发明名称 Oxazole substituted indazoles as pi3-kinase inhibitors
摘要 596071 Disclosed is a substituted indazole compound of formula (I) where the substituents are as disclosed in the specification. Examples of a compounds of formula (I) are: N-[5-[4-(5-{ [(2R,6S)-2,6-dimethyl-4-morpholinyl]methyl} -1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]methanesulfonamide; 6-(1H-indol-4-yl)-4-(5-{ [4-(1-methylethyl)-1-piperazinyl]methyl} -1,3-oxazol-2-yl)-1H-indazole and 2,4-difluoro-N-[5-[4-(5-{ [4-(1-methylethyl)-1-piperazinyl]methyl} -1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide. Also disclosed are pharmaceutical compositions comprising a compound of formula (I) and the use of a compound of formula (I) in the manufacture of a medicament. The medicament is useful in the treatment or use in the treatment of a disorder mediated by inappropriate PI3-kinase activity such as asthma, chronic obstructive pulmonary disease (COPD), idiopathic pulmonary fibrosis (IPF), viral respiratory tract infections, viral exacerbation of respiratory diseases, aspergillosis, leishmaniasis and allergic rhinitis.
申请公布号 NZ596071(A) 申请公布日期 2013.12.20
申请号 NZ20100596071 申请日期 2010.04.28
申请人 GLAXO GROUP LIMITED 发明人 MITCHELL CHARLOTTE JANE;KEELING SUZANNE ELAINE;PARR NIGEL JAMES;JONES PAUL SPENCER;HAMBLIN JULIE NICOLE;LE JOELLE
分类号 C07D413/14;A61K31/422;A61K31/4439;A61P11/00;A61P31/12;A61P35/00;A61P37/00 主分类号 C07D413/14
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