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 cascade

Info

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
Application number
AU2001219236A
Inventor
Darin E. Jones
Melvin L. Rueppel
Michael S. South
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pharmacia LLC
Original Assignee
Pharmacia LLC
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Pharmacia LLC filed Critical Pharmacia LLC
Publication of AU2001219236A1 publication Critical patent/AU2001219236A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C07D239/545Two 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D253/00Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
    • C07D253/02Heterocyclic 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
    • C07D253/061,2,4-Triazines
    • C07D253/0651,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
    • C07D253/071,2,4-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
    • C07D253/075Two hetero atoms, in positions 3 and 5
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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)
AU2001219236A 2000-05-18 2000-11-20 Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade Abandoned AU2001219236A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US09574207 2000-05-18
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
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 (7)

* Cited by examiner, † Cited by third party
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.
MXPA06015273A (en) * 2004-06-29 2007-03-15 Pfizer Prod Inc Method for preparing 5-`4-(2-hydroxy -ethyl)-3, 5-dioxo-4, 5-dihydro-3h-`1, 2, 4!-triazin-2 -yl!benzamide derivatives with p2x7 inhibiting activity by reaction of the derivative unsubstituted in 4-position of the triazine with an oxiran in the presen
SI2724722T1 (en) * 2006-10-20 2017-07-31 Neurendo Pharma, Llc Method of restoring 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
CN107405343A (en) 2014-11-07 2017-11-28 明尼苏达大学董事会 Salt and composition available for treatment disease
CN116410143A (en) * 2021-12-29 2023-07-11 杭州奥默医药股份有限公司 Polysubstituted uracil derivative, preparation method and application thereof

Family Cites Families (55)

* Cited by examiner, † Cited by third party
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
DE69314169T2 (en) 1992-04-16 1998-01-15 Zeneca Ltd PEPTIDES WITH AN ALPHAAMINOBORONAIRE GROUP AND THEIR USE AS AN ELASTASE INHIBITOR
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 Int 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
KR100400639B1 (en) 1995-04-27 2003-12-31 미쯔비시 웰 파마 가부시키가이샤 Heterocyclic amide compounds and their medicinal uses
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
CA2224437A1 (en) 1995-06-27 1997-01-16 Merck & Co., Inc. Pyridinone-thrombin inhibitors
CA2245811A1 (en) 1996-02-22 1997-08-28 Merck & Co., Inc. Pyridinone thrombin inhibitors
JP3140790B2 (en) 1996-04-23 2001-03-05 メルク エンド カンパニー インコーポレーテッド Pyrazinone thrombin inhibitors
US5668289A (en) 1996-06-24 1997-09-16 Merck & Co., Inc. Pyridinone thrombin inhibitors
EP0934305A4 (en) 1996-08-29 2001-04-11 Merck & Co Inc Integrin antagonists
CN1169791C (en) 1996-09-06 2004-10-06 日本化药株式会社 Novel acetamide derivatives and protease inhibitors
US5872138A (en) 1996-09-13 1999-02-16 Merck & Co., Inc. Thrombin inhibitors
EP0927035A4 (en) 1996-09-13 2002-11-13 Merck & Co Inc Thrombin inhibitors
AU743544B2 (en) 1996-10-11 2002-01-31 Millennium Pharmaceuticals, Inc. Selective factor Xa inhibitors
EP0932615A1 (en) 1996-10-11 1999-08-04 Cor Therapeutics, Inc. SELECTIVE FACTOR Xa INHIBITORS
US5869487A (en) 1996-10-24 1999-02-09 Merck & Co., Inc. Pyrido 3,4-B!pyrazines for use as thrombin inhibitors
ATE234091T1 (en) 1996-10-24 2003-03-15 Merck & Co Inc THROMBIN INHIBITORS
CN1088706C (en) 1996-10-25 2002-08-07 卫福有限公司 Novel heterocyclic amide compound and medical use thereof
JP2001508796A (en) 1997-01-22 2001-07-03 メルク エンド カンパニー インコーポレーテッド Thrombin inhibitors
US5792779A (en) 1997-02-19 1998-08-11 Merck & Co., Inc. Pyridinone thrombin inhibitors
EP0969840A4 (en) 1997-03-24 2001-02-28 Merck & Co Inc 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
AU729910B2 (en) 1997-05-02 2001-02-15 Akzo Nobel N.V. Serine protease inhibitors
CA2295153A1 (en) 1997-06-26 1999-01-07 Gerald Floyd Smith Antithrombotic agents
IL133621A0 (en) 1997-06-26 2001-04-30 Lilly Co Eli Antithrombotic agents
IL133623A0 (en) 1997-06-26 2001-04-30 Lilly Co Eli Antithrombotic agents
EP1017393A4 (en) 1997-09-05 2002-01-23 Merck & Co Inc Pyrazinone thrombin inhibitors
AU1605699A (en) 1997-11-26 1999-06-15 Corvas International, Inc. Substituted 3-amino-2-hydroxyphenylacetamide derivatives as enzyme inhibitors (ii)
AU751412B2 (en) 1997-11-26 2002-08-15 3-Dimensional Pharmaceuticals, Inc. Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors
ATE232536T1 (en) 1998-01-20 2003-02-15 Warner Lambert Co N-(2-(5-BENZYLOXYCARBONYL-AMINO-6-OXO-2-(4-
WO1999059591A1 (en) 1998-05-19 1999-11-25 Merck & Co., Inc. Pyrazinone thrombin inhibitors
AU742178B2 (en) 1998-05-26 2001-12-20 Merck & Co., Inc. Imidazopyridine thrombin inhibitors
JP2003520185A (en) 1998-06-03 2003-07-02 コーテック インコーポレーテッド Α-Ketooxadiazoles as serine protease inhibitors
CA2334679C (en) 1998-06-11 2012-10-23 3-Dimensional Pharmaceuticals, Inc. Pyrazinone protease inhibitors
ATE253076T1 (en) * 1998-08-14 2003-11-15 Pfizer ANTITHROMBOTIC DRUGS
AU758237B2 (en) 1998-09-28 2003-03-20 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
AU747776B2 (en) 1998-10-30 2002-05-23 Merck & Co., Inc. Thrombin inhibitors
FR2786482B1 (en) 1998-11-27 2002-08-09 Synthelabo NOVEL 2-PYRIDONE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
AU3127900A (en) 1998-12-23 2000-07-31 Du Pont Pharmaceuticals Company Thrombin or factor xa inhibitors
CA2373614A1 (en) 1999-05-19 2000-11-23 Pharmacia Corporation Substituted polycyclic aryl and heteroaryl pyrymidinones useful as anticoagulants
AU771928B2 (en) 1999-05-19 2004-04-08 Pharmacia Corporation Substituted polycyclic aryl and heteroaryl pyridones useful for selective inhibition of the coagulation cascade
BR0011273A (en) 1999-05-19 2002-06-18 Pharmacia Corp Heteroaryl and polycyclic aryl uracils substituted as anticoagulant agents

Also Published As

Publication number Publication date
US20030023086A1 (en) 2003-01-30
US6458952B1 (en) 2002-10-01
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
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
PL352368A1 (en) Substituted polycyclic aryl and heteroaryl pyrazinones useful for selective inhibition of the coagulation cascade
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
AU2001288360A1 (en) Genomics-assisted rapid identification of targets
AU2001219236A1 (en) Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade
AU2002367752A1 (en) Substituted 5-membered polycyclic compounds useful for selective inhibition of the coagulation cascade
AU2001255754A1 (en) Methods and compositions for the manufacture of molecular beacons
AU2001262111A1 (en) Aryl and heteroaryl sulfonates
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
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
AU2001225523A1 (en) Novel arylpropionaldehyde derivatives and production and use of the same
AU2001286584A1 (en) Inhibition of protein-protein interaction
AU2002334854A1 (en) 6-membered heterocyclic compounds useful for selective inhibition of the coagulation cascade
WO2003020115A9 (en) Methods and compositions for the detection of cancer
AU2002220591A1 (en) Means for the identification of compounds capable of inhibiting karap-transduced signals