KR20090021215A - 암의 치료를 위한 화합물 및 조성물 - Google Patents
암의 치료를 위한 화합물 및 조성물 Download PDFInfo
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- KR20090021215A KR20090021215A KR1020097000459A KR20097000459A KR20090021215A KR 20090021215 A KR20090021215 A KR 20090021215A KR 1020097000459 A KR1020097000459 A KR 1020097000459A KR 20097000459 A KR20097000459 A KR 20097000459A KR 20090021215 A KR20090021215 A KR 20090021215A
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
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| US20100048609A1 (en) * | 2006-08-01 | 2010-02-25 | Jacobs Jeffrey W | Pharmaceutical dosage forms for (+)-1,4-dihydro-7-[(3s,4s)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid |
| AU2008317400B2 (en) | 2007-10-22 | 2014-10-02 | Sunesis Pharmaceuticals, Inc. | Methods of using (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino) -1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3- carboxylic acid in combination therapy |
| CA2708264C (en) | 2007-12-10 | 2018-07-03 | Sunesis Pharmaceuticals, Inc. | Methods of using (+)-1,4-dihydro-7-[(3s,4s)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid for treatment of antecedent hematologic disorders |
| RU2548031C2 (ru) * | 2008-12-31 | 2015-04-10 | Санесис Фармасьютикалз, Инк. | Способ получения (+)-1,4-дигидро-7-[(3s,4s)-3-метокси-4-(метиламино)-1-пирролидинил]-4-оксо-1-(2-тиазолил)-1,8-нафтиридин-3-карбоновой кислоты |
| RU2558835C2 (ru) | 2009-02-27 | 2015-08-10 | Санесис Фармасьютикалз, Инк. | Способы применения sns-595 для лечения субъектов с онкологическими заболеваниями, имеющих сниженную активность brca2 |
| UA110465C2 (en) * | 2009-09-04 | 2016-01-12 | Sunesis Pharmaceutecals Inc | Stable sns-595 composition |
| AU2013202641B2 (en) * | 2009-09-04 | 2015-07-23 | Sunesis Pharmaceuticals, Inc. | Stable sns-595 compositions and methods of preparation |
| US8470817B2 (en) * | 2009-10-26 | 2013-06-25 | Sunesis Pharmaceuticals, Inc. | Compounds and methods for treatment of cancer |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4261989A (en) * | 1979-02-19 | 1981-04-14 | Kaken Chemical Co. Ltd. | Geldanamycin derivatives and antitumor drug |
| US5391485A (en) * | 1985-08-06 | 1995-02-21 | Immunex Corporation | DNAs encoding analog GM-CSF molecules displaying resistance to proteases which cleave at adjacent dibasic residues |
| US5078996A (en) * | 1985-08-16 | 1992-01-07 | Immunex Corporation | Activation of macrophage tumoricidal activity by granulocyte-macrophage colony stimulating factor |
| JPS63500636A (ja) * | 1985-08-23 | 1988-03-10 | 麒麟麦酒株式会社 | 多分化能性顆粒球コロニー刺激因子をコードするdna |
| US4810643A (en) | 1985-08-23 | 1989-03-07 | Kirin- Amgen Inc. | Production of pluripotent granulocyte colony-stimulating factor |
| KR0166088B1 (ko) | 1990-01-23 | 1999-01-15 | . | 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도 |
| US5078966A (en) | 1990-08-14 | 1992-01-07 | Nalco Chemical Company | Carbohydrazide to prevent hydrogen blistering and corrosion of metal surfaces in contact with refinery overhead condensates |
| US5360352A (en) | 1992-12-24 | 1994-11-01 | The Whitaker Corporation | Wire retainer for current mode coupler |
| PL181867B1 (pl) * | 1994-06-14 | 2001-09-28 | Dainippon Pharmaceutical Co | Nowe zwiazki, sposoby ich wytwarzania i srodki przeciw nowotworowe PL |
| JP4323574B2 (ja) * | 1995-12-13 | 2009-09-02 | 大日本住友製薬株式会社 | 抗腫瘍剤 |
| JPH10173986A (ja) | 1996-12-16 | 1998-06-26 | Sony Corp | 移動体撮影装置 |
| DE69813194T2 (de) | 1997-01-13 | 2004-02-05 | Kudos Pharmaceuticals Ltd. | Assay, verbindungen, therapie und nachweisverfahren um zelluläre dns-reparatur-aktivität zu modulieren |
| US20020032216A1 (en) * | 1997-03-21 | 2002-03-14 | Lg Chemical Ltd. | Salt of naphthyridine carboxylic acid derivative |
| JP2001523977A (ja) * | 1997-06-05 | 2001-11-27 | ザ ユニバーシティ オブ テキサス システム ボード オブ リージェンツ | Apaf−1、ced−4ヒト相同体、カスパーゼ−3の活性化因子 |
| US6171857B1 (en) * | 1997-10-17 | 2001-01-09 | Brown University Research Foundatiion | Leucine zipper protein, KARP-1 and methods of regulating DNA dependent protein kinase activity |
| US5968921A (en) * | 1997-10-24 | 1999-10-19 | Orgegon Health Sciences University | Compositions and methods for promoting nerve regeneration |
| IL124015A0 (en) * | 1998-04-08 | 1999-01-26 | Yeda Res & Dev | Pharmaceutical compositions comprising a protein |
| JP4294121B2 (ja) | 1998-06-05 | 2009-07-08 | 大日本住友製薬株式会社 | ピリドンカルボン酸誘導体の製造方法およびその中間体 |
| CA2363621A1 (en) * | 1999-02-26 | 2000-08-31 | The Johns Hopkins University | A novel inhibitor of programmed cell death |
| US6670144B1 (en) * | 1999-02-26 | 2003-12-30 | Cyclacel, Ltd. | Compositions and methods for monitoring the phosphorylation of natural binding partners |
| US7163801B2 (en) | 1999-09-01 | 2007-01-16 | The Burnham Institute | Methods for determining the prognosis for cancer patients using tucan |
| US6479541B1 (en) | 2000-03-30 | 2002-11-12 | Baxter International | Amiodarone-containing parenteral administration |
| WO2002020500A2 (en) | 2000-09-01 | 2002-03-14 | Icos Corporation | Materials and methods to potentiate cancer treatment |
| AU2001296558A1 (en) * | 2000-10-03 | 2002-04-15 | Oncopharmaceutical, Inc. | Inhibitors of angiogenesis and tumor growth for local and systemic administration |
| WO2002036171A1 (en) * | 2000-11-02 | 2002-05-10 | Sloan Kettering Institute For Cancer Research | Methods for enhancing the efficacy of cytotoxic agents through the use of hsp90 inhibitors |
| US20030016887A1 (en) * | 2001-07-18 | 2003-01-23 | Fu-Long Su | Receiving bag with seal opening and sealing clip |
| WO2004085418A2 (en) | 2003-03-24 | 2004-10-07 | Luitpold Pharmaceuticals, Inc. | Xanthones, thioxanthones and acridinones as dna-pk inhibitors |
| JP5317472B2 (ja) * | 2004-03-15 | 2013-10-16 | サネシス ファーマシューティカルズ, インコーポレイテッド | Sns−595、及びその使用方法 |
| US7387499B2 (en) | 2004-08-13 | 2008-06-17 | Gateway Inc. | System and method for testing the operation of a cooling fan |
| KR20080041298A (ko) | 2005-09-02 | 2008-05-09 | 선에시스 파마슈티컬스 인코포레이티드 | 암 치료를 위한(+)-1,4-디히드로-7-[(3s,4s)-3-메톡시-4-(메틸아미노)-1-피롤리디닐]-4-옥소-1-(2-티아졸릴)-1,8-나프티리딘-3-카르복실산의 사용 방법 |
| CA2654876A1 (en) * | 2006-06-12 | 2007-12-21 | Sunesis Pharmaceuticals, Inc. | 1-8-naphthyridine compounds for the treatment of cancer |
| US20100048609A1 (en) | 2006-08-01 | 2010-02-25 | Jacobs Jeffrey W | Pharmaceutical dosage forms for (+)-1,4-dihydro-7-[(3s,4s)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid |
| HUE026693T2 (hu) * | 2006-08-02 | 2016-07-28 | Sunesis Pharmaceuticals Inc | (+)-1,4-dihidro-7-[(3S,4S)-3-metoxi-4-(metilamino)-1-pirrolidinil]-4-oxo-1-(2-tiazolil) -1,8-naftiridin-3-karbonsav és cytarabin (Ara-C) kombinált alkalmazása leukémia kezelésére |
| AU2008317400B2 (en) | 2007-10-22 | 2014-10-02 | Sunesis Pharmaceuticals, Inc. | Methods of using (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino) -1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3- carboxylic acid in combination therapy |
| CA2708264C (en) | 2007-12-10 | 2018-07-03 | Sunesis Pharmaceuticals, Inc. | Methods of using (+)-1,4-dihydro-7-[(3s,4s)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid for treatment of antecedent hematologic disorders |
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2007
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- 2007-06-12 CN CN201410211154.5A patent/CN104027333B/zh not_active Expired - Fee Related
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- 2007-06-12 JP JP2009515473A patent/JP2009539994A/ja active Pending
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- 2007-06-12 MX MX2008015775A patent/MX2008015775A/es active IP Right Grant
- 2007-06-12 BR BRPI0713637-4A patent/BRPI0713637A2/pt not_active Application Discontinuation
- 2007-06-12 EP EP07796066A patent/EP2043645A2/en not_active Withdrawn
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2012
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2013
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| JP2013209398A (ja) | 2013-10-10 |
| WO2007146335A2 (en) | 2007-12-21 |
| CA2654876A1 (en) | 2007-12-21 |
| US20100029708A1 (en) | 2010-02-04 |
| US20150150858A1 (en) | 2015-06-04 |
| US20120245198A1 (en) | 2012-09-27 |
| BRPI0713637A2 (pt) | 2012-10-23 |
| US8124773B2 (en) | 2012-02-28 |
| EP2043645A2 (en) | 2009-04-08 |
| AU2007258280B2 (en) | 2013-05-02 |
| IL195883A0 (en) | 2009-09-01 |
| US8765954B2 (en) | 2014-07-01 |
| CN104027333B (zh) | 2017-05-17 |
| US20170101404A1 (en) | 2017-04-13 |
| JP2009539994A (ja) | 2009-11-19 |
| CN104027333A (zh) | 2014-09-10 |
| CN101505753A (zh) | 2009-08-12 |
| AU2007258280A1 (en) | 2007-12-21 |
| IL243294A0 (en) | 2016-02-29 |
| WO2007146335A3 (en) | 2009-02-12 |
| CN101505753B (zh) | 2014-05-21 |
| MX2008015775A (es) | 2009-04-17 |
| US9676774B2 (en) | 2017-06-13 |
| JP2016094434A (ja) | 2016-05-26 |
| EP2354138A1 (en) | 2011-08-10 |
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