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AU2001239791A1 - Succinoylamino carbocycles and heterocycles as inhibitors of abeta protein production - Google Patents

Succinoylamino carbocycles and heterocycles as inhibitors of abeta protein production

Info

Publication number
AU2001239791A1
AU2001239791A1AU2001239791AAU3979101AAU2001239791A1AU 2001239791 A1AU2001239791 A1AU 2001239791A1AU 2001239791 AAU2001239791 AAU 2001239791AAU 3979101 AAU3979101 AAU 3979101AAU 2001239791 A1AU2001239791 A1AU 2001239791A1
Authority
AU
Australia
Prior art keywords
succinoylamino
carbocycles
heterocycles
inhibitors
protein production
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
AU2001239791A
Inventor
Wei Deng
Hong Liu
Thomas P. MADUSKUIE JR.
Richard E. Olson
Andrew J. Tebben
Lorin Andrew Thompson
Nenghui Wang
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.)
Bristol Myers Squibb Pharma Co
Original Assignee
DuPont Merck Pharmaceutical Co
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 DuPont Merck Pharmaceutical CofiledCriticalDuPont Merck Pharmaceutical Co
Publication of AU2001239791A1publicationCriticalpatent/AU2001239791A1/en
Abandonedlegal-statusCriticalCurrent

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AU2001239791A2000-02-172001-02-16Succinoylamino carbocycles and heterocycles as inhibitors of abeta protein productionAbandonedAU2001239791A1 (en)

Applications Claiming Priority (3)

Application NumberPriority DateFiling DateTitle
US18318600P2000-02-172000-02-17
US601831862000-02-17
PCT/US2001/005236WO2001060826A2 (en)2000-02-172001-02-16SUCCINOYLAMINO CARBOCYCLES AND HETEROCYCLES AS INHIBITORS OF Aβ PROTEIN PRODUCTION

Publications (1)

Publication NumberPublication Date
AU2001239791A1true AU2001239791A1 (en)2001-08-27

Family

ID=22671796

Family Applications (1)

Application NumberTitlePriority DateFiling Date
AU2001239791AAbandonedAU2001239791A1 (en)2000-02-172001-02-16Succinoylamino carbocycles and heterocycles as inhibitors of abeta protein production

Country Status (6)

CountryLink
US (1)US6525044B2 (en)
EP (1)EP1261610A2 (en)
JP (1)JP2003523345A (en)
AU (1)AU2001239791A1 (en)
CA (1)CA2395862A1 (en)
WO (1)WO2001060826A2 (en)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
HRP990246A2 (en)1998-08-072000-06-30Du Pont Pharm CoSuccinoylamino benzodiazepines as inhibitors of a beta protein production
NZ525513A (en)1998-08-072004-09-24Pont Pharmaceuticals DuSuccinoylamino lactams as inhibitors of Abeta protein production
EP1313426A2 (en)1998-12-242003-05-28Bristol-Myers Squibb Pharma CompanySuccinoylamino benzodiazepines as inhibitors of a-beta protein production
CA2395862A1 (en)2000-02-172001-08-23Hong LiuSuccinoylamino carbocycles and heterocycles as inhibitors of a.beta. protein production
MXPA02009755A (en)2000-04-032003-03-27Bristol Myers Squibb Pharma CoCYCLIC LACTAMS AS INHIBITORS OF Abeta PROTEIN PRODUCTION.
MXPA02009729A (en)2000-04-032003-03-27Bristol Myers Squibb Pharma CoCYCLIC LACTAMS AS INHIBITORS OF A beta PROTEIN PRODUCTION.
US7640062B2 (en)2000-05-082009-12-29Brainsgate Ltd.Methods and systems for management of alzheimer's disease
US7146209B2 (en)*2000-05-082006-12-05Brainsgate, Ltd.Stimulation for treating eye pathologies
AU2001261728A1 (en)2000-05-172001-11-26Bristol-Myers Squibb Pharma CompanyUse of small molecule radioligands for diagnostic imaging
BR0106717A (en)2000-06-012002-04-16Bristol Myers Squibb Pharma Co Compounds, pharmaceutical composition and uses of innovative lactam compounds
EP1466898A4 (en)*2001-12-272005-12-07Daiichi Seiyaku CoBeta-amyloid protein production/secretion inhibitors
US7684859B2 (en)*2002-04-252010-03-23Brainsgate Ltd.Stimulation of the OTIC ganglion for treating medical conditions
JP2006500318A (en)*2002-04-252006-01-05ブレインスゲート リミテッド Method and apparatus for adjusting the characteristics of BBB and cerebral circulation using nerve excitatory and / or neurosuppressive effects of odorants on the intracranial nerve
EP1585430B1 (en)*2002-11-142017-01-11Brainsgate Ltd.Surgical tools and techniques for stimulation
US8055347B2 (en)2005-08-192011-11-08Brainsgate Ltd.Stimulation for treating brain events and other conditions
US8010189B2 (en)*2004-02-202011-08-30Brainsgate Ltd.SPG stimulation for treating complications of subarachnoid hemorrhage
US9233245B2 (en)2004-02-202016-01-12Brainsgate Ltd.SPG stimulation
WO2006021957A2 (en)*2004-08-232006-03-02Brainsgate Ltd.Concurrent bilateral spg modulation
EP1966169A2 (en)*2005-12-292008-09-10Immupharma France SACompositions and methods for the inhibition of phospholipase a2
CA2635359A1 (en)*2005-12-292007-07-05Immupharma France SaCompositions and methods for synthesizing heterocyclic therapeutic compounds
US20090210026A1 (en)*2006-08-172009-08-20Brainsgate Ltd.Spg stimulation for enhancing neurogenesis and brain metabolism
US20100204230A1 (en)2007-02-122010-08-12Peter BlurtonPiperazine derivatives for treatment of ad and related conditions
CN101284828B (en)*2007-04-122011-04-27中国科学院上海药物研究所 Cycloheptanepyridine compounds, their preparation method, use and pharmaceutical composition containing such compounds
US7860569B2 (en)2007-10-182010-12-28Brainsgate, Ltd.Long-term SPG stimulation therapy for prevention of vascular dementia
CN101945853B (en)2007-12-212014-08-20配体药物公司Selective androgen receptor modulators (sarms) and uses thereof
EP2291181B9 (en)2008-04-182013-09-11University College Dublin National University Of Ireland, DublinCaptodiamine for the treatment of depression symptoms
CA2767764A1 (en)2009-07-132011-01-20Takeda Pharmaceutical Company LimitedHeterocyclic compound and use thereof
CN103249733A (en)2010-09-022013-08-14武田药品工业株式会社Fused triazoles for the treatment or prophylaxis of mild cognitive impairment
TWI530489B (en)2011-03-222016-04-21必治妥美雅史谷比公司 Bis(fluoroalkyl)-1,4-benzodiazepine compound
GB201116559D0 (en)2011-09-262011-11-09Univ Leuven KathNovel viral replication inhibitors
US9242941B2 (en)2012-09-212016-01-26Bristol-Myers Squibb CompanyAlkyl, fluoroalkyl-1,4-benzodiazepinone compounds
US9242940B2 (en)2012-09-212016-01-26Bristol-Myers Squibb CompanyN-substituted bis(fluoroalkyl)-1,4-benzodiazepinone compounds
US9427442B2 (en)2012-09-212016-08-30Bristol-Myers Squibb CompanyFluoroalkyl and fluorocycloalkyl 1,4-benzodiazepinone compounds
EP2897944B1 (en)*2012-09-212016-10-26Bristol-Myers Squibb CompanySubstituted 1,5-benzodiazepinone compounds
JP2015529250A (en)2012-09-212015-10-05ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Fluoroalkyldibenzodiazepinone compounds
TWI614238B (en)*2012-09-212018-02-11必治妥美雅史谷比公司 Bis(fluoroalkyl)-1,4-benzodiazepine compounds and prodrugs thereof
JP2015529251A (en)2012-09-212015-10-05ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Tricyclic heterocyclic compounds as NOTCH inhibitors
JP2015531792A (en)2012-09-212015-11-05ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Prodrugs of 1,4-benzodiazepinone compounds
WO2014047392A1 (en)2012-09-212014-03-27Bristol-Myers Squibb CompanyFluoroalkyl-1,4-benzodiazepinone compounds
EP2981267A1 (en)2013-04-042016-02-10Bristol-Myers Squibb CompanyCombination therapy for the treatment of proliferative diseases
US9675796B2 (en)2013-11-102017-06-13Brainsgate Ltd.Implant and delivery system for neural stimulator
US10441567B2 (en)2014-01-172019-10-15Ligand Pharmaceuticals IncorporatedMethods and compositions for modulating hormone levels
US10271907B2 (en)2015-05-132019-04-30Brainsgate Ltd.Implant and delivery system for neural stimulator
JP2022529341A (en)2019-04-192022-06-21リガンド・ファーマシューティカルズ・インコーポレイテッド The crystalline form of the compound and the method for producing the crystalline form of the compound.

Family Cites Families (77)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
FR2630440B1 (en)*1988-04-251991-09-20Jouveinal Sa BENZODIAZEPINES, THEIR PREPARATION PROCESS AND INTERMEDIATES AND THEIR THERAPEUTIC APPLICATIONS
EP0411668B2 (en)1989-08-041998-11-11MERCK SHARP & DOHME LTD.Central cholecystokinin antagonists for treatment of psychiatric disorders
CA2026856A1 (en)1989-10-051991-04-06Mark G. Bock3-substituted-1,4-benzodiazepines useful as oxytocin
CA2032427A1 (en)1989-12-181991-06-19Mark G. BockBenzodiazepines analogs
GB9107368D0 (en)1991-04-081991-05-22Smithkline Beecham PlcNovel compounds
JP3457312B2 (en)1992-07-292003-10-14メルク シヤープ エンド ドーム リミテツド Benzodiasepine derivative
US5283241A (en)1992-08-281994-02-01Merck & Co., Inc.Benzo-fused lactams promote release of growth hormone
CN1041921C (en)1992-12-211999-02-03史密丝克莱恩比彻姆公司 bicyclic fibrinogen antagonist
MX9308016A (en)1992-12-221994-08-31Lilly Co Eli HUMAN IMMUNODEFICIENCY VIRUS PROTEASE INHIBITING COMPOUNDS, PROCEDURE FOR THEIR PREPARATION AND PHARMACEUTICAL FORMULATION CONTAINING THEM.
CA2160786A1 (en)1993-05-141994-11-24James C. Marsters, Jr.Ras farnesyl transferase inhibitors
AU7102394A (en)1993-06-091995-01-03Smithkline Beecham CorporationBicyclic fibrinogen antagonists
US5602156A (en)1993-09-171997-02-11The United States Of America As Represented By The Department Of Health And Human ServicesMethod for inhibiting metalloproteinase expression
US5545735A (en)1993-10-041996-08-13Merck & Co., Inc.Benzo-Fused Lactams promote release of growth hormone
US5426185A (en)1993-11-221995-06-20Merck & Co., Inc.Antiarrhythmic benzodiazepines
US5770573A (en)1993-12-061998-06-23Cytel CorporationCS-1 peptidomimetics, compositions and methods of using the same
CA2196062A1 (en)1994-07-291996-02-15Yoshinari SatoBenzodiazepine derivatives
US5661161A (en)1994-09-291997-08-26Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
JPH11505509A (en)1994-12-091999-05-21スミスクライン・ビーチャム・コーポレイション Bicyclic fibrinogen antagonist
US5639746A (en)1994-12-291997-06-17The Procter & Gamble CompanyHydroxamic acid-containing inhibitors of matrix metalloproteases
WO1996018602A1 (en)1994-12-131996-06-20Smithkline Beecham CorporationBicyclic fibrinogen antagonists
US5672598A (en)*1995-03-211997-09-30The Procter & Gamble CompanyLactam-containing hydroxamic acids
US5856326A (en)1995-03-291999-01-05Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
US5578629A (en)1995-03-291996-11-26Merck & Co., Inc.Benzamide-containing inhibitors of farnesyl-protein transferase
GB9507799D0 (en)1995-04-181995-05-31British Biotech PharmMetalloproteinase inhibitors
US5710171A (en)1995-05-241998-01-20Merck & Co., Inc.Bisphenyl inhibitors of farnesyl-protein transferase
EP0828754B1 (en)1995-05-292005-02-02Pfizer Inc.Dipeptides which promote release of growth hormone
US5756528A (en)1995-06-061998-05-26Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
EP0761680A3 (en)1995-09-121999-05-06Ono Pharmaceutical Co., Ltd.Tetrazole compounds having Interleukin-1beta converting enzyme inhibitory activity
AU7139996A (en)1995-10-051997-04-28Chiroscience LimitedMercaptoamide derivatives and their therapeutic use
WO1997019053A1 (en)1995-11-231997-05-29British Biotech Pharmaceuticals LimitedMetalloproteinase inhibitors
JP2000504014A (en)1996-01-302000-04-04メルク エンド カンパニー インコーポレーテッド Farnesyl-protein transferase inhibitor
US5891889A (en)1996-04-031999-04-06Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
US5919785A (en)1996-04-031999-07-06Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
AU715603B2 (en)1996-04-032000-02-03Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
US5965578A (en)1996-04-031999-10-12Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
US5885995A (en)1996-04-031999-03-23Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
US5869682A (en)1996-04-031999-02-09Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
US5859012A (en)1996-04-031999-01-12Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
AU2555997A (en)1996-04-031997-10-22Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
US5852010A (en)1996-04-031998-12-22Merck & Co., Inc.Inhibitors of farnesyl-protein transferase
CA2250460A1 (en)1996-04-031997-10-09John H. HutchinsonInhibitors of farnesyl-protein transferase
CA2251955A1 (en)1996-04-181997-10-23Nancy E. KohlA method of treating cancer
EP0934270A1 (en)1996-05-301999-08-11Merck & Co., Inc.A method of treating cancer
US5703129A (en)1996-09-301997-12-30Bristol-Myers Squibb Company5-amino-6-cyclohexyl-4-hydroxy-hexanamide derivatives as inhibitors of β-amyloid protein production
JP2001504810A (en)1996-10-112001-04-10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
PL323130A1 (en)1996-11-151998-05-25Hoechst AgApplication of heterocyclic compounds in production of a pharmaceutic agent, novel heterocyclic compounds and pharmaceutic agent as such
ATE296797T1 (en)1996-11-222005-06-15Elan Pharm Inc N-(ARYL/HETEROARYL/ALKYLACETYL) AMINO ACID AMIDES, PHARMACEUTICAL COMPOSITIONS THEREFOR, AND METHODS FOR INHIBITING BETA-AMYLOID PEPTIDE RELEASE OR SYNTHESIS
IL129238A0 (en)1996-11-222000-02-17Elan Pharm IncN-(aryl/heteroarylacetyl) amino acid esters pharmaceutical compositions comprising same and methods for inhibiting b-amyloid peptide release and/ or its synthesis by use of such compounds
NZ335157A (en)1996-11-222001-01-26Elan Pharm IncN-(aryl/heteroaryl) amino acid derivatives and methods for inhibiting beta-amyloid peptide release or its synthesis
AU5585198A (en)1996-11-221998-06-10Athena Pharmaceuticals, Inc.N-(aryl/heteroaryl) amino acid esters, pharmaceutical compositions, and ethods for inhibiting beta-amyloid peptide release and/or its synthesis
TW523506B (en)1996-12-182003-03-11Ono Pharmaceutical CoSulfonamide or carbamide derivatives and drugs containing the same as active ingredients
EA002100B1 (en)*1996-12-232001-12-24Элан Фармасьютикалз, Инк.CYCLOALKYL, LACTAM, LACTONE AND RELATED COMPOUNDS, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, AND METHOD FOR INHIBITING beta-AMYLOID PEPTIDE RELEASE AND/OR ITS SYNTHESISBY USE OF SUCH COMPOUNDS
CA2276081A1 (en)1996-12-301998-07-09Lekhanh O. TranInhibitors of farnesyl-protein transferase
EP0968206B8 (en)1997-02-192007-01-24Berlex, Inc.N-heterocyclic derivatives as nos inhibitors
WO1998041510A1 (en)1997-03-141998-09-24Shionogi & Co., Ltd.Novel benzolactam derivatives and medicinal compositions comprising the same
US5985900A (en)*1997-04-011999-11-16Agouron Pharmaceuticals, Inc.Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses
EP0973396A4 (en)1997-04-072001-02-07Merck & Co IncA method of treating cancer
US6060038A (en)1997-05-152000-05-09Merck & Co., Inc.Radiolabeled farnesyl-protein transferase inhibitors
DE19726427A1 (en)1997-06-231998-12-24Boehringer Mannheim Gmbh Pyrimidine-2,4,6-trione derivatives, processes for their preparation and medicaments containing these compounds
GB9715030D0 (en)1997-07-181997-09-24British Biotech PharmMetalloproteinase inhibitors
JP2001515842A (en)1997-08-112001-09-25シーオーアール セラピューティクス インコーポレイテッド Selective factor Xa inhibitor
ATE211482T1 (en)1997-08-112002-01-15Cor Therapeutics Inc SELECTIVE INHIBITORS OF FACTOR X CONTAINING AN AZEPINE STRUCTURE
AU735366B2 (en)1997-09-292001-07-05Bristol-Myers Squibb CompanyInhibitors of farnesyl protein transferase
US6297239B1 (en)1997-10-082001-10-02Merck & Co., Inc.Inhibitors of prenyl-protein transferase
US6440965B1 (en)1997-10-152002-08-27Krenitsky Pharmaceuticals, Inc.Substituted pyrimidine derivatives, their preparation and their use in the treatment of neurodegenerative or neurological disorders of the central nervous system
AU1277799A (en)*1997-12-221999-07-12Elan Pharmaceuticals, Inc.Polycyclic alpha-amino-$m(e)-caprolactams and related compounds
NZ505800A (en)1998-02-202002-09-27Deep Video Imaging LtdA multi-layer display and a method for extracting depth from 2D video data
PA8469501A1 (en)*1998-04-102000-09-29Pfizer Prod Inc HYDROXAMIDES OF THE ACID (4-ARILSULFONILAMINO) -TETRAHIDROPIRAN-4-CARBOXILICO
AU5204799A (en)1998-06-222000-01-10Elan Pharmaceuticals, Inc.Compounds for inhibiting beta-amyloid peptide release and/or its synthesis
CA2324475A1 (en)1998-06-221999-12-29Elan Pharmaceuticals, Inc.Cyclic amino acid compounds, pharmaceutical compositions comprising same, and methods for inhibiting .beta.-amyloid peptide release and/or its synthesis by use of such compounds
WO1999067221A1 (en)1998-06-221999-12-29Elan Pharmaceuticals, Inc.Compounds for inhibiting beta-amyloid peptide release and/or its synthesis
EP1089977A1 (en)1998-06-222001-04-11Elan Pharmaceuticals, Inc.Compounds for inhibiting beta-amyloid peptide release and/or its synthesis
WO2000002903A1 (en)*1998-07-102000-01-20Cytel CorporationCs-1 peptidomimetics, compositions and methods of using the same
HRP990246A2 (en)1998-08-072000-06-30Du Pont Pharm CoSuccinoylamino benzodiazepines as inhibitors of a beta protein production
AU1618000A (en)1998-11-122000-05-29Du Pont Pharmaceuticals CompanyUse of radioligands to screen inhibitors of amyloid-beta peptide production
EP1313426A2 (en)1998-12-242003-05-28Bristol-Myers Squibb Pharma CompanySuccinoylamino benzodiazepines as inhibitors of a-beta protein production
CA2395862A1 (en)2000-02-172001-08-23Hong LiuSuccinoylamino carbocycles and heterocycles as inhibitors of a.beta. protein production

Also Published As

Publication numberPublication date
US20020055501A1 (en)2002-05-09
JP2003523345A (en)2003-08-05
EP1261610A2 (en)2002-12-04
WO2001060826A2 (en)2001-08-23
CA2395862A1 (en)2001-08-23
US6525044B2 (en)2003-02-25
WO2001060826A3 (en)2002-01-17

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