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1. 发明授权

US6055369A Apparatus for visual programming with screen flow 失效
标题翻译：屏幕流程视觉编程设备
公开(公告)号：US6055369A
公开(公告)日：2000-04-25
申请号：US852033
申请日：1997-05-06
申请人： Tomoharu Sawahata , Wei-Tek Tsai , Akira K. Onoma , Tao Jiang
发明人： Tomoharu Sawahata , Wei-Tek Tsai , Akira K. Onoma , Tao Jiang
IPC分类号： G06F9/06 , G06F9/44 , G06F9/445
CPC分类号： G06F8/34
摘要： An apparatus is disclosed for visual programming for creating a program with a visual user interface. The visual programming apparatus has a screen storage unit for storing multiple screens to be employed with the program; a screen creating unit for creating the multiple screens to be employed with the program and storing the multiple screens in the screen storage unit; a screen flow creating unit for creating a screen flow indicating a flow of processes by displaying on an edit screen the multiple screens stored in the screen storage unit in a compressed manner and specifying a link between the multiple compressed screens on the edit screen; a screen flow information extracting unit for extracting data of a link from the screen flow created by the screen flow creating unit; and a code creating unit for creating a source code from the data of the link extracted by the screen flow information extracting unit and from data of the screen.
摘要翻译：公开了一种用于可视化编程的装置，用于创建具有可视用户界面的程序。视觉编程装置具有屏幕存储单元，用于存储要与节目一起使用的多个屏幕; 用于创建要与程序一起使用的多个屏幕并将多个屏幕存储在屏幕存储单元中的屏幕创建单元; 屏幕流创建单元，用于通过在编辑屏幕上以压缩的方式显示存储在屏幕存储单元中的多个屏幕并指定编辑屏幕上的多个压缩屏幕之间的链接来创建指示流程的屏幕流程; 屏幕流信息提取单元，用于从由屏幕流创建单元创建的屏幕流提取链接的数据; 以及代码创建单元，用于从由屏幕流信息提取单元提取的链接的数据和从屏幕的数据创建源代码。

2. 外观设计

USD946004S1 Screen swivel mount 有权
公开(公告)号：USD946004S1
公开(公告)日：2022-03-15
申请号：US29796129
申请日：2021-06-22
申请人： Tao Jiang
设计人： Tao Jiang

3. 发明授权

US08592432B2 Compounds and compositions as protein kinase inhibitors 失效
标题翻译：化合物和组合物作为蛋白激酶抑制剂
公开(公告)号：US08592432B2
公开(公告)日：2013-11-26
申请号：US12936199
申请日：2009-04-03
申请人： Bei Chen , Tao Jiang , Thomas H. Marsilje , Pierre-Yves Michellys , Truc Ngoc Nguyen , Wei Pei , Baogen Wu , Zhaobo Gao , Yonghui Ge , Chen Huang , Yuncheng Li , Xuefeng Zhu
发明人： Bei Chen , Tao Jiang , Thomas H. Marsilje , Pierre-Yves Michellys , Truc Ngoc Nguyen , Wei Pei , Baogen Wu , Zhaobo Gao , Yonghui Ge , Chen Huang , Yuncheng Li , Xuefeng Zhu
IPC分类号： A61K31/506 , A61K31/5377 , C07D239/42 , C07D239/30 , C07D295/108 , C07D487/04 , A61P35/00 , A61P35/02 , A61P35/04
CPC分类号： C07D239/48 , C07D403/12 , C07D403/14 , C07D487/04
摘要： The invention provides novel pyrimidine derivatives and pharmaceutical compositions thereof, and methods for using such compounds. For example, the pyrimidine derivatives of the invention may be used to treat, ameliorate or prevent a condition which responds to inhibition of anaplastic lymphoma kinase (ALK) activity, c-ros oncogene (ROS), insulin-like growth factor (IGF-1R), and/or insulin receptor (InsR) or a combination thereof.
摘要翻译：本发明提供新颖的嘧啶衍生物及其药物组合物，以及使用这些化合物的方法。例如，本发明的嘧啶衍生物可用于治疗，改善或预防对间变性淋巴瘤激酶（ALK）活性，c-ros致癌基因（ROS），胰岛素样生长因子（IGF-1R ）和/或胰岛素受体（InsR）或其组合。

4. 发明授权

US08524904B2 Process for the preparation of 6-alpha-hydroxy-N-alkylated opiates 有权
标题翻译： 6-α-羟基-N-烷基化阿片剂的制备方法
公开(公告)号：US08524904B2
公开(公告)日：2013-09-03
申请号：US12630192
申请日：2009-12-03
申请人： Christopher W. Grote , Peter X. Wang , Tao Jiang , Gary L. Cantrell , Frank W. Moser , Catherine E. Thomasson
发明人： Christopher W. Grote , Peter X. Wang , Tao Jiang , Gary L. Cantrell , Frank W. Moser , Catherine E. Thomasson
IPC分类号： C07D489/08 , C07D489/02
CPC分类号： C07D489/02 , Y02P20/55
摘要： The present invention is directed to the preparation of 6-hydroxy morphinans having formula (II) or N-alkylated 6-hydroxy morphinans having formula (III).
摘要翻译：本发明涉及具有式（II）的6-羟基吗啡烷或具有式（III）的N-烷基化的6-羟基吗啡喃的制备。

5. 发明申请

US20130131699A1 POROUS METAL DEVICE FOR REGENERATING SOFT TISSUE-TO-BONE INTERFACE 有权
公开(公告)号：US20130131699A1
公开(公告)日：2013-05-23
申请号：US13679041
申请日：2012-11-16
申请人： Tao Jiang , Jian Q. Yao , Hali Wang , Timothy A. Hoeman , Ray Zubok , John Chernosky , Keith A. Roby
发明人： Tao Jiang , Jian Q. Yao , Hali Wang , Timothy A. Hoeman , Ray Zubok , John Chernosky , Keith A. Roby
IPC分类号： A61B17/68
CPC分类号： A61F2/0811 , A61B17/68 , A61F2002/0858 , A61F2002/0888 , A61F2250/0021 , A61F2250/0023 , A61F2250/0026 , A61L27/04 , A61L27/56
摘要： The present disclosure relates, in some aspects, to orthopaedic implants for securing soft tissue to bone and methods for using the same. One particular implant comprises a first exposed porous surface region, having pores for promoting bone ingrowth, and a second exposed porous surface, having pores for promoting soft tissue ingrowth. At least some of the pores of the first exposed porous surface region may be seeded with osteocytic factors and at least some of the pores of the second exposed porous surface region may be seeded with fibrocytic factors. Such orthopaedic implants can advantageously facilitate regeneration of the soft tissue to bone interface.

6. 发明申请

US20130005748A1 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS 有权
公开(公告)号：US20130005748A1
公开(公告)日：2013-01-03
申请号：US13610422
申请日：2012-09-11
申请人： Pierre-Yves Michellys , Wei Pei , Thomas H. Marsilje , Wenshuo Lu , Bei Chen , Tetsuo Uno , Yunho Jin , Tao Jiang
发明人： Pierre-Yves Michellys , Wei Pei , Thomas H. Marsilje , Wenshuo Lu , Bei Chen , Tetsuo Uno , Yunho Jin , Tao Jiang
IPC分类号： A61K31/519 , A61P31/00 , A61P35/00 , A61P37/06 , A61K31/52 , A61K31/517
CPC分类号： A61K31/506 , A61K31/5377 , A61K45/06 , C07D213/74 , C07D239/48 , C07D239/95 , C07D401/12 , C07D401/14 , C07D403/12 , C07D403/14 , C07D405/14 , C07D413/12 , C07D417/12 , C07D451/02 , C07D453/02 , C07D471/04 , C07D473/16 , C07D487/04 , C07D487/08
摘要： The invention provides novel pyrimidine and pyridine derivatives and pharmaceutical compositions thereof, and methods for using such compounds. For example, the pyrimidine and pyridine derivatives of the invention may be used to treat, ameliorate or prevent a condition which responds to inhibition of anaplastic lymphoma kinase (ALK) activity, focal adhesion kinase (FAK), zeta-chain-associated protein kinase 70 (ZAP-70), insulin-like growth factor (IGF-1R), or a combination thereof.

7. 发明授权

US08252928B2 Processes for the synthesis of five and six membered heterocyclic rings 有权
标题翻译：合成五元和六元杂环的方法
公开(公告)号：US08252928B2
公开(公告)日：2012-08-28
申请号：US12558646
申请日：2009-09-14
申请人： Peter X. Wang , Tao Jiang , David W. Berberich
发明人： Peter X. Wang , Tao Jiang , David W. Berberich
IPC分类号： C07D489/02 , C07D489/08
CPC分类号： C07D489/02 , C07D489/00
摘要： The present invention provides processes for the synthesis of five and six membered rings. In particular, the present invention provides processes for the synthesis of five and six membered rings in alkaloids.
摘要翻译：本发明提供合成五元和六元环的方法。特别地，本发明提供了合成生物碱中五元和六元环的方法。

8. 发明授权

US08202971B2 Process for preparing compounds of chitosan saccharified with aminosugar 失效
标题翻译：用氨基糖糖化糖壳化合物的方法
公开(公告)号：US08202971B2
公开(公告)日：2012-06-19
申请号：US12499767
申请日：2009-07-08
申请人： Xiguang Chen , Jing Li , Xiaojie Cheng , Tao Jiang
发明人： Xiguang Chen , Jing Li , Xiaojie Cheng , Tao Jiang
IPC分类号： C08B37/08
CPC分类号： C08B37/003
摘要： A process for preparing compounds of chitosan saccharified with aminosugar, adopts chitosan derivatives, aminosugar derivatives and anhydride derivatives as raw materials to synthesize target products. The process comprises: covalently bonding an anhydride derivative as a bonding arm to an aminosugar derivative, so as to form a monosaccharide derivative having an end group of carboxyl; and then covalently bonding the monosaccharide derivative having an end group of carboxyl to a primary amino group of a chitosan derivative via the carboxyl, so as to form a compound of chitosan saccharified with aminosugar.
摘要翻译：用氨基糖糖化糖壳化合物的方法，采用壳聚糖衍生物，氨基糖衍生物和酸酐衍生物为原料合成目标产物。该方法包括：将作为结合臂的酸酐衍生物与氨基糖衍生物共价键合，形成具有羧基端基的单糖衍生物; 然后通过羧基将具有羧基末端基团的单糖衍生物共价键合到壳聚糖衍生物的伯氨基上，以形成用氨基糖糖化的壳聚糖化合物。

9. 发明申请

US20120134931A1 PEPTIDES WHOSE UPTAKE IN CELLS IS CONTROLLABLE 有权
标题翻译：细胞摄取的细胞是可控的
公开(公告)号：US20120134931A1
公开(公告)日：2012-05-31
申请号：US13384591
申请日：2010-07-15
申请人： Roger Tsien , Tood Aguilera , Emilia Olson , Tao Jiang , Quyen Nguyen
发明人： Roger Tsien , Tood Aguilera , Emilia Olson , Tao Jiang , Quyen Nguyen
IPC分类号： A61K49/06 , C07K9/00 , C07K7/02 , A61K49/00
CPC分类号： A61K47/64 , A61K47/595 , A61K47/60 , A61K47/62 , A61K47/6911 , A61K49/0032 , A61K49/0056 , C07K7/06
摘要： Disclosed herein, in certain embodiments, is a selective transport molecule with increased in vivo circulation. In some embodiments, a selective transport molecule disclosed herein has the formula (A-X-B-C)-M, wherein C is a cargo moiety; A is a peptide with a sequence comprising 5 to 9 consecutive acidic amino acids, wherein the amino acids are selected from: aspartates and glutamates; B is a peptide with a sequence comprising 5 to 20 consecutive basic amino acids; X is a linker; and M is a macromolecular carrier.
摘要翻译：在某些实施方案中，本文公开了具有增加的体内循环的选择性转运分子。在一些实施方案中，本文公开的选择性转运分子具有式（A-X-B-C）-M，其中C是货物部分; A是具有包含5至9个连续酸性氨基酸的序列的肽，其中所述氨基酸选自：天冬氨酸和谷氨酸; B是具有包含5至20个连续碱性氨基酸的序列的肽; X是一个连接子; M是大分子载体。

10. 发明授权

US08101757B2 Processes for the preparation of normorphinan salts 有权
标题翻译：制备正高霉素盐的方法
公开(公告)号：US08101757B2
公开(公告)日：2012-01-24
申请号：US12316887
申请日：2008-12-17
申请人： Peter X. Wang , Tao Jiang , Gary L. Cantrell , David W. Berberich , Jian Bao , Bobby N. Trawick
发明人： Peter X. Wang , Tao Jiang , Gary L. Cantrell , David W. Berberich , Jian Bao , Bobby N. Trawick
IPC分类号： C07D489/02 , C07D489/08
CPC分类号： C07D489/08
摘要： The invention provides a process for the conversion of opioid derivatives into normorphinan compounds useful for making “nal” compound analgesics and antagonists. In particular, the process may be used for the production of pure normorphinan salts from crude opioid substrates.
摘要翻译：本发明提供了一种将阿片样物质衍生物转化成可用于制备“nal”复合镇痛药和拮抗剂的正大脑啡肽化合物的方法。特别地，该方法可用于从粗制阿片样物质底物生产纯的正大脑啡肽。

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