公开(公告)号：US20100216841A1

公开(公告)日：2010-08-26

申请号：US11922399

申请日：2006-06-28

Applicant: James C. Barrow ,  Craig W. Lindsley ,  William D. Shipe ,  Zhiqiang Yang ,  David Wisnoski

Inventor： James C. Barrow ,  Craig W. Lindsley ,  William D. Shipe ,  Zhiqiang Yang ,  David Wisnoski

IPC: A61K31/445 ,  C07D211/34 ,  C07D405/06 ,  C07D403/06 ,  C07D413/06 ,  C07D417/06 ,  A61K31/453 ,  A61K31/454 ,  A61P25/00

CPC classification number: C07D211/38

Abstract: The present invention is directed to 4-fluoro-piperidine compounds which are antagonists of T-type calcium channels, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which T-type calcium channels are involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which T-type calcium channels are involved.

Abstract translation: 本发明涉及作为T型钙通道拮抗剂的4-氟哌啶化合物，其可用于治疗或预防涉及T型钙通道的神经和精神疾病及疾病。 本发明还涉及包含这些化合物的药物组合物以及这些化合物和组合物在预防或治疗涉及T型钙通道的疾病中的用途。

公开(公告)号：US20180162874A1

公开(公告)日：2018-06-14

申请号：US15579115

申请日：2016-06-20

Applicant: Gregori J. MORRIELLO ,  Lehua CHANG ,  Ashley FORSTER ,  Yili CHEN ,  Michael P. DWYER ,  Richard BERGER ,  Ming WANG ,  Kausik K. NADA ,  Jaime L. BUNDA ,  William D. SHIPE ,  Merck Sharp & Dohme Corp.

Inventor： Gregori J. Morriello ,  Michael P. Dwyer ,  Lehua Chang ,  Yili Chen ,  Ming Wang ,  Ashley Forster ,  Richard Berger ,  Kausik k Nanda ,  Jaime L Bunda ,  William D Shipe

IPC: C07D498/04 ,  C07D473/34 ,  A61P25/18 ,  A61P25/16 ,  A61P25/28

CPC classification number: C07D498/04 ,  A61P25/06 ,  A61P25/16 ,  A61P25/18 ,  A61P25/28 ,  C07D473/34 ,  C07D487/04

Abstract: The present invention is directed to pyrimidine carboxamide compounds of formula I which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 2 (PDE2). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis, Parkinson's disease, Parkinson's disease dementia (PDD), or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

公开(公告)号：US20130203756A1

公开(公告)日：2013-08-08

申请号：US13825616

申请日：2011-10-24

Applicant: Jamie L. Bunda ,  Christopher D. Cox ,  Vadim Y. Dudkin ,  Hannah D. Fiji ,  Michael J. Kelly ,  Mark E. Layton ,  Joseph E. Pero ,  William D. Shipe ,  Justin T. Sheen

Inventor： Jamie L. Bunda ,  Christopher D. Cox ,  Vadim Y. Dudkin ,  Hannah D. Fiji ,  Michael J. Kelly ,  Mark E. Layton ,  Joseph E. Pero ,  William D. Shipe ,  Justin T. Sheen

IPC: C07D403/06 ,  C07D519/00 ,  C07D417/14 ,  C07D413/14 ,  C07D471/04

CPC classification number: C07D403/06 ,  A61K31/44 ,  C07D413/14 ,  C07D417/14 ,  C07D471/04 ,  C07D519/00

Abstract: The present invention is directed to isoindolinone compounds which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

Abstract translation: 本发明涉及可用作治疗与磷酸二酯酶10（PDE10）相关的中枢神经系统疾病的治疗剂的异吲哚啉酮化合物。 本发明还涉及这些化合物用于治疗神经和精神疾病如精神分裂症，精神病或亨廷顿病以及与纹状体功能减退或基底神经节功能障碍相关的疾病的用途。

公开(公告)号：US20130158056A1

公开(公告)日：2013-06-20

申请号：US13820648

申请日：2011-09-26

Applicant: Christopher D. Cox ,  Izzat T. Raheem ,  William D. Shipe ,  Cory R. Theberge

Inventor： Christopher D. Cox ,  Izzat T. Raheem ,  William D. Shipe ,  Cory R. Theberge

IPC: C07D513/04 ,  C07D495/04 ,  C07D417/14 ,  C07D471/04 ,  C07D401/14

CPC classification number: A61K31/505 ,  A61K31/506 ,  A61K31/513 ,  C07D239/30 ,  C07D239/48 ,  C07D239/52 ,  C07D239/56 ,  C07D401/14 ,  C07D403/12 ,  C07D403/14 ,  C07D413/14 ,  C07D417/12 ,  C07D417/14 ,  C07D471/04 ,  C07D495/04 ,  C07D513/04

Abstract: The present invention is directed to 2-alkoxy pyrimidine compounds which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

Abstract translation: 本发明涉及可用作治疗与磷酸二酯酶10（PDE10）相关的中枢神经系统疾病的治疗剂的2-烷氧基嘧啶化合物。 本发明还涉及这些化合物用于治疗神经和精神疾病如精神分裂症，精神病或亨廷顿病以及与纹状体功能减退或基底神经节功能障碍相关的疾病的用途。

公开(公告)号：US08389720B2

公开(公告)日：2013-03-05

申请号：US13127898

申请日：2009-11-03

Applicant: James C. Barrow ,  Mark T. Bilodeau ,  Christopher D. Cox ,  John C. Hartnett ,  Nathan R. Kett ,  Yiwei Li ,  Peter J. Manley ,  Jeffrey Melamed ,  William D. Shipe ,  B. Wesley Trotter ,  Amy Zartman

Inventor： James C. Barrow ,  Mark T. Bilodeau ,  Christopher D. Cox ,  John C. Hartnett ,  Nathan R. Kett ,  Yiwei Li ,  Peter J. Manley ,  Jeffrey Melamed ,  William D. Shipe ,  B. Wesley Trotter ,  Amy Zartman

IPC: A61K31/551 ,  A61K31/5355 ,  A61K31/497 ,  A61K31/519 ,  A61K31/4412 ,  A61K31/4704 ,  C07D243/08 ,  C07D413/14 ,  C07D471/04 ,  C07D401/14 ,  C07D401/12 ,  C07D405/14

CPC classification number: A61K31/47 ,  C07D401/12 ,  C07D405/12

Abstract: The present invention is directed to quinolone compounds which are antagonists of neuropeptide S receptors, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which the neuropeptide S receptor is involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the neuropeptide S receptor is involved.

Abstract translation: 本发明涉及作为神经肽S受体的拮抗剂的喹诺酮化合物，其可用于治疗或预防神经和精神疾病以及涉及神经肽S受体的疾病。 本发明还涉及包含这些化合物的药物组合物以及这些化合物和组合物在预防或治疗涉及神经肽S受体的疾病中的用途。

公开(公告)号：US08293914B2

公开(公告)日：2012-10-23

申请号：US12990014

申请日：2009-04-23

Applicant: Scott D. Kuduk ,  Christina Ng Di Marco ,  William D. Shipe

Inventor： Scott D. Kuduk ,  Christina Ng Di Marco ,  William D. Shipe

IPC: C07D215/38

CPC classification number: C07D401/14 ,  C07D401/06 ,  C07D405/14 ,  C07D409/14 ,  C07D413/14 ,  C07D417/14

Abstract: The present invention is directed to compounds of formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, schizophrenia, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases mediated by the M1 receptor.

Abstract translation: 本发明涉及作为M1受体阳性变构调节剂的式（I）化合物，其可用于治疗涉及M1受体的疾病，例如阿尔茨海默氏病，精神分裂症，疼痛或睡眠障碍。 本发明还涉及包含该化合物的药物组合物，以及该化合物和组合物在治疗由M1受体介导的疾病中的用途。

公开(公告)号：US20110212946A1

公开(公告)日：2011-09-01

申请号：US13127898

申请日：2009-11-03

Applicant: James C. Barrow ,  Mark T. Bilodeau ,  Christopher D. Cox ,  John C. Hartnett ,  Nathan R. Kett ,  Yiwei Li ,  Peter J. Manley ,  Jeffrey Melamed ,  William D. Shipe ,  B. Wesley Trotter ,  Amy Zartman

Inventor： James C. Barrow ,  Mark T. Bilodeau ,  Christopher D. Cox ,  John C. Hartnett ,  Nathan R. Kett ,  Yiwei Li ,  Peter J. Manley ,  Jeffrey Melamed ,  William D. Shipe ,  B. Wesley Trotter ,  Amy Zartman

IPC: A61K31/4704 ,  C07D405/14 ,  A61K31/496 ,  A61K31/55 ,  C07D401/12 ,  A61K31/4709 ,  C07D413/12 ,  A61K31/5377 ,  C07D215/227 ,  A61P25/00

CPC classification number: A61K31/47 ,  C07D401/12 ,  C07D405/12

Abstract: The present invention is directed to quinolone compounds which are antagonists of neuropeptide S receptors, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which the neuropeptide S receptor is involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the neuropeptide S receptor is involved.

Abstract translation: 本发明涉及作为神经肽S受体的拮抗剂的喹诺酮化合物，其可用于治疗或预防神经和精神疾病以及涉及神经肽S受体的疾病。 本发明还涉及包含这些化合物的药物组合物以及这些化合物和组合物在预防或治疗涉及神经肽S受体的疾病中的用途。

公开(公告)号：US20100009962A1

公开(公告)日：2010-01-14

申请号：US12308929

申请日：2007-06-27

Applicant: Craig Lindsley ,  William D. Shipe ,  Feng Yang ,  Jaime Lynn Bunda

Inventor： Craig Lindsley ,  William D. Shipe ,  Feng Yang ,  Jaime Lynn Bunda

IPC: A61K31/5377 ,  C07D401/10 ,  A61K31/4709 ,  C07D413/14 ,  C07D401/14 ,  A61K31/497 ,  A61P25/28

CPC classification number: C07D401/10 ,  C07D215/56 ,  C07D405/10 ,  C07D417/10

Abstract: The present invention is directed to benzyl-substituted quinolone compounds of general formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the treatment of diseases in which the M1 receptor is involved.

Abstract translation: 本发明涉及通式（I）的苄基取代喹诺酮化合物，它是M1受体阳性变构调节剂，可用于治疗涉及M1受体的疾病，例如阿尔茨海默病，疼痛或睡眠障碍 。 本发明还涉及包含这些化合物的药物组合物以及这些化合物和组合物在治疗涉及M1受体的疾病中的用途。