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
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2007536043A
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English (en)
Japanese (ja)
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JP2008516902A (ja
JP4875623B2 (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
DE102004050196A DE102004050196A1 (de) 2004-10-15 2004-10-15 Substituierte 2-Pyridon-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Medikament
DE102004050196.3 2004-10-15
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 (enExample) 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 (enExample)
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)
DE (2) DE102004050196A1 (enExample)
DK (1) DK1802578T3 (enExample)
ES (1) ES2304721T3 (enExample)
IL (1) IL182093A (enExample)
MX (1) MX2007003360A (enExample)
PT (1) PT1802578E (enExample)
WO (1) WO2006042638A1 (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
SG164368A1 (en) 2005-07-18 2010-09-29 Bipar Sciences Inc Treatment of cancer
AU2007292387A1 (en) 2006-09-05 2008-03-13 Bipar Sciences, Inc. Treatment of cancer
WO2008030891A2 (en) * 2006-09-05 2008-03-13 Bipar Sciences, Inc. Inhibition of fatty acid synthesis by parp inhibitors and methods of treatment thereof
EP2173743A2 (en) 2007-07-13 2010-04-14 Icagen, Inc. Sodium channel inhibitors
JP2011503111A (ja) 2007-11-12 2011-01-27 バイパー サイエンシズ,インコーポレイティド Parp阻害剤単独又は抗腫瘍剤との組み合わせによる乳がんの治療
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
HUE045916T2 (hu) 2015-07-23 2020-01-28 Inst Curie Dbait molekula és PARP inhibitorok kombinációjának alkalmazása rák kezelésében
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
WO2018197461A1 (en) 2017-04-28 2018-11-01 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
SG11202000230VA (en) 2017-07-11 2020-02-27 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
WO2020146612A1 (en) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Esters and carbamates as modulators of sodium channels
WO2020146682A1 (en) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Carboxamides 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
CA3159461A1 (en) 2019-11-25 2021-06-03 Iwao Ojima Combination therapy using fabp5 inhibitors with taxanes for treatment of cancer
US20230348401A1 (en) * 2020-01-15 2023-11-02 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
AU2024312126A1 (en) 2023-06-21 2025-12-11 Tetragon Biosciences Ltd. Combination comprising a deoxycytidine derivative and a parp inhibitor for use in a method of treating hr proficient cancer

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
KR0170534B1 (ko) * 1993-11-10 1999-02-18 미즈노 시게루 크로만 유도체 및 그의 제약학적 용도
MXPA02003436A (es) * 1999-10-07 2002-08-20 Amgen Inc Inhibidores de triazina cinasa.
AU2002331621B2 (en) * 2001-08-15 2008-06-05 Icos Corporation 2H-phthalazin-1-ones and methods for use thereof
AUPS019702A0 (en) 2002-01-29 2002-02-21 Fujisawa Pharmaceutical Co., Ltd. Condensed heterocyclic compounds

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