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公开(公告)号:US08729079B2
公开(公告)日:2014-05-20
申请号:US13592511
申请日:2012-08-23
申请人: Aranapakam Venkatesan , Roger Astbury Smith , Subramanya Hosahalli , Vijay Potluri , Sunil Kumar Panigrahi , Vishnu Basetti , Karunasree Kunta
发明人: Aranapakam Venkatesan , Roger Astbury Smith , Subramanya Hosahalli , Vijay Potluri , Sunil Kumar Panigrahi , Vishnu Basetti , Karunasree Kunta
IPC分类号: C07D487/04 , C07D519/00 , A61K31/519 , A61P29/00
CPC分类号: C07D487/04 , C07D519/00 , C07F9/6561
摘要: The present application provides novel pyrimido-pyridazinone compounds and methods for preparing and using these compounds. These compounds are useful in treating inflammation in patients by administering one or more of the compounds to a patient. In one embodiment, the novel pyrimido-pyridazinone compound is of Formula (I) and R1 and R2 are defined herein.
摘要翻译: 本申请提供了新的嘧啶并哒嗪酮化合物及其制备和使用方法。 这些化合物可用于通过向患者施用一种或多种化合物来治疗患者的炎症。 在一个实施方案中,新的嘧啶并哒嗪酮化合物具有式(I),并且R 1和R 2在本文中定义。
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公开(公告)号:US20070015665A1
公开(公告)日:2007-01-18
申请号:US11480032
申请日:2006-06-30
申请人: Vijay Potluri , Saibal Das , Pradip Sasmal , Javed Iqbal , Parimal Misra , Ranjan Chakrabarti , Rashmi Talwar
发明人: Vijay Potluri , Saibal Das , Pradip Sasmal , Javed Iqbal , Parimal Misra , Ranjan Chakrabarti , Rashmi Talwar
IPC分类号: C07D417/02 , A01N43/78
CPC分类号: C07D277/42
摘要: The present application provides novel thiazole derivatives that are useful as activators of Adenosine 5′-Monophosphate-Activated Protein Kinase and pharmaceutical compositions containing such compounds.
摘要翻译: 本申请提供了可用作腺苷5'-单磷酸激活蛋白激酶的激活剂的新型噻唑衍生物和含有这些化合物的药物组合物。
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公开(公告)号:US09303027B2
公开(公告)日:2016-04-05
申请号:US13811020
申请日:2011-07-19
申请人: Pradip Kumar Sasmal , Vamsee Krishna Chintakunta , Vijay Potluri , Ish Kumar Khanna , Ashok Tehim , Mahaboobi Jaleel , Thomas Hogberg , Oystein Rist , Lisbeth Elster , Thomas Michael Frimurer , Lars-Ole Gerlach
发明人: Pradip Kumar Sasmal , Vamsee Krishna Chintakunta , Vijay Potluri , Ish Kumar Khanna , Ashok Tehim , Mahaboobi Jaleel , Thomas Hogberg , Oystein Rist , Lisbeth Elster , Thomas Michael Frimurer , Lars-Ole Gerlach
IPC分类号: C07D419/12 , C07D207/09 , C07D401/12 , C07D403/12 , C07D413/12 , C07D413/14 , C07D417/12 , C07D207/12 , C07D209/34 , C07D213/76 , C07D215/12 , C07D215/227 , C07D231/56 , C07D249/18 , C07D261/20 , C07D263/56 , C07D263/58 , C07D275/06 , C07D277/30 , C07D279/02 , C07D295/13
CPC分类号: C07D419/12 , C07D207/09 , C07D207/12 , C07D209/34 , C07D213/76 , C07D215/12 , C07D215/227 , C07D231/56 , C07D249/18 , C07D261/20 , C07D263/56 , C07D263/58 , C07D275/06 , C07D277/30 , C07D279/02 , C07D295/13 , C07D401/12 , C07D403/12 , C07D413/12 , C07D413/14 , C07D417/12
摘要: The present invention relates to a series of substituted compounds having the general formula (I), including their stereoisomers and/or their pharmaceutically acceptable salts. (I) Wherein A, m, R1s, R2, R3, R4 are as defined herein. This invention also relates to methods of making these compounds including intermediates. The compounds of this invention are effective at the kappa (κ) opioid receptor (KOR) site. Therefore, the compounds of this invention are useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of central nervous system disorders (CNS), including but not limited to acute and chronic pain, and associated disorders, particularly functioning peripherally at the CNS.
摘要翻译: 本发明涉及一系列具有通式(I)的取代的化合物,包括其立体异构体和/或其药学上可接受的盐。 (I)其中A,m,R 1,R 2,R 3,R 4如本文所定义。 本发明还涉及制备这些化合物包括中间体的方法。 本发明的化合物在κ(αKα)阿片受体(KOR)位点是有效的。 因此,本发明的化合物可用作药物,特别是用于治疗和/或预防各种中枢神经系统疾病(CNS),包括但不限于急性和慢性疼痛以及相关疾病,特别是周边功能 在CNS。
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公开(公告)号:US20130303525A1
公开(公告)日:2013-11-14
申请号:US13811020
申请日:2011-07-19
申请人: Pradip Kumar Sasmal , Vamsee Krishna Chintakunta , Vijay Potluri , Ish Kumar Khanna , Ashok Tehim , Mahaboobi Jaleel , Thomas Hogberg , Oystein Rist , Lisbeth Elster , Thomas Michael Frimurer , Lars-Ole Gerlach
发明人: Pradip Kumar Sasmal , Vamsee Krishna Chintakunta , Vijay Potluri , Ish Kumar Khanna , Ashok Tehim , Mahaboobi Jaleel , Thomas Hogberg , Oystein Rist , Lisbeth Elster , Thomas Michael Frimurer , Lars-Ole Gerlach
IPC分类号: C07D419/12 , C07D401/12 , C07D413/14 , C07D403/12 , C07D207/09 , C07D417/12 , C07D413/12
CPC分类号: C07D419/12 , C07D207/09 , C07D207/12 , C07D209/34 , C07D213/76 , C07D215/12 , C07D215/227 , C07D231/56 , C07D249/18 , C07D261/20 , C07D263/56 , C07D263/58 , C07D275/06 , C07D277/30 , C07D279/02 , C07D295/13 , C07D401/12 , C07D403/12 , C07D413/12 , C07D413/14 , C07D417/12
摘要: The present invention relates to a series of substituted compounds having the general formula (I), including their stereoisomers and/or their pharmaceutically acceptable salts. (I) Wherein A, m, R1s, R2, R3, R4 are as defined herein. This invention also relates to methods of making these compounds including intermediates. The compounds of this invention are effective at the kappa (κ) opioid receptor (KOR) site. Therefore, the compounds of this invention are useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of central nervous system disorders (CNS), including but not limited to acute and chronic pain, and associated disorders, particularly functioning peripherally at the CNS.
摘要翻译: 本发明涉及一系列具有通式(I)的取代的化合物,包括其立体异构体和/或其药学上可接受的盐。 (I)其中A,m,R 1,R 2,R 3,R 4如本文所定义。 本发明还涉及制备这些化合物包括中间体的方法。 本发明的化合物在κ(κ)阿片样物质受体(KOR)位点是有效的。 因此,本发明的化合物可用作药物,特别是用于治疗和/或预防各种中枢神经系统疾病(CNS),包括但不限于急性和慢性疼痛以及相关疾病,特别是周边功能 在CNS。
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公开(公告)号:US20130053346A1
公开(公告)日:2013-02-28
申请号:US13592511
申请日:2012-08-23
申请人: Aranapakam Venkatesan , Roger Astbury Smith , Subramanya Hosahalli , Vijay Potluri , Sunil Kumar Panigrahi , Vishnu Basetti , Karunasree Kunta
发明人: Aranapakam Venkatesan , Roger Astbury Smith , Subramanya Hosahalli , Vijay Potluri , Sunil Kumar Panigrahi , Vishnu Basetti , Karunasree Kunta
IPC分类号: A61K31/519 , A61K31/5377 , C07D519/00 , A61K31/541 , A61K31/55 , A61K31/551 , C07F9/6561 , A61K31/675 , A61P29/00 , A61P19/08 , A61P3/00 , A61P11/06 , A61P5/00 , A61P37/08 , A61P25/00 , C07D487/04
CPC分类号: C07D487/04 , C07D519/00 , C07F9/6561
摘要: The present application provides novel pyrimido-pyridazinone compounds and methods for preparing and using these compounds. These compounds are useful in treating inflammation in patients by administering one or more of the compounds to a patient. In one embodiment, the novel pyrimido-pyridazinone compound is of Formula (I) and R1 and R2 are defined herein.
摘要翻译: 本申请提供了新的嘧啶并哒嗪酮化合物及其制备和使用方法。 这些化合物可用于通过向患者施用一种或多种化合物来治疗患者的炎症。 在一个实施方案中,新的嘧啶并哒嗪酮化合物具有式(I),并且R 1和R 2在本文中定义。
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