AU2001296854A1 - Pyrazole compounds, pharmaceutical compositions, and methods for modulating or inhibiting erab or hadh2 activity - Google Patents

Pyrazole compounds, pharmaceutical compositions, and methods for modulating or inhibiting erab or hadh2 activity

Info

Publication number
AU2001296854A1
AU2001296854A1 AU2001296854A AU9685401A AU2001296854A1 AU 2001296854 A1 AU2001296854 A1 AU 2001296854A1 AU 2001296854 A AU2001296854 A AU 2001296854A AU 9685401 A AU9685401 A AU 9685401A AU 2001296854 A1 AU2001296854 A1 AU 2001296854A1
Authority
AU
Australia
Prior art keywords
hadh2
erab
modulating
inhibiting
activity
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
AU2001296854A
Inventor
Melwyn A Abreo
Charles Scott Agree
Jerry J. Meng
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.)
Agouron Pharmaceuticals LLC
Original Assignee
Agouron Pharmaceuticals 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 Agouron Pharmaceuticals LLC filed Critical Agouron Pharmaceuticals LLC
Publication of AU2001296854A1 publication Critical patent/AU2001296854A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • 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
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A90/00—Technologies having an indirect contribution to adaptation to climate change
    • Y02A90/10—Information and communication technologies [ICT] supporting adaptation to climate change, e.g. for weather forecasting or climate simulation
AU2001296854A 2000-08-18 2001-08-17 Pyrazole compounds, pharmaceutical compositions, and methods for modulating or inhibiting erab or hadh2 activity Abandoned AU2001296854A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US22612300P 2000-08-18 2000-08-18
US60226123 2000-08-18
PCT/US2001/041795 WO2002016365A1 (en) 2000-08-18 2001-08-17 Pyrazole compounds, pharmaceutical compositions, and methods for modulating or inhibiting erab or hadh2 activity

Publications (1)

Publication Number Publication Date
AU2001296854A1 true AU2001296854A1 (en) 2002-03-04

Family

ID=22847647

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2001296854A Abandoned AU2001296854A1 (en) 2000-08-18 2001-08-17 Pyrazole compounds, pharmaceutical compositions, and methods for modulating or inhibiting erab or hadh2 activity

Country Status (14)

Country Link
US (2) US6964957B2 (en)
EP (2) EP1311511A1 (en)
JP (2) JP2004506737A (en)
AR (1) AR035486A1 (en)
AU (1) AU2001296854A1 (en)
BR (1) BR0113461A (en)
CA (2) CA2354653A1 (en)
GT (1) GT200100169A (en)
HK (1) HK1046288A1 (en)
MX (1) MXPA03001455A (en)
PA (1) PA8525801A1 (en)
PE (1) PE20020394A1 (en)
UY (1) UY26895A1 (en)
WO (1) WO2002016365A1 (en)

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DE10221052A1 (en) * 2002-05-10 2003-12-04 Transmit Technologietransfer Active substances for therapy, diagnostics and prophylaxis of diseases in which abnormal protein structures occur
CA2565308A1 (en) * 2003-05-06 2004-11-25 New Century Pharmaceuticals Albumin binding sites for evaluating drug interactions and methods of evaluating or designing drugs based on their albumin binding properties
WO2005041895A2 (en) * 2003-11-03 2005-05-12 New Century Pharmaceuticals, Inc. Albumin binding sites for evaluating drug interactions and methods of evaluating or designing drugs based on their albumin binding properties
US20080274975A1 (en) * 2004-04-12 2008-11-06 The Trustees Of Columbia University In The City Of New Yourk Methods and Compositions for Inhibiting Abad/Abeta Protein Interaction
CA2583439C (en) * 2004-09-24 2016-05-10 University Of Maryland, Baltimore Method of treating organophosphorous poisoning
US9132135B2 (en) * 2004-09-24 2015-09-15 University Of Maryland, Baltimore Method of treating organophosphorous poisoning
WO2010118367A2 (en) * 2009-04-10 2010-10-14 Progenics Pharmaceuticals, Inc. Antiviral pyrimidines
MA41291A (en) 2014-12-30 2017-11-07 Forma Therapeutics Inc PYRROLOTRIAZINONE AND IMIDAZOTRIAZINONE DERIVATIVES AS UBIQUE-SPECIFIC PROTEASE INHIBITORS No. 7 (USP7) FOR THE TREATMENT OF CANCER
TWI698436B (en) 2014-12-30 2020-07-11 美商佛瑪治療公司 Pyrrolo and pyrazolopyrimidines as ubiquitin-specific protease 7 inhibitors
WO2016126926A1 (en) 2015-02-05 2016-08-11 Forma Therapeutics, Inc. Quinazolinones and azaquinazolinones as ubiquitin-specific protease 7 inhibitors
EP3253759A1 (en) 2015-02-05 2017-12-13 Forma Therapeutics, Inc. Isothiazolopyrimidinones, pyrazolopyrimidinones, and pyrrolopyrimidinones as ubiquitin-specific protease 7 inhibitors
US9932351B2 (en) 2015-02-05 2018-04-03 Forma Therapeutics, Inc. Thienopyrimidinones as ubiquitin-specific protease 7 inhibitors
WO2023146880A1 (en) * 2022-01-25 2023-08-03 Board Of Regents Of The University Of Nebraska Functionalized allopurinol derivatives for treatment of alzheimer's disease

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US3165520A (en) 1965-01-12 Certificate of correction
US4666908A (en) 1985-04-05 1987-05-19 Warner-Lambert Company 5-Substituted pyrazolo[4,3-d]pyrimidine-7-ones and methods of use
DE68908786T2 (en) 1988-06-16 1994-03-17 Smith Kline French Lab Condensed pyrimidine derivatives, processes and intermediates for their preparation and pharmaceutical preparations containing them.
US5109119A (en) * 1989-06-06 1992-04-28 Schering Corporation Crystalline r-h-gm-csf and method
GB9013750D0 (en) 1990-06-20 1990-08-08 Pfizer Ltd Therapeutic agents
GB9114760D0 (en) 1991-07-09 1991-08-28 Pfizer Ltd Therapeutic agents
US5294612A (en) 1992-03-30 1994-03-15 Sterling Winthrop Inc. 6-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-ones and compositions and method of use thereof
US5322933A (en) * 1992-05-07 1994-06-21 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Crystal structure of TGF-β-2
PH31122A (en) 1993-03-31 1998-02-23 Eisai Co Ltd Nitrogen-containing fused-heterocycle compounds.
US5294611A (en) 1993-04-23 1994-03-15 American Cyanamid Company Angiotensin II receptor blocking 2,3,6 substituted quinazolinones
GB9301192D0 (en) 1993-06-09 1993-06-09 Trott Francis W Flower shaped mechanised table
US5556778A (en) * 1994-04-28 1996-09-17 Albert Einstein College Of Medicine Of Yeshiva University, A Division Of Yeshiva University Crystalline Inha Enzyme-NADH Complex
CN1056611C (en) 1994-06-16 2000-09-20 美国辉瑞有限公司 Pyrazolo and pyrrolopyridines
US5756466A (en) 1994-06-17 1998-05-26 Vertex Pharmaceuticals, Inc. Inhibitors of interleukin-1β converting enzyme
GB9423910D0 (en) 1994-11-26 1995-01-11 Pfizer Ltd Therapeutic agents
US5656629A (en) 1995-03-10 1997-08-12 Sanofi Winthrop, Inc. 6-substituted pyrazolo (3,4-d)pyrimidin-4-ones and compositions and methods of use thereof
US6555651B2 (en) 1997-10-09 2003-04-29 The Trustees Of Columbia University In The City Of New York Ligand binding site of rage and uses thereof
US6153652A (en) 1996-11-22 2000-11-28 Elan Pharmaceuticals, Inc. N-(aryl/heteroaryl/alkylacetyl) amino acid amides, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
US6268479B1 (en) * 1997-03-12 2001-07-31 The Trustees Of Columbia University In The City Of New York Intracellular amyloid-beta peptide binding (ERAB) polypeptide
BR9808845A (en) 1997-03-14 2000-08-01 Otsuka Pharma Co Ltd Pyrimidine derivative, agents for curing an allergic disease, asthma and atopic dermatitis, agents for inhibiting the production of tnf-alpha, cytokines and 5-lipoxygenase, processes for curing an allergic disease, asthma and atopic dermatitis and to inhibit the production of no, tnf-alpha and cytokines and 5-lipoxygenase and uses of a compound
PL336586A1 (en) 1997-04-25 2000-07-03 Pfizer Pyrazoylpyrimidinones inhibiting the cyclic guanosine 3',5'-monophosphate phosphodiesterase of type 5 (cgmp pde5) for treating sexual disorders
US6020162A (en) * 1997-06-13 2000-02-01 The Rockefeller University Crystal of a protein-ligand complex containing an N-terminal truncated eIF4E, and methods of use thereof
US5872011A (en) * 1997-06-13 1999-02-16 The Rockefeller University Crystal of a protein-ligand complex containing an N-terminal truncated eIF4E, and methods of use thereof
ATE355841T1 (en) 1997-12-13 2007-03-15 Bristol Myers Squibb Co USE OF PYRAZOLO (3,4-B)PYRIDINE AS A CYCLINE-DEPENDENT KINASE INHIBITOR
US6194410B1 (en) 1998-03-11 2001-02-27 Hoffman-La Roche Inc. Pyrazolopyrimidine and pyrazolines and process for preparation thereof
GB9822238D0 (en) 1998-10-12 1998-12-09 Pfizer Ltd Process for preparation of pyrazolo[4,3-D]pyrimidin-7-ones and intermediates thereof
AUPP672198A0 (en) 1998-10-23 1998-11-19 Fujisawa Pharmaceutical Co., Ltd. Pyrazolopyridine compound and pharmaceutical use thereof
MXPA01011112A (en) 1999-06-10 2002-06-04 Warner Lambert Co Method of inhibiting amyloid protein aggregation and imaging amyloid deposits using isoindoline derivatives.
MXPA01009863A (en) 1999-06-10 2002-05-06 Warner Lambert Co Rhodanine derivatives and their use in inhibiting and imaging amyloids.
BR0011441A (en) 1999-06-10 2002-07-16 Warner Lambert Co Rhodanine derivatives for use in a method of inhibiting amyloid protein aggregation and imaging amyloid deposits
CA2382095A1 (en) 1999-08-13 2001-02-22 The Trustees Of Columbia University In The City Of New York Methods of inhibiting binding of .beta.-sheet fibril to rage and consequences thereof

Also Published As

Publication number Publication date
CA2354653A1 (en) 2002-02-18
BR0113461A (en) 2003-07-01
PE20020394A1 (en) 2002-06-21
EP1223176A2 (en) 2002-07-17
JP2002360269A (en) 2002-12-17
EP1311511A1 (en) 2003-05-21
PA8525801A1 (en) 2002-08-29
GT200100169A (en) 2002-05-16
EP1223176A3 (en) 2002-10-23
UY26895A1 (en) 2002-04-26
HK1046288A1 (en) 2003-01-03
WO2002016365A1 (en) 2002-02-28
MXPA03001455A (en) 2004-05-04
CA2415182A1 (en) 2002-02-28
JP2004506737A (en) 2004-03-04
AR035486A1 (en) 2004-06-02
US20020065292A1 (en) 2002-05-30
US6964957B2 (en) 2005-11-15
US20020132319A1 (en) 2002-09-19

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