1/68
    • C07K14/005A61K2039/5254A61K2039/54C12N7/00C12N2770/28022C12N2770/28034C12Q1/707G01N33/576
    • The present invention relates to a novel isolated avian hepatitis E virus having a nucleotide sequence set forth in SEQ ID NO:1 or its complementary strand. The invention further concerns immunogenic compositions comprising this new virus or recombinant products such as the nucleic acid and vaccines that protect an avian or mammalian species from viral infection or hepatitis-splenomegaly syndrome caused by the hepatitis E virus. Also included in the scope of the invention is a method for propagating, inactivating or attenuating a hepatitis E virus comprising inoculating an embryonated chicken egg with a live, pathogenic hepatitis E virus and recovering the virus or serially passing the pathogenic virus through additional embryonated chicken eggs until the virus is rendered inactivated or attenuated. Further, this invention concerns diagnostic reagents for detecting an avian hepatitis E viral infection or diagnosing hepatitis-splenomegaly syndrome in an avian or mammalian species comprising an antibody raised or produced against the immunogenic compositions and antigens such as ORF2 proteins expressed in a baculovirus vector, E. coli, etc. The invention additionally encompasses methods for detecting avian HEV nucleic acid sequences using nucleic acid hybridization probes or oligonucleotide primers for polymerase chain reaction (PCR).
    • 本发明涉及具有SEQ ID NO:1所示核苷酸序列或其互补链的新颖的分离型禽类戊型肝炎病毒。 本发明还涉及包含这种新病毒或重组产物(例如核酸和疫苗)的免疫原性组合物,其保护禽类或哺乳动物物种免受由戊型肝炎病毒引起的病毒感染或肝炎 - 脾肿大综合症。 本发明的范围还包括传播,灭活或减毒戊型肝炎病毒的方法,包括用活的致病性戊型肝炎病毒接种含胚鸡蛋,并回收该病毒或通过另外的含胚鸡蛋串联通过病原性病毒 直到病毒灭活或减毒。 此外,本发明涉及用于检测禽流感病毒感染或诊断禽流感或哺乳动物物种中的肝炎 - 脾肿大综合征的诊断试剂,其包含针对免疫原性组合物产生或产生的抗体,例如杆状病毒载体中表达的ORF2蛋白 大肠杆菌等。本发明另外包括使用核酸杂交探针或用于聚合酶链反应(PCR)的寡核苷酸引物检测禽类HEV核酸序列的方法。