PE59399A1 - Compuestos heterociclicos, composiciones farmaceuticas que los comprenden y metodos para inhibir la liberacion del peptido � - amiloide y/o su sintesis mediante el uso de dichos compuestos - Google Patents

Compuestos heterociclicos, composiciones farmaceuticas que los comprenden y metodos para inhibir la liberacion del peptido � - amiloide y/o su sintesis mediante el uso de dichos compuestos

Info

Publication number
PE59399A1
PE59399A1 PE1998000144A PE00014498A PE59399A1 PE 59399 A1 PE59399 A1 PE 59399A1 PE 1998000144 A PE1998000144 A PE 1998000144A PE 00014498 A PE00014498 A PE 00014498A PE 59399 A1 PE59399 A1 PE 59399A1
Authority
PE
Peru
Prior art keywords
alkyl
alkynyl
formula
optionally substituted
compounds
Prior art date
Application number
PE1998000144A
Other languages
English (en)
Inventor
James E Audia
Lee H Latimer
Warren J Porter
James Droste
Eugene D Thorsett
Jeffrey S Nissen
Original Assignee
Athena Neurosciences Inc
Lilly Co Eli
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 Athena Neurosciences Inc, Lilly Co Eli filed Critical Athena Neurosciences Inc
Publication of PE59399A1 publication Critical patent/PE59399A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D257/00Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04Five-membered rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/061,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/08Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D277/10Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/08Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D277/12Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Abstract

SE REFIERE A UN COMPUESTO DE FORMULA A-B-C; A ES A(i), R1 ES ALQUILO, ALQUENILO, ALQUINILO, OPCIONALMENTE SUSTITUIDOS, ENTRE OTROS; Z ES a)UN GRUPO DE FORMULA -CX`X''-CO-, X', X'' SON H, OH, F o FORMAN UN GRUPO OXO; b)UN GRUPO DE FORMULA -T-CX'X''-CO-; T ES O, S, NR3; R3 ES H, ACILO, ALQUILO, ENTRE OTROS; c)UN GRUPO DE FORMULA CX'X''T(CO), R2 ES ALQUILO, ALQUENILO, ALQUINILO OPCIONALMENTE SUSTITUIDOS, ENTRE OTROS; R6 ES ALQUILO, ALQUENILO, ALQUINILO OPCIONALMENTE SUSTITUIDOS, m Y p SON 0-1; Aii) R1 ES ALQUILO, ALQUENILO, ALQUINILO, ENTRE OTROS; T' ES UN ENLACE, O, S, NR3; W, X SON (CR7R7)q, O, S, NR8, q ES 1-2; R7 Y R8 SON H, ALQUILO, CICLOALQUILO, ENTRE OTROS; R4 ES H, ALQUILO, ALQUENILO, OPCIONALMENTE SUSTITUIDOS, ENTRE OTROS; B ES -CO-NH-CR5; R5 ES ALQUILO, ALQUENILO, ALQUINILO, OPCIONALMENTE SUSTITUIDOS; B(ii); B(iii); B(iv), SI A ES LA FORMULA A(ii) O A(iii), B PUEDE SER UN ENLACE. C ES -C(O)Y o -C(S)Y, Y ES ALQUILO o CICLOALQUILO, NHSO2R8, ENTRE OTROS; C(ii) CR11R11Y', R11 ES H, ALQUILO, CICLOALQUILO OPCIONALMENTE SUSTITUIDO, ENTRE OTROS; Y' ES OH, ALCOXI, AMINO, ENTRE OTROS; C(iii) OPCIONALMENTE FUSIONADO. UN COMPUESTO PREFERIDO ES (S)-2-[1-(3,5-DIFLUORFENILACETAMIDO)ETIL]-4-METOXICARBONIL-4-FENILMETIL-2-IMIDAZOLINA; ENTRE OTROS. PUEDE PREVENIR EL INICIO O TRATAR LA ENFERMEDAD DE ALZHEIMER (AD)
PE1998000144A 1997-02-28 1998-02-27 Compuestos heterociclicos, composiciones farmaceuticas que los comprenden y metodos para inhibir la liberacion del peptido � - amiloide y/o su sintesis mediante el uso de dichos compuestos PE59399A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US80826397A 1997-02-28 1997-02-28

Publications (1)

Publication Number Publication Date
PE59399A1 true PE59399A1 (es) 1999-06-21

Family

ID=25198310

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1998000144A PE59399A1 (es) 1997-02-28 1998-02-27 Compuestos heterociclicos, composiciones farmaceuticas que los comprenden y metodos para inhibir la liberacion del peptido � - amiloide y/o su sintesis mediante el uso de dichos compuestos

Country Status (22)

Country Link
EP (1) EP0968198A1 (es)
JP (1) JP2001513107A (es)
KR (1) KR20000075767A (es)
CN (1) CN1253554A (es)
AR (1) AR011164A1 (es)
AU (1) AU6662298A (es)
BR (1) BR9807876A (es)
CA (1) CA2278674A1 (es)
CO (1) CO4920244A1 (es)
EA (1) EA199900778A1 (es)
HR (1) HRP980093A2 (es)
HU (1) HUP0001293A3 (es)
ID (1) ID22873A (es)
IL (1) IL130851A0 (es)
NO (1) NO994016L (es)
NZ (1) NZ336613A (es)
PE (1) PE59399A1 (es)
PL (1) PL335424A1 (es)
TR (1) TR199902071T2 (es)
WO (1) WO1998038177A1 (es)
YU (1) YU7998A (es)
ZA (1) ZA981627B (es)

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US6635632B1 (en) 1996-12-23 2003-10-21 Athena Neurosciences, Inc. Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
KR20010033408A (ko) * 1997-12-22 2001-04-25 진 엠. 듀발 폴리시클릭 α-아미노-ε-카프롤락탐 및 관련 화합물
US6774125B2 (en) 1998-06-22 2004-08-10 Elan Pharmaceuticals, Inc. Deoxyamino acid compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
US6552013B1 (en) 1998-06-22 2003-04-22 Elan Pharmaceuticals, Inc. Deoxyamino acid compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
AU4707999A (en) * 1998-06-22 2000-01-10 Elan Pharmaceuticals, Inc. Compounds for inhibiting beta-amyloid peptide release and/or its synthesis
US6569851B1 (en) 1998-06-22 2003-05-27 Elan Pharmaceutials, Inc. Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
US6509331B1 (en) 1998-06-22 2003-01-21 Elan Pharmaceuticals, Inc. Deoxyamino acid compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
US6528505B1 (en) 1998-06-22 2003-03-04 Elan Pharmaceuticals, Inc. Cyclic amino acid compounds pharmaceutical compositions comprising same and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
US6737038B1 (en) 1998-11-12 2004-05-18 Bristol-Myers Squibb Company Use of small molecule radioligands to discover inhibitors of amyloid-beta peptide production and for diagnostic imaging
US6395897B1 (en) 1999-03-02 2002-05-28 Boehringer Ingelheim Pharmaceuticals, Inc. Nitrile compounds useful as reversible inhibitors of #9 cathepsin 5
US7160880B1 (en) * 1999-05-14 2007-01-09 Cenes Limited Short-acting benzodiazepines
GB9911803D0 (en) * 1999-05-20 1999-07-21 Merck Sharp & Dohme Therapeutic combination
EP1210338A2 (en) * 1999-08-05 2002-06-05 IGT Pharma Inc. 1,4-diazepine derivatives for the treatment of diseases related to the central nervous system
US6420364B1 (en) 1999-09-13 2002-07-16 Boehringer Ingelheim Pharmaceuticals, Inc. Compound useful as reversible inhibitors of cysteine proteases
WO2001087354A2 (en) 2000-05-17 2001-11-22 Bristol-Myers Squibb Pharma Company Use of small molecule radioligands for diagnostic imaging
BR0106717A (pt) 2000-06-01 2002-04-16 Bristol Myers Squibb Pharma Co Compostos, composição farmacêutica e usos dos compostos de lactama inovadora
DE10029077A1 (de) * 2000-06-13 2001-12-20 Bayer Ag Thiazolylsubstituierte Heterocyclen
US6432944B1 (en) 2000-07-06 2002-08-13 Bristol-Myers Squibb Company Benzodiazepinone β-amyloid inhibitors: arylacetamidoalanyl derivatives
FR2840899B1 (fr) * 2002-06-12 2005-02-25 Sanofi Synthelabo Derives d'acylaminothiazole, leur preparation et leur utilisation en therapeutique
AR039059A1 (es) 2001-08-06 2005-02-09 Sanofi Aventis Compuesto derivado de acilaminotiazol, su utilizacion, procedimientos para prepararlo, composicion farmaceutica que lo comprende, y compuestos intermediarios
EP1550725A4 (en) 2002-06-05 2010-08-25 Kaneka Corp PROCESS FOR PRODUCING OPTICALLY ACTIVE alpha-METHYLCYSTEINE DERIVATIVE
NZ584773A (en) 2004-09-17 2012-07-27 Whitehead Biomedical Inst Compounds, Compositions and Methods of Inhibiting Alpha-Synuclein Toxicity
US7449486B2 (en) 2004-10-19 2008-11-11 Array Biopharma Inc. Mitotic kinesin inhibitors and methods of use thereof
UA95907C2 (en) 2005-05-02 2011-09-26 Эррей Биофарма Инк. Mitotic kinesin inhibitors and methods of use thereof
EP1757290A1 (en) 2005-08-16 2007-02-28 Zentaris GmbH Novel triazole derivatives as ghrelin analogue ligands of growth hormone secretagogue receptors
WO2008042928A2 (en) 2006-10-03 2008-04-10 Array Biopharma, Inc. Oxadiazole and thiadiazole derivatives as mitotic kinesin inhibitors and methods of use thereof
ES2700613T3 (es) * 2008-07-16 2019-02-18 Bitop Ag Síntesis de amidinas cíclicas
AR081331A1 (es) 2010-04-23 2012-08-08 Cytokinetics Inc Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos
AR081626A1 (es) 2010-04-23 2012-10-10 Cytokinetics Inc Compuestos amino-piridazinicos, composiciones farmaceuticas que los contienen y uso de los mismos para tratar trastornos musculares cardiacos y esqueleticos
US9133123B2 (en) 2010-04-23 2015-09-15 Cytokinetics, Inc. Certain amino-pyridines and amino-triazines, compositions thereof, and methods for their use
EP2431035A1 (en) 2010-09-16 2012-03-21 Æterna Zentaris GmbH Novel Triazole Derivatives with Improved Receptor Activity and Bioavailability Properties as Ghrelin Antagonists of Growth Hormone Secretagogue Receptors
US8759380B2 (en) 2011-04-22 2014-06-24 Cytokinetics, Inc. Certain heterocycles, compositions thereof, and methods for their use
US8809372B2 (en) 2011-09-30 2014-08-19 Asana Biosciences, Llc Pyridine derivatives
CN103435549A (zh) * 2013-08-14 2013-12-11 无锡惠飞生物医药技术有限公司 5-甲基-7-氨基-5H,7H-二苯并[b,d]氮杂环庚-6-酮的制备方法
CN105646208B (zh) * 2016-02-24 2018-10-16 潍坊晶润化工股份有限公司 丙酮酸甲酯的制备方法

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JPH11506923A (ja) * 1995-06-06 1999-06-22 アセナ ニューロサイエンシーズ,インコーポレイテッド 新しいカテプシンならびにその阻害のための方法および組成物

Also Published As

Publication number Publication date
CA2278674A1 (en) 1998-09-03
YU7998A (sh) 2002-06-19
ZA981627B (en) 1999-10-05
KR20000075767A (ko) 2000-12-26
WO1998038177A1 (en) 1998-09-03
CO4920244A1 (es) 2000-05-29
CN1253554A (zh) 2000-05-17
NO994016D0 (no) 1999-08-19
EP0968198A1 (en) 2000-01-05
HUP0001293A3 (en) 2000-09-28
JP2001513107A (ja) 2001-08-28
IL130851A0 (en) 2001-01-28
NO994016L (no) 1999-10-18
ID22873A (id) 1999-12-16
PL335424A1 (en) 2000-04-25
HRP980093A2 (en) 1998-12-31
HUP0001293A1 (hu) 2000-08-28
BR9807876A (pt) 2000-02-29
AR011164A1 (es) 2000-08-02
AU6662298A (en) 1998-09-18
NZ336613A (en) 2001-10-26
TR199902071T2 (xx) 2000-01-21
EA199900778A1 (ru) 2000-04-24

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