CN101035761B - 作为聚(adp-核糖)聚合酶(parp)抑制剂、治疗由坏死或细胞程序死亡导致的组织损伤或疾病的3,6-取代的5-芳基氨基-1h-吡啶-2-酮衍生物和相关化合物 - Google Patents

作为聚(adp-核糖)聚合酶(parp)抑制剂、治疗由坏死或细胞程序死亡导致的组织损伤或疾病的3,6-取代的5-芳基氨基-1h-吡啶-2-酮衍生物和相关化合物 Download PDF

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CN101035761B
CN101035761B CN2005800338248A CN200580033824A CN101035761B CN 101035761 B CN101035761 B CN 101035761B CN 2005800338248 A CN2005800338248 A CN 2005800338248A CN 200580033824 A CN200580033824 A CN 200580033824A CN 101035761 B CN101035761 B CN 101035761B
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alkyl
ethyl
pyridin
methyl
amino
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CN101035761A (zh
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S·波伊克特
S·居斯雷根
A·霍德梅斯特尔
H·施罗伊德
U·施万
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Sanofi Aventis Deutschland GmbH
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    • 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
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • 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
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CN2005800338248A 2004-10-15 2005-10-05 作为聚(adp-核糖)聚合酶(parp)抑制剂、治疗由坏死或细胞程序死亡导致的组织损伤或疾病的3,6-取代的5-芳基氨基-1h-吡啶-2-酮衍生物和相关化合物 Expired - Fee Related CN101035761B (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE102004050196.3 2004-10-15
DE102004050196A DE102004050196A1 (de) 2004-10-15 2004-10-15 Substituierte 2-Pyridon-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Medikament
PCT/EP2005/010697 WO2006042638A1 (de) 2004-10-15 2005-10-05 3,6-substituierte 5-arylamino-1h-pyidin-2-on derivative und verwandte verbindungen als poly(adp-ribose)polymerase (parp) inhibitoren zur behandlung von durch nekose oder apoptose verursachten gewebeschäden oder erkankungen

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CN101035761A CN101035761A (zh) 2007-09-12
CN101035761B true CN101035761B (zh) 2010-06-02

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CN2005800338248A Expired - Fee Related CN101035761B (zh) 2004-10-15 2005-10-05 作为聚(adp-核糖)聚合酶(parp)抑制剂、治疗由坏死或细胞程序死亡导致的组织损伤或疾病的3,6-取代的5-芳基氨基-1h-吡啶-2-酮衍生物和相关化合物

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EP (1) EP1802578B1 (enExample)
JP (1) JP4875623B2 (enExample)
KR (1) KR20070063005A (enExample)
CN (1) CN101035761B (enExample)
AT (1) ATE393146T1 (enExample)
AU (1) AU2005297570C1 (enExample)
BR (1) BRPI0516516A (enExample)
CA (1) CA2583565A1 (enExample)
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WO2011058367A2 (en) 2009-11-13 2011-05-19 Astrazeneca Ab Diagnostic test for predicting responsiveness to treatment with poly(adp-ribose) polymerase (parp) inhibitor
WO2011141909A2 (en) 2010-05-10 2011-11-17 Radikal Therapeutics Inc. Lipoic acid and nitroxide derivatives and uses thereof
TW201512171A (zh) 2013-04-19 2015-04-01 Pfizer Ltd 化學化合物
AU2016296905B2 (en) 2015-07-23 2018-07-05 Centre National De La Recherche Scientifique Use of a combination of Dbait molecule and parp inhibitors to treat cancer
GB201519573D0 (en) 2015-11-05 2015-12-23 King S College London Combination
WO2018162439A1 (en) 2017-03-08 2018-09-13 Onxeo New predictive biomarker for the sensitivity to a treatment of cancer with a dbait molecule
EP3615026B1 (en) 2017-04-28 2021-03-03 Akribes Biomedical GmbH A parp inhibitor in combination with a glucocorticoid and/or ascorbic acid and/or a protein growth factor for the treatment of impaired wound healing
ES3008911T3 (en) 2017-07-11 2025-03-25 Vertex Pharma Carboxamides as modulators of sodium channels
JP7534218B2 (ja) 2018-03-13 2024-08-14 ヴァレリオ・セラピューティクス がんの治療における獲得耐性に対抗するdbait分子
WO2020012357A1 (en) * 2018-07-10 2020-01-16 Integral Biosciences Pvt. Ltd. Heterocyclic compounds and methods of use
WO2020146682A1 (en) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Carboxamides as modulators of sodium channels
WO2020146612A1 (en) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Esters and carbamates as modulators of sodium channels
JP7646643B2 (ja) * 2019-10-04 2025-03-17 アンスティトゥート・ナシオナル・ドゥ・ラ・サンテ・エ・ドゥ・ラ・ルシャルシュ・メディカル・(インセルム) 新規なピリジン-2(1h)オン誘導体、その調製、及び疼痛を処置するためのその使用
CA3159461A1 (en) 2019-11-25 2021-06-03 Iwao Ojima Combination therapy using fabp5 inhibitors with taxanes for treatment of cancer
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ATE393146T1 (de) 2008-05-15
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AU2005297570C1 (en) 2012-06-07
KR20070063005A (ko) 2007-06-18
WO2006042638A1 (de) 2006-04-27
CN101035761A (zh) 2007-09-12
EP1802578B1 (de) 2008-04-23
MX2007003360A (es) 2007-05-23
AU2005297570A1 (en) 2006-04-27
JP2008516902A (ja) 2008-05-22
JP4875623B2 (ja) 2012-02-15
DK1802578T3 (da) 2008-08-11
US7863280B2 (en) 2011-01-04

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