CN101325956B - 治疗心房颤动的化合物 - Google Patents
治疗心房颤动的化合物 Download PDFInfo
- Publication number
- CN101325956B CN101325956B CN200680046601XA CN200680046601A CN101325956B CN 101325956 B CN101325956 B CN 101325956B CN 200680046601X A CN200680046601X A CN 200680046601XA CN 200680046601 A CN200680046601 A CN 200680046601A CN 101325956 B CN101325956 B CN 101325956B
- Authority
- CN
- China
- Prior art keywords
- receptor
- adenosine
- atrial fibrillation
- calcium
- antagonists
- 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.)
- Expired - Fee Related
Links
- AFXKLUCTBPZBAJ-UHFFFAOYSA-N NC(CCSc1nc(N)c(cn[n]2-c3ccccc3)c2n1)=O Chemical compound NC(CCSc1nc(N)c(cn[n]2-c3ccccc3)c2n1)=O AFXKLUCTBPZBAJ-UHFFFAOYSA-N 0.000 description 2
- BCGFASHRDSXLNN-UHFFFAOYSA-N CC(C)c1nc(-c2ncc[s]2)c2[s]ccc2n1 Chemical compound CC(C)c1nc(-c2ncc[s]2)c2[s]ccc2n1 BCGFASHRDSXLNN-UHFFFAOYSA-N 0.000 description 1
- GACDSQLJMZANKT-UHFFFAOYSA-N CC[n]1c(Br)nc2c(N)ncnc12 Chemical compound CC[n]1c(Br)nc2c(N)ncnc12 GACDSQLJMZANKT-UHFFFAOYSA-N 0.000 description 1
- CLJSIBKRVMNALR-UHFFFAOYSA-N Cc(cc1N(C2=NN3c4ccccc4)C3=O)cc(NCc3ccccc3)c1N=C2N Chemical compound Cc(cc1N(C2=NN3c4ccccc4)C3=O)cc(NCc3ccccc3)c1N=C2N CLJSIBKRVMNALR-UHFFFAOYSA-N 0.000 description 1
- ANTQNVKQQVGUDR-UHFFFAOYSA-N NC(N1N=C(c2ccc[o]2)NC11)=Nc2c1cn[n]2CCCC1C=CC=CC1 Chemical compound NC(N1N=C(c2ccc[o]2)NC11)=Nc2c1cn[n]2CCCC1C=CC=CC1 ANTQNVKQQVGUDR-UHFFFAOYSA-N 0.000 description 1
- MSJODEOZODDVGW-UHFFFAOYSA-N Nc([n]1nc(-c2ccc[o]2)nc1c1c2)nc1ccc2Cl Chemical compound Nc([n]1nc(-c2ccc[o]2)nc1c1c2)nc1ccc2Cl MSJODEOZODDVGW-UHFFFAOYSA-N 0.000 description 1
- SKBCBSVLFJCUKC-UHFFFAOYSA-N Nc1nc(NCc(cc2)ccc2O)nc2nc(-c3ccc[o]3)n[n]12 Chemical compound Nc1nc(NCc(cc2)ccc2O)nc2nc(-c3ccc[o]3)n[n]12 SKBCBSVLFJCUKC-UHFFFAOYSA-N 0.000 description 1
- UTLPKQYUXOEJIL-UHFFFAOYSA-N Nc1nc([n](CCc2ccccc2)nc2)c2c2nc(-c3ccc[o]3)n[n]12 Chemical compound Nc1nc([n](CCc2ccccc2)nc2)c2c2nc(-c3ccc[o]3)n[n]12 UTLPKQYUXOEJIL-UHFFFAOYSA-N 0.000 description 1
- WRXAWLLASUJMMD-UHFFFAOYSA-N Nc1nc([n](Cc(cc2)ccc2F)nc2)c2c2nc(-c3ccc[o]3)n[n]12 Chemical compound Nc1nc([n](Cc(cc2)ccc2F)nc2)c2c2nc(-c3ccc[o]3)n[n]12 WRXAWLLASUJMMD-UHFFFAOYSA-N 0.000 description 1
- BJALMNZBJQDVQK-UHFFFAOYSA-N Nc1nc2n[n](Cc(cc3)ccc3F)cc2c2nc(-c3ccc[o]3)n[n]12 Chemical compound Nc1nc2n[n](Cc(cc3)ccc3F)cc2c2nc(-c3ccc[o]3)n[n]12 BJALMNZBJQDVQK-UHFFFAOYSA-N 0.000 description 1
- XEEQGYMUWCZPDN-CVRLYYSRSA-N O[C@H](C1NCCCC1)c1c(cccc2C(F)(F)F)c2nc(C(F)(F)F)c1 Chemical compound O[C@H](C1NCCCC1)c1c(cccc2C(F)(F)F)c2nc(C(F)(F)F)c1 XEEQGYMUWCZPDN-CVRLYYSRSA-N 0.000 description 1
- XEEQGYMUWCZPDN-DOMZBBRYSA-N O[C@H]([C@@H]1NCCCC1)c1c(cccc2C(F)(F)F)c2nc(C(F)(F)F)c1 Chemical compound O[C@H]([C@@H]1NCCCC1)c1c(cccc2C(F)(F)F)c2nc(C(F)(F)F)c1 XEEQGYMUWCZPDN-DOMZBBRYSA-N 0.000 description 1
Images
Classifications
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
-
- 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
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
- A61P9/06—Antiarrhythmics
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Cardiology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ESP200502545 | 2005-10-14 | ||
| ES200502545A ES2273599B1 (es) | 2005-10-14 | 2005-10-14 | Compuestos para el tratamiento de la fibrilacion auricular. |
| PCT/ES2006/000564 WO2007045705A2 (es) | 2005-10-14 | 2006-10-10 | Compuestos para el tratamiento de la fibrilación auricular |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101325956A CN101325956A (zh) | 2008-12-17 |
| CN101325956B true CN101325956B (zh) | 2012-02-29 |
Family
ID=37962872
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200680046601XA Expired - Fee Related CN101325956B (zh) | 2005-10-14 | 2006-10-10 | 治疗心房颤动的化合物 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US8012973B2 (enExample) |
| EP (1) | EP1949903B8 (enExample) |
| JP (1) | JP2009511551A (enExample) |
| CN (1) | CN101325956B (enExample) |
| AT (1) | ATE553763T1 (enExample) |
| AU (1) | AU2006303240B2 (enExample) |
| BR (1) | BRPI0617369A2 (enExample) |
| CA (1) | CA2626020A1 (enExample) |
| DK (1) | DK1949903T3 (enExample) |
| ES (2) | ES2273599B1 (enExample) |
| MX (1) | MX2008004886A (enExample) |
| RU (1) | RU2445099C2 (enExample) |
| WO (1) | WO2007045705A2 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3088900B1 (en) * | 2011-10-17 | 2020-08-12 | Roche Diagniostics GmbH | Troponin as marker for intermittent atrial fibrillation |
| CZ2014307A3 (cs) * | 2014-05-06 | 2016-01-13 | Vysoká škola chemicko- technologická v Praze | Kofein-8-hydrazony jako nová cytostatika pro léčbu onkologických onemocnění |
| WO2017008205A1 (en) * | 2015-07-10 | 2017-01-19 | Merck Sharp & Dohme Corp. | Substituted aminoquinazoline compounds as a2a antagonist |
| CN108570054B (zh) * | 2017-03-07 | 2021-07-16 | 广州再极医药科技有限公司 | 氨基嘧啶并五元杂环化合物、其中间体、制备方法、药物组合物及应用 |
| JP7478673B2 (ja) | 2018-06-04 | 2024-05-07 | エクスシエンティア・エルティーディー | アデノシン受容体アンタゴニストとしてのピラゾロピリミジン化合物 |
| CN108864114B (zh) * | 2018-06-04 | 2020-11-06 | 应世生物科技(南京)有限公司 | 选择性a2a受体拮抗剂 |
| EP4146341A4 (en) * | 2020-05-06 | 2024-06-26 | Ohio State Innovation Foundation | Compositions and methods for treating atrial fibrillation |
| KR102675647B1 (ko) * | 2021-06-30 | 2024-06-18 | 단국대학교 천안캠퍼스 산학협력단 | 인간치아줄기세포의 상아모세포로의 분화를 위한 신규 화합물 및 이의 의학적 용도 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US599387A (en) * | 1898-02-22 | Cabinet | ||
| US4772607A (en) * | 1986-05-20 | 1988-09-20 | Warner-Lambert Company | Dialkenyl derivatives of xanthine, pharmaceutical compositions and methods of use therefor |
| US20030022890A1 (en) * | 1999-12-06 | 2003-01-30 | Atwal Karnail S. | Heterocyclic dihydropyrimidine compounds |
Family Cites Families (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4780464A (en) * | 1986-12-08 | 1988-10-25 | Warner-Lambert Company | (1,2,4)triazolo(4,3-a)quinoxaline-4-amines |
| EP0559893B1 (en) | 1990-10-18 | 1999-02-03 | Kyowa Hakko Kogyo Co., Ltd. | Xanthine derivative |
| GB9124968D0 (en) * | 1991-11-25 | 1992-01-22 | Ici Plc | Chemical process |
| US5484920A (en) | 1992-04-08 | 1996-01-16 | Kyowa Hakko Kogyo Co., Ltd. | Therapeutic agent for Parkinson's disease |
| CA2116967C (en) | 1992-07-08 | 2003-08-19 | Fumio Suzuki | Antidepressants |
| IT1264901B1 (it) | 1993-06-29 | 1996-10-17 | Schering Plough S P A | Analoghi eterociclici di 1,2,4-triazolo(15-c)pirimidine ad attivita' antagonista per il recettore a2 dell'adenosina |
| WO1995003806A1 (en) | 1993-07-27 | 1995-02-09 | Kyowa Hakko Kogyo Co., Ltd. | Remedy for parkinson's disease |
| US5736528A (en) * | 1993-10-28 | 1998-04-07 | University Of Florida Research Foundation, Inc. | N6 -(epoxynorborn-2-yl) adenosines as A1 adenosine receptor agonists |
| US5703085A (en) | 1994-02-23 | 1997-12-30 | Kyowa Hakko Kogyo Co., Ltd. | Xanthine derivatives |
| IT1277392B1 (it) | 1995-07-28 | 1997-11-10 | Schering Plough S P A | Analoghi eterociclici di 1,2,4-triazolo(1,5-c]pirimidine ad attivita' antagonista per il recettore a2a dell'adenosina |
| US6051578A (en) * | 1996-02-12 | 2000-04-18 | Pfizer Inc. | Pyrazolopyrimidines for treatment of CNS disorders |
| US6060478A (en) * | 1996-07-24 | 2000-05-09 | Dupont Pharmaceuticals | Azolo triazines and pyrimidines |
| JP4195729B2 (ja) | 1997-03-24 | 2008-12-10 | 協和醗酵工業株式会社 | [1,2,4]トリアゾロ[1,5−c]ピリミジン誘導体 |
| IT1291372B1 (it) | 1997-05-21 | 1999-01-07 | Schering Plough S P A | Uso di analoghi eterociclici di 1,2,4-triazolo (1,5-c) pirimidine per la preparazione di medicamenti utili per il trattamento delle malattie |
| ES2264210T3 (es) | 1997-09-05 | 2006-12-16 | Kyowa Hakko Kogyo Co., Ltd. | Derivados de xantina para el tratamiento de la isquemia cerebral. |
| EP0975345A1 (en) | 1997-11-26 | 2000-02-02 | Cerebrus Pharmaceuticals Limited | (-)-mefloquine to block purinergic receptors and to treat movement or neurodegenerative disorders |
| WO1999035147A1 (en) | 1998-01-05 | 1999-07-15 | Eisai Co., Ltd. | Purine derivatives and adenosine a2 receptor antagonists serving as preventives/remedies for diabetes |
| AU2639299A (en) | 1998-02-24 | 1999-09-15 | Kyowa Hakko Kogyo Co. Ltd. | Remedies/preventives for parkinson's disease |
| DE19930558A1 (de) | 1998-07-24 | 2000-01-27 | Marquardt Gmbh | Elektrischer Schalter |
| GB9819384D0 (en) | 1998-09-04 | 1998-10-28 | Cerebrus Ltd | Chemical compounds II |
| GB9819382D0 (en) | 1998-09-04 | 1998-10-28 | Cerebrus Ltd | Chemical compounds I |
| AU748612B2 (en) * | 1998-09-04 | 2002-06-06 | Procter & Gamble Company, The | Substituted dihydrobenzopyrans useful as antiarrhythmic agents |
| AU4431000A (en) | 1999-05-12 | 2000-12-05 | Fujisawa Pharmaceutical Co., Ltd. | Novel use |
| US6545002B1 (en) | 1999-06-01 | 2003-04-08 | University Of Virginia Patent Foundation | Substituted 8-phenylxanthines useful as antagonists of A2B adenosine receptors |
| GB9915437D0 (en) | 1999-07-01 | 1999-09-01 | Cerebrus Ltd | Chemical compounds III |
| ES2246867T3 (es) | 1999-07-02 | 2006-03-01 | Eisai Co., Ltd. | Compuestos de imidazol condensados y medicamentos contra la diabetes mellitus. |
| JP3347691B2 (ja) * | 1999-07-05 | 2002-11-20 | プロクター、エンド、ギャンブル、ファーマスーティカルズ、インコーポレーテッド | 抗不整脈及び抗細動剤として有用な新規4−オキソ環式尿素類 |
| HK1049835B (zh) | 1999-08-31 | 2005-04-08 | 范德比尔特大学 | A2b腺苷受体的选择性拮抗剂 |
| US6355653B1 (en) | 1999-09-06 | 2002-03-12 | Hoffmann-La Roche Inc. | Amino-triazolopyridine derivatives |
| DE19947154A1 (de) | 1999-10-01 | 2001-10-04 | Bayer Ag | Substituierte 2-Thio-3,5-dicyano-4-aryl-6-aminopyridine und ihre Verwendung |
| US6194366B1 (en) | 1999-11-16 | 2001-02-27 | Esc, Inc. | Post chemical-mechanical planarization (CMP) cleaning composition |
| AUPQ441499A0 (en) | 1999-12-02 | 2000-01-06 | Fujisawa Pharmaceutical Co., Ltd. | Novel compound |
| US6258793B1 (en) * | 1999-12-03 | 2001-07-10 | Cv Therapeutics, Inc. | N6 heterocyclic 5′ modified adenosine derivatives |
| EP1261327B1 (en) | 2000-02-25 | 2005-04-27 | F.Hoffmann-La Roche Ag | Adenosine receptor modulators |
| WO2001080893A1 (en) | 2000-04-26 | 2001-11-01 | Eisai Co., Ltd. | Medicinal compositions promoting bowel movement |
| IL152726A0 (en) | 2000-05-26 | 2003-06-24 | Schering Corp | Adenosine a2a receptor antagonists |
| JP3886897B2 (ja) | 2000-06-21 | 2007-02-28 | エフ.ホフマン−ラ ロシュ アーゲー | ベンゾチアゾール誘導体 |
| HUP0700086A2 (en) | 2000-08-11 | 2007-05-29 | Eisai Co Ltd | 2-aminopyridine compounds, use thereof as drugs and pharmaceutical compositions containing them |
| GB0100620D0 (en) * | 2001-01-10 | 2001-02-21 | Vernalis Res Ltd | Chemical cokpounds V |
| AR037243A1 (es) | 2001-10-15 | 2004-11-03 | Schering Corp | Antagonistas del receptor de adenosina a2a,a5-amino-imidazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]pirimidina, composiciones farmaceuticas y el uso de dichos compuestos para la preparacion de un medicamento |
| US6599901B1 (en) * | 2001-11-19 | 2003-07-29 | Hoffman-La Roche Inc. | Pyridone substituted benzothiazole derivatives |
| HUP0402324A3 (en) | 2001-11-30 | 2008-09-29 | Schering Corp | [1,2,4]triazolo[1,5-a]pyridine and [1,2,4]triazolo[1,5-c]pyrimidine derivatives as adenosine a2a receptor antagonists and pharmaceutical compositions containing them |
| PE20030739A1 (es) | 2001-11-30 | 2003-08-28 | Schering Corp | Antagonistas del receptor de adenosina a2a |
| HUP0402018A3 (en) | 2001-11-30 | 2008-06-30 | Schering Corp | 5-amino-7h-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine derivatives, their use and pharmaceutical compositions containing them |
| ES2279903T3 (es) | 2001-12-18 | 2007-09-01 | Cv Therapeutics, Inc. | Antagonistas del receptor a2a de adenosina. |
| US20050043315A1 (en) | 2002-01-02 | 2005-02-24 | Hideo Tsutsumi | Aminopyrimidine compounds, processes for their preparation and pharmaceutical compositions containing them |
| ES2208063B1 (es) | 2002-04-01 | 2005-10-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de la 4-(pirrolopirimidin-6-il)bencenosulfonamida. |
| AU2002950853A0 (en) | 2002-08-19 | 2002-09-12 | Fujisawa Pharmaceutical Co., Ltd. | Aminopyrimidine compound and pharmaceutical use thereof |
| CA2496920A1 (en) | 2002-08-30 | 2004-03-11 | Kyowa Hakko Kogyo Co., Ltd. | Adenosine a2a receptor antagonists for treating restless legs syndrome or related disorders |
| WO2004029056A1 (ja) | 2002-09-24 | 2004-04-08 | Kyowa Hakko Kogyo Co., Ltd. | [1,2,4]トリアゾロ[1,5−c]ピリミジン誘導体 |
| EP2295047A3 (en) | 2002-12-19 | 2011-05-18 | Schering Corporation | Use of adenosine A2a receptor antagonists for the treatment of restless leg syndrome and other movement disorders |
| CA2520251A1 (en) * | 2003-03-27 | 2004-10-07 | Pfizer Products Inc. | Substituted 4-amino[1,2,4]triazolo[4,3-a]quinoxalines |
| WO2004092177A1 (en) | 2003-04-09 | 2004-10-28 | Biogen Idec Ma Inc. | Triazolopyrazines and methods of making and using the same |
| PT1622912E (pt) | 2003-04-23 | 2009-08-17 | Schering Corp | Antagonistas 2-alcinil- e 2-alcenilpirazolo-[4,3-b]-1,2,4- triazolo-[1,5-c]-pirimidina do receptor a2a da adenosina |
| DK1673354T3 (da) | 2003-10-03 | 2009-07-27 | Ortho Mcneil Janssen Pharm | Arylindenopyridiner og arylindenopyrimidiner og deres anvendelse som adenosin-A2a-receptorantagonister |
| CA2543644A1 (en) | 2003-10-27 | 2005-05-06 | Astellas Pharma Inc. | Pyrazine derivatives and pharmaceutical use thereof |
| TW200524887A (en) | 2003-10-27 | 2005-08-01 | Lundbeck & Co As H | N-thiazol-2-yl-benzamide derivatives |
| ATE377599T1 (de) | 2003-12-01 | 2007-11-15 | Schering Corp | Verfahren zur herstellung von substituierten 5- aminopyrazolo(4,3-e)-1,2,4-triazolo(1,5- c)pyrimidinen |
| AU2004299461A1 (en) | 2003-12-15 | 2005-06-30 | Almirall Ag | 2, 6 bisheteroaryl-4-aminopyrimidines as adenosine receptor antagonists |
-
2005
- 2005-10-14 ES ES200502545A patent/ES2273599B1/es not_active Expired - Fee Related
-
2006
- 2006-10-10 MX MX2008004886A patent/MX2008004886A/es active IP Right Grant
- 2006-10-10 AT AT06830873T patent/ATE553763T1/de active
- 2006-10-10 JP JP2008535047A patent/JP2009511551A/ja active Pending
- 2006-10-10 ES ES06830873T patent/ES2386377T3/es active Active
- 2006-10-10 BR BRPI0617369-1A patent/BRPI0617369A2/pt not_active IP Right Cessation
- 2006-10-10 AU AU2006303240A patent/AU2006303240B2/en not_active Ceased
- 2006-10-10 US US12/090,115 patent/US8012973B2/en not_active Expired - Fee Related
- 2006-10-10 CA CA002626020A patent/CA2626020A1/en not_active Abandoned
- 2006-10-10 EP EP06830873A patent/EP1949903B8/en not_active Not-in-force
- 2006-10-10 CN CN200680046601XA patent/CN101325956B/zh not_active Expired - Fee Related
- 2006-10-10 WO PCT/ES2006/000564 patent/WO2007045705A2/es not_active Ceased
- 2006-10-10 DK DK06830873.3T patent/DK1949903T3/da active
- 2006-10-10 RU RU2008118995/15A patent/RU2445099C2/ru not_active IP Right Cessation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US599387A (en) * | 1898-02-22 | Cabinet | ||
| US4772607A (en) * | 1986-05-20 | 1988-09-20 | Warner-Lambert Company | Dialkenyl derivatives of xanthine, pharmaceutical compositions and methods of use therefor |
| US20030022890A1 (en) * | 1999-12-06 | 2003-01-30 | Atwal Karnail S. | Heterocyclic dihydropyrimidine compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2006303240A1 (en) | 2007-04-26 |
| ATE553763T1 (de) | 2012-05-15 |
| ES2273599A1 (es) | 2007-05-01 |
| US20090312332A1 (en) | 2009-12-17 |
| EP1949903B1 (en) | 2012-04-18 |
| AU2006303240B2 (en) | 2012-07-12 |
| CA2626020A1 (en) | 2007-04-26 |
| RU2445099C2 (ru) | 2012-03-20 |
| CN101325956A (zh) | 2008-12-17 |
| ES2273599B1 (es) | 2008-06-01 |
| EP1949903B8 (en) | 2012-05-23 |
| ES2386377T3 (es) | 2012-08-20 |
| MX2008004886A (es) | 2009-03-02 |
| BRPI0617369A2 (pt) | 2011-07-26 |
| US8012973B2 (en) | 2011-09-06 |
| RU2008118995A (ru) | 2009-11-20 |
| JP2009511551A (ja) | 2009-03-19 |
| WO2007045705A2 (es) | 2007-04-26 |
| DK1949903T3 (da) | 2012-07-30 |
| EP1949903A2 (en) | 2008-07-30 |
| WO2007045705A3 (es) | 2007-06-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2457842C2 (ru) | Способ предотвращения и лечения болезни печени с использованием антагонистов рецептора аденозина a2b | |
| O'callaghan et al. | Treatment of pulmonary arterial hypertension with targeted therapies | |
| Zhao et al. | Diminished α7 nicotinic acetylcholine receptor (α7nAChR) rescues amyloid-β induced atrial remodeling by oxi-CaMKII/MAPK/AP-1 axis-mediated mitochondrial oxidative stress | |
| CN101325956B (zh) | 治疗心房颤动的化合物 | |
| US20220362251A1 (en) | Treatment of tachycardia | |
| Chen et al. | Stachydrine hydrochloride alleviates pressure overload-induced heart failure and calcium mishandling on mice | |
| TW202342050A (zh) | 用於治療進行性纖維化間質性肺病之新穎治療組合 | |
| Schulz et al. | Minimal α1-and α2-adrenoceptor-mediated coronary vasoconstriction in the anaesthetized swine | |
| Michel | Treatment of myocardial ischemia | |
| KR20140022052A (ko) | 심근 경색 후 환자에서의 심부전 및 부정맥 치료를 위한 a2b 아데노신 수용체 안타고니스트의 용도 | |
| AU2006230674A8 (en) | Methods for the Treatment of Synucleinopathies | |
| Sastry et al. | Tonic inhibitory influence of a supraspinal monoaminergic system on recurrent inhibition of an extensor monosynaptic reflex | |
| KR20130088834A (ko) | 폐 고혈압의 치료를 위한 a2b 아데노신 수용체 길항제의 용도 | |
| JP2025511786A (ja) | 筋線維症の治療 | |
| KR20220100544A (ko) | PI3K/Akt 매개 후기 나트륨 전류 억제를 통한 부정맥 치료용 약학 조성물 및 치료방법 | |
| US20120015968A1 (en) | Use of pyrimidylaminobenzamide derivatives for the treatment of disorders mediated by the leucine zipper-and sterile alpha motif-containing kinase (zak) | |
| Fei et al. | The regulation of AMPKα1/Nrf2/HO-1 pathway mediated by galantamine hydrobromide lycoremine in myocardial ischemia reperfusion rats | |
| Lawless et al. | PDE5 inhibition improves symptom-free survival and restores transverse tubule loss and catecholamine responsiveness in heart failure | |
| Doisne et al. | Articles in PresS. Am J Physiol Heart Circ Physiol (May 8, 2009). doi: 10.1152/ajpheart. 00256.2009 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20120229 Termination date: 20131010 |