MX2008010931A - Quinolonas utiles como inhibidores de sintasa de oxido nitrico inducibles. - Google Patents
Quinolonas utiles como inhibidores de sintasa de oxido nitrico inducibles.Info
- Publication number
- MX2008010931A MX2008010931A MX2008010931A MX2008010931A MX2008010931A MX 2008010931 A MX2008010931 A MX 2008010931A MX 2008010931 A MX2008010931 A MX 2008010931A MX 2008010931 A MX2008010931 A MX 2008010931A MX 2008010931 A MX2008010931 A MX 2008010931A
- Authority
- MX
- Mexico
- Prior art keywords
- nitric oxide
- oxide synthase
- synthase inhibitors
- inducible nitric
- quinolones
- Prior art date
Links
- 102000011779 Nitric Oxide Synthase Type II Human genes 0.000 title abstract 2
- 108010076864 Nitric Oxide Synthase Type II Proteins 0.000 title abstract 2
- 150000007660 quinolones Chemical class 0.000 title abstract 2
- 239000000236 nitric oxide synthase inhibitor Substances 0.000 title 1
- CSYSULGPHGCBQD-UHFFFAOYSA-N s-ethylisothiouronium diethylphosphate Chemical compound CCSC(N)=N.CCOP(O)(=O)OCC CSYSULGPHGCBQD-UHFFFAOYSA-N 0.000 title 1
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 230000002194 synthesizing effect Effects 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4704—2-Quinolinones, e.g. carbostyril
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- A—HUMAN NECESSITIES
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/227—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
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- Pain & Pain Management (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
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- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
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Abstract
La presente invención se refiere a quinolonas novedosas de la Fórmula (I) (ver fórmula (I)) que inhiben la sintasa NOS inducible junto con métodos para sintetizar y usar los compuestos que incluye métodos para inhibir o modular la síntesis del óxido nítrico y/o reducir los niveles de óxido nítrico en un paciente al administrar los compuestos para el tratamiento de la enfermedad.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US77656106P | 2006-02-24 | 2006-02-24 | |
| US84869606P | 2006-10-02 | 2006-10-02 | |
| PCT/US2007/062769 WO2007117778A2 (en) | 2006-02-24 | 2007-02-23 | Quinolones useful as inducible nitric oxide synthase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2008010931A true MX2008010931A (es) | 2008-09-03 |
Family
ID=38581716
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2008010931A MX2008010931A (es) | 2006-02-24 | 2007-02-23 | Quinolonas utiles como inhibidores de sintasa de oxido nitrico inducibles. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20080139558A1 (es) |
| EP (1) | EP1986747A2 (es) |
| JP (1) | JP2009529496A (es) |
| KR (1) | KR20080108478A (es) |
| AR (1) | AR059622A1 (es) |
| AU (1) | AU2007235132A1 (es) |
| BR (1) | BRPI0707028A2 (es) |
| CA (1) | CA2643011A1 (es) |
| IL (1) | IL193526A0 (es) |
| MX (1) | MX2008010931A (es) |
| TW (1) | TW200803855A (es) |
| WO (1) | WO2007117778A2 (es) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CA2608116A1 (en) | 2005-05-10 | 2006-11-16 | Intermune, Inc. | Method of modulating stress-activated protein kinase system |
| AU2007229637A1 (en) * | 2006-03-28 | 2007-10-04 | Novartis Ag | Amide derivatives and their application for the treatment of G protein related diseases |
| WO2008103615A1 (en) * | 2007-02-21 | 2008-08-28 | Kalypsys, Inc. | Isoquinolines useful as inducible nitric oxide synthase inhibitors |
| WO2008113006A1 (en) * | 2007-03-14 | 2008-09-18 | Xenon Pharmaceuticals Inc. | Methods of using quinolinone compounds in treating sodium channel-mediated diseases or conditions |
| AR067744A1 (es) | 2007-07-31 | 2009-10-21 | Bayer Cropscience Sa | Derivados fungicidas de (hetero) aril- metilen -n- cicloalquil carboxamida condensados de 6 elementos con n |
| WO2009029592A1 (en) * | 2007-08-27 | 2009-03-05 | Kalypsys, Inc. | Heterobicyclic-substituted quinolones useful as nitric oxide synthase inhibitors |
| WO2009029617A1 (en) * | 2007-08-27 | 2009-03-05 | Kalypsys, Inc. | Diarylamine-substituted quinolones useful as inducible nitric oxide synthase inhibitors |
| WO2009029625A1 (en) * | 2007-08-27 | 2009-03-05 | Kalypsys, Inc. | 4- [heterocyclyl-methyl] -8-fluoro-quinolin-2-ones useful as nitric oxide synthase inhibitors |
| CN104402773A (zh) * | 2008-02-12 | 2015-03-11 | 柳韩洋行 | 2-甲基-2’-苯基丙酸衍生物的制备方法和中间体化合物 |
| CA3034994A1 (en) | 2008-06-03 | 2009-12-10 | Intermune, Inc. | Substituted aryl-2 pyridone compounds and use thereof for treating inflammatory and fibrotic disorders |
| US8389720B2 (en) * | 2008-11-13 | 2013-03-05 | Merck Sharp & Dohme Corp. | Quinolone neuropeptide S receptor antagonists |
| CA2803842C (en) | 2010-06-30 | 2020-01-07 | Fujifilm Corporation | Nicotinamide derivative or salt thereof as syk-inhibitors |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| CN103121969A (zh) * | 2012-12-04 | 2013-05-29 | 中国科学院昆明植物研究所 | 苯并咪唑及其衍生物,其药物组合物及其应用 |
| CN103121970B (zh) * | 2012-12-04 | 2015-04-29 | 中国科学院昆明植物研究所 | 苯并咪唑及其衍生物,其药物组合物及其在制备抗抑郁药物中的应用 |
| CA2943363A1 (en) | 2014-04-02 | 2015-10-08 | Intermune, Inc. | Anti-fibrotic pyridinones |
| WO2015157471A1 (en) | 2014-04-08 | 2015-10-15 | The Methodist Hospital | Inos-inhibitory compositions and their use as breast cancer therapeutics |
| MX373789B (es) | 2014-09-19 | 2020-03-23 | Forma Therapeutics Inc | Derivados de piridinil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh). |
| ES2706888T3 (es) | 2014-09-19 | 2019-04-01 | Forma Therapeutics Inc | Referencia cruzada a aplicaciones relacionadas |
| ES2953347T3 (es) | 2014-09-19 | 2023-11-10 | Forma Therapeutics Inc | Derivados de piridin-2(1H)-ona quinolinona como inhibidores de isocitrato deshidrogenasa mutante |
| WO2016044781A1 (en) | 2014-09-19 | 2016-03-24 | Forma Therapeutics, Inc. | Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors |
| WO2016171755A1 (en) | 2015-04-21 | 2016-10-27 | Forma Therapeutics, Inc. | Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors |
| US10407419B2 (en) | 2015-04-21 | 2019-09-10 | Forma Therapeutics, Inc. | Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors |
| GB201512635D0 (en) | 2015-07-17 | 2015-08-26 | Ucl Business Plc | Uses of therapeutic compounds |
| US11311527B2 (en) | 2018-05-16 | 2022-04-26 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1) |
| WO2019222551A1 (en) | 2018-05-16 | 2019-11-21 | Forma Therapeutics, Inc. | Solid forms of ((s)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile |
| US11013734B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation |
| HUE061331T2 (hu) | 2018-05-16 | 2023-06-28 | Forma Therapeutics Inc | Mutáns IDH-1 gátlása |
| US11013733B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1) |
| EP3807264A1 (en) | 2018-06-12 | 2021-04-21 | Ryvu Therapeutics S.A. | Modulators of stimulator of interferon genes (sting) |
| CN110903267B (zh) * | 2018-09-14 | 2023-09-22 | 中国科学院宁波材料技术与工程研究所 | 一种含(四氢)呋喃取代基的烯酸化合物的合成方法 |
| IL288868B2 (en) | 2019-06-12 | 2025-02-01 | Ryvu Therapeutics S A | Next generation of stimulator of interferon genes (STING) modulators |
| AU2020400010B2 (en) * | 2019-12-11 | 2024-01-25 | Ryvu Therapeutics S.A. | Heterocyclic compounds as modulators of Stimulator of Interferon Genes (STING) |
| US20230295116A1 (en) * | 2020-08-11 | 2023-09-21 | Board Of Trustees Of Michigan State University | Proteasome enhancers and uses thereof |
| WO2022090481A1 (en) | 2020-11-02 | 2022-05-05 | Boehringer Ingelheim International Gmbh | Substituted 1h-pyrazolo[4,3-c]pyridines and derivatives as egfr inhibitors |
| JP2024520752A (ja) * | 2021-06-07 | 2024-05-24 | ユーダブリューエム・リサーチ・ファウンデーション,インコーポレーテッド | 炎症状態の治療における置換5-(4-メチル-6-フェニル-4H-ベンゾ[f]イミダゾ[1,5-a][1,4]ジアゼピン-3-イル)-1,2,4-オキサジアゾールの使用 |
| US20250387385A1 (en) * | 2022-06-24 | 2025-12-25 | Zydus Lifesciences Limited | Treatment for glomerular diseases |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS5929668A (ja) * | 1982-08-13 | 1984-02-16 | Otsuka Pharmaceut Co Ltd | カルボスチリル誘導体 |
| JPS60142959A (ja) * | 1983-12-28 | 1985-07-29 | Otsuka Pharmaceut Co Ltd | キノリン誘導体 |
| JPS6463518A (en) * | 1987-09-02 | 1989-03-09 | Otsuka Pharma Co Ltd | Antiarrhythmic agent |
| FR2637591B1 (fr) * | 1988-10-11 | 1992-10-23 | Synthelabo | Derives de quinoleinone, leur preparation et leur application en therapeutique |
| JP3122671B2 (ja) * | 1990-05-23 | 2001-01-09 | 協和醗酵工業株式会社 | 複素環式化合物 |
| US5457099A (en) * | 1992-07-02 | 1995-10-10 | Sawai Pharmaceutical Co., Ltd. | Carbostyril derivatives and antiallergic agent |
| JPH08502503A (ja) * | 1992-10-27 | 1996-03-19 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 抗ヘリコバクター活性を有する4−キノリニル誘導体 |
| JPH06239858A (ja) * | 1993-02-16 | 1994-08-30 | Otsuka Pharmaceut Co Ltd | 末梢血管拡張剤 |
| US6235748B1 (en) * | 1997-09-03 | 2001-05-22 | Guilford Pharmaceuticals Inc. | Oxo-substituted compounds, process of making, and compositions and methods for inhibiting parp activity |
| WO2001070227A1 (en) * | 2000-03-17 | 2001-09-27 | Merck & Co., Inc. | Antagonists of gonadotropin releasing hormone |
| ATE386736T1 (de) * | 2000-09-11 | 2008-03-15 | Novartis Vaccines & Diagnostic | Verfahren zur herstellung von benzimidazol-2-yl - chinolinonderivaten |
| ATE319704T1 (de) * | 2000-12-27 | 2006-03-15 | Janssen Pharmaceutica Nv | Farnesyltransferase hemmende, in der 4-stellung substituierte chinolin- und chinazolinderivate |
| JP2003146972A (ja) * | 2001-11-14 | 2003-05-21 | Teikoku Hormone Mfg Co Ltd | カルボスチリル誘導体 |
| KR101150449B1 (ko) * | 2002-08-21 | 2012-06-01 | 베링거 잉겔하임 파르마 게엠베하 운트 코 카게 | 8-[3-아미노-피페리딘-1-일]-크산틴, 이의 제조방법 및 이를 포함하는 약제학적 조성물 |
| WO2004078731A1 (en) * | 2003-03-06 | 2004-09-16 | 'chemical Diversity Research Institute', Ltd. | Quinoline-carboxylic acids and the derivatives thereof, a focused library |
| WO2005077369A1 (en) * | 2004-02-05 | 2005-08-25 | Schering Corporation | Piperidine derivatives useful as ccr3 antagonists |
-
2007
- 2007-02-16 TW TW096106270A patent/TW200803855A/zh unknown
- 2007-02-23 JP JP2008556576A patent/JP2009529496A/ja active Pending
- 2007-02-23 BR BRPI0707028-4A patent/BRPI0707028A2/pt not_active Application Discontinuation
- 2007-02-23 KR KR1020087023220A patent/KR20080108478A/ko not_active Withdrawn
- 2007-02-23 AR ARP070100770A patent/AR059622A1/es unknown
- 2007-02-23 EP EP07757450A patent/EP1986747A2/en not_active Withdrawn
- 2007-02-23 US US11/678,572 patent/US20080139558A1/en not_active Abandoned
- 2007-02-23 CA CA002643011A patent/CA2643011A1/en not_active Abandoned
- 2007-02-23 MX MX2008010931A patent/MX2008010931A/es unknown
- 2007-02-23 AU AU2007235132A patent/AU2007235132A1/en not_active Abandoned
- 2007-02-23 WO PCT/US2007/062769 patent/WO2007117778A2/en not_active Ceased
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2008
- 2008-08-18 IL IL193526A patent/IL193526A0/en unknown
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|---|---|
| US20080139558A1 (en) | 2008-06-12 |
| WO2007117778A9 (en) | 2009-05-22 |
| WO2007117778A8 (en) | 2008-12-31 |
| AU2007235132A1 (en) | 2007-10-18 |
| BRPI0707028A2 (pt) | 2011-04-12 |
| EP1986747A2 (en) | 2008-11-05 |
| WO2007117778A3 (en) | 2008-02-07 |
| WO2007117778A2 (en) | 2007-10-18 |
| JP2009529496A (ja) | 2009-08-20 |
| KR20080108478A (ko) | 2008-12-15 |
| CA2643011A1 (en) | 2007-10-18 |
| IL193526A0 (en) | 2009-08-03 |
| TW200803855A (en) | 2008-01-16 |
| AR059622A1 (es) | 2008-04-16 |
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