JP2013525473A5 - - Google Patents

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Publication number
JP2013525473A5
JP2013525473A5 JP2013508559A JP2013508559A JP2013525473A5 JP 2013525473 A5 JP2013525473 A5 JP 2013525473A5 JP 2013508559 A JP2013508559 A JP 2013508559A JP 2013508559 A JP2013508559 A JP 2013508559A JP 2013525473 A5 JP2013525473 A5 JP 2013525473A5
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JP
Japan
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group
ortho
meta
optionally substituted
trifluoromethyl
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JP2013508559A
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English (en)
Japanese (ja)
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JP5812541B2 (ja
JP2013525473A (ja
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Publication date
Priority claimed from HU1000243A external-priority patent/HUP1000243A2/hu
Application filed filed Critical
Publication of JP2013525473A publication Critical patent/JP2013525473A/ja
Publication of JP2013525473A5 publication Critical patent/JP2013525473A5/ja
Application granted granted Critical
Publication of JP5812541B2 publication Critical patent/JP5812541B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2013508559A 2010-05-06 2011-05-06 8−ヒドロキシキノリン誘導体 Active JP5812541B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
HU1000243A HUP1000243A2 (en) 2010-05-06 2010-05-06 8-hidroxy-quinoline derivatives
HUP1000243 2010-05-06
PCT/HU2011/000043 WO2011148208A1 (en) 2010-05-06 2011-05-06 8-hydroxy-quinoline derivatives

Publications (3)

Publication Number Publication Date
JP2013525473A JP2013525473A (ja) 2013-06-20
JP2013525473A5 true JP2013525473A5 (cg-RX-API-DMAC7.html) 2014-06-26
JP5812541B2 JP5812541B2 (ja) 2015-11-17

Family

ID=89989711

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013508559A Active JP5812541B2 (ja) 2010-05-06 2011-05-06 8−ヒドロキシキノリン誘導体

Country Status (21)

Country Link
US (1) US8871937B2 (cg-RX-API-DMAC7.html)
EP (1) EP2566849B1 (cg-RX-API-DMAC7.html)
JP (1) JP5812541B2 (cg-RX-API-DMAC7.html)
KR (1) KR101837974B1 (cg-RX-API-DMAC7.html)
CN (1) CN102985407B (cg-RX-API-DMAC7.html)
AU (1) AU2011256989B2 (cg-RX-API-DMAC7.html)
CA (1) CA2798419C (cg-RX-API-DMAC7.html)
CY (1) CY1122426T1 (cg-RX-API-DMAC7.html)
DK (1) DK2566849T3 (cg-RX-API-DMAC7.html)
EA (1) EA021026B1 (cg-RX-API-DMAC7.html)
ES (1) ES2761832T3 (cg-RX-API-DMAC7.html)
HR (1) HRP20192278T1 (cg-RX-API-DMAC7.html)
HU (2) HUP1000243A2 (cg-RX-API-DMAC7.html)
MX (1) MX337999B (cg-RX-API-DMAC7.html)
NZ (1) NZ603967A (cg-RX-API-DMAC7.html)
PL (1) PL2566849T3 (cg-RX-API-DMAC7.html)
PT (1) PT2566849T (cg-RX-API-DMAC7.html)
RS (1) RS59678B1 (cg-RX-API-DMAC7.html)
SI (1) SI2566849T1 (cg-RX-API-DMAC7.html)
SM (1) SMT201900710T1 (cg-RX-API-DMAC7.html)
WO (1) WO2011148208A1 (cg-RX-API-DMAC7.html)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUP1500098A2 (hu) 2015-03-09 2016-09-28 Avidin Kft 8-hidroxikinolin származékok új enantiomerjei és szintézisük
EP3361871A4 (en) * 2015-10-12 2019-06-26 Health Research, Inc. PROCESS FOR INDUCING APOPTOSIS IN CANCER CELLS
CN105367553A (zh) * 2015-12-04 2016-03-02 广东工业大学 一种他克林-8-羟(胺)基喹啉衍生物及其应用
HUP1600234A2 (en) 2016-04-05 2017-12-28 Mta Termeszettudomanyi Kutatokoezpont Mdr-reversing 8-hydroxy-quinoline derivatives
WO2024073624A2 (en) * 2022-09-28 2024-04-04 The Research Foundation For The State University Of New York Antiproliferative betti bases and prodrugs thereof

Family Cites Families (31)

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WO1999015179A1 (en) 1997-09-25 1999-04-01 Regents Of The University Of Minnesota Methods of limiting apoptosis of cells
US6184210B1 (en) 1997-10-10 2001-02-06 Cytovia, Inc. Dipeptide apoptosis inhibitors and the use thereof
JP2002501018A (ja) 1998-01-26 2002-01-15 マイトコー ミトコンドリア関連疾患を処置するためのミトコンドリア保護剤
US6737511B1 (en) 1999-08-16 2004-05-18 The United States Of America As Represented By The Department Of Health And Human Services Receptor-mediated uptake of an extracellular BCL-xL fusion protein inhibits apoptosis
KR20020033777A (ko) 1999-08-27 2002-05-07 추후보정 치환된 α-히드록시 산 카스파제 억제제 및 이의 용도
US6890896B1 (en) 1999-11-18 2005-05-10 Ceremedix, Inc. Compositions and methods for counteracting effects of reactive oxygen species and free radicals
US6476048B1 (en) 1999-12-07 2002-11-05 Inotek Pharamaceuticals Corporation Substituted phenanthridinones and methods of use thereof
US6531464B1 (en) 1999-12-07 2003-03-11 Inotek Pharmaceutical Corporation Methods for the treatment of neurodegenerative disorders using substituted phenanthridinone derivatives
US6534651B2 (en) 2000-04-06 2003-03-18 Inotek Pharmaceuticals Corp. 7-Substituted isoindolinone inhibitors of inflammation and reperfusion injury and methods of use thereof
GB0011095D0 (en) 2000-05-08 2000-06-28 Black James Foundation astrin and cholecystokinin receptor ligands (III)
WO2002030411A2 (en) 2000-10-13 2002-04-18 Johns Hopkins University Treatment of apoptotic cell death
US6552076B2 (en) 2000-12-15 2003-04-22 Mitokor Compounds for altering mitochondrial function and cellular responses
US7601846B2 (en) 2001-06-26 2009-10-13 The Regents Of The University Of California Compounds having activity as inhibitors of apoptosis
CA2452005C (en) 2001-07-10 2011-03-15 Idec Pharmaceutical Corporation Inhibition of apoptosis process and improvement of cell performance
DE10144153A1 (de) 2001-09-07 2003-03-27 Newfrey Llc Halteclip mit versetzten Rastfingern
AU2003211102B2 (en) 2002-02-13 2010-03-04 Beth Israel Deaconess Medical Center, Inc. Methods of treating vascular disease
US7217709B2 (en) 2003-02-28 2007-05-15 Inotek Pharmaceuticals Corporation Tetracyclic benzamide derivatives and methods of use thereof
US7449464B2 (en) 2003-03-12 2008-11-11 Kudos Pharmaceuticals Limited Phthalazinone derivatives
JP4824566B2 (ja) 2003-05-28 2011-11-30 エーザイ インコーポレーテッド Parpを阻害するための化合物、方法、および医薬組成物
NZ549393A (en) 2004-01-23 2009-07-31 Cornell Res Foundation Inc Methods for reducing oxidative damage
TWI375673B (en) 2005-04-11 2012-11-01 Abbott Lab 1h-benzimidazole-4-carboxamides substituted with a quaternary carbon at the 2-position are potent parp inhibitors
CN101309908A (zh) 2005-11-15 2008-11-19 艾博特公司 作为有效parp抑制剂的取代的1h-苯并咪唑-4-甲酰胺化合物
US7528174B2 (en) 2006-01-06 2009-05-05 University Of Pittsburgh-Of The Commonwealth System Of Higher Education Selective targeting agents for mitochondria
CN101611009A (zh) * 2006-07-25 2009-12-23 伊维沃制药股份有限公司 喹啉衍生物
US8609649B2 (en) * 2007-03-20 2013-12-17 Brandeis University Compositions and methods for the diagnosis, treatment, and prevention of amyotrophic lateral sclerosis and related neurological diseases
US8183236B2 (en) * 2007-04-12 2012-05-22 University Of Southern California Compounds with HIV-1 integrase inhibitory activity and use thereof as anti-HIV/AIDS therapeutics
CA2687187A1 (en) 2007-05-25 2008-12-18 Burnham Institute For Medical Research Inhibitors of thapsigargin-induced cell death
US8138356B2 (en) * 2007-10-16 2012-03-20 Angiogeney, Inc. Chemical inhibitors of inhibitors of differentiation
US10301265B2 (en) * 2008-05-28 2019-05-28 Virginia I. Roxas-Duncan Small molecule inhibitors of botulinum neurotoxins
US8658170B2 (en) * 2010-01-06 2014-02-25 Joseph P. Errico Combination therapy with MDM2 and EFGR inhibitors
AU2011204368B2 (en) * 2010-01-06 2014-11-27 Joseph P. Errico Methods and compositions of targeted drug development

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