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BR0313122A - Vegfr-2 and vegfr-3 inhibiting anthranilamidopyridines - Google Patents

Vegfr-2 and vegfr-3 inhibiting anthranilamidopyridines

Info

Publication number
BR0313122A
BR0313122A BR0313122-0A BR0313122A BR0313122A BR 0313122 A BR0313122 A BR 0313122A BR 0313122 A BR0313122 A BR 0313122A BR 0313122 A BR0313122 A BR 0313122A
Authority
BR
Brazil
Prior art keywords
vegfr
diseases
arthritis
preparation
compounds according
Prior art date
Application number
BR0313122-0A
Other languages
Portuguese (pt)
Inventor
Andreas Huth
Martin Kr Ger
Ludwig Zorn
Stuart Ince
Karl-Heinz Thierauch
Andreas Menrad
Martin Haberey
Holger Hess-Stump
Original Assignee
Schering Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE10235690A external-priority patent/DE10235690A1/en
Priority claimed from DE10328036A external-priority patent/DE10328036A1/en
Application filed by Schering Ag filed Critical Schering Ag
Publication of BR0313122A publication Critical patent/BR0313122A/en

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
    • C07D213/75Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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Abstract

"ANTRANILAMIDOPIRIDINAS INIBIDORAS DE VEGFR-2 E VEGFR-3". A presente invenção refere-se à antranilamidopiridinamidas inibidoras de VEGFR-2 e VEGFR-3, sua preparação e emprego como medicamento para o tratamento de doenças, que são provocadas pela angiogênese persistente bem como produtos intermediários para a preparação dos compostos. Os compostos de acordo com a invenção, são empregáveis como ou no crescimento do tumor ou metástase, psoríase, sarcoma de Kaposi, restenose tal como restenose induzida pelo stent, endometriose, doença de Crohn, doença de Hodgkins, leucemia, artrite, tal como artrite reumatóide, hemangioma, angiofibroma, doenças dos olhos, tais como retinopatia diabética, glaucoma neovascular, doenças renais, tais como glomerulonefrite, nefropatia diabética, nefroscierose maligna, síndrome microangiopática trómbica, rejeições de transplantes e glomerulopatia, doenças fibróticas, tal como cirrose hepática, doenças proliferativas das células mesangiais, arteriosclerose, lesões do tecido nervoso e inibição da reoclusão de vasos após tratamento com cateter de balão, na prótese vascular ou após o implante de dispositivos mecânicos para manter a abertura dos vasos, tal como por exemplo, stents, como imunossupressívos, para o auxílio na cura de feridas sem cicatriz, manchas de velhice e dermatite de contato. Os compostos de acordo com a invenção, são igualmente aplicáveis como inibidores de VEGFR-3 na linfangiogênese."VEGFR-2 AND VEGFR-3 INHIBITOR ANTRANYLAMIDOPYRIDES". The present invention relates to VEGFR-2 and VEGFR-3 inhibiting anthranilamidopyridinamides, their preparation and use as a medicament for the treatment of diseases which are caused by persistent angiogenesis as well as intermediate products for the preparation of the compounds. The compounds according to the invention are employed as either in tumor growth or metastasis, psoriasis, Kaposi's sarcoma, restenosis such as stent-induced restenosis, endometriosis, Crohn's disease, Hodgkins disease, leukemia, arthritis, such as arthritis. rheumatoid, hemangioma, angiofibroma, eye diseases such as diabetic retinopathy, neovascular glaucoma, renal diseases such as glomerulonephritis, diabetic nephropathy, malignant nephrosclerosis, transplant rejections and glomerulopathy, fibrosis diseases, such as cirrhotic diseases such as cirrhosis mesangial cell proliferation, arteriosclerosis, nerve tissue damage and inhibition of vessel reocclusion after balloon catheter treatment, vascular prosthesis or after implantation of mechanical devices to maintain vessel opening, such as stents such as immunosuppressive , to aid in healing non-scarred wounds, stains of old age and contact dermatitis. The compounds according to the invention are also applicable as inhibitors of VEGFR-3 in lymphangiogenesis.

BR0313122-0A 2002-07-31 2003-07-22 Vegfr-2 and vegfr-3 inhibiting anthranilamidopyridines BR0313122A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10235690A DE10235690A1 (en) 2002-07-31 2002-07-31 New N-benzyl-anthranilic acid (hetero)arylamide derivatives and analogs, are tyrosine kinase KDR and FLT inhibitors and angiogenesis inhibitors, useful e.g. for treating tumors, psoriasis or restenosis
DE10328036A DE10328036A1 (en) 2003-06-19 2003-06-19 New N-benzyl-anthranilic acid (hetero)arylamide derivatives and analogs, are tyrosine kinase KDR and FLT inhibitors and angiogenesis inhibitors, useful e.g. for treating tumors, psoriasis or restenosis
PCT/EP2003/007964 WO2004013102A1 (en) 2002-07-31 2003-07-22 Vegfr-2 and vegfr-3 inhibitory anthranylamidopyridines

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BR0313122A true BR0313122A (en) 2005-07-05

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BR0313122-0A BR0313122A (en) 2002-07-31 2003-07-22 Vegfr-2 and vegfr-3 inhibiting anthranilamidopyridines

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EP (1) EP1594841A1 (en)
JP (2) JP4777648B2 (en)
KR (1) KR20050026535A (en)
CN (1) CN1671666A (en)
AU (1) AU2003281855A1 (en)
BR (1) BR0313122A (en)
CA (1) CA2493026C (en)
CO (1) CO5720998A2 (en)
CR (1) CR7673A (en)
EC (1) ECSP055631A (en)
HR (1) HRP20050187A2 (en)
IL (1) IL166377A0 (en)
MX (1) MXPA04012948A (en)
NO (1) NO20051035L (en)
PL (1) PL374610A1 (en)
RS (1) RS20050084A (en)
RU (1) RU2005105683A (en)
WO (1) WO2004013102A1 (en)

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US7615565B2 (en) 2002-07-31 2009-11-10 Bayer Schering Pharma Aktiengesellschaft VEGFR-2 and VEGFR-3 inhibitory anthranilamide pyridines
GB0229022D0 (en) * 2002-12-12 2003-01-15 Novartis Ag Organic Compounds
AU2004206860B2 (en) 2003-01-14 2010-03-18 Cytokinetics, Inc. Compounds, compositions and methods
DE102004009238A1 (en) * 2004-02-26 2005-09-08 Merck Patent Gmbh New aryl amide compounds are kinase inhibitors useful for the treatment and/or prophylaxis of e.g. tumors, psoriasis, rheumatoid arthritis, contact dermatitis, inflammations, endometriosis, scar and benign prostatic hyperplasia
NZ552404A (en) * 2004-06-17 2010-04-30 Cytokinetics Inc Compounds, compositions and methods
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