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1. 发明授权

US08805566B2 Product line management system and method thereof 有权
标题翻译：产品线管理系统及其方法
公开(公告)号：US08805566B2
公开(公告)日：2014-08-12
申请号：US13040235
申请日：2011-03-03
申请人： Shih-Fang Wong , Xin Lu , Fei Wang , Peng Tang , Jia-Hong Yang , Hui-Feng Liu
发明人： Shih-Fang Wong , Xin Lu , Fei Wang , Peng Tang , Jia-Hong Yang , Hui-Feng Liu
IPC分类号： G06F19/00
CPC分类号： G05B19/418 , G05B2219/32183 , G05B2219/32196 , Y02P90/02 , Y02P90/14 , Y02P90/22
摘要： A method testing the quality of products applied to a system is provided. Each product includes a unique identification number. The system includes a data storage device and test devices. The data storage device includes a first table recording identification numbers, test types, and test results, each test device stores a second table records the identification numbers and the test types. The method includes: obtaining the identification number; obtaining the test type; determining whether a test type previous to the test type exists; and generating first information to prompt the operator to return the to-be-tested product to the workstation of previous test type when the test result corresponding to the existed previous test type does not exist or the test result corresponding to the existed previous test type is a first value.
摘要翻译：提供了一种测试应用于系统的产品质量的方法。每个产品都包含唯一的识别号码。该系统包括一个数据存储设备和测试设备。数据存储装置包括记录识别号，测试类型和测试结果的第一表，每个测试设备存储第二表记录标识号和测试类型。该方法包括：获取识别号码; 获得测试类型; 确定是否存在测试类型之前的测试类型; 并且当不存在与现有的先前测试类型相对应的测试结果或者与现有的测试类型相对应的测试结果是生成第一信息以提示操作者将待测试产品返回到先前测试类型的工作站第一个值。

2. 发明授权

US08745129B2 Client with standby server connection function and method thereof 有权
标题翻译：客户端具有备用服务器连接功能及其方法
公开(公告)号：US08745129B2
公开(公告)日：2014-06-03
申请号：US13155393
申请日：2011-06-08
申请人： Shih-Fang Wong , Xin Lu , Peng Tang , Jia-Hong Yang , Hui-Feng Liu
发明人： Shih-Fang Wong , Xin Lu , Peng Tang , Jia-Hong Yang , Hui-Feng Liu
IPC分类号： G06F15/16
CPC分类号： H04L43/0811 , H04L1/22 , H04L41/0668 , H04L67/141
摘要： A process giving a client the capability of fixing the time within which it may attempt to connect itself to a standby server and a method thereof are provided. The client records the length of time preceding every successful-connection to at least one standby server within a predetermined period, determines an average connection setup time relating to the at least one standby server calculated from all the recorded connection setup times, detects in real time whether the client is successfully connected to a master server, and switches the connection attempts of the client away to each standby server in turn, according to the average connection setup time applying to each standby server respectively, once the client has lost its connection with the master server.
摘要翻译：提供给客户端修复可能尝试将自身连接到备用服务器的时间的能力及其方法。客户端在预定时间段内记录每个成功连接之前的时间长度至少一个备用服务器，确定与从所有记录的连接建立时间计算的至少一个备用服务器相关的平均连接建立时间，实时检测客户端是否成功连接到主服务器，并且根据分别应用于每个备用服务器的平均连接建立时间，将客户端的连接尝试依次切换到每个备用服务器，一旦客户端已经失去与主服务器

3. 发明授权

US08457921B2 Electronic device tester and testing method 有权
标题翻译：电子设备测试仪和测试方法
公开(公告)号：US08457921B2
公开(公告)日：2013-06-04
申请号：US12955908
申请日：2010-11-30
申请人： Shih-Fang Wong , Xin Lu , Jia-Hong Yang , Peng Tang , Hui-Feng Liu
发明人： Shih-Fang Wong , Xin Lu , Jia-Hong Yang , Peng Tang , Hui-Feng Liu
IPC分类号： G01R31/00 , G06F19/00
CPC分类号： H04M1/24 , G01R31/00
摘要： An electronic device tester is connected to an electronic device needed to be tested. A test program is stored in a data storage of the tester. The test program includes a number of test instructions. The tester encapsulates the test instructions of the test program to a number of script files, stores the script files to the data storage, and records a name of each script file to the test program. After the test instruction is encapsulated, the tester selects desired script files of the test program and calls the selected script files according to the names of the script files to implement the test program to test the electronic device.
摘要翻译：电子设备测试仪连接到需要测试的电子设备。测试程序存储在测试仪的数据存储器中。测试程序包括许多测试指令。测试程序将测试程序的测试指令封装到多个脚本文件，将脚本文件存储到数据存储中，并将每个脚本文件的名称记录到测试程序中。测试指令封装后，测试人员将选择测试程序的所需脚本文件，并根据脚本文件的名称调用所选脚本文件，以实施测试程序来测试电子设备。

4. 发明申请

US20060088905A1 Methods for the synthesis of zeazanthin 审中-公开
标题翻译：合成玉米黄质的方法
公开(公告)号：US20060088905A1
公开(公告)日：2006-04-27
申请号：US11242639
申请日：2005-10-03
申请人： Samuel Lockwood , Peng Tang , Geoff Nadolski , Henry Jackson , Zhiqiang Fang , Yishu Du , Min Yang , William Geiss , Richard Williams , David Burdick
发明人： Samuel Lockwood , Peng Tang , Geoff Nadolski , Henry Jackson , Zhiqiang Fang , Yishu Du , Min Yang , William Geiss , Richard Williams , David Burdick
IPC分类号： C12P23/00 , C07C45/45
CPC分类号： C07C403/24 , C07B2200/07 , C07B2200/09 , C07C29/143 , C07C45/298 , C07C45/511 , C07C45/61 , C07C45/64 , C07C45/673 , C07C45/70 , C07C45/71 , C07C47/21 , C07C49/713 , C07C49/753 , C07C403/08 , C07C2601/16 , C07D319/06 , C07F7/188 , C07F7/1892 , C07F9/113 , C07F9/5442 , C12P23/00 , C07C49/603 , C07C33/02 , C07C35/08 , C07C35/21
摘要： A method used for synthesizing intermediates for use in the synthesis of carotenoids and carotenoid analogs, and/or carotenoid derivatives. In some embodiments, the invention includes methods for synthesizing optically active intermediates useful for the synthesis of optically active carotenoids. Synthesis of optically active carotenoids, in one embodiment, may be accomplished by forming an optically active dihydroxy intermediate from ketoisopherone. The optically active dihydroxy intermediate may be converted into optically active zeaxanthin.
摘要翻译：用于合成用于合成类胡萝卜素和类胡萝卜素类似物的中间体和/或类胡萝卜素衍生物的方法。在一些实施方案中，本发明包括用于合成可用于合成光学活性类胡萝卜素的光学活性中间体的方法。在一个实施方案中，光学活性类胡萝卜素的合成可以通过从酮糖酮形成光学活性的二羟基中间体来完成。光学活性的二羟基中间体可以转化成光学活性的玉米黄质。

5. 发明申请

US20060009493A1 Indolinone hydrazides as c-Met inhibitors 审中-公开
标题翻译：吲哚酮酰肼作为c-Met抑制剂
公开(公告)号：US20060009493A1
公开(公告)日：2006-01-12
申请号：US10875508
申请日：2004-06-25
申请人： Marcel Koenig , Jingrong Cui , Chung Wei , Steven Do , Fang-Jie Zhang , Tomas Vojkovsky , John Ramphal , Guang Yang , Matthew Mattson , Christopher Nelson , Peng Tang
发明人： Marcel Koenig , Jingrong Cui , Chung Wei , Steven Do , Fang-Jie Zhang , Tomas Vojkovsky , John Ramphal , Guang Yang , Matthew Mattson , Christopher Nelson , Peng Tang
IPC分类号： C07D43/02 , A61K31/4439
CPC分类号： C07D209/40 , C07D209/34 , C07D401/04 , C07D401/06 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/12 , C07D471/04
摘要： The present invention relates to compounds of the formulae (I)-(XII), wherein R1-R71, A, B, X, Y, G, L and Z are defined herein, and their pharmaceutically acceptable salts. These compounds modulate the activity of c-Met and are therefore expected to be useful in the prevention and treatment of c-Met related disorders such as cancer.
摘要翻译：本发明涉及式（I） - （XII）的化合物，其中R 1 -R 71，A，B，X，Y，G，L和 Z在本文中定义，及其药学上可接受的盐。这些化合物调节c-Met的活性，因此预期可用于预防和治疗c-Met相关疾病如癌症。

6. 发明申请

US20060293545A1 Methods for synthesis of carotenoids, including analogs, derivatives, and synthetic and biological intermediates 有权
标题翻译：合成类胡萝卜素的方法，包括类似物，衍生物和合成和生物中间体
公开(公告)号：US20060293545A1
公开(公告)日：2006-12-28
申请号：US11415375
申请日：2006-05-01
申请人： Samuel Lockwood , Peng Tang , Geoff Nadolski , Henry Jackson , Zhiqiang Fang , Yishu Du , Min Yang , William Geiss , Richard Williams , David Burdick
发明人： Samuel Lockwood , Peng Tang , Geoff Nadolski , Henry Jackson , Zhiqiang Fang , Yishu Du , Min Yang , William Geiss , Richard Williams , David Burdick
IPC分类号： C07C403/00
CPC分类号： C07C29/147 , C07C11/21 , C07C33/02 , C07C45/298 , C07C47/21 , C07C49/743 , C07C67/08 , C07C67/30 , C07C67/343 , C07C67/39 , C07C69/40 , C07C69/602 , C07C403/24 , C07C2601/16 , C07F9/113 , C07F9/65515 , C07C69/73 , C07C35/21
摘要： A method for synthesizing intermediates for use in the synthesis of carotenoid synthetic intermediates, carotenoid analogs, and/or carotenoid derivatives. The carotenoid analog, derivative, or intermediate may be administered to a subject for the inhibition and/or amelioration of any disease that involves production of reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals. In some embodiments, the invention may include methods for synthesizing chemical compounds including an analog or derivative of a carotenoid. Carotenoid analogs or derivatives may include acyclic end groups. In some embodiments, a carotenoid analog or derivative may include at least one substituent. The substituent may enhance the solubility of the carotenoid analog or derivative such that the carotenoid analog or derivative at least partially dissolves in water.
摘要翻译：用于合成用于合成类胡萝卜素合成中间体，类胡萝卜素类似物和/或类胡萝卜素衍生物的中间体的方法。类胡萝卜素类似物，衍生物或中间体可以施用于受试者以抑制和/或改善涉及产生活性氧，活性氮物质，自由基和/或非自由基的任何疾病。在一些实施方案中，本发明可以包括合成包括类胡萝卜素类似物或衍生物的化合物的方法。类胡萝卜素类似物或衍生物可包括无环端基。在一些实施方案中，类胡萝卜素类似物或衍生物可包括至少一个取代基。取代基可以增强类胡萝卜素类似物或衍生物的溶解度，使得类胡萝卜素类似物或衍生物至少部分地溶解在水中。

7. 发明申请

US20060111580A1 Methods for the synthesis of chiral dihydroxy ketone intermediates useful for the chiral synthesis of carotenoids 审中-公开
标题翻译：用于手性合成类胡萝卜素的手性二羟基酮中间体的合成方法
公开(公告)号：US20060111580A1
公开(公告)日：2006-05-25
申请号：US11242627
申请日：2005-10-03
申请人： Samuel Lockwood , Peng Tang , Geoff Nadolski , Henry Jackson , Zhiqiang Fang , Yishu Du , Min Yang , William Geiss , Richard Williams , David Burdick
发明人： Samuel Lockwood , Peng Tang , Geoff Nadolski , Henry Jackson , Zhiqiang Fang , Yishu Du , Min Yang , William Geiss , Richard Williams , David Burdick
IPC分类号： C07F7/04 , C07C45/00
CPC分类号： C07C403/24 , C07B2200/07 , C07B2200/09 , C07C29/143 , C07C45/298 , C07C45/511 , C07C45/61 , C07C45/64 , C07C45/673 , C07C45/70 , C07C45/71 , C07C47/21 , C07C49/713 , C07C49/753 , C07C403/08 , C07C2601/16 , C07D319/06 , C07F7/188 , C07F7/1892 , C07F9/113 , C07F9/5442 , C12P23/00 , C07C49/603 , C07C33/02 , C07C35/08 , C07C35/21
摘要： A method used for synthesizing intermediates for use in the synthesis of carotenoids and carotenoid analogs, and/or carotenoid derivatives. In some embodiments, the invention includes methods for synthesizing optically active intermediates useful for the synthesis of optically active carotenoids. Synthesis of optically active carotenoids, in one embodiment, may be accomplished by forming an optically active dihydroxy ketone intermediate from ketoisopherone.
摘要翻译：用于合成用于合成类胡萝卜素和类胡萝卜素类似物的中间体和/或类胡萝卜素衍生物的方法。在一些实施方案中，本发明包括用于合成可用于合成光学活性类胡萝卜素的光学活性中间体的方法。在一个实施方案中，光学活性类胡萝卜素的合成可以通过从酮酮中形成光学活性的二羟基酮中间体来完成。

8. 发明申请

US20060183185A1 Method for the synthesis of astaxanthin 审中-公开
标题翻译：虾青素合成方法
公开(公告)号：US20060183185A1
公开(公告)日：2006-08-17
申请号：US11242645
申请日：2005-10-03
申请人： Samuel Lockwood , Peng Tang , Geoff Nadolski , Henry Jackson , Zhiqiang Fang , Yishu Du , Min Yang , William Geiss , Richard Williams , David Burdick
发明人： Samuel Lockwood , Peng Tang , Geoff Nadolski , Henry Jackson , Zhiqiang Fang , Yishu Du , Min Yang , William Geiss , Richard Williams , David Burdick
IPC分类号： C12P23/00 , C07C45/45
CPC分类号： C07C403/24 , C07B2200/07 , C07B2200/09 , C07C29/143 , C07C45/298 , C07C45/511 , C07C45/61 , C07C45/64 , C07C45/673 , C07C45/70 , C07C45/71 , C07C47/21 , C07C49/713 , C07C49/753 , C07C403/08 , C07C2601/16 , C07D319/06 , C07F7/188 , C07F7/1892 , C07F9/113 , C07F9/5442 , C12P23/00 , C07C49/603 , C07C33/02 , C07C35/08 , C07C35/21
摘要： A method used for synthesizing intermediates for use in the synthesis of carotenoids and carotenoid analogs, and/or carotenoid derivatives. In some embodiments, the invention includes methods for synthesizing optically active intermediates useful for the synthesis of optically active carotenoids. Synthesis of optically active carotenoids, in one embodiment, may be accomplished by forming an optically active unsaturated ketone intermediate from ketoisopherone. The optically active unsaturated ketone may be converted into optically active astaxanthin derivatives.
摘要翻译：用于合成用于合成类胡萝卜素和类胡萝卜素类似物的中间体和/或类胡萝卜素衍生物的方法。在一些实施方案中，本发明包括用于合成可用于合成光学活性类胡萝卜素的光学活性中间体的方法。在一个实施方案中，光学活性类胡萝卜素的合成可以通过从酮酸成岩得到光学活性的不饱和酮中间体来完成。旋光不饱和酮可以转化成光学活性的虾青素衍生物。

9. 发明申请

US20050197382A1 Indolinone combinatorial libraries and related products and methods for the treatment of disease 有权
标题翻译：吲哚酮组合文库及相关产品及治疗方法
公开(公告)号：US20050197382A1
公开(公告)日：2005-09-08
申请号：US10784917
申请日：2004-02-24
申请人： Peng Tang , Li Sun , Gerald McMahon , Klaus Hirth , Laura Shawver
发明人： Peng Tang , Li Sun , Gerald McMahon , Klaus Hirth , Laura Shawver
IPC分类号： C07D209/34 , A61K31/404 , G01N33/53 , G01N33/543
CPC分类号： C07D209/34
摘要： The present invention relates to organic molecules capable of modulating, regulating and/or inhibiting protein kinase signal transduction. Such compounds are useful for the treatment of diseases related to unregulated protein kinase signal transduction, including cell proliferative diseases such as cancer, atherosclerosis, arthritis and restenosis and metabolic diseases such as diabetes. The present invention features indolinone compounds that potently inhibit protein kinases and related products and methods. Inhibitors specific to the FLK protein kinase can be obtained by adding chemical substituents to the 3-[(indole-3-yl)methylene]-2-indolinone, in particular at the 1′ position of the indole ring. Indolinone compounds that specifically inhibit the FLK and platelet derived growth factor protein kinases can harbor a tetrahydroindole or cyclopentano-b-pyrrol moiety. Indolinone compounds that are modified with substituents, particularly at the 5 position of the oxindole ring, can effectively activate protein kinases. This invention also features novel hydrosoluble indolinone compounds that are tyrosine kinase inhibitors and related products and methods.
摘要翻译：本发明涉及能够调节，调节和/或抑制蛋白激酶信号转导的有机分子。这些化合物可用于治疗与未调节的蛋白激酶信号转导相关的疾病，包括细胞增殖性疾病如癌症，动脉粥样硬化，关节炎和再狭窄以及诸如糖尿病的代谢疾病。本发明具有抑制蛋白激酶及相关产物和方法的吲哚啉酮化合物。可以通过向3 - [（吲哚-3-基）亚甲基] -2-二氢吲哚酮，特别是在吲哚环的1'位置添加化学取代基来获得对FLK蛋白激酶特异性的抑制剂。特异性抑制FLK和血小板衍生生长因子蛋白激酶的吲哚酮化合物可以含有四氢吲哚或环戊基-b-吡咯部分。被取代基修饰的吲哚啉酮化合物，特别是在羟吲哚环的5位，可以有效地激活蛋白激酶。本发明还具有酪氨酸激酶抑制剂和相关产物和方法的新型水溶性吲哚啉酮化合物。

10. 发明申请

US20050038066A1 Geometrically restricted 3-cyclopentylidene-1,3-dihydroindol-2-ones as potent protein tyrosine kinase inhibitors 失效
标题翻译：几何限制3-亚环戊基-1,3-二氢吲哚-2-酮作为有效的蛋白酪氨酸激酶抑制剂
公开(公告)号：US20050038066A1
公开(公告)日：2005-02-17
申请号：US10911637
申请日：2004-08-05
申请人： Fang-Jie Zhang , Jingrong Cui , Chung Chen Wei , Peng Tang
发明人： Fang-Jie Zhang , Jingrong Cui , Chung Chen Wei , Peng Tang
IPC分类号： A61K31/404 , A61K31/4745 , C07D20060101 , C07D209/34 , C07D209/42 , C07D403/04 , C07D403/06 , C07D403/14 , C07D471/02 , C07D471/04 , C07D43/02
CPC分类号： C07D209/34 , C07D209/42 , C07D403/06 , C07D403/14 , C07D471/04
摘要： The present invention relates to certain sulfonamido-substituted geometrically restricted indolinones of the formula: wherein R1-R12 and X are variables defined herein. The sulfonamido-substituted geometrically restricted indolinones of the preferred embodiments of the present invention modulate the activity of protein kinases (“PKs”). The compounds of this invention are therefore useful in treating disorders related to abnormal PK activity. Pharmaceutical compositions comprising these compounds, methods of treating diseases utilizing pharmaceutical compositions comprising these compounds and methods of preparing them are also disclosed.
摘要翻译：本发明涉及下列通式的某些亚磺酰氨基取代的几何受限的二氢吲哚酮：其中R1-R12和X是本文定义的变量。本发明优选实施方案的亚磺酰氨基取代的几何限制性二氢吲哚酮调节蛋白激酶（“PKs”）的活性。因此，本发明的化合物可用于治疗与异常PK活性相关的疾病。还公开了包含这些化合物的药物组合物，利用包含这些化合物的药物组合物治疗疾病的方法及其制备方法。

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