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NO20042719L - Substituerte 2-amino-cykloalkankarboksamider og deres anvendelse som protease-inhibitorer - Google Patents

Substituerte 2-amino-cykloalkankarboksamider og deres anvendelse som protease-inhibitorer

Info

Publication number
NO20042719L
NO20042719L NO20042719A NO20042719A NO20042719L NO 20042719 L NO20042719 L NO 20042719L NO 20042719 A NO20042719 A NO 20042719A NO 20042719 A NO20042719 A NO 20042719A NO 20042719 L NO20042719 L NO 20042719L
Authority
NO
Norway
Prior art keywords
cycloalkanecarboxamides
amino
substituted
protease inhibitors
protease
Prior art date
Application number
NO20042719A
Other languages
English (en)
Norwegian (no)
Inventor
David Bernard Smith
Thomas Gabriel
Nancy Elisabeth Krauss
Taraneh Mirzadegan
Wylie Solang Palmer
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of NO20042719L publication Critical patent/NO20042719L/no

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    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P19/00Drugs for skeletal disorders
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • A61P33/02Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A61P33/06Antimalarials
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P35/00Antineoplastic agents
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    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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    • A61P9/06Antiarrhythmics
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    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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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    • C07D213/81Amides; Imides
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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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    • C07D215/40Nitrogen atoms attached in position 8
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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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    • C07D241/40Benzopyrazines
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    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
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  • Organic Chemistry (AREA)
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  • Health & Medical Sciences (AREA)
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  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Heart & Thoracic Surgery (AREA)
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  • Tropical Medicine & Parasitology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Virology (AREA)
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  • AIDS & HIV (AREA)
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  • Ophthalmology & Optometry (AREA)
  • Vascular Medicine (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Indole Compounds (AREA)
NO20042719A 2001-12-04 2004-06-28 Substituerte 2-amino-cykloalkankarboksamider og deres anvendelse som protease-inhibitorer NO20042719L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US33675001P 2001-12-04 2001-12-04
PCT/EP2002/013221 WO2003048123A1 (fr) 2001-12-04 2002-11-25 2-amino-cycloalkanecarboxamides substitues et leur utilisation en tant qu'inhibiteurs de la cysteine protease

Publications (1)

Publication Number Publication Date
NO20042719L true NO20042719L (no) 2004-06-28

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NO20042719A NO20042719L (no) 2001-12-04 2004-06-28 Substituerte 2-amino-cykloalkankarboksamider og deres anvendelse som protease-inhibitorer

Country Status (25)

Country Link
US (1) US6747053B2 (fr)
EP (1) EP1453801B1 (fr)
JP (1) JP2005517640A (fr)
KR (1) KR20050044660A (fr)
CN (1) CN1315806C (fr)
AR (1) AR037683A1 (fr)
AT (1) ATE357432T1 (fr)
AU (1) AU2002352126A1 (fr)
BR (1) BR0214642A (fr)
CA (1) CA2467435A1 (fr)
DE (1) DE60219068T2 (fr)
ES (1) ES2282497T3 (fr)
GT (1) GT200200253A (fr)
HU (1) HUP0402344A2 (fr)
IL (1) IL161992A0 (fr)
MX (1) MXPA04005263A (fr)
NO (1) NO20042719L (fr)
PA (1) PA8559701A1 (fr)
PE (1) PE20030723A1 (fr)
PL (1) PL370766A1 (fr)
RU (1) RU2004120784A (fr)
TW (1) TW200303861A (fr)
UY (1) UY27561A1 (fr)
WO (1) WO2003048123A1 (fr)
ZA (1) ZA200404343B (fr)

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WO2000042213A1 (fr) * 1999-01-13 2000-07-20 The Research Foundation Of State University Of New York Nouveau procede d'identification d'inhibiteurs de proteines kinase
US7005445B2 (en) * 2001-10-22 2006-02-28 The Research Foundation Of State University Of New York Protein kinase and phosphatase inhibitors and methods for designing them
GB0128996D0 (en) 2001-12-04 2002-01-23 Novartis Ag Organic compounds
EP1474425B9 (fr) * 2002-01-07 2008-07-02 Eisai Co., Ltd. Deazapurines et leurs utilisations
SE0203712D0 (sv) 2002-12-13 2002-12-13 Astrazeneca Ab Novel compounds
GB0403038D0 (en) * 2004-02-11 2004-03-17 Novartis Ag Organic compounds
WO2006007664A1 (fr) * 2004-07-22 2006-01-26 Genomics Research Partners Pty Ltd Agents et methodes de diagnostic de l'osteoarthrite
US20100179122A1 (en) * 2005-06-28 2010-07-15 Lindsley Craig W Non-Nucleoside Reverse Transcriptase Inhibitors
EP1749822B1 (fr) * 2005-08-05 2008-10-15 Hybrigenics S.A. Nouvelles inhibiteurs de cysteine protease et leur utilisation therapeutique
CA2617725C (fr) * 2005-08-05 2012-04-03 Hybrigenics Sa Nouveaux inhibiteurs des proteases a cysteine et leurs applications therapeutiques
WO2007041775A1 (fr) * 2005-10-10 2007-04-19 The University Of Queensland Inhibiteurs de cystéine protéase incorporant des groupements azide
WO2007081530A2 (fr) * 2006-01-03 2007-07-19 Med Institute, Inc. Appareil médical endoluminal pour livraison locale d'inhibiteurs de la cathepsine et méthode pour construire un tel appareil
JP4012239B2 (ja) 2006-01-11 2007-11-21 生化学工業株式会社 オキサゾロン誘導体
US7838542B2 (en) * 2006-06-29 2010-11-23 Kinex Pharmaceuticals, Llc Bicyclic compositions and methods for modulating a kinase cascade
WO2009001129A1 (fr) * 2007-06-26 2008-12-31 Astrazeneca Ab Dérivés de 1-cyanocyclopropyle utilisés comme inhibiteurs de la cathepsine k
CN101591327B (zh) * 2008-05-26 2012-07-25 华东理工大学 苯烷酰胺类化合物及其用途
WO2013014204A2 (fr) * 2011-07-26 2013-01-31 Sanofi Dérivés d'acide 3-hétéroaroylaminopropionique et leur utilisation comme produits pharmaceutiques
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HUP0402344A2 (hu) 2005-02-28
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AU2002352126A1 (en) 2003-06-17
ZA200404343B (en) 2006-07-26
MXPA04005263A (es) 2004-10-11
US20030212097A1 (en) 2003-11-13
DE60219068D1 (de) 2007-05-03
BR0214642A (pt) 2004-11-03
ATE357432T1 (de) 2007-04-15
PE20030723A1 (es) 2003-08-29
EP1453801B1 (fr) 2007-03-21
GT200200253A (es) 2003-07-03
TW200303861A (en) 2003-09-16
UY27561A1 (es) 2003-06-30
PL370766A1 (en) 2005-05-30
CN1639119A (zh) 2005-07-13
PA8559701A1 (es) 2003-07-28
ES2282497T3 (es) 2007-10-16
US6747053B2 (en) 2004-06-08
IL161992A0 (en) 2005-11-20
CN1315806C (zh) 2007-05-16
CA2467435A1 (fr) 2003-06-12
KR20050044660A (ko) 2005-05-12
EP1453801A1 (fr) 2004-09-08
AR037683A1 (es) 2004-12-01
DE60219068T2 (de) 2007-12-13

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