JP2008516902A5 - - Google Patents

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Publication number
JP2008516902A5
JP2008516902A5 JP2007536043A JP2007536043A JP2008516902A5 JP 2008516902 A5 JP2008516902 A5 JP 2008516902A5 JP 2007536043 A JP2007536043 A JP 2007536043A JP 2007536043 A JP2007536043 A JP 2007536043A JP 2008516902 A5 JP2008516902 A5 JP 2008516902A5
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JP
Japan
Prior art keywords
alkyl
heteroaryl
phenyl
fluorine
methyl
Prior art date
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Granted
Application number
JP2007536043A
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English (en)
Japanese (ja)
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JP4875623B2 (ja
JP2008516902A (ja
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Publication date
Priority claimed from DE102004050196A external-priority patent/DE102004050196A1/de
Application filed filed Critical
Publication of JP2008516902A publication Critical patent/JP2008516902A/ja
Publication of JP2008516902A5 publication Critical patent/JP2008516902A5/ja
Application granted granted Critical
Publication of JP4875623B2 publication Critical patent/JP4875623B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2007536043A 2004-10-15 2005-10-05 壊死又はアポトーシスによって生じた組織損傷又は疾患の治療におけるポリ(adp−リボース)ポリメラーゼ(parp)阻害剤としての3,6−置換された5−アリールアミノ−1h−ピリジン−2−オン誘導体及び関連化合物 Expired - Fee Related JP4875623B2 (ja)

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

Publications (3)

Publication Number Publication Date
JP2008516902A JP2008516902A (ja) 2008-05-22
JP2008516902A5 true JP2008516902A5 (en:Method) 2008-11-06
JP4875623B2 JP4875623B2 (ja) 2012-02-15

Family

ID=35414525

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007536043A Expired - Fee Related JP4875623B2 (ja) 2004-10-15 2005-10-05 壊死又はアポトーシスによって生じた組織損傷又は疾患の治療におけるポリ(adp−リボース)ポリメラーゼ(parp)阻害剤としての3,6−置換された5−アリールアミノ−1h−ピリジン−2−オン誘導体及び関連化合物

Country Status (16)

Country Link
US (1) US7863280B2 (en:Method)
EP (1) EP1802578B1 (en:Method)
JP (1) JP4875623B2 (en:Method)
KR (1) KR20070063005A (en:Method)
CN (1) CN101035761B (en:Method)
AT (1) ATE393146T1 (en:Method)
AU (1) AU2005297570C1 (en:Method)
BR (1) BRPI0516516A (en:Method)
CA (1) CA2583565A1 (en:Method)
DE (2) DE102004050196A1 (en:Method)
DK (1) DK1802578T3 (en:Method)
ES (1) ES2304721T3 (en:Method)
IL (1) IL182093A (en:Method)
MX (1) MX2007003360A (en:Method)
PT (1) PT1802578E (en:Method)
WO (1) WO2006042638A1 (en:Method)

Families Citing this family (24)

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AU2003284237A1 (en) * 2002-10-16 2004-05-04 Transport Systems, Inc. Monorail sortation system
US7961081B2 (en) * 2003-05-22 2011-06-14 John Tomlienovic Anti-theft system and method
CA2615374A1 (en) 2005-07-18 2007-01-25 Ernest Kun Kun Treatment of cancer
US8143447B2 (en) 2006-09-05 2012-03-27 Bipar Sciences, Inc. Treatment of cancer
US7994222B2 (en) 2006-09-05 2011-08-09 Bipar Sciences, Inc. Monitoring of the inhibition of fatty acid synthesis by iodo-nitrobenzamide compounds
EP2173743A2 (en) * 2007-07-13 2010-04-14 Icagen, Inc. Sodium channel inhibitors
AU2008321128A1 (en) 2007-11-12 2009-05-22 Bipar Sciences, Inc. Treatment of breast cancer with a PARP inhibitor alone or in combination with anti-tumor agents
WO2011058367A2 (en) 2009-11-13 2011-05-19 Astrazeneca Ab Diagnostic test for predicting responsiveness to treatment with poly(adp-ribose) polymerase (parp) inhibitor
AU2011251622A1 (en) 2010-05-10 2012-12-20 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
PT3325623T (pt) 2015-07-23 2019-09-04 Inst Curie Utilização de uma combinação de molécula dbait e de inibidores de parp para o tratamento do cancro
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
US20200129476A1 (en) 2017-04-28 2020-04-30 Akribes Biomedical Gmbh 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
AU2019235337A1 (en) 2018-03-13 2020-08-27 Centre National De La Recherche Scientifique A Dbait molecule against acquired resistance in the treatment of cancer
US20200247812A1 (en) * 2018-07-10 2020-08-06 Integral Biosciences Private Limited 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
US12351556B2 (en) 2019-10-04 2025-07-08 Inserm (Institut National De La Sante Et De La Recherche Medicale) Pyridin-2(1H)one derivatives, their preparation and their use for the treatment of pain
EP4065099A4 (en) 2019-11-25 2023-11-29 The Research Foundation for The State University of New York COMBINATION THERAPY USING FABP5 INHIBITORS WITH TAXANS FOR THE TREATMENT OF CANCER
WO2021146543A1 (en) * 2020-01-15 2021-07-22 The Trustees Of Princeton University Inhibitors of glucose-6-phosphate dehydrogenase and uses thereof
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
CN121398822A (zh) 2023-06-21 2026-01-23 四方生物科学有限公司 用于在治疗hr功能正常的癌症的方法中的用途的包含脱氧胞苷衍生物和parp抑制剂的组合

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL70169A0 (en) * 1982-11-18 1984-02-29 Sterling Drug Inc 2(1h)-pyridinones,their preparation and pharmaceutical compositions containing them
GB9121651D0 (en) * 1991-10-11 1991-11-27 Smithkline Beecham Plc Chemical compounds
CA2153498A1 (en) * 1993-11-10 1995-05-18 Hidetsura Cho Chroman derivative and medicinal use thereof
CA2386218A1 (en) * 1999-10-07 2001-04-12 Amgen Inc. Triazine kinase inhibitors
JP2005501848A (ja) * 2001-08-15 2005-01-20 アイコス コーポレイション 2h−フタラジン−1−オンおよびその使用方法
AUPS019702A0 (en) * 2002-01-29 2002-02-21 Fujisawa Pharmaceutical Co., Ltd. Condensed heterocyclic compounds

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