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公开(公告)号:US20130345180A1
公开(公告)日:2013-12-26
申请号:US13837137
申请日:2013-03-15
Applicant: Novartis AG
Inventor: Rolf BAENTELI , Gerhard ZENKE , Nigel Graham COOKE , Rudolf DUTHALER , Gebhard THOMA , Anette VON MATT , Toshiyuki HONDA , Naoko MATSUURA , Kazuhiko NONOMURA , Osamu OHMORI , Ichiro UMEMURA , Klaus HINTERDING , Christos PAPAGEORGIOU
IPC: C07D239/48 , A61K31/506 , C07D403/12 , C07D401/12 , A61K31/55 , A61K31/5377 , C07D417/12 , A61K45/06 , A61K31/505
CPC classification number: C07D239/48 , A61K31/505 , A61K31/506 , A61K31/5377 , A61K31/55 , A61K45/06 , C07D231/12 , C07D233/56 , C07D249/08 , C07D401/12 , C07D401/14 , C07D403/12 , C07D417/12
Abstract: There are provided compounds of formula I wherein X, R1, R2, R3, R4, R5, R6, R7, R8 and R9 are as indicated in claim 1, useful in disorders where ZAP-70 and/or Syk inhibition plays a role or caused by a malfunction of signal cascades connected with FAK.
Abstract translation: 提供式I化合物,其中X,R 1,R 2,R 3,R 4,R 5,R 6,R 7,R 8和R 9如权利要求1所述,其可用于ZAP-70和/或Syk抑制起作用或 由与FAK连接的信号级联故障引起的。
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公开(公告)号:US20150342951A1
公开(公告)日:2015-12-03
申请号:US14365512
申请日:2012-12-14
Applicant: NOVARTIS AG
Inventor: Nigel Graham COOKE , Paulo Antonio FERNANDES GOMES DOS SANTOS , Pascal FURET , Christina HEBACH , Klemens HOGENAUER , Gregory HOLLINGWORTH , Christoph KALIS , Ian LEWIS , Alexander Baxter SMITH , Nicolas SOLDERMANN , Frederic STAUFFER , Ross STRANG , Frank STOWASSER , Nicola TUFFILLI , Anette VON MATT , Romain WOLF , Frederic ZECRI
IPC: A61K31/519 , A61K31/551 , A61K31/541 , A61K31/5377 , A61K31/517
CPC classification number: A61K31/519 , A61K31/517 , A61K31/5377 , A61K31/541 , A61K31/551 , C07D239/74 , C07D401/04 , C07D401/14 , C07D403/04 , C07D413/14 , C07D487/08 , Y02A50/409 , Y02A50/411 , Y02A50/414
Abstract: The invention relates to new uses of PI3K inhibitors, wherein said inhibitors have an inhibitory action on the PI3K isoform delta for the treatment of immunopathology in a subject suffering from a disease or disorder selected from malaria, leishmaniasis, trypanosomiasis, toxoplasmosis and/or neurocysticercosis, via functional inhibition of TLR9 of the infected subject.
Abstract translation: 本发明涉及PI3K抑制剂的新用途,其中所述抑制剂对PI3K同种型δ具有抑制作用,用于治疗患有选自疟疾,利什曼病,锥虫病,弓形虫病和/或神经囊尾erc病的疾病或病症的受试者的免疫病理学, 通过功能抑制受感染受试者的TLR9。
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