NO993098L - Sykloalkyl, laktam, lakton og beslektede forbindelser, farmasöytiske sammensetninger som omfatter disse, og fremgangsmåter for å inhibere <beta>-amyloid peptid frigivning og/eller syntese av disse ved anvendelse av slike forbindelser - Google Patents

Sykloalkyl, laktam, lakton og beslektede forbindelser, farmasöytiske sammensetninger som omfatter disse, og fremgangsmåter for å inhibere <beta>-amyloid peptid frigivning og/eller syntese av disse ved anvendelse av slike forbindelser

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Publication number
NO993098L
NO993098L NO993098A NO993098A NO993098L NO 993098 L NO993098 L NO 993098L NO 993098 A NO993098 A NO 993098A NO 993098 A NO993098 A NO 993098A NO 993098 L NO993098 L NO 993098L
Authority
NO
Norway
Prior art keywords
compounds
lactam
lactone
cycloalkyl
beta
Prior art date
Application number
NO993098A
Other languages
English (en)
Norwegian (no)
Other versions
NO993098D0 (no
Inventor
Jing Wu
Jay S Tung
Eugene D Thorsett
Michael A Pleiss
Jeffrey S Nissen
Jeffrey Neitz
Lee H Latimer
Varghese John
Stephen Freedman
Thomas C Britton
James E Audia
Jon K Reel
Thomas E Mabry
Bruce A Dressman
Cynthia L Cwi
James J Droste
Steven S Henry
Stacey L Mcdaniel
William Leonard Scott
Russell D Stucky
Warren J Porter
Original Assignee
Elan Pharm 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 Elan Pharm Inc, Lilly Co Eli filed Critical Elan Pharm Inc
Publication of NO993098D0 publication Critical patent/NO993098D0/no
Publication of NO993098L publication Critical patent/NO993098L/no

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    • C07—ORGANIC CHEMISTRY
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    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/273—2-Pyrrolidones 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 other ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
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    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/78—Ring systems having three or more relevant rings
    • C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
    • C07D311/82—Xanthenes
    • C07D311/90—Xanthenes with hydrocarbon radicals, substituted by amino radicals, directly attached in position 9
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00—Drugs for disorders of the nervous system
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    • C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
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    • C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
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    • C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D267/14—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
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    • C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom 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
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    • C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, 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
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
NO993098A 1996-12-23 1999-06-22 Sykloalkyl, laktam, lakton og beslektede forbindelser, farmasöytiske sammensetninger som omfatter disse, og fremgangsmåter for å inhibere <beta>-amyloid peptid frigivning og/eller syntese av disse ved anvendelse av slike forbindelser NO993098L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US78002596A 1996-12-23 1996-12-23
PCT/US1997/022986 WO1998028268A2 (fr) 1996-12-23 1997-12-22 CYCLOALKYLE, LACTAME ET COMPOSES ASSOCIES, COMPOSITIONS PHARMACEUTIQUES CONTENANT CES COMPOSES, ET PROCEDES D'INHIBITION DE LA LIBERATION DU PEPTIDE β-AMYLOIDE ET/OU DE SA SYNTHESE AU MOYEN DE TELS COMPOSES

Publications (2)

Publication Number Publication Date
NO993098D0 NO993098D0 (no) 1999-06-22
NO993098L true NO993098L (no) 1999-08-20

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NO993098A NO993098L (no) 1996-12-23 1999-06-22 Sykloalkyl, laktam, lakton og beslektede forbindelser, farmasöytiske sammensetninger som omfatter disse, og fremgangsmåter for å inhibere <beta>-amyloid peptid frigivning og/eller syntese av disse ved anvendelse av slike forbindelser

Country Status (28)

Country Link
EP (1) EP0951466B1 (fr)
JP (1) JP3812952B2 (fr)
KR (1) KR20000069654A (fr)
CN (2) CN1616432A (fr)
AR (1) AR010854A1 (fr)
AT (1) ATE421509T1 (fr)
AU (1) AU749658C (fr)
BR (1) BR9714517A (fr)
CA (1) CA2272305A1 (fr)
CO (1) CO4930282A1 (fr)
DE (1) DE69739236D1 (fr)
DK (1) DK0951466T3 (fr)
EA (1) EA002100B1 (fr)
ES (1) ES2319239T3 (fr)
HR (1) HRP970705A2 (fr)
HU (1) HUP0001232A3 (fr)
ID (1) ID22177A (fr)
IL (2) IL129820A0 (fr)
NO (1) NO993098L (fr)
NZ (1) NZ335583A (fr)
PE (1) PE52799A1 (fr)
PL (1) PL196641B1 (fr)
PT (1) PT951466E (fr)
SI (1) SI0951466T1 (fr)
TR (1) TR199901343T2 (fr)
TW (1) TW568914B (fr)
WO (1) WO1998028268A2 (fr)
ZA (1) ZA9711537B (fr)

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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
CA2307221A1 (fr) * 1997-12-22 1999-07-01 Elan Pharmaceuticals, Inc. E-caprolactames .alpha.-amino polycycliques et composes connexes
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
US6958330B1 (en) 1998-06-22 2005-10-25 Elan Pharmaceuticals, Inc. Polycyclic α-amino-ε-caprolactams and related 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
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
NZ509241A (en) 1998-08-07 2003-08-29 Du Pont Pharm Co Succinoylamino lactams as inhibitors of alpha-beta protein production
HRP990246A2 (en) 1998-08-07 2000-06-30 Du Pont Pharm Co Succinoylamino benzodiazepines as inhibitors of a beta protein production
AU6278099A (en) 1998-09-30 2000-04-17 Elan Pharmaceuticals, Inc. Biological reagents and methods for determining the mechanism in the generation of beta-amyloid peptide
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
JP4615727B2 (ja) 1998-12-24 2011-01-19 ブリストル−マイヤーズ スクイブ ファーマ カンパニー Ａβタンパク質生成の阻害剤としてのスクシノイルアミノベンゾジアゼピン
JP2003503476A (ja) * 1999-07-06 2003-01-28 バーテックス ファーマシューティカルズ インコーポレイテッド 環化アミド誘導体
WO2001010846A2 (fr) * 1999-08-05 2001-02-15 Igt Pharma Inc. Nouveaux composes de 1,4-benzodiazepine et derives de ces derniers
US6960576B2 (en) 1999-09-13 2005-11-01 Bristol-Myers Squibb Pharma Company Hydroxyalkanoylaminolactams and related structures as inhibitors of Aβ protein production
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HUP0001232A3 (en) 2001-02-28
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