公开(公告)号：US07161003B1

公开(公告)日：2007-01-09

申请号：US10654546

申请日：2003-09-03

申请人： Timothy J. Guzi ,  Kamil Paruch ,  Michael P. Dwyer ,  Ronald J. Doll ,  Viyyoor M. Girijavallabhan ,  Alan Mallams ,  Carmen S. Alvarez ,  Kartik M. Keertikar ,  Jocelyn Rivera ,  Tin-Yau Chan ,  Vincent Madison ,  Thierry O. Fischmann ,  Lawrence W. Dillard ,  Vinh D. Tran ,  Zhen Min He ,  Ray Anthony James ,  Haengsoon Park ,  Vidyadhar M. Paradkar ,  Douglas Walsh Hobbs

发明人： Timothy J. Guzi ,  Kamil Paruch ,  Michael P. Dwyer ,  Ronald J. Doll ,  Viyyoor M. Girijavallabhan ,  Alan Mallams ,  Carmen S. Alvarez ,  Kartik M. Keertikar ,  Jocelyn Rivera ,  Tin-Yau Chan ,  Vincent Madison ,  Thierry O. Fischmann ,  Lawrence W. Dillard ,  Vinh D. Tran ,  Zhen Min He ,  Ray Anthony James ,  Haengsoon Park ,  Vidyadhar M. Paradkar ,  Douglas Walsh Hobbs

IPC分类号： C07D487/04

CPC分类号： C07D487/04

摘要： In its many embodiments, the present invention provides a novel class of pyrazolo[1,5-a]pyrimidine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions.

摘要翻译： 在其许多实施方案中，本发明提供了一类新颖的吡唑并[1,5-a]嘧啶化合物作为细胞周期蛋白依赖性激酶的抑制剂，制备此类化合物的方法，含有一种或多种此类化合物的药物组合物，制备药物制剂的方法 包括一种或多种这样的化合物，以及使用这些化合物或药物组合物治疗，预防，抑制或改善与CDK相关的一种或多种疾病的方法。

公开(公告)号：US07807683B2

公开(公告)日：2010-10-05

申请号：US11396001

申请日：2006-03-31

申请人： Timothy J. Guzi ,  Kamil Paruch ,  Michael P. Dwyer ,  Ronald J. Doll ,  Viyyoor M. Girijavallabhan ,  Alan Mallams ,  Carmen S. Alvarez ,  Kartik M. Keertikar ,  Jocelyn Rivera ,  Tin Yau Chan ,  Vincent Madison ,  Thierry O. Fischmann ,  Lawrence W. Dillard ,  Vinh D. Tran ,  Zhen Min He ,  Ray Anthony James ,  Haengsoon Park ,  Vidyadhar M. Paradkar ,  Douglas Walsh Hobbs

发明人： Timothy J. Guzi ,  Kamil Paruch ,  Michael P. Dwyer ,  Ronald J. Doll ,  Viyyoor M. Girijavallabhan ,  Alan Mallams ,  Carmen S. Alvarez ,  Kartik M. Keertikar ,  Jocelyn Rivera ,  Tin Yau Chan ,  Vincent Madison ,  Thierry O. Fischmann ,  Lawrence W. Dillard ,  Vinh D. Tran ,  Zhen Min He ,  Ray Anthony James ,  Haengsoon Park ,  Vidyadhar M. Paradkar ,  Douglas Walsh Hobbs

IPC分类号： A61K31/519 ,  A61P35/04 ,  A61P35/02 ,  C07D487/04 ,  A61P35/00

CPC分类号： C07D487/04

摘要： In its many embodiments, the present invention provides a novel class of pyrazolo[1,5-a]pyrimidine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions.

摘要翻译： 在其许多实施方案中，本发明提供了一类新颖的吡唑并[1,5-a]嘧啶化合物作为细胞周期蛋白依赖性激酶的抑制剂，制备此类化合物的方法，含有一种或多种此类化合物的药物组合物，制备药物制剂的方法 包括一种或多种这样的化合物，以及使用这些化合物或药物组合物治疗，预防，抑制或改善与CDK相关的一种或多种疾病的方法。

公开(公告)号：US07119200B2

公开(公告)日：2006-10-10

申请号：US10776988

申请日：2004-02-11

申请人： Timothy J. Guzi ,  Kamil Paruch ,  Michael P. Dwyer ,  Ronald J. Doll ,  Viyyoor M. Girijavallabhan ,  Alan Mallams ,  Carmen S. Alvarez ,  Kartik M. Keertikar ,  Jocelyn Rivera ,  Tin-Yau Chan ,  Vincent Madison ,  Thierry O. Fischmann ,  Lawrence W. Dillard ,  Vinh D. Tran ,  Zhen Min He ,  Ray Anthony James ,  Haengsoon Park ,  Vidyadhar M. Hobbs ,  Douglas Walsh Hobbs

发明人： Timothy J. Guzi ,  Kamil Paruch ,  Michael P. Dwyer ,  Ronald J. Doll ,  Viyyoor M. Girijavallabhan ,  Alan Mallams ,  Carmen S. Alvarez ,  Kartik M. Keertikar ,  Jocelyn Rivera ,  Tin-Yau Chan ,  Vincent Madison ,  Thierry O. Fischmann ,  Lawrence W. Dillard ,  Vinh D. Tran ,  Zhen Min He ,  Ray Anthony James ,  Haengsoon Park ,  Vidyadhar M. Hobbs ,  Douglas Walsh Hobbs

IPC分类号： C07D487/04

CPC分类号： C07D487/04 ,  A61K31/495

摘要： In its many embodiments, the present invention provides a novel class of pyrazolo[1,5-a]pyrimidine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions.

公开(公告)号：US08673924B2

公开(公告)日：2014-03-18

申请号：US11788847

申请日：2007-04-20

申请人： Timothy J. Guzi ,  Kamil Paruch ,  Michael P. Dwyer ,  Ronald J. Doll ,  Viyyoor M. Girijavallabhan ,  Alan Mallams ,  Carmen S. Alvarez ,  Kartik M. Keertikar ,  Jocelyn Rivera ,  Tin-Yau Chan ,  Vincent S. Madison ,  Thierry O. Fischmann ,  Lawrence W. Dillard ,  Vinh D. Tran ,  Zhenmin He ,  Ray Anthony James ,  Haengsoon Park ,  Vidyadhar M. Paradkar ,  Douglas Walsh Hobbs ,  Paul Kirschmeier ,  Rajat Bannerji

发明人： Timothy J. Guzi ,  Kamil Paruch ,  Michael P. Dwyer ,  Ronald J. Doll ,  Viyyoor M. Girijavallabhan ,  Alan Mallams ,  Carmen S. Alvarez ,  Kartik M. Keertikar ,  Jocelyn Rivera ,  Tin-Yau Chan ,  Vincent S. Madison ,  Thierry O. Fischmann ,  Lawrence W. Dillard ,  Vinh D. Tran ,  Zhenmin He ,  Ray Anthony James ,  Haengsoon Park ,  Vidyadhar M. Paradkar ,  Douglas Walsh Hobbs ,  Paul Kirschmeier ,  Rajat Bannerji

IPC分类号： C07D487/04 ,  A61K31/519 ,  A61P35/00

CPC分类号： A61K31/33 ,  A61K31/4965 ,  A61K31/497 ,  A61K31/519 ,  A61K31/535 ,  A61K31/555 ,  A61K31/56 ,  A61K31/655 ,  A61K31/675 ,  A61K31/7004 ,  A61K33/24 ,  A61K45/06 ,  A61K2300/00

摘要： In its many embodiments, the present invention provides a method of inhibiting one or more cyclin dependent kinases in a patient comprising administering to said patient a therapeutically effective amount of at least one pyrazolo[1,5-a]pyrimidine compound or a pharmaceutical composition comprising such compound, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions. An example pyrazolo[1,5-a]pyrimidine compound useful in the present invention is shown below:

摘要翻译： 在其许多实施方案中，本发明提供了抑制患者中一种或多种细胞周期蛋白依赖性激酶的方法，包括向所述患者施用治疗有效量的至少一种吡唑并[1,5-a]嘧啶化合物或包含 以及使用这些化合物或药物组合物治疗，预防，抑制或改善与CDK相关的一种或多种疾病的方法。 用于本发明的吡唑并[1,5-a]嘧啶化合物的实例如下所示：

公开(公告)号：US07550467B2

公开(公告)日：2009-06-23

申请号：US11247635

申请日：2005-10-11

申请人： Tao Guo ,  Huizhong Gu ,  Douglas Walsh Hobbs

发明人： Tao Guo ,  Huizhong Gu ,  Douglas Walsh Hobbs

IPC分类号： A61K31/497

CPC分类号： C07D213/75 ,  C07D295/13 ,  C07D311/58

摘要： The present invention discloses compounds of Formula I wherein V, W, Y, Z, R1, R2, R3, R4, d, m, n, p and r are herein defined, said compounds being novel antagonists for melanin-concentrating hormone (MCH), as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising such MCH antagonists as well as methods of using them to treat obesity, metabolic disorders, eating disorders such as hyperphagia, and diabetes. An illustrative compound is shown below:

摘要翻译： 本发明公开了式I化合物，其中V，W，Y，Z，R 1，R 2，R 3，R 4，d，m，n，p和r在本文中定义，所述化合物是黑色素浓缩激素 ），以及制备这些化合物的方法。 在另一个实施方案中，本发明公开了包含这样的MCH拮抗剂的药物组合物以及使用它们治疗肥胖，代谢紊乱，进食障碍如食欲过盛和糖尿病的方法。 示例性化合物如下所示：

公开(公告)号：US07034056B2

公开(公告)日：2006-04-25

申请号：US10101136

申请日：2002-03-19

申请人： Douglas Walsh Hobbs ,  Tao Guo ,  Rachael C. Hunter ,  Huizhong Gu

发明人： Douglas Walsh Hobbs ,  Tao Guo ,  Rachael C. Hunter ,  Huizhong Gu

IPC分类号： A61K31/17 ,  C07C275/40

CPC分类号： C07D207/08 ,  C07C233/78 ,  C07C237/20 ,  C07C255/58 ,  C07C255/60 ,  C07C271/54 ,  C07C275/28 ,  C07C275/30 ,  C07C275/32 ,  C07C311/06 ,  C07C311/07 ,  C07C311/08 ,  C07C311/18 ,  C07C311/19 ,  C07C2601/02 ,  C07C2601/04 ,  C07C2601/08 ,  C07C2601/14 ,  C07D207/12 ,  C07D207/14 ,  C07D209/16 ,  C07D211/58 ,  C07D213/40 ,  C07D213/89 ,  C07D261/18 ,  C07D295/13 ,  C07D295/155 ,  C07D295/205 ,  C07D317/58 ,  C07D333/20 ,  C07D333/38 ,  C07D409/12

摘要： In one embodiment, this invention provides a novel class of compounds as antagonists of the MCH receptor, methods of preparing such compounds, pharmaceutical compositions containing one or more of the compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention or amelioration or one or more of diseases associated with the MCH receptor. An illustrative inventive compound is shown below: