ATE478664T1 - Azaphenanthridone-derivate und deren verwendung als parp-inhibitoren - Google Patents
Azaphenanthridone-derivate und deren verwendung als parp-inhibitorenInfo
- Publication number
- ATE478664T1 ATE478664T1 AT01986053T AT01986053T ATE478664T1 AT E478664 T1 ATE478664 T1 AT E478664T1 AT 01986053 T AT01986053 T AT 01986053T AT 01986053 T AT01986053 T AT 01986053T AT E478664 T1 ATE478664 T1 AT E478664T1
- Authority
- AT
- Austria
- Prior art keywords
- azaphenanthridone
- derivatives
- parp inhibitors
- compounds
- parp
- Prior art date
Links
- 239000012661 PARP inhibitor Substances 0.000 title 1
- 229940121906 Poly ADP ribose polymerase inhibitor Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229920000776 Poly(Adenosine diphosphate-ribose) polymerase Polymers 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/06—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/06—Peri-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Virology (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Communicable Diseases (AREA)
- Psychiatry (AREA)
- Emergency Medicine (AREA)
- Tropical Medicine & Parasitology (AREA)
- Hospice & Palliative Care (AREA)
- AIDS & HIV (AREA)
- Endocrinology (AREA)
- Psychology (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25013200P | 2000-12-01 | 2000-12-01 | |
| US31027401P | 2001-08-07 | 2001-08-07 | |
| PCT/US2001/044815 WO2002044183A2 (en) | 2000-12-01 | 2001-11-30 | Benzoazepine and benzodiazepine derivatives and their use as parp inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE478664T1 true ATE478664T1 (de) | 2010-09-15 |
Family
ID=26940622
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT01986053T ATE478664T1 (de) | 2000-12-01 | 2001-11-30 | Azaphenanthridone-derivate und deren verwendung als parp-inhibitoren |
Country Status (10)
| Country | Link |
|---|---|
| US (5) | US6887996B2 (de) |
| EP (1) | EP1339402B1 (de) |
| JP (1) | JP4323802B2 (de) |
| AT (1) | ATE478664T1 (de) |
| AU (1) | AU3652102A (de) |
| CA (1) | CA2430363C (de) |
| DE (1) | DE60142921D1 (de) |
| ES (1) | ES2354249T3 (de) |
| MX (1) | MXPA03004832A (de) |
| WO (1) | WO2002044183A2 (de) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MXPA03004832A (es) | 2000-12-01 | 2004-05-04 | Guilford Pharm Inc | Compuestos y sus usos. |
| US7247641B2 (en) * | 2001-08-07 | 2007-07-24 | Mgi Gp, Inc. | Compounds, derivatives, compositions, preparation and uses |
| US8563592B2 (en) | 2001-11-01 | 2013-10-22 | Spectrum Pharmaceuticals, Inc. | Bladder cancer treatment and methods |
| WO2003037314A2 (en) | 2001-11-01 | 2003-05-08 | Spectrum Pharmaceuticals, Inc. | Medical compositions for intravesical treatment of bladder cancer |
| AU2003201573B2 (en) * | 2002-01-22 | 2009-02-26 | Biomatera Inc. | Method of drying biodegradable polymers |
| CA2503844A1 (en) * | 2002-10-30 | 2004-05-21 | Merck & Co., Inc. | Piperidinyl-alpha-aminoamide modulators of chemokine receptor activity |
| PL378372A1 (pl) | 2003-01-09 | 2006-04-03 | Pfizer Inc. | Tricykliczne związki jako inhibitory kinaz białkowych do wzmacniania skuteczności środków przeciwnowotworowych i radioterapii |
| US20050192321A1 (en) * | 2003-09-15 | 2005-09-01 | Meythaler Jay M. | Treatment of neuropathy with rapid release aminopyridine |
| US7399765B2 (en) | 2003-09-19 | 2008-07-15 | Abbott Laboratories | Substituted diazabicycloalkane derivatives |
| US20050171079A1 (en) * | 2004-02-04 | 2005-08-04 | Schrimpf Michael R. | Amino-substituted tricyclic derivatives and methods of use |
| US7365193B2 (en) | 2004-02-04 | 2008-04-29 | Abbott Laboratories | Amino-substituted tricyclic derivatives and methods of use |
| AU2006230582A1 (en) * | 2005-03-31 | 2006-10-05 | Spectrum Pharmaceuticals, Inc. | Indoloquinone tumor radiation sensitization |
| US20070023994A1 (en) * | 2005-08-01 | 2007-02-01 | Xerox Corporation | Media registration systems and methods |
| AU2006279034A1 (en) * | 2005-08-05 | 2007-02-15 | Astrazeneca Ab | Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators |
| WO2007051119A1 (en) * | 2005-10-26 | 2007-05-03 | Mgi Gp, Inc. | Methods and compositions of parp inhibitors as potentiators in cancer therapy |
| EP2774925B1 (de) | 2005-11-08 | 2016-12-28 | Vertex Pharmaceuticals Incorporated | Heterocyclische Modulatoren von ATP-bindenden Kassettentransportern |
| US7956064B2 (en) * | 2006-09-01 | 2011-06-07 | Cylene Pharmaceuticals, Inc. | Fused tricyclic compounds as serine-threonine protein kinase and PARP modulators |
| WO2008141119A2 (en) | 2007-05-09 | 2008-11-20 | Vertex Pharmaceuticals Incorporated | Modulators of cftr |
| HUE031913T2 (en) | 2007-12-07 | 2017-08-28 | Vertex Pharma | Solid forms of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl) benzoic acid |
| PL2231606T3 (pl) * | 2007-12-07 | 2013-07-31 | Vertex Pharma | Sposoby wytwarzania kwasów cykloalkilokarboksyamidopirydynobenzoesowych |
| DE602008004820D1 (de) * | 2007-12-18 | 2011-03-17 | Meiji Seika Kaisha | Vorbeuge- oder heilmittel für entzündliche darmerkrankungen |
| AU2009219376B2 (en) * | 2008-02-28 | 2014-09-25 | Merck Patent Gmbh | Protein kinase inhibitors and use thereof |
| JP5523352B2 (ja) | 2008-02-28 | 2014-06-18 | バーテックス ファーマシューティカルズ インコーポレイテッド | Cftr修飾因子としてのへテロアリール誘導体 |
| GB0804755D0 (en) * | 2008-03-14 | 2008-04-16 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| BRPI0913188A2 (pt) | 2008-05-29 | 2016-01-12 | Albany Molecular Res Inc | moduladores de receptores 5-ht3, métodos de fabricação, e uso dos mesmos |
| ES2550101T3 (es) * | 2008-12-17 | 2015-11-04 | Merck Patent Gmbh | Inhibidores de proteína quinasa de benzonaftiridinona tricíclica modificada con anillo C y su uso |
| MA33053B1 (fr) * | 2009-01-23 | 2012-02-01 | Tadeka Pharmaceutical Company Ltd | Inhibiteurs de la poly(adp-ribose) polymerase (parp) |
| JP5715625B2 (ja) | 2009-07-30 | 2015-05-07 | 武田薬品工業株式会社 | ポリ(adp−リボース)ポリメラーゼ(parp)阻害剤 |
| RS62767B1 (sr) | 2010-04-07 | 2022-01-31 | Vertex Pharma | Farmaceutski sastavi 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioksol-5-il) ciklopropankarboksamido)-3-metilpiriodin-2-il)benzojeve kiseline i njihova primena |
| EP2569307A2 (de) | 2010-05-10 | 2013-03-20 | Radikal Therapeutics Inc. | Liponsäure- und nitroxidderivate sowie ihre verwendung |
| WO2011145669A1 (ja) * | 2010-05-19 | 2011-11-24 | 大日本住友製薬株式会社 | アミド誘導体 |
| DK3012329T3 (da) | 2010-06-18 | 2017-11-20 | Myriad Genetics Inc | Fremgangsmåder og materialer til at vurdere tab af heterozygositet |
| DK2609216T3 (en) | 2010-08-24 | 2016-09-12 | Dana Farber Cancer Inst Inc | Methods to predict anti-cancer response |
| GB201106814D0 (en) | 2011-04-21 | 2011-06-01 | Astex Therapeutics Ltd | New compounds |
| EP3693473B1 (de) | 2011-06-17 | 2025-02-19 | Myriad Genetics, Inc. | Methoden und materialien zur beurteilung des allelischen ungleichgewichts |
| US9173395B2 (en) | 2011-07-04 | 2015-11-03 | Bayer Intellectual Property Gmbh | Use of substituted isoquinolinones, isoquinolindiones, isoquinolintriones and dihydroisoquinolinones or in each case salts thereof as active agents against abiotic stress in plants |
| BR112014015152A2 (pt) | 2011-12-21 | 2017-07-04 | Myriad Genetics Inc | métodos e materiais para a avaliação da perda de heterozigosidade |
| NO2797921T3 (de) | 2011-12-31 | 2018-02-03 | ||
| SG11201403538TA (en) | 2011-12-31 | 2014-09-26 | Beigene Ltd | Fused tetra or penta-cyclic pyridophthalazinones as parp inhibitors |
| MX355183B (es) | 2012-01-25 | 2018-04-09 | Vertex Pharma | Formulaciones de acido 3- (6- (1- (2.2- difluorobenzo [d] [1,3] dioxol-5-il) ciclopropancarboxamido) -3- metilpiridin-2-il) benzoico. |
| DK3415915T3 (da) | 2012-02-23 | 2024-11-04 | Childrens Medical Center | Fremgangsmåde til at forudsige respons til PARP-inhibitorer |
| AU2013273466B2 (en) | 2012-06-07 | 2018-11-01 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Methods for detecting inactivation of the homologous recombination pathway (BRCA1/2) in human tumors |
| JP2015533783A (ja) * | 2012-09-05 | 2015-11-26 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 非生物的な植物ストレスに対する活性物質としてのベンゾジアゼピノン類及びベンゾアゼピノン類又はそれらの塩の使用 |
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| DK2981624T3 (da) | 2013-04-05 | 2020-03-02 | Myriad Genetics Inc | Fremgangsmåder til vurdering af homolog rekombinationsdeficiens og forudsigelse af respons på cancerbehandling |
| HRP20210516T2 (hr) | 2013-11-12 | 2021-10-01 | Vertex Pharmaceuticals Incorporated | Postupak proizvodnje farmaceutskih pripravaka za liječenje bolesti koje su posredovane putem cftr |
| WO2015086473A1 (en) | 2013-12-09 | 2015-06-18 | Institut Curie | Methods for detecting inactivation of the homologous recombination pathway (brca1/2) in human tumors |
| ES2946251T3 (es) | 2014-08-15 | 2023-07-14 | Myriad Genetics Inc | Métodos y materiales para evaluar la deficiencia de recombinación homóloga |
| KR102576006B1 (ko) | 2014-11-18 | 2023-09-06 | 버텍스 파마슈티칼스 인코포레이티드 | 고처리량 시험 고성능 액체 크로마토그래피의 수행 방법 |
| AU2015357498B2 (en) * | 2014-12-06 | 2019-09-12 | Intra-Cellular Therapies, Inc. | Organic compounds |
| ES2879434T3 (es) | 2015-07-23 | 2021-11-22 | Inst Curie | Uso de una combinación de molécula Dbait e inhibidores de PARP para tratamiento del cáncer |
| IL257442B2 (en) | 2015-08-25 | 2023-03-01 | Beigene Ltd | Process for preparing parp inhibitor, crystalline forms and their uses |
| GB201519573D0 (en) | 2015-11-05 | 2015-12-23 | King S College London | Combination |
| US10213511B2 (en) | 2016-03-02 | 2019-02-26 | Frequency Therapeutics, Inc. | Thermoreversible compositions for administration of therapeutic agents |
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| US9913848B2 (en) * | 2016-03-02 | 2018-03-13 | Frequency Therapeutics, Inc. | Methods for controlled proliferation of stem cells / generating inner ear hair cells using 1,2,3,4-tetrahydro-[1,4]diazepino[6,7, 1-hi]indolyl based compounds |
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| EP4141127B1 (de) | 2021-08-30 | 2024-10-09 | Zentrum Familiärer Brust- und Eierstockkrebs Universitätsklinik Köln | Verfahren zur bewertung des mangels an homologer rekombination in eierstockkrebszellen |
| 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 |
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| CN119504590A (zh) * | 2024-11-20 | 2025-02-25 | 鹤壁市宝瑞德化工有限公司 | 一种1-甲基-3-三氟甲基-4-氯甲基-5-二氟甲氧基-1-h-吡唑及其制备方法 |
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| US3300499A (en) * | 1964-01-27 | 1967-01-24 | Sterling Drug Inc | 4-alkyl (or alkenyl)-1, 4-dihydro-1-oxobenzo [f] [1, 7] naphthyridine 2-carboxylic acid derivatives |
| US3398551A (en) * | 1966-10-03 | 1968-08-27 | Carrier Corp | Compressor control including pressure equalizer and overpressure means |
| US3700673A (en) * | 1971-02-12 | 1972-10-24 | Morton Norwich Products Inc | 3-4-dihydrobenzo(b) (1,7)naphthyridin-1(2h)-ones |
| US6197785B1 (en) * | 1997-09-03 | 2001-03-06 | Guilford Pharmaceuticals Inc. | Alkoxy-substituted compounds, methods, and compositions for inhibiting PARP activity |
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| CA2332239A1 (en) * | 1998-05-15 | 1999-11-25 | Guilford Pharmaceuticals Inc. | Fused tricyclic compounds which inhibit parp activity |
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-
2001
- 2001-11-30 MX MXPA03004832A patent/MXPA03004832A/es active IP Right Grant
- 2001-11-30 JP JP2002546553A patent/JP4323802B2/ja not_active Expired - Fee Related
- 2001-11-30 DE DE60142921T patent/DE60142921D1/de not_active Expired - Lifetime
- 2001-11-30 EP EP01986053A patent/EP1339402B1/de not_active Expired - Lifetime
- 2001-11-30 AT AT01986053T patent/ATE478664T1/de not_active IP Right Cessation
- 2001-11-30 AU AU3652102A patent/AU3652102A/xx not_active Withdrawn
- 2001-11-30 US US09/996,776 patent/US6887996B2/en not_active Ceased
- 2001-11-30 CA CA2430363A patent/CA2430363C/en not_active Expired - Fee Related
- 2001-11-30 ES ES01986053T patent/ES2354249T3/es not_active Expired - Lifetime
- 2001-11-30 WO PCT/US2001/044815 patent/WO2002044183A2/en not_active Ceased
-
2005
- 2005-02-28 US US11/066,478 patent/US20050148575A1/en not_active Abandoned
- 2005-08-30 US US11/213,712 patent/US7915280B2/en not_active Expired - Fee Related
-
2006
- 2006-02-21 US US11/357,334 patent/US7235557B2/en not_active Expired - Fee Related
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2008
- 2008-01-10 US US12/007,463 patent/USRE41150E1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2002044183A2 (en) | 2002-06-06 |
| ES2354249T3 (es) | 2011-03-11 |
| US7235557B2 (en) | 2007-06-26 |
| US6887996B2 (en) | 2005-05-03 |
| US20050148575A1 (en) | 2005-07-07 |
| JP2004517831A (ja) | 2004-06-17 |
| DE60142921D1 (de) | 2010-10-07 |
| CA2430363A1 (en) | 2002-06-06 |
| US20030022883A1 (en) | 2003-01-30 |
| WO2002044183A3 (en) | 2003-05-22 |
| CA2430363C (en) | 2010-04-13 |
| JP4323802B2 (ja) | 2009-09-02 |
| US20060003987A1 (en) | 2006-01-05 |
| AU3652102A (en) | 2002-06-11 |
| USRE41150E1 (en) | 2010-02-23 |
| US7915280B2 (en) | 2011-03-29 |
| MXPA03004832A (es) | 2004-05-04 |
| EP1339402B1 (de) | 2010-08-25 |
| US20060142266A1 (en) | 2006-06-29 |
| EP1339402A2 (de) | 2003-09-03 |
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