ATE303387T1 - Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitus - Google Patents
Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitusInfo
- Publication number
- ATE303387T1 ATE303387T1 AT00940909T AT00940909T ATE303387T1 AT E303387 T1 ATE303387 T1 AT E303387T1 AT 00940909 T AT00940909 T AT 00940909T AT 00940909 T AT00940909 T AT 00940909T AT E303387 T1 ATE303387 T1 AT E303387T1
- Authority
- AT
- Austria
- Prior art keywords
- group
- diabetes mellitus
- alkyl group
- adenosine
- substituted
- Prior art date
Links
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical class C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title abstract 3
- 239000003814 drug Substances 0.000 title abstract 2
- 206010012601 diabetes mellitus Diseases 0.000 title 1
- 229940079593 drug Drugs 0.000 title 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title 1
- 208000002249 Diabetes Complications Diseases 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 229940124049 Adenosine A2 receptor antagonist Drugs 0.000 abstract 2
- 206010012655 Diabetic complications Diseases 0.000 abstract 2
- 239000003449 adenosine A2 receptor antagonist Substances 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- -1 imidazole compound Chemical class 0.000 abstract 1
- 230000003449 preventive effect Effects 0.000 abstract 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical group OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 abstract 1
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical group OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/18—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18848499 | 1999-07-02 | ||
| JP2000143495 | 2000-05-16 | ||
| JP2000182786 | 2000-06-19 | ||
| PCT/JP2000/004358 WO2001002400A1 (en) | 1999-07-02 | 2000-06-30 | Fused imidazole compounds and remedies for diabetes mellitus |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE303387T1 true ATE303387T1 (de) | 2005-09-15 |
Family
ID=27326046
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT00940909T ATE303387T1 (de) | 1999-07-02 | 2000-06-30 | Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitus |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6841549B1 (de) |
| EP (1) | EP1221444B1 (de) |
| JP (1) | JP4324338B2 (de) |
| KR (1) | KR100694684B1 (de) |
| CN (1) | CN1166666C (de) |
| AT (1) | ATE303387T1 (de) |
| AU (1) | AU778450B2 (de) |
| CA (1) | CA2376835C (de) |
| DE (1) | DE60022366T2 (de) |
| DK (1) | DK1221444T3 (de) |
| ES (1) | ES2246867T3 (de) |
| NZ (1) | NZ516260A (de) |
| PT (1) | PT1221444E (de) |
| WO (1) | WO2001002400A1 (de) |
Families Citing this family (70)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9915437D0 (en) | 1999-07-01 | 1999-09-01 | Cerebrus Ltd | Chemical compounds III |
| IL152023A0 (en) | 2000-04-26 | 2003-04-10 | Eisai Co Ltd | Compounds having adenosine a2 receptor antagonism and pharmaceutical compositions containing the same |
| GB0100623D0 (en) | 2001-01-10 | 2001-02-21 | Vernalis Res Ltd | Chemical compounds IV |
| GB0100624D0 (en) | 2001-01-10 | 2001-02-21 | Vernalis Res Ltd | Chemical compounds VII |
| GB0100620D0 (en) | 2001-01-10 | 2001-02-21 | Vernalis Res Ltd | Chemical cokpounds V |
| TWI301834B (en) | 2001-10-22 | 2008-10-11 | Eisai R&D Man Co Ltd | Pyrimidone compound and pharmaceutical composition including the same |
| TWI330183B (de) | 2001-10-22 | 2010-09-11 | Eisai R&D Man Co Ltd | |
| US7189730B2 (en) * | 2001-12-18 | 2007-03-13 | Cv Therapeutics, Inc. | A2A adenosine receptor antagonists |
| BR0306919A (pt) | 2002-01-28 | 2004-11-09 | Kyowa Hakko Kogyo Kk | Métodos para reduzir ou suprimir a efetividade adversa da terapia de l-dopa e/ou do agonista da dopamina, e para tratamento moderado de l-dopa, composição para tratamento moderado de l-dopa, método para tratar doença de parkinson e/ou complicações motoras de l-dopa, composição para o tratamento da doença de parkinson, e, métodos para prolongar o tratamento eficaz da doença de parkinson, e para tratar os distúrbios de movimento |
| US7129239B2 (en) | 2002-10-28 | 2006-10-31 | Pfizer Inc. | Purine compounds and uses thereof |
| US7674791B2 (en) | 2003-04-09 | 2010-03-09 | Biogen Idec Ma Inc. | Triazolopyrazines and methods of making and using the same |
| WO2004092170A2 (en) | 2003-04-09 | 2004-10-28 | Biogen Idec Ma Inc. | Triazolotriazines and pyrazolotriazines useful as a2a adenosine receptor antagon ists |
| DE602004018637D1 (de) | 2003-04-09 | 2009-02-05 | Biogen Idec Inc | A2a-adenosinrezeptorantagonisten |
| CN100372844C (zh) * | 2003-05-13 | 2008-03-05 | 弗·哈夫曼-拉罗切有限公司 | 作为腺苷受体配体的2-咪唑-苯并噻唑 |
| WO2005058898A2 (en) * | 2003-12-16 | 2005-06-30 | Ranbaxy Laboratories Limited | Purine compounds which can be used as phosphodiesterase (pde) type iv inhibitors |
| JP2007535560A (ja) * | 2004-04-28 | 2007-12-06 | シーブイ・セラピューティクス・インコーポレイテッド | A1アデノシンレセプターアンタゴニスト |
| AR049384A1 (es) * | 2004-05-24 | 2006-07-26 | Glaxo Group Ltd | Derivados de purina |
| EP1758895A1 (de) | 2004-06-17 | 2007-03-07 | Wyeth a Corporation of the State of Delaware | Gonadotropin-freisetzende hormonrezeptor-antagonisten |
| CA2570693A1 (en) * | 2004-06-17 | 2006-01-26 | Wyeth | Processes for preparing gonadotropin releasing hormone receptor antagonists |
| GT200500281A (es) * | 2004-10-22 | 2006-04-24 | Novartis Ag | Compuestos organicos. |
| GB0423551D0 (en) * | 2004-10-22 | 2004-11-24 | Novartis Ag | Organic compounds |
| MX2007005765A (es) * | 2004-11-23 | 2007-07-19 | Wyeth Corp | Antagonistas del receptor de la hormona que libera gonadotropina. |
| US7538113B2 (en) * | 2005-02-18 | 2009-05-26 | Wyeth | 4-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor |
| US7534796B2 (en) * | 2005-02-18 | 2009-05-19 | Wyeth | Imidazo[4,5-b]pyridine antagonists of gonadotropin releasing hormone receptor |
| US7582634B2 (en) * | 2005-02-18 | 2009-09-01 | Wyeth | 7-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor |
| US20060189619A1 (en) * | 2005-02-24 | 2006-08-24 | Wyeth | 3-({4-[2-(4-Tert-butylphenyl)-1h-benzimidazol-4-yl]piperazin-1-yl}methyl)pyrido[2,3-b]]pyrazi ne compounds |
| US7531542B2 (en) | 2005-05-18 | 2009-05-12 | Wyeth | Benzooxazole and benzothiazole antagonists of gonadotropin releasing hormone receptor |
| US7582636B2 (en) * | 2005-05-26 | 2009-09-01 | Wyeth | Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of Gonadotropin Releasing Hormone receptor |
| GB0514809D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
| ES2270715B1 (es) | 2005-07-29 | 2008-04-01 | Laboratorios Almirall S.A. | Nuevos derivados de pirazina. |
| JP2007063225A (ja) * | 2005-09-01 | 2007-03-15 | Takeda Chem Ind Ltd | イミダゾピリジン化合物 |
| US20090023723A1 (en) * | 2005-09-21 | 2009-01-22 | Pharmacopeia Drug Discovery, Inc. | Purinone derivatives for treating neurodegenerative diseases |
| ES2274712B1 (es) * | 2005-10-06 | 2008-03-01 | Laboratorios Almirall S.A. | Nuevos derivados imidazopiridina. |
| ES2273599B1 (es) | 2005-10-14 | 2008-06-01 | Universidad De Barcelona | Compuestos para el tratamiento de la fibrilacion auricular. |
| US7989459B2 (en) | 2006-02-17 | 2011-08-02 | Pharmacopeia, Llc | Purinones and 1H-imidazopyridinones as PKC-theta inhibitors |
| AR063141A1 (es) | 2006-10-04 | 2008-12-30 | Pharmacopeia Inc | Derivados de 2- ( benzimidazolil ) purina 8- sustituida para inmunosupresion |
| US7902187B2 (en) | 2006-10-04 | 2011-03-08 | Wyeth Llc | 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression |
| TW200831104A (en) | 2006-10-04 | 2008-08-01 | Pharmacopeia Inc | 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression |
| ES2303776B1 (es) * | 2006-12-29 | 2009-08-07 | Laboratorios Almirall S.A. | Derivados de 5-fenil-6-piridin-4-il-1,3-dihidro-2h-imidazo(4,5-b)piridin-2-ona utiles como antagonistas del receptor de adenosina a2b. |
| NZ579635A (en) * | 2007-03-20 | 2011-07-29 | Curis Inc | Fused amino pyridine as hsp90 inhibitors |
| GB0906579D0 (en) | 2009-04-16 | 2009-05-20 | Vernalis R&D Ltd | Pharmaceuticals, compositions and methods of making and using the same |
| WO2010036380A1 (en) | 2008-09-26 | 2010-04-01 | Intellikine, Inc. | Heterocyclic kinase inhibitors |
| RU2539568C2 (ru) | 2008-10-31 | 2015-01-20 | Дженентек, Инк. | Пиразолопиримидиновые соединения-ингибиторы jak и способы |
| EP2246335A1 (de) * | 2009-02-17 | 2010-11-03 | Bayer CropScience AG | Aminopyrimidinamide als Schädlingsbekämpfungsmittel |
| HUE025704T2 (en) * | 2009-03-20 | 2016-04-28 | Sigma Tau Ind Farmaceuti | Oxidized triazolyl purine derivatives used as adenosine A2A receptor ligands and their use as medicaments |
| UA110324C2 (en) | 2009-07-02 | 2015-12-25 | Genentech Inc | Jak inhibitory compounds based on pyrazolo pyrimidine |
| ES2574253T3 (es) | 2009-12-18 | 2016-06-16 | Mitsubishi Tanabe Pharma Corporation | Nuevo agente antiplaquetario |
| US20130096104A1 (en) * | 2010-03-17 | 2013-04-18 | Genentech, Inc. | Imidazopyridine compounds, compositions and methods of use |
| ES2365960B1 (es) | 2010-03-31 | 2012-06-04 | Palobiofarma, S.L | Nuevos antagonistas de los receptores de adenosina. |
| RU2013114352A (ru) | 2010-09-15 | 2014-10-20 | Ф. Хоффманн-Ля Рош Аг | Азабензотиазолы, композиции и способы применения |
| CA2817785A1 (en) | 2010-11-19 | 2012-05-24 | Toby Blench | Pyrazolopyridines and pyrazolopyridines and their use as tyk2 inhibitors |
| WO2012070601A1 (ja) * | 2010-11-24 | 2012-05-31 | ヤマサ醤油株式会社 | 新規な2-アルキニル-n9-プロパギルアデニンおよびその医薬用途 |
| US8901313B2 (en) * | 2011-03-16 | 2014-12-02 | Genentech, Inc. | 6,5-heterocyclic propargylic alcohol compounds and uses therefor |
| CN103044337A (zh) * | 2011-10-13 | 2013-04-17 | 南京理工大学 | 2-(n-烷基)氨基咪唑衍生物的合成方法 |
| CN103664704B (zh) * | 2012-08-31 | 2016-05-18 | 南京理工大学 | 一种合成n,n’-二取代基脲的方法 |
| EP2818472A1 (de) * | 2013-06-27 | 2014-12-31 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Imidazo[4,5-c]pyridin- und Pyrrolo[3,2-c]pyridinverbindungen als Modulatoren der G-Protein-Gekoppelte Rezeptoren Kinase 5 (GRK5) |
| NZ718190A (en) | 2013-08-23 | 2017-10-27 | Neupharma Inc | Substituted quinazolines for inhibiting kinase activity |
| PE20211782A1 (es) | 2014-05-23 | 2021-09-08 | Hoffmann La Roche | Compuestos de 5-cloro-2-difluorometoxifenil pirazolopirimidina, composiciones y metodos de uso de los mismos |
| CA3021947A1 (en) * | 2016-04-26 | 2017-11-02 | Sumitomo Dainippon Pharma Co., Ltd. | Substituted purine derivative |
| AU2017312561B2 (en) * | 2016-08-15 | 2022-06-30 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| TW202332436A (zh) | 2017-04-18 | 2023-08-16 | 美商塞爾基因定量細胞研究公司 | 治療用化合物 |
| RU2769696C2 (ru) | 2017-05-22 | 2022-04-05 | Ф. Хоффманн-Ля Рош Аг | Терапевтические соединения и композиции и способы их применения |
| KR102717280B1 (ko) | 2017-08-01 | 2024-10-14 | 메르크 파텐트 게엠베하 | 아데노신 수용체 길항제로서의 티아졸로피리딘 유도체 |
| CN110944994B (zh) | 2017-08-21 | 2023-06-09 | 默克专利股份公司 | 作为腺苷受体拮抗剂的喹喔啉衍生物 |
| TWI791593B (zh) | 2017-08-21 | 2023-02-11 | 德商馬克專利公司 | 做為腺苷受體拮抗劑之苯并咪唑衍生物 |
| KR20210083287A (ko) | 2018-10-25 | 2021-07-06 | 메르크 파텐트 게엠베하 | 아데노신 수용체 안타고니스트로서의 5-아자인다졸 유도체 |
| CA3117512A1 (en) | 2018-10-25 | 2020-04-30 | Merck Patent Gmbh | 5-azaindazole derivatives as adenosine receptor antagonists |
| AR117844A1 (es) | 2019-01-22 | 2021-09-01 | Merck Patent Gmbh | Derivados de tiazolopiridina como antagonistas del receptor de adenosina |
| KR20210061202A (ko) * | 2019-11-19 | 2021-05-27 | 일동제약(주) | 벤조나이트릴이 치환된 축합 피리미딘 유도체 및 그의 의약 용도 |
| US11806350B2 (en) | 2020-11-19 | 2023-11-07 | Ildong Pharmaceutical Co., Ltd. | Prevention and/or treatment of CNS disorders |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL264338A (de) * | 1960-05-04 | |||
| GB1004073A (en) * | 1962-08-13 | 1965-09-08 | Merck & Co Inc | Veterinary antihelmintic compositions comprising benzimidazole derivatives |
| JPS5441331A (en) * | 1977-06-29 | 1979-04-02 | Sandoz Ag | Antiistout agent |
| US4212876A (en) * | 1978-06-21 | 1980-07-15 | Sandoz, Inc. | Substituted or unsubstituted 2-phenylbenzimidazoles as anti-obesity agents |
| JPS60260579A (ja) * | 1984-01-13 | 1985-12-23 | Yoshitomi Pharmaceut Ind Ltd | プリン誘導体 |
| JPS61158983A (ja) * | 1984-12-28 | 1986-07-18 | Yoshitomi Pharmaceut Ind Ltd | プリン誘導体 |
| SU1282506A1 (ru) | 1985-05-11 | 1997-12-10 | Институт физико-органической химии и углехимии АН УССР | 2-(3',4',5'-триметоксифенил)-1-метилимидазо (4,5-с)пиридингидрохлорид, обладающий спазмолитической и гипотензивной активностью |
| US4772600A (en) * | 1986-06-09 | 1988-09-20 | A. H. Robins Company, Inc. | Fused imidazoheterocyclic compounds and pharmaceutical compositions |
| US4714762A (en) * | 1986-10-31 | 1987-12-22 | Warner-Lambert Company | Antiarteriosclerotic substituted benzimidazol-2-yl-and 3H-imidazo[4,5-b]pyridin-2-yl-phenoxy-alkanoic acids and salts and esters thereof |
| JP2869561B2 (ja) | 1989-05-22 | 1999-03-10 | 大塚製薬株式会社 | 血小板粘着抑制剤 |
| US5117830A (en) * | 1990-11-08 | 1992-06-02 | Whitby Research, Inc. | Method of determining viability of tissue |
| GB9125001D0 (en) * | 1991-11-25 | 1992-01-22 | Ici Plc | Heterocyclic compounds |
| HUT76280A (en) | 1993-12-29 | 1997-07-28 | Fujisawa Pharmaceutical Co | Pyrazolopyridine derivatives, pharmaceutical compositions containing them, process for proiducing them and their use |
| JPH07243069A (ja) * | 1994-03-08 | 1995-09-19 | Murata:Kk | 金属表面の電解処理方法 |
| US5552426A (en) | 1994-04-29 | 1996-09-03 | Eli Lilly And Company | Methods for treating a physiological disorder associated with β-amyloid peptide |
| JPH11508267A (ja) | 1995-06-26 | 1999-07-21 | 藤沢薬品工業株式会社 | ピラゾール化合物および医薬組成物 |
| CA2248013A1 (en) | 1996-03-11 | 1997-09-18 | Eli Lilly And Company | Methods of treating or preventing interstitial cystitis |
| ES2161455T3 (es) * | 1996-04-02 | 2001-12-01 | Microfibres Inc | Tejido de pelo flocado estampado mejorado y metodo para fabricar el mismo. |
| AU3255097A (en) | 1996-07-05 | 1998-02-02 | Novo Nordisk A/S | Novel (n)-alkoxyadenine derivatives acting as cytokine inhibitors |
| AUPO111096A0 (en) | 1996-07-18 | 1996-08-08 | Fujisawa Pharmaceutical Co., Ltd. | New compound |
| JP4021964B2 (ja) * | 1996-12-26 | 2007-12-12 | トーアエイヨー株式会社 | ピリダジノン誘導体、その製造法およびそれを含有するアデノシンa1拮抗剤 |
| US6284748B1 (en) * | 1997-03-07 | 2001-09-04 | Metabasis Therapeutics, Inc. | Purine inhibitors of fructose 1,6-bisphosphatase |
| CA2315736A1 (en) * | 1998-01-05 | 1999-07-15 | Eisai Co., Ltd. | Purine compounds and adenosine a2 receptor antagonist as preventive or therapeutic for diabetes mellitus |
| JP3990061B2 (ja) * | 1998-01-05 | 2007-10-10 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | プリン誘導体および糖尿病の予防・治療剤としてのアデノシンa2受容体拮抗剤 |
| WO1999057103A1 (en) | 1998-04-30 | 1999-11-11 | Nippon Chemiphar Co., Ltd. | Condensed imidazole derivative and therapeutic agent for liver disease |
-
2000
- 2000-06-30 NZ NZ516260A patent/NZ516260A/en not_active IP Right Cessation
- 2000-06-30 KR KR1020017016643A patent/KR100694684B1/ko not_active Expired - Fee Related
- 2000-06-30 CN CNB008098603A patent/CN1166666C/zh not_active Expired - Fee Related
- 2000-06-30 CA CA002376835A patent/CA2376835C/en not_active Expired - Fee Related
- 2000-06-30 JP JP2001507837A patent/JP4324338B2/ja not_active Expired - Fee Related
- 2000-06-30 WO PCT/JP2000/004358 patent/WO2001002400A1/ja not_active Ceased
- 2000-06-30 AT AT00940909T patent/ATE303387T1/de not_active IP Right Cessation
- 2000-06-30 EP EP00940909A patent/EP1221444B1/de not_active Expired - Lifetime
- 2000-06-30 AU AU55717/00A patent/AU778450B2/en not_active Ceased
- 2000-06-30 US US10/018,688 patent/US6841549B1/en not_active Expired - Fee Related
- 2000-06-30 DE DE60022366T patent/DE60022366T2/de not_active Expired - Lifetime
- 2000-06-30 PT PT00940909T patent/PT1221444E/pt unknown
- 2000-06-30 ES ES00940909T patent/ES2246867T3/es not_active Expired - Lifetime
- 2000-06-30 DK DK00940909T patent/DK1221444T3/da active
Also Published As
| Publication number | Publication date |
|---|---|
| JP4324338B2 (ja) | 2009-09-02 |
| PT1221444E (pt) | 2005-11-30 |
| KR100694684B1 (ko) | 2007-03-13 |
| CN1166666C (zh) | 2004-09-15 |
| NZ516260A (en) | 2004-08-27 |
| DE60022366D1 (de) | 2005-10-06 |
| CA2376835C (en) | 2009-09-15 |
| KR20020015060A (ko) | 2002-02-27 |
| DK1221444T3 (da) | 2005-11-14 |
| EP1221444A1 (de) | 2002-07-10 |
| AU5571700A (en) | 2001-01-22 |
| DE60022366T2 (de) | 2006-06-14 |
| WO2001002400A1 (en) | 2001-01-11 |
| CN1365361A (zh) | 2002-08-21 |
| WO2001002400A8 (en) | 2001-04-05 |
| CA2376835A1 (en) | 2001-01-11 |
| AU778450B2 (en) | 2004-12-09 |
| EP1221444A4 (de) | 2003-05-07 |
| EP1221444B1 (de) | 2005-08-31 |
| US6841549B1 (en) | 2005-01-11 |
| ES2246867T3 (es) | 2006-03-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ATE303387T1 (de) | Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitus | |
| EE200300403A (et) | N-asendatud mittearomaatne heterotsükliline ühend, seda sisaldav ravimkompositsioon ning ühendi kasutamine ravimina | |
| ATE388958T1 (de) | 4'-c-substituierte 2-haloadenosinderivate | |
| DK1213296T3 (da) | Glucopyranosyloxpyrazolderivater, lægemidler indeholdende samme samt mellemprodukter til fremstilling heraf | |
| WO2004048345A3 (en) | 2,5-diketopiperazines for the treatment of obesity | |
| PT976748E (pt) | Derivados de pirrolidina com actividade inibidora de fosfolipase a2 | |
| IL192605A0 (en) | 1,2-dihydropyridin-2-one derivatives and pharmaceutical compositions containing the same | |
| DE60012751D1 (de) | Verwendung von ep4 rezeptorliganden zur behandlung von neuropathischen schmerz | |
| NO985518L (no) | Morfinanderivater og medisinsk anvendelse derav | |
| CY1112899T1 (el) | Παραγωγα θειαδιαζολινης για τη θεραπεια του καρκινου | |
| NO20052074L (no) | Substituerte benzoksazinoner og anvendelser derav. | |
| ATE503746T1 (de) | Neue imidazolidinderivate | |
| DE60025616D1 (de) | Isoindolderivate | |
| NO20025035D0 (no) | Oksadiazolderivater som har anticancer-effekter | |
| DE60032016D1 (de) | Zyklische aminverbindungen als ccr5-rezeptor antagonisten | |
| DE60330758D1 (de) | Bestimmte pharmazeutisch wertvolle substituierte aminoalkyl-heterocyclen | |
| ATE402151T1 (de) | 2-(arylphenyl)amino-imidazolin-derivate | |
| WO2004080411A3 (en) | Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto | |
| IL169577A0 (en) | Oligosaccharide derivatives and pharmaceutical compostions containing the same | |
| ATE319452T1 (de) | Arzneimittel gegen essstörungen | |
| WO2007000392A3 (en) | Chloro-substituted guanidines | |
| DE60238847D1 (de) | Pyrimidinderivate enthaltendes medikament | |
| ATE262522T1 (de) | Benzimidazolverbindungen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| UEP | Publication of translation of european patent specification |
Ref document number: 1221444 Country of ref document: EP |
|
| EEIH | Change in the person of patent owner | ||
| REN | Ceased due to non-payment of the annual fee |