CN1856476A - 异喹啉酮钾通道抑制剂 - Google Patents
异喹啉酮钾通道抑制剂 Download PDFInfo
- Publication number
- CN1856476A CN1856476A CNA2004800273696A CN200480027369A CN1856476A CN 1856476 A CN1856476 A CN 1856476A CN A2004800273696 A CNA2004800273696 A CN A2004800273696A CN 200480027369 A CN200480027369 A CN 200480027369A CN 1856476 A CN1856476 A CN 1856476A
- Authority
- CN
- China
- Prior art keywords
- phenyl
- ketone
- alkyl
- replace
- 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.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
- C07D217/24—Oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/03—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/04—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing a quinolizine ring system condensed with only one six-membered carbocyclic ring, e.g. julolidine
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50510103P | 2003-09-23 | 2003-09-23 | |
| US60/505,101 | 2003-09-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1856476A true CN1856476A (zh) | 2006-11-01 |
Family
ID=34392976
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2004800273696A Pending CN1856476A (zh) | 2003-09-23 | 2004-09-17 | 异喹啉酮钾通道抑制剂 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US7723352B2 (OSRAM) |
| EP (1) | EP1667982B1 (OSRAM) |
| JP (1) | JP4718467B2 (OSRAM) |
| CN (1) | CN1856476A (OSRAM) |
| AU (1) | AU2004276236B2 (OSRAM) |
| CA (1) | CA2539814C (OSRAM) |
| WO (1) | WO2005030791A2 (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101573338B (zh) * | 2006-12-27 | 2013-03-20 | 塞诺菲-安万特股份有限公司 | 环烷基胺取代的异喹诺酮和异喹啉酮衍生物 |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2539541C (en) * | 2003-09-23 | 2010-06-29 | Merck & Co., Inc. | Isoquinolinone potassium channel inhibitors |
| CA2539729C (en) * | 2003-09-23 | 2010-09-07 | Merck & Co., Inc. | Isoquinolinone potassium channel inhibitors |
| WO2005030791A2 (en) * | 2003-09-23 | 2005-04-07 | Merck & Co., Inc. | Isoquinolinone potassium channel inhibitors |
| US7709476B2 (en) * | 2003-09-23 | 2010-05-04 | Merck Sharp & Dohme Corp. | Isoquinolinone potassium channel inhibitors |
| AU2004276268B2 (en) * | 2003-09-23 | 2009-01-29 | Merck Sharp & Dohme Corp. | Isoquinoline potassium channel inhibitors |
| US7723290B2 (en) | 2004-10-22 | 2010-05-25 | Bioincept, Llc | Compositions and methods for modulating the immune system |
| WO2006015159A2 (en) | 2004-07-29 | 2006-02-09 | Merck & Co., Inc. | Potassium channel inhibitors |
| US7569589B2 (en) | 2004-07-29 | 2009-08-04 | Merck & Co., Inc. | Potassium channel inhibitors |
| DE102005028862A1 (de) * | 2005-06-22 | 2007-01-11 | Sanofi-Aventis Deutschland Gmbh | Substituierte Heterocyclen, ihre Verwendung als Medikament sowie sie enthaltende pharmazeutische Zubereitungen |
| WO2007000240A1 (en) | 2005-06-28 | 2007-01-04 | Sanofi-Aventis | Isoquinoline derivatives as inhibitors of rho-kinase |
| UA93882C2 (ru) | 2005-07-26 | 2011-03-25 | Санофи-Авентис | Пиперидинил-замещенные производные изохинолона kak ингибиторы rho-киназы |
| JP5049970B2 (ja) | 2005-07-26 | 2012-10-17 | サノフイ | Rho−キナーゼ阻害剤としてのシクロヘキシルアミンイソキノロン誘導体 |
| GB0525164D0 (en) | 2005-12-09 | 2006-01-18 | Xention Discovery Ltd | Compounds |
| EP1989197A1 (en) * | 2006-02-17 | 2008-11-12 | Janssen Pharmaceutica, N.V. | Pyrazolylquinazolinones as potassium channel openers |
| NZ577980A (en) | 2006-12-27 | 2012-01-12 | Sanofi Aventis | Cycloalkylamine substituted isoquinolone derivatives |
| KR101545533B1 (ko) | 2006-12-27 | 2015-08-19 | 사노피 | 치환된 이소퀴놀린 및 Rho-키나아제 억제제로서의 이의 용도 |
| WO2008077552A1 (en) | 2006-12-27 | 2008-07-03 | Sanofi-Aventis | Substituted isoquinoline and isoquinolinone derivatives |
| WO2008077556A1 (en) | 2006-12-27 | 2008-07-03 | Sanofi-Aventis | Cycloalkylamine substituted isoquinoline and isoquinolinone derivatives |
| JP5405316B2 (ja) | 2006-12-27 | 2014-02-05 | サノフイ | シクロアルキルアミン置換イソキノリン誘導体 |
| MY150746A (en) | 2006-12-27 | 2014-02-28 | Sanofi Aventis | Substituted isoquinoline and isoquinolinone derivatives as inhibitors of rho-kinase |
| US9623021B2 (en) * | 2007-01-22 | 2017-04-18 | Gtx, Inc. | Nuclear receptor binding agents |
| US9604931B2 (en) | 2007-01-22 | 2017-03-28 | Gtx, Inc. | Nuclear receptor binding agents |
| CN103432133B (zh) | 2007-01-22 | 2016-08-10 | Gtx公司 | 核受体结合剂的用途 |
| HUE026617T2 (en) | 2008-06-24 | 2016-06-28 | Sanofi Sa | Substituted isoquinolines and isoquinolinones as RHO kinase inhibitors |
| WO2009156099A1 (en) | 2008-06-24 | 2009-12-30 | Sanofi-Aventis | 6-substituted isoquinolines and isoquinolinones |
| ES2434121T3 (es) | 2008-06-24 | 2013-12-13 | Sanofi | Derivados de isoquinolina e isoquinolinona bi- y policíclicos sustituidos como inhibidores de rho cinasa |
| GB0815781D0 (en) | 2008-08-29 | 2008-10-08 | Xention Ltd | Novel potassium channel blockers |
| GB0815782D0 (en) | 2008-08-29 | 2008-10-08 | Xention Ltd | Novel potassium channel blockers |
| GB0815784D0 (en) | 2008-08-29 | 2008-10-08 | Xention Ltd | Novel potassium channel blockers |
| EP2680872B1 (en) | 2011-03-02 | 2018-08-15 | BioIncept LLC | Use of pif peptides for treating infections, atherosclerosis and peritonitis |
| WO2013142390A1 (en) * | 2012-03-21 | 2013-09-26 | Gtx, Inc. | Aldo-keto reductase subfamily 1c3 (akr1c3) inhibitors |
| HRP20200341T1 (hr) * | 2013-10-18 | 2020-06-12 | Celgene Quanticel Research, Inc. | Bromodomenski (bet) inhibitori |
| EA038715B1 (ru) * | 2014-01-24 | 2021-10-08 | Селджен Квонтисел Рисёрч, Инк. | Ингибиторы бромодомена |
| AR104259A1 (es) | 2015-04-15 | 2017-07-05 | Celgene Quanticel Res Inc | Inhibidores de bromodominio |
| US11096987B2 (en) | 2015-08-28 | 2021-08-24 | Bioincept, Llc | Mutant peptides and methods of treating subjects using the same |
| EP3341006A4 (en) | 2015-08-28 | 2019-03-13 | BioIncept LLC | COMPOSITIONS AND METHODS FOR TREATING NERVE DAMAGE |
| AU2017252276A1 (en) | 2016-04-18 | 2018-11-15 | Celgene Quanticel Research, Inc. | Therapeutic compounds |
| US10150754B2 (en) | 2016-04-19 | 2018-12-11 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| EP4126819A1 (en) * | 2020-04-03 | 2023-02-08 | Vertex Pharmaceuticals Incorporated | 7- or 8-hydroxy-isoquinoline and 7- or 8-hydroxy-quinoline derivatives as alpha-1 -antitrypsin modulators for treating alpha-1 -antitrypsin deficiency (aatd) |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3594380A (en) * | 1969-02-18 | 1971-07-20 | American Home Prod | Isoquinolin-1(2h)-ones |
| US3878215A (en) * | 1971-12-01 | 1975-04-15 | Sandoz Ag | 2-Alkyl-3-substituted-4-aryl isoquinolines |
| US4897391A (en) * | 1988-06-17 | 1990-01-30 | Schering Corporation | Tricyclic anti-allergy, antiinflammatory and anti-hyperproliferative compounds |
| NO179904C (no) * | 1992-09-04 | 1997-01-08 | Takeda Chemical Industries Ltd | Kondenserte heterocykliske forbindelser og deres anvendelse |
| US5728712A (en) * | 1995-05-19 | 1998-03-17 | Chiroscience Limited | 3,4-disubstituted-phenylsulphonamides and their therapeutic use |
| DE60132606T2 (de) | 2000-09-20 | 2009-02-19 | Merck & Co., Inc. | Isochinolinone als kalium-kanal-inhibitoren |
| EP1396488A1 (en) | 2001-05-23 | 2004-03-10 | Mitsubishi Pharma Corporation | Fused heterocyclic compound and medicinal use thereof |
| CA2476162A1 (en) * | 2002-02-13 | 2003-08-21 | Takeda Chemical Industries, Ltd. | Jnk inhibitor |
| CA2539541C (en) * | 2003-09-23 | 2010-06-29 | Merck & Co., Inc. | Isoquinolinone potassium channel inhibitors |
| WO2005030791A2 (en) * | 2003-09-23 | 2005-04-07 | Merck & Co., Inc. | Isoquinolinone potassium channel inhibitors |
| CA2539729C (en) * | 2003-09-23 | 2010-09-07 | Merck & Co., Inc. | Isoquinolinone potassium channel inhibitors |
| AU2004276268B2 (en) * | 2003-09-23 | 2009-01-29 | Merck Sharp & Dohme Corp. | Isoquinoline potassium channel inhibitors |
| US7709476B2 (en) * | 2003-09-23 | 2010-05-04 | Merck Sharp & Dohme Corp. | Isoquinolinone potassium channel inhibitors |
-
2004
- 2004-09-17 WO PCT/US2004/030431 patent/WO2005030791A2/en not_active Ceased
- 2004-09-17 EP EP04788811.0A patent/EP1667982B1/en not_active Expired - Lifetime
- 2004-09-17 CN CNA2004800273696A patent/CN1856476A/zh active Pending
- 2004-09-17 JP JP2006528067A patent/JP4718467B2/ja not_active Expired - Fee Related
- 2004-09-17 CA CA2539814A patent/CA2539814C/en not_active Expired - Fee Related
- 2004-09-17 US US10/571,870 patent/US7723352B2/en not_active Expired - Fee Related
- 2004-09-17 AU AU2004276236A patent/AU2004276236B2/en not_active Ceased
-
2010
- 2010-04-02 US US12/753,572 patent/US8338449B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101573338B (zh) * | 2006-12-27 | 2013-03-20 | 塞诺菲-安万特股份有限公司 | 环烷基胺取代的异喹诺酮和异喹啉酮衍生物 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005030791A3 (en) | 2005-05-26 |
| CA2539814C (en) | 2010-07-06 |
| EP1667982A2 (en) | 2006-06-14 |
| EP1667982B1 (en) | 2013-07-31 |
| US20070027177A1 (en) | 2007-02-01 |
| EP1667982A4 (en) | 2008-08-13 |
| US8338449B2 (en) | 2012-12-25 |
| US7723352B2 (en) | 2010-05-25 |
| JP4718467B2 (ja) | 2011-07-06 |
| AU2004276236A1 (en) | 2005-04-07 |
| US20100256698A1 (en) | 2010-10-07 |
| CA2539814A1 (en) | 2005-04-07 |
| AU2004276236B2 (en) | 2008-01-24 |
| JP2007516218A (ja) | 2007-06-21 |
| WO2005030791A2 (en) | 2005-04-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1856476A (zh) | 异喹啉酮钾通道抑制剂 | |
| CN1856307A (zh) | 喹啉钾通道抑制剂 | |
| CN100337626C (zh) | 酰化的、杂芳基-稠合的环烯基胺和它们作为药物的用途 | |
| CN1151136C (zh) | 缩合哒嗪系化合物 | |
| CN1856474A (zh) | 异喹啉钾通道抑制剂 | |
| CN1273451C (zh) | 哌啶mch拮抗剂及其治疗肥胖症的用途 | |
| CN1856475A (zh) | 异喹啉钾通道抑制剂 | |
| CN1191249C (zh) | 用于治疗、特别是治疗良性前列腺增生的喹啉和喹唑啉化合物 | |
| CN1993347A (zh) | 钾通道抑制剂 | |
| HK1040712A1 (en) | Substituted pyrazole derivatives condensed with six-membered heterocyclic rings | |
| CN1960975A (zh) | 作为多聚(adp-核糖)聚合酶(parp)抑制剂的取代的吡啶酮 | |
| CN1950371A (zh) | 用作组胺h3受体配体的四氢萘啶衍生物 | |
| CN101031559A (zh) | 氨基环脲衍生物和其制法及作为激酶抑制剂的医药用途 | |
| CN1856477A (zh) | 异喹啉钾通道抑制剂 | |
| CN1351497A (zh) | 用作山梨醇脱氢酶抑制剂的氨基嘧啶类化合物 | |
| CN87100652A (zh) | 抗心律不齐剂 | |
| CN1688577A (zh) | 三氮杂螺[5.5]十一烷衍生物及以它为活性成分的药物 | |
| CN1665811A (zh) | 氨基甲酸酯-取代的吡唑并吡啶类化合物 | |
| CN1675209A (zh) | 二氢吡唑并吡啶化合物 | |
| CN1856473A (zh) | 异喹啉酮钾通道抑制剂 | |
| CN1856310A (zh) | 喹唑啉钾通道抑制剂 | |
| CN1968929A (zh) | 取代的四氢-2h-异喹啉-1-酮衍生物、其制备方法以及其作为药物的用途 | |
| CN1202171A (zh) | 吡啶并[2,3-d]嘧啶衍生物及其医药组合物 | |
| CN1886402A (zh) | 嘧啶-2-胺衍生物及其作为a2b腺苷受体拮抗剂的用途 | |
| CN1816541A (zh) | Vr-1拮抗剂取代-1-酞嗪胺 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |