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公开(公告)号:US09034879B2
公开(公告)日:2015-05-19
申请号:US14343861
申请日:2012-09-14
申请人: Kamlesh Jagdis Bala , Rebecca Butler , Stephen Paul Collingwood , Edward Charles Hall , Lee Edwards , Darren Mark Legrand , Katrin Spiegel
发明人: Kamlesh Jagdis Bala , Rebecca Butler , Stephen Paul Collingwood , Edward Charles Hall , Lee Edwards , Darren Mark Legrand , Katrin Spiegel
IPC分类号: A61K31/497 , C07D417/04 , C07D413/04 , A61K31/4439 , A61K45/06
CPC分类号: A61K31/497 , A61K31/4439 , A61K45/06 , C07D413/04 , C07D417/04
摘要: The present invention provides pyridin-oxadiazole/thiadiazole derivatives of Formula I wherein A is N or CR 4a; and (ii) or (iii) which restore or enhance the function of mutant and/or wild type CFTR to treat cystic fibrosis, primary ciliary dyskinesia, chronic bronchitis, chronic obstructive pulmonary disease, asthma, respiratory tract infections, lung carcinoma, xerostomia and keratoconjunctivitis sire, or constipation (IBS, IBD, opioid induced). Pharmaceutical compositions comprising such derivatives are also encompassed.
摘要翻译: 本发明提供式I的吡啶并恶二唑/噻二唑衍生物,其中A为N或CR 4a; 和(ii)或(iii)其恢复或增强突变和/或野生型CFTR的功能以治疗囊性纤维化,原发性纤毛运动障碍,慢性支气管炎,慢性阻塞性肺病,哮喘,呼吸道感染,肺癌,口腔干燥症和 角膜结膜炎或便秘(IBS,IBD,阿片样物质诱发)。 还包括包含这些衍生物的药物组合物。
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公开(公告)号:US20140228376A1
公开(公告)日:2014-08-14
申请号:US14343861
申请日:2012-09-14
申请人: Kamlesh Jagdis Bala , Rebecca Butler , Stephen Paul Collingwood , Edward Charles Hall , Lee Edwards , Darren Mark Legrand , Katrin Spiegel
发明人: Kamlesh Jagdis Bala , Rebecca Butler , Stephen Paul Collingwood , Edward Charles Hall , Lee Edwards , Darren Mark Legrand , Katrin Spiegel
IPC分类号: A61K31/497 , C07D417/04 , A61K45/06 , C07D413/04 , A61K31/4439
CPC分类号: A61K31/497 , A61K31/4439 , A61K45/06 , C07D413/04 , C07D417/04
摘要: The present invention provides pyridin-oxadiazole/thiadiazole derivatives of Formula I wherein A is N or CR 4a; and (ii) or (iii) which restore or enhance the function of mutant and/or wild type CFTR to treat cystic fibrosis, primary ciliary dyskinesia, chronic bronchitis, chronic obstructive pulmonary disease, asthma, respiratory tract infections, lung carcinoma, xerostomia and keratoconjunctivitis sire, or constipation (IBS, IBD, opioid induced). Pharmaceutical compositions comprising such derivatives are also encompassed.
摘要翻译: 本发明提供式I的吡啶并恶二唑/噻二唑衍生物,其中A为N或CR 4a; 和(ii)或(iii)其恢复或增强突变和/或野生型CFTR的功能以治疗囊性纤维化,原发性纤毛运动障碍,慢性支气管炎,慢性阻塞性肺病,哮喘,呼吸道感染,肺癌,口腔干燥症和 角膜结膜炎或便秘(IBS,IBD,阿片样物质诱发)。 还包括包含这些衍生物的药物组合物。
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公开(公告)号:US10112926B2
公开(公告)日:2018-10-30
申请号:US15303879
申请日:2014-04-24
申请人: Benjamin Richard Bellenie , Graham Charles Bloomfield , Ian Bruce , Andrew James Culshaw , Edward Charles Hall , Gregory John Hollingworth , James Neef , Matthew Spendiff , Simon James Watson
发明人: Benjamin Richard Bellenie , Graham Charles Bloomfield , Ian Bruce , Andrew James Culshaw , Edward Charles Hall , Gregory John Hollingworth , James Neef , Matthew Spendiff , Simon James Watson
IPC分类号: C07D401/14 , C07D413/14 , C07D401/04 , C07D413/04 , C07D417/04 , C07D417/14 , C07D213/73 , C07D491/107 , A61K31/4439 , A61K31/444 , A61K31/4545 , A61K31/496 , A61K31/5377 , A61K31/55
摘要: The present invention provides compounds of formula (I) which inhibit the activity of PI 3-kinase gamma isoform, which are useful for the treatment of diseases mediated by the activation of PI 3-kinase gamma isoform.
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公开(公告)号:US10004732B2
公开(公告)日:2018-06-26
申请号:US15303868
申请日:2014-04-24
申请人: Benjamin Richard Bellenie , Graham Charles Bloomfield , Ian Bruce , Andrew James Culshaw , Edward Charles Hall , Gregory John Hollingworth , James Neef , Matthew Spendiff , Simon James Watson
发明人: Benjamin Richard Bellenie , Graham Charles Bloomfield , Ian Bruce , Andrew James Culshaw , Edward Charles Hall , Gregory John Hollingworth , James Neef , Matthew Spendiff , Simon James Watson
IPC分类号: C07D401/04 , C07D401/14 , C07D403/14 , C07D405/04 , C07D405/14 , C07D409/04 , C07D409/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , A61K31/497 , A61K31/5377 , C07D403/04
CPC分类号: A61K31/497 , A61K31/5377 , C07D401/04 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/04 , C07D405/14 , C07D409/04 , C07D409/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14
摘要: The present invention provides compounds of formula (I) which inhibit the activity of PI 3-kinase gamma isoform, which are useful for the treatment of diseases mediated by the activation of PI 3-kinase gamma isoform.
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