AU2001219236A1 - Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade - Google Patents
Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascadeInfo
- Publication number
- AU2001219236A1 AU2001219236A1 AU2001219236A AU1923601A AU2001219236A1 AU 2001219236 A1 AU2001219236 A1 AU 2001219236A1 AU 2001219236 A AU2001219236 A AU 2001219236A AU 1923601 A AU1923601 A AU 1923601A AU 2001219236 A1 AU2001219236 A1 AU 2001219236A1
- Authority
- AU
- Australia
- Prior art keywords
- useful
- coagulation cascade
- selective inhibition
- polycyclic aryl
- substituted polycyclic
- 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.)
- Abandoned
Links
- 230000015271 coagulation Effects 0.000 title 1
- 238000005345 coagulation Methods 0.000 title 1
- 125000001072 heteroaryl group Chemical group 0.000 title 1
- 230000005764 inhibitory process Effects 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
- C07D239/545—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
- C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
- C07D253/06—1,2,4-Triazines
- C07D253/065—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
- C07D253/07—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members 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
- C07D253/075—Two hetero atoms, in positions 3 and 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Chemical Kinetics & Catalysis (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)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/574,207 US6458952B1 (en) | 1999-05-19 | 2000-05-18 | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade |
| US09574207 | 2000-05-18 | ||
| PCT/US2000/031885 WO2001087852A1 (en) | 2000-05-18 | 2000-11-20 | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2001219236A1 true AU2001219236A1 (en) | 2001-11-26 |
Family
ID=24295129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2001219236A Abandoned AU2001219236A1 (en) | 2000-05-18 | 2000-11-20 | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade |
Country Status (3)
| Country | Link |
|---|---|
| US (2) | US6458952B1 (en) |
| AU (1) | AU2001219236A1 (en) |
| WO (1) | WO2001087852A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7015230B1 (en) * | 1999-05-19 | 2006-03-21 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade |
| PA8591801A1 (en) * | 2002-12-31 | 2004-07-26 | Pfizer Prod Inc | BENZAMID INHIBITORS OF THE P2X7 RECEIVER. |
| US7214825B2 (en) | 2003-10-17 | 2007-05-08 | Honeywell International Inc. | O-(3-chloropropenyl) hydroxylamine free base |
| KR20070115583A (en) * | 2004-06-29 | 2007-12-06 | 화이자 프로덕츠 인코포레이티드 | Unsubstituted 5- [4- (2-hydroxy-ethyl) -3,5-dioxo-4,5-dihydro-3H- [1,2,3-substituted at the 4-position of the triazine in the presence of a Lewis acid 4] Production method of the derivative having P2X7 inhibitory activity by reaction of triazin-2-yl] -benzamide derivative with oxirane |
| ES2618500T3 (en) | 2006-10-20 | 2017-06-21 | Neurendo Pharma, Llc | Method to restore the incretin effect |
| UA112897C2 (en) | 2012-05-09 | 2016-11-10 | Байєр Фарма Акцієнгезелльшафт | BICYCLIC SUBSTITUTED URATILES AND THEIR APPLICATIONS FOR THE TREATMENT AND / OR PREVENTION OF DISEASES |
| ES2787223T3 (en) | 2014-11-07 | 2020-10-15 | Univ Minnesota | Salts and compositions useful for treating diseases |
| CN116410143A (en) * | 2021-12-29 | 2023-07-11 | 杭州奥默医药股份有限公司 | A kind of multi-substituted uracil derivative and its preparation method and application |
Family Cites Families (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5910541A (en) * | 1982-07-09 | 1984-01-20 | Takeda Chem Ind Ltd | Quinone compound |
| JPS60255749A (en) * | 1984-05-31 | 1985-12-17 | Univ Nagoya | Quinone derivative |
| US5304658A (en) * | 1984-08-01 | 1994-04-19 | Takeda Chemical Industries, Ltd. | Quinone derivatives, their production and use |
| IL81264A (en) * | 1986-01-30 | 1990-11-05 | Takeda Chemical Industries Ltd | Quinone derivatives,their production and pharmaceutical compositions containing them |
| US5008267A (en) * | 1988-10-29 | 1991-04-16 | Mitsui Toatsu Chemicals, Incorporated | Pyrimidinedione compounds, method of producing the same and antiarrythmic agents containing the same |
| GB9216272D0 (en) | 1991-08-15 | 1992-09-09 | Ici Plc | Substituted heterocycles |
| CA2133657A1 (en) | 1992-04-16 | 1993-10-28 | Peter R. Bernstein | Substituted derivatives |
| US5441960A (en) | 1992-04-16 | 1995-08-15 | Zeneca Limited | 1-pyrimidinylacetamide human leukocyte elastate inhibitors |
| US5618792A (en) | 1994-11-21 | 1997-04-08 | Cortech, Inc. | Substituted heterocyclic compounds useful as inhibitors of (serine proteases) human neutrophil elastase |
| DE69526677T2 (en) | 1994-12-13 | 2002-12-05 | Corvas International, Inc. | AROMATIC HETEROCYCLIC DERIVATIVES AS ENZYMINHIBITORS |
| US5656645A (en) | 1994-12-13 | 1997-08-12 | Corvas International, Inc. | Aromatic heterocyclic derivatives as enzyme inhibitors |
| US5658930A (en) | 1994-12-13 | 1997-08-19 | Corvas International, Inc. | Aromatic heterocyclic derivatives as enzyme inhibitors |
| US6011158A (en) | 1994-12-13 | 2000-01-04 | Corvas International, Inc. | Aromatic heterocyclic derivatives as enzyme inhibitors |
| US5948785A (en) | 1995-04-27 | 1999-09-07 | The Green Cross Corporation | Heterocyclic amide compounds and pharmaceutical use of the same |
| US5612378A (en) | 1995-06-06 | 1997-03-18 | 3-Dimensional Pharmaceuticals, Inc. | Bis-arylsulfonylaminobenzamide derivatives and the use thereof as factor Xa inhibitors |
| US5741819A (en) | 1995-06-07 | 1998-04-21 | 3-Dimensional Pharmaceuticals, Inc. | Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors |
| JPH11508558A (en) | 1995-06-27 | 1999-07-27 | メルク エンド カンパニー インコーポレーテッド | Pyridinone thrombin inhibitor |
| AU720616B2 (en) | 1996-02-22 | 2000-06-08 | Merck & Co., Inc. | Pyridinone thrombin inhibitors |
| EE9800353A (en) | 1996-04-23 | 1999-04-15 | Merck & Co., Inc. | Pyrazinones thrombin inhibitors |
| US5668289A (en) | 1996-06-24 | 1997-09-16 | Merck & Co., Inc. | Pyridinone thrombin inhibitors |
| AU724191B2 (en) | 1996-08-29 | 2000-09-14 | Merck & Co., Inc. | Integrin antagonists |
| CA2263198A1 (en) | 1996-09-06 | 1998-03-12 | Nippon Kayaku Kabushiki Kaisha | Novel acetamide derivatives and protease inhibitors |
| WO1998010763A1 (en) | 1996-09-13 | 1998-03-19 | Merck & Co., Inc. | Thrombin inhibitors |
| US5872138A (en) | 1996-09-13 | 1999-02-16 | Merck & Co., Inc. | Thrombin inhibitors |
| JP2001502674A (en) | 1996-10-11 | 2001-02-27 | シーオーアール・セラピューティックス・インコーポレーテッド | Selective factor Xa inhibitor |
| CA2268381A1 (en) | 1996-10-11 | 1998-04-23 | Cor Therapeutics, Inc. | Selective factor xa inhibitors |
| AU715305B2 (en) | 1996-10-24 | 2000-01-20 | Merck & Co., Inc. | Thrombin inhibitors |
| US5869487A (en) | 1996-10-24 | 1999-02-09 | Merck & Co., Inc. | Pyrido 3,4-B!pyrazines for use as thrombin inhibitors |
| CN1088706C (en) | 1996-10-25 | 2002-08-07 | 卫福有限公司 | Novel heterocyclic amide compound and its medical application |
| AU722429B2 (en) | 1997-01-22 | 2000-08-03 | Merck & Co., Inc. | Thrombin inhibitors |
| US5792779A (en) | 1997-02-19 | 1998-08-11 | Merck & Co., Inc. | Pyridinone thrombin inhibitors |
| JP2001518932A (en) | 1997-03-24 | 2001-10-16 | メルク エンド カンパニー インコーポレーテッド | Thrombin inhibitors |
| US5866573A (en) | 1997-04-21 | 1999-02-02 | Merck & Co., Inc. | Pyrazinone thrombin inhibitors |
| IL123986A (en) | 1997-04-24 | 2011-10-31 | Organon Nv | Serine protease inhibiting antithrombotic agents and pharmaceutical compositions comprising them |
| KR20010012174A (en) | 1997-05-02 | 2001-02-15 | 에프.지.엠. 헤르만스 ; 이.에이치. 리링크 | Serine protease inhibitors |
| IL133621A0 (en) | 1997-06-26 | 2001-04-30 | Lilly Co Eli | Antithrombotic agents |
| ES2241151T3 (en) | 1997-06-26 | 2005-10-16 | Eli Lilly And Company | ANTITROMBOTIC AGENTS. |
| EP0999834B1 (en) | 1997-06-26 | 2005-10-12 | Eli Lilly And Company | Antithrombotic agents |
| CA2301520A1 (en) | 1997-09-05 | 1999-03-11 | Merck & Co., Inc. | Pyrazinone thrombin inhibitors |
| US6037356A (en) | 1997-11-26 | 2000-03-14 | 3-Dimensional Pharmaceuticals, Inc. | Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors |
| AU1605699A (en) | 1997-11-26 | 1999-06-15 | Corvas International, Inc. | Substituted 3-amino-2-hydroxyphenylacetamide derivatives as enzyme inhibitors (ii) |
| JP2002509153A (en) | 1998-01-20 | 2002-03-26 | ワーナー−ランバート・カンパニー | N- [2- (5-benzyloxycarbonyl-amino-6-oxo-2- (4-fluorophenyl) -1,6-dihydro-1-) as an in vivo inhibitor of interleukin-1β converting enzyme (ICE) Pyrimidinyl) acetoxyl] -L-aspartic aldehyde |
| AU753479B2 (en) | 1998-05-19 | 2002-10-17 | Merck & Co., Inc. | Pyrazinone thrombin inhibitors |
| JP2002516326A (en) | 1998-05-26 | 2002-06-04 | メルク エンド カムパニー インコーポレーテッド | Imidazopyridine thrombin inhibitors |
| EP1089752A4 (en) | 1998-06-03 | 2002-01-02 | Cortech Inc | Alpha-keto oxadiazoles as serine protease inhibitors |
| EP1589029B1 (en) | 1998-06-11 | 2010-03-17 | Ortho-McNeil Pharmaceuticals, Inc. | Pyrazinone protease inhibitors |
| DK0997474T3 (en) | 1998-08-14 | 2004-02-09 | Pfizer | Antithrombotic agents |
| CA2343109A1 (en) | 1998-09-28 | 2000-04-06 | Merck & Co., Inc. | Thrombin inhibitors |
| AU747776B2 (en) | 1998-10-30 | 2002-05-23 | Merck & Co., Inc. | Thrombin inhibitors |
| JP2002528542A (en) | 1998-10-30 | 2002-09-03 | メルク エンド カムパニー インコーポレーテッド | Thrombin inhibitor |
| FR2786482B1 (en) | 1998-11-27 | 2002-08-09 | Synthelabo | NOVEL 2-PYRIDONE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
| WO2000038683A1 (en) | 1998-12-23 | 2000-07-06 | Du Pont Pharmaceuticals Company | THROMBIN OR FACTOR Xa INHIBITORS |
| JP2002544263A (en) | 1999-05-19 | 2002-12-24 | ファルマシア・コーポレイション | Substituted polycyclic aryl and heteroaryl uracils as anticoagulants |
| NZ514875A (en) | 1999-05-19 | 2004-10-29 | Pharmacia Corp | Substituted polycyclic aryl and heteroaryl pyridones useful for selective inhibition of the coagulation cascade |
| PL352827A1 (en) | 1999-05-19 | 2003-09-08 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrymidinones useful as anticoagulants |
-
2000
- 2000-05-18 US US09/574,207 patent/US6458952B1/en not_active Expired - Fee Related
- 2000-11-20 WO PCT/US2000/031885 patent/WO2001087852A1/en not_active Ceased
- 2000-11-20 AU AU2001219236A patent/AU2001219236A1/en not_active Abandoned
-
2002
- 2002-08-08 US US10/215,292 patent/US20030023086A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US6458952B1 (en) | 2002-10-01 |
| US20030023086A1 (en) | 2003-01-30 |
| WO2001087852A1 (en) | 2001-11-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IL146244A0 (en) | Substituted polycyclic aryl and heteroaryl pyridones useful for selective inhibition of the coagulation cascade | |
| IL146245A0 (en) | Substituted polycyclic aryl and heteroaryl pyrazinones useful for selective inhibition of the coagulation cascade | |
| AU2001265141A1 (en) | Multifunctional periodic cellular solids and the method of making thereof | |
| AU2002256418A1 (en) | Inhibitors of bace | |
| AU2001238426A1 (en) | Prepaints and methods of preparing paints from the prepaints | |
| AU2862100A (en) | Materials and methods for the purification of polyelectrolytes | |
| AU2001275870A1 (en) | Methods and kits for the detection of arginine compounds | |
| AU2001243598A1 (en) | Polycyclic aryl and heteroaryl substituted benzenes useful for selective inhibition of the coagulation cascade | |
| AU2003303926A1 (en) | Ceramics and methods of making the same | |
| AU2002211370A1 (en) | Inhibition of tgf-beta and uses thereof | |
| AU2001219236A1 (en) | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade | |
| AU2002214189A1 (en) | Methods of identifying inhibitory compounds and uses thereof | |
| AU2002367752A1 (en) | Substituted 5-membered polycyclic compounds useful for selective inhibition of the coagulation cascade | |
| AU2001222501A1 (en) | Substituted polycyclic aryl and heteroaryl pyrimidinones useful for selective inhibition of the coagulation cascade | |
| AU2002337843A1 (en) | Processes for the preparation of substituted isoxazoles and 2-isoxazolines | |
| AU2001262111A1 (en) | Aryl and heteroaryl sulfonates | |
| AU2001217827A1 (en) | Substituted polycyclic aryl and heteroaryl pyridones useful for selective inhibition of the coagulation cascade | |
| AU2002359792A1 (en) | Methods and compositions for the inhibition of viral release | |
| AU2002338989A1 (en) | Substituted C-furan-2-yl-methylamine and C-thiophen-2-yl-methylamine derivatives | |
| HK1047092A (en) | Substituted polycyclic aryl and heteroaryl pyrazinones useful for selective inhibition of the coagulation cascade | |
| AU2001286584A1 (en) | Inhibition of protein-protein interaction | |
| AU2002334854A1 (en) | 6-membered heterocyclic compounds useful for selective inhibition of the coagulation cascade | |
| AU2002360614A1 (en) | Methods of inhibiting fertility | |
| AU2002220591A1 (en) | Means for the identification of compounds capable of inhibiting karap-transduced signals | |
| AU2001283789A1 (en) | Trap for the purification of drainwater |