CA2285567A1 - Lactones gamma alpha-methylene utilisees comme inhibiteurs selectifs de la cyclooxygenase-2 - Google Patents

Lactones gamma alpha-methylene utilisees comme inhibiteurs selectifs de la cyclooxygenase-2 Download PDF

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Publication number
CA2285567A1
CA2285567A1 CA002285567A CA2285567A CA2285567A1 CA 2285567 A1 CA2285567 A1 CA 2285567A1 CA 002285567 A CA002285567 A CA 002285567A CA 2285567 A CA2285567 A CA 2285567A CA 2285567 A1 CA2285567 A1 CA 2285567A1
Authority
CA
Canada
Prior art keywords
phenyl
furanone
methylsulfonyl
compound
cox
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
CA002285567A
Other languages
English (en)
Inventor
Serge Leger
Erich Grimm
Petpiboon Prasit
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.)
Merck Frosst Canada and Co
Original Assignee
Individual
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
Priority claimed from GBGB9709356.1A external-priority patent/GB9709356D0/en
Application filed by Individual filed Critical Individual
Publication of CA2285567A1 publication Critical patent/CA2285567A1/fr
Abandoned legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D405/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00Sulfones; Sulfoxides
    • C07C317/14Sulfones; Sulfoxides having sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00Sulfones; Sulfoxides
    • C07C317/24Sulfones; Sulfoxides having sulfone or sulfoxide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D307/58One oxygen atom, e.g. butenolide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/04Systems containing only non-condensed rings with a four-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

L'invention concerne un nouveau composé de formule (I) et un procédé de traitement des maladies induites par COX-2 consistant à administrer à un patient une quantité non toxique thérapeutiquement efficace d'un composé de formule (I). L'invention concerne aussi certaines compositions pharmaceutiques destinées au traitement de maladies induites par COX-2 comprenant des composés de formule (I).
CA002285567A 1997-04-02 1998-03-31 Lactones gamma alpha-methylene utilisees comme inhibiteurs selectifs de la cyclooxygenase-2 Abandoned CA2285567A1 (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US4253597P 1997-04-02 1997-04-02
US60/042,535 1997-04-02
GB9709356.1 1997-05-07
GBGB9709356.1A GB9709356D0 (en) 1997-05-07 1997-05-07 Alpha-methylene gamma lactones as selective cyclooxygenase-2 inhibitors
PCT/CA1998/000302 WO1998043966A1 (fr) 1997-04-02 1998-03-31 Lactones gamma alpha-methylene utilisees comme inhibiteurs selectifs de la cyclooxygenase-2

Publications (1)

Publication Number Publication Date
CA2285567A1 true CA2285567A1 (fr) 1998-10-08

Family

ID=26311502

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002285567A Abandoned CA2285567A1 (fr) 1997-04-02 1998-03-31 Lactones gamma alpha-methylene utilisees comme inhibiteurs selectifs de la cyclooxygenase-2

Country Status (5)

Country Link
EP (1) EP0971910A1 (fr)
JP (1) JP2001518087A (fr)
AU (1) AU6818298A (fr)
CA (1) CA2285567A1 (fr)
WO (1) WO1998043966A1 (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6180651B1 (en) 1996-04-04 2001-01-30 Bristol-Myers Squibb Diarylmethylidenefuran derivatives, processes for their preparation and their uses in therapeutics
CN100488500C (zh) 2000-07-20 2009-05-20 劳拉斯有限公司 Cox-2抑制剂预防免疫缺陷的用途
AU2002306150B2 (en) 2001-06-13 2008-02-14 Magnachem International Laboratories, Inc. Lactone formulations and method of use
JP4869597B2 (ja) 2002-11-05 2012-02-08 マグナケム インターナショナル ラボラトリーズ, インコーポレイテッド 合成ラクトン処方物ならびに使用方法
ATE342722T1 (de) 2003-05-07 2006-11-15 Osteologix As Behandlung von knorpel/knochen-erkrankungen mit wasserlöslichen strontiumsalzen
WO2005102315A1 (fr) 2004-04-23 2005-11-03 Magnachem International Laboratories, Inc. Formulations de lactone synthetique pour maitrise la douleur
EP2350645A2 (fr) 2008-10-24 2011-08-03 Magnachem International Laboratories, Inc. Procédé d'analyse de composés interagissant de manière sélective avec rad9
CA3209491A1 (fr) 2021-03-15 2022-09-22 Saul Yedgar Dipalmitoyl-phosphatidyl-ethanol-amine conjuguee a l'acide hyaluronique en combinaison avec des medicaments anti-inflammatoires non steroidiens (ains) pour traiter ou soulager des maladies inflammatoire
WO2023150719A1 (fr) * 2022-02-03 2023-08-10 Purdue Research Foundation Alpha-méthylène et alpha-aminométhyl lactones et lactames pour le traitement d'une infection à clostridium difficile (cdi)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2747123B1 (fr) * 1996-04-04 1998-06-26 Union Pharma Scient Appl Nouveaux derives diarylmethylidene tetrahydrofurane, leurs procedes de preparation, et leurs utilisations en therapeutique
FR2751964B1 (fr) * 1996-08-01 1998-10-30 Union Pharma Scient Appl Nouveaux derives diarylmethylene carbocycliques, leurs procedes de preparation, et leurs utilisations en therapeutique

Also Published As

Publication number Publication date
JP2001518087A (ja) 2001-10-09
AU6818298A (en) 1998-10-22
EP0971910A1 (fr) 2000-01-19
WO1998043966A1 (fr) 1998-10-08

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