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11. 发明申请

US20080004442A1 Tetrazole-substituted arylamides as P2X3 and P2X2/3 antagonists 有权
标题翻译：四唑取代的芳酰胺如P2X3和P2X2 / 3拮抗剂
公开(公告)号：US20080004442A1
公开(公告)日：2008-01-03
申请号：US11823808
申请日：2007-06-28
申请人： Michael Dillon , Ronald Hawley , Li Chen , Lichun Feng , Minmin Yang
发明人： Michael Dillon , Ronald Hawley , Li Chen , Lichun Feng , Minmin Yang
IPC分类号： C07D257/04 , C07D401/10 , C07D401/14 , C07D413/10
CPC分类号： A61K31/41 , A61K31/4439 , A61K31/497 , A61K31/5377 , C07D241/12 , C07D257/04 , C07D401/10 , C07D401/12 , C07D401/14 , C07D403/10 , C07D403/12 , C07D403/14 , C07D405/12 , C07D407/10 , C07D409/12 , C07D413/10 , C07D417/10 , C07D417/12 , C07D471/04 , C07D491/10 , C07D491/107 , C07D498/08
摘要： Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is optionally substituted tetrazolyl, R2 is optionally substituted phenyl, optionally substituted pyridinyl or optionally substituted thienyl, and R3, R4, R5 and R6 are as defined herein. Also provided are methods of using the compounds for treating diseases associated with the P2X3 and/or a P2X2/3 receptor antagonist and methods of making the compounds.
摘要翻译：式I化合物或其药学上可接受的盐，其中R 1是任选取代的四唑基，R 2是任选取代的苯基，任选取代的吡啶基或任选取代的噻吩基，R 3，R 4，R 5和R 6如本文所定义。还提供了使用该化合物治疗与P2X 3和/或P2X 2/3受体拮抗剂相关的疾病的方法和制备该化合物的方法。

12. 发明授权

US07235675B2 Conjugates of mycophenolic acid 失效
标题翻译：霉酚酸的结合物
公开(公告)号：US07235675B2
公开(公告)日：2007-06-26
申请号：US10900447
申请日：2004-07-27
申请人： Mitali Ghoshal , Gerald Sigler , Raymond A. Hui , Ronald Hawley , Eva Hoess , Erasmus J. Huber , John W. Patterson , Salvatore J. Salamone , Allan Dorn
发明人： Mitali Ghoshal , Gerald Sigler , Raymond A. Hui , Ronald Hawley , Eva Hoess , Erasmus J. Huber , John W. Patterson , Salvatore J. Salamone , Allan Dorn
IPC分类号： C07D307/00 , C07D407/00
CPC分类号： C07D405/12 , C07D307/88 , C07D473/08 , C07H15/20 , C07H15/22 , C07H15/24 , C07J17/00 , C07J19/005 , C07J41/0005 , C07J41/0055 , C07J43/003 , G01N33/53 , G01N33/535 , G01N33/5735 , G01N33/581 , G01N33/78 , G01N33/9453 , G01N2333/904
摘要： The present invention provides a method for the measurement of an analyte in biological samples whereby an uncompetitive inhibitor is coupled to a ligand and utilized in a homogeneous assay. The analyte can be a drug or drug derivative, hormone, polypeptide, or oligonucleotide.The present invention also provides novel compounds, assay reagents and packaged kits useful for performing such measurements.
摘要翻译：本发明提供了一种用于测量生物样品中分析物的方法，由此使非竞争性抑制剂与配体偶联并用于均匀测定。分析物可以是药物或药物衍生物，激素，多肽或寡核苷酸。本发明还提供了可用于进行这种测量的新型化合物，测定试剂和包装的试剂盒。

13. 发明申请

US20070142631A1 ENZYME INHIBITON IMMUNOASSAY 失效
公开(公告)号：US20070142631A1
公开(公告)日：2007-06-21
申请号：US11673180
申请日：2007-02-09
申请人： Mitali Ghoshal , Gerald Sigler , Raymond Hui , Ronald Hawley , Eva Hoess , Erasmus Huber , John Patterson , Salvatore Salamone , Allan Dorn
发明人： Mitali Ghoshal , Gerald Sigler , Raymond Hui , Ronald Hawley , Eva Hoess , Erasmus Huber , John Patterson , Salvatore Salamone , Allan Dorn
IPC分类号： C07J17/00 , C07H15/22 , C07D473/04 , C07H15/24 , C07H15/20
CPC分类号： C07D405/12 , C07D307/88 , C07D473/08 , C07H15/20 , C07H15/22 , C07H15/24 , C07J17/00 , C07J19/005 , C07J41/0005 , C07J41/0055 , C07J43/003 , G01N33/53 , G01N33/535 , G01N33/5735 , G01N33/581 , G01N33/78 , G01N33/9453 , G01N2333/904
摘要： The present invention provides a method for the measurement of an analyte in biological samples whereby an uncompetitive inhibitor is coupled to a ligand and utilized in a homogeneous assay. The analyte can be a drug or drug derivative, hormone, polypeptide, or oligonucleotide. The present invention also provides novel compounds, assay reagents and packaged kits useful for performing such measurements.
摘要翻译：本发明提供了一种用于测量生物样品中分析物的方法，由此使非竞争性抑制剂与配体偶联并用于均匀测定。分析物可以是药物或药物衍生物，激素，多肽或寡核苷酸。本发明还提供了可用于进行这种测量的新型化合物，测定试剂和包装的试剂盒。

14. 发明授权

US07571947B2 Device and method for extending truck cargo space 失效
标题翻译：扩大卡车货物的装置和方法
公开(公告)号：US07571947B2
公开(公告)日：2009-08-11
申请号：US11843037
申请日：2007-08-22
申请人： Ronald Hawley
发明人： Ronald Hawley
IPC分类号： B60P7/06
CPC分类号： B62D33/0273
摘要： The present invention extends the truck bed, thus increasing cargo space by the length of the truck tailgate. One embodiment of the invention comprises rotatably attaching an end panel to the tailgate, with rotatable and storable support members. Another embodiment comprises right and left side panels rotatably attached to the end panel. When the assembly is stored, either the support members or the side panels are rotated inward to rest against the inner surface of the end panel and the end panel is rotated downwardly and secured against the upper surface of the tailgate. When the assembly is deployed, the end panel is unsecured from the tailgate and is rotated upwardly until approximately perpendicular with the tailgate and the cargo space bed. The support members or side panels are rotated outwardly and secured to complete deployment. In certain embodiments, the end panel may be removed easily and quickly, or lowered down and out of the way, to allow and facilitate loading of longer items in the cargo space, and then reattached and deployed. The mounting bracket and/or end panel may comprise molded reinforced plastic composite material.
摘要翻译：本发明延伸了卡车底盘，从而将货物空间增加了卡车尾门的长度。本发明的一个实施例包括以可旋转和可存储的支撑构件将端板可旋转地附接到后挡板。另一个实施例包括可旋转地附接到端板的右侧板和左侧板。当组件被存储时，支撑构件或侧板向内旋转以抵靠端板的内表面，并且端板向下旋转并固定在后挡板的上表面上。当组件部署时，端板不受后挡板的影响，并向上旋转直到大约垂直于后挡板和货物空间床。支撑构件或侧板向外旋转并固定以完全展开。在某些实施例中，可以容易地，快速地或者降下端面板去除端面板，以允许并便于在货物空间中装载更长的物品，然后重新附接和展开。安装支架和/或端板可以包括模制的增强塑料复合材料。

15. 发明申请

US20070049609A1 Methods of using diaminopyrimidine P2X3 and P2X2/3 receptor modulators for treatment of respiratory and gastrointestinal diseases 有权
标题翻译：使用二氨基嘧啶P2X3和P2X2 / 3受体调节剂治疗呼吸道和胃肠道疾病的方法
公开(公告)号：US20070049609A1
公开(公告)日：2007-03-01
申请号：US11509921
申请日：2006-08-25
申请人： Chris Broka , David Carter , Michael Dillon , Anthony Ford , Ronald Hawley , Alam Jahangir , Amy Moore , Daniel Parish
发明人： Chris Broka , David Carter , Michael Dillon , Anthony Ford , Ronald Hawley , Alam Jahangir , Amy Moore , Daniel Parish
IPC分类号： A61K31/513
CPC分类号： A61K31/506 , A61K31/505 , A61K31/513 , A61K31/538 , Y10S514/826
摘要： Methods for treating respiratory and gastrointestinal diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): or a pharmaceutically acceptable salt thereof, wherein D, X, Y, R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein.
摘要翻译：用于治疗由P2X 3和/或P2X 3/3受体拮抗剂介导的呼吸道和胃肠道疾病的方法，所述方法包括向有需要的受试者施用有效量的式（I）化合物或其药学上可接受的盐，其中D，X，Y，R 1，R 2，R 3， R 4，R 4，R 5，R 6，R 7和R 8， SUP>如本文所定义。

16. 发明申请

US20050209260A1 Diaminopyrimidines as P2X3 and P2X2/3 antagonists 有权
标题翻译：二氨基嘧啶作为P2X3和P2X2 / 3拮抗剂
公开(公告)号：US20050209260A1
公开(公告)日：2005-09-22
申请号：US11071555
申请日：2005-03-03
申请人： Chris Broka , David Carter , Michael Dillon , Ronald Hawley , Alam Jahangir , Clara Lin , Daniel Parish
发明人： Chris Broka , David Carter , Michael Dillon , Ronald Hawley , Alam Jahangir , Clara Lin , Daniel Parish
IPC分类号： A61K31/505 , A61K31/506 , C07D239/48 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12 , C07D43/02
CPC分类号： C07D239/49 , A61K31/505 , A61K31/506 , C07D239/48 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12
摘要： Compounds and methods for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): or a pharmaceutically acceptable salt, solvate or prodrug thereof, wherein D, X, Y, R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein.
摘要翻译：用于治疗由P2X 3和/或P2X 3/3受体拮抗剂介导的疾病的化合物和方法，所述方法包括向有需要的受试者施用有效量的式（I）化合物或其药学上可接受的盐，溶剂化物或前药，其中D，X，Y，R 1，R 2，R 2， R 4，R 4，R 5，R 6，R 7和R 9， 8“如本文所定义。

17. 发明授权

US06811998B2 Conjugates of uncompetitive inhibitors of inosine monophosphate dehydrogenase 失效
标题翻译：肌苷单磷酸脱氢酶的竞争性抑制剂的结合物
公开(公告)号：US06811998B2
公开(公告)日：2004-11-02
申请号：US10341692
申请日：2003-01-14
申请人： Mitali Ghoshal , Gerald Sigler , Raymond A. Hui , Ronald Hawley , Eva Hoess , Erasmus J. Huber , John W. Patterson , Salvatore J. Salamone , Allan Dorn
发明人： Mitali Ghoshal , Gerald Sigler , Raymond A. Hui , Ronald Hawley , Eva Hoess , Erasmus J. Huber , John W. Patterson , Salvatore J. Salamone , Allan Dorn
IPC分类号： C12Q132
CPC分类号： C07D405/12 , C07D307/88 , C07D473/08 , C07H15/20 , C07H15/22 , C07H15/24 , C07J17/00 , C07J19/005 , C07J41/0005 , C07J41/0055 , C07J43/003 , G01N33/53 , G01N33/535 , G01N33/5735 , G01N33/581 , G01N33/78 , G01N33/9453 , G01N2333/904
摘要： The present invention provides a method for the measurement of an analyte in biological samples whereby an uncompetitive inhibitor is coupled to a ligand and utilized in a homogeneous assay. The analyte can be a drug or drug derivative, hormone, polypeptide, or oligonucleotide. The present invention also provides novel compounds, assay reagents and packaged kits useful for performing such measurements.
摘要翻译：本发明提供了一种用于测量生物样品中分析物的方法，由此使非竞争性抑制剂与配体偶联并用于均匀测定。分析物可以是药物或药物衍生物，激素，多肽或寡核苷酸。本发明还提供了可用于进行这种测量的新型化合物，测定试剂和包装的试剂盒。

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