发明公开
EP1392680A2 SELEKTIVE ANTHRANYLAMIDPYRIDINAMIDE ALS VEGFR-2 UND VEGFR-3 INHIBITOREN
有权
选择性ANTHRANYLAMIDPYRIDINAMIDE AS VEGFR-2和VEGFR-3抑制剂
- 专利标题: SELEKTIVE ANTHRANYLAMIDPYRIDINAMIDE ALS VEGFR-2 UND VEGFR-3 INHIBITOREN
- 专利标题(英): Selective anthranilamide pyridine amides as inhibitors of vegfr-2 and vegfr-3
- 专利标题(中): 选择性ANTHRANYLAMIDPYRIDINAMIDE AS VEGFR-2和VEGFR-3抑制剂
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申请号: EP02735333.3申请日: 2002-05-03
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公开(公告)号: EP1392680A2公开(公告)日: 2004-03-03
- 发明人: ERNST, Alexander , HUTH, Andreas , KRÜGER, Martin , THIERAUCH, Karl-Heinz , MENRAD, Andreas , HABEREY, Martin
- 申请人: SCHERING AKTIENGESELLSCHAFT
- 申请人地址: Müllerstrasse 178 13342 Berlin DE
- 专利权人: SCHERING AKTIENGESELLSCHAFT
- 当前专利权人: SCHERING AKTIENGESELLSCHAFT
- 当前专利权人地址: Müllerstrasse 178 13342 Berlin DE
- 优先权: DE10123574 20010508; DE10125294 20010515; DE10164590 20011221
- 国际公布: WO2002090352 20021114
- 主分类号: C07D401/14
- IPC分类号: C07D401/14 ; C07D401/12 ; C07D407/12 ; C07D409/14 ; A61K31/47 ; A61K31/44 ; A61P29/00
摘要:
The invention relates to selective anthranilamide pyridine amides as inhibitors of VEGFR-2 and VEGFR-3 and to their production and use as medicaments for treating diseases that are caused by persistent angiogenesis. The inventive compounds can be used for example in cases of psoriasis, Kaposi's sarcoma, restenosis, such as e.g. stent-induced restenosis, endometriosis, Crohn's disease, Hodgkin's disease, leukaemia, arthritis, such as rheumatoid arthritis, haemangioma, angiofibromatosis, in eye diseases such as diabetic retinopathy, neovascular glaucoma, in kidney diseases such as glomerulonephritis, diabetic nephropathy, malign nephrosclerosis, thrombic micro-angiopathic syndrome, transplant rejection and glomerulopathy, in fibrotic diseases such as hepatic cirrhosis, mesangial-cell proliferative diseases, arteriosclerosis, damage to the nerve tissue and inhibition of the re-occlusion of vessels after balloon catheter treatment, in vessel prosthetics or after the use of mechanical devices for keeping vessels open, e.g. stents, as immunosuppressants, to support wound healing without scars and in cases of age spots and contact dermatitis. The inventive compounds can also be used as inhibitors of VEGFR-3 in lymphangiogenesis for hyperplastic and dysplastic changes in the lymphatic system.
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