NO933918L - 2- og 5-alkyl-og fenylsubstituerte 4- (1-hydroksy-, 1-acyloksy- e ller 1- karbamoyloksy)-5-hydroksy-2(5H)- furanoner som anti-inflammatorisk e midler - Google Patents

2- og 5-alkyl-og fenylsubstituerte 4- (1-hydroksy-, 1-acyloksy- e ller 1- karbamoyloksy)-5-hydroksy-2(5H)- furanoner som anti-inflammatorisk e midler

Info

Publication number
NO933918L
NO933918L NO933918A NO933918A NO933918L NO 933918 L NO933918 L NO 933918L NO 933918 A NO933918 A NO 933918A NO 933918 A NO933918 A NO 933918A NO 933918 L NO933918 L NO 933918L
Authority
NO
Norway
Prior art keywords
alkyl
phenyl
hydroxy
substituted phenyl
carbons
Prior art date
Application number
NO933918A
Other languages
English (en)
Other versions
NO933918D0 (no
Inventor
Gary C M Lee
Michael E Garst
George Sachs
Inc Allergan
Original Assignee
Lee Gary C. M.
Garst Michael E.
George Sachs
Inc Allergan
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 Lee Gary C. M., Garst Michael E., George Sachs, Inc Allergan filed Critical Lee Gary C. M.
Publication of NO933918D0 publication Critical patent/NO933918D0/no
Publication of NO933918L publication Critical patent/NO933918L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic 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
    • C07D307/56—Heterocyclic 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
    • C07D307/60—Two oxygen atoms, e.g. succinic anhydride
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • C07F7/0814—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
    • C07F9/65515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pain & Pain Management (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Rheumatology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Furan Compounds (AREA)

Abstract

Nye anti-inflammatoriske furanonforbindelser har følgende formel hvor R1 uavhengig er H, fenyl, C^-Ctalkylsubstituert fenyl, halogensubstituert fenyl, eller alkyl med l til 6 karbon- atomer, og n er et helt tall med verdier på l eller 2, og hvor når n er l, er Ri-gruppen bundet enten til 3- eller 5-still- ingen i 2-furanonet, når n er 2, er Rj. bundet til både 3- og 5- stillingen, under den forutsetning at når n er l, er R! ikke H; Y! er H, alkyl med l til 20 karbonatomer, fenyl-Ci-C^alkyl, C±- C20alkenyl inneholdende en eller flere olefinbindinger, PO(OH)2, PO(OH)OR2, PO(OH)R2, PO(OR2)2, hvor R2 uavhengig er alkyl med l til 20 karbonatomer, fenyl, eller halogensubsti- tuert fenyl eller Ci-Cjalkylsubstituert fenyl, YL videre er CO- R3, CO-OR3, CONHR3, S02R3, S02NHR3, (CH2)p-O-R3, eller (CH2)p-O- (CH2)m-0-R3, hvor p og m er hele tall og uavhengig er l til 20, og R3 er H, Cj_-C20alkyl, Ci-Czoalkenyl inneholdende en eller flere olefinbindinger, fenyl, halogensubstituert fenyl eller Ci-C6alkylsubstituert fenyl, under den forutsetning at når Y! er CO-R3, CO-ORj og CONHR3, er R3 ikke hydrogen; Y2 er H, en alkylgruppe med l til 25 karbonatomer, fenyl, naftyl, fenyl(CL C20)alkyl-, naftyl (C^-CZQ) alkyl-, halogensubstituert fenyl, G!~ C6akyl-substituert fenyl, halogensubstituert naftyl, C^-CjSub- stituert naftyl; Y3 er H, alkyl med l til 20 karbonatomer, CO- Rt, CO-0-R4, CO-NH-RA, PO(ORJZ eller PO(ORJR4, hvor R4 uavhen- gig er H, alkyl med l til 20 karbonatomer, fenyl eller halo- gensubstituert fenyl eller Ci-Cealkylsubstituert fenyl.
NO933918A 1991-04-30 1993-10-29 2- og 5-alkyl-og fenylsubstituerte 4- (1-hydroksy-, 1-acyloksy- e ller 1- karbamoyloksy)-5-hydroksy-2(5H)- furanoner som anti-inflammatorisk e midler NO933918L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US07/693,204 US5183906A (en) 1991-04-30 1991-04-30 2- and 5-alkyl and phenyl substituted 4-(1-hydroxy, 1-acyloxy or 1-carbamoyloxy)-5-hydroxy-2 (5h)-furanones as anti-inflammatory agents
PCT/US1992/003623 WO1992019610A1 (en) 1991-04-30 1992-04-29 2- and 5-alkyl and phenyl substituted 4-(1-hydroxy, 1-acyloxy or 1-carbamoyloxy)-5-hydroxy-2(5h)-furanones as anti-inflammatory agents

Publications (2)

Publication Number Publication Date
NO933918D0 NO933918D0 (no) 1993-10-29
NO933918L true NO933918L (no) 1993-12-28

Family

ID=24783742

Family Applications (1)

Application Number Title Priority Date Filing Date
NO933918A NO933918L (no) 1991-04-30 1993-10-29 2- og 5-alkyl-og fenylsubstituerte 4- (1-hydroksy-, 1-acyloksy- e ller 1- karbamoyloksy)-5-hydroksy-2(5H)- furanoner som anti-inflammatorisk e midler

Country Status (10)

Country Link
US (1) US5183906A (no)
EP (1) EP0579769B1 (no)
JP (1) JP3181054B2 (no)
AT (1) ATE172459T1 (no)
AU (1) AU1923892A (no)
CA (1) CA2109064A1 (no)
DE (1) DE69227366T2 (no)
ES (1) ES2124261T3 (no)
NO (1) NO933918L (no)
WO (1) WO1992019610A1 (no)

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US5268387A (en) * 1992-04-24 1993-12-07 Allergan, Inc. Pharmaceutical compositions and method for administering 3 and 4-substituted 2(5H)-furanones to a mammal for inhibiting bone loss
WO1994026279A1 (en) * 1993-05-18 1994-11-24 The Upjohn Company Bisphosphonate esters for treating gastric disorders
EP0714391A1 (en) * 1993-08-19 1996-06-05 Warner-Lambert Company Substituted 2(5h)furanone, 2(5h)thiophenone and 2(5h)pyrrolone derivatives, their preparation and their use as endothelin antagonists
US5464865A (en) * 1993-12-22 1995-11-07 Ortho Pharmaceutical Corporation 4-aryl- and 4-arylthio-5-hydroxy-2(5H)-furanones as inhibitors of phospholipase A2
US5451686A (en) * 1994-04-15 1995-09-19 Allergan, Inc. 3 and 5 alkyl and phenyl 4-(hydroxy or acyloxy)-alkyl substituted 2(5H)-furanones as anti-inflammatory agents
US5639468A (en) * 1995-06-07 1997-06-17 University Of Southern California Method for reducing or preventing post-surgical adhesion formation using manoalide and analogs thereof
US5922759A (en) * 1996-06-21 1999-07-13 Warner-Lambert Company Butenolide endothelin antagonists
US5998468A (en) * 1995-08-24 1999-12-07 Warner-Lambert Company Furanone endothelin antagonists
US5891892A (en) * 1996-10-29 1999-04-06 Warner-Lambert Company Small molecule biaryl compounds as inhibitors of endothelin converting enzyme
ATE445838T1 (de) 2001-07-25 2009-10-15 Raptor Pharmaceutical Inc Zusammensetzungen und verfahren zur modulation des transports durch die blut-hirn-schranke
CA2571710A1 (en) 2004-06-24 2006-11-02 Nicholas Valiante Small molecule immunopotentiators and assays for their detection
DK1889198T3 (da) 2005-04-28 2015-02-09 Proteus Digital Health Inc Farma-informatiksystem
WO2008036682A2 (en) 2006-09-18 2008-03-27 Raptor Pharmaceutical Inc. Treatment of liver disorders by administration of receptor-associated protein (rap)-conjugates
ES2728225T3 (es) 2009-02-20 2019-10-23 2 Bbb Medicines B V Sistema de administración de fármacos a base de glutatión
US8445002B2 (en) 2009-05-06 2013-05-21 Laboratory Skin Care, Inc. Dermal delivery compositions comprising active agent-calcium phosphate particle complexes and methods of using the same
US20120077778A1 (en) 2010-09-29 2012-03-29 Andrea Bourdelais Ladder-Frame Polyether Conjugates
FR2978963A1 (fr) 2011-08-11 2013-02-15 Ascorbix Nouveaux derives des furanones et composition pharmaceutique les contenant

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US2359096A (en) * 1941-03-21 1944-09-26 Lilly Co Eli beta-substituted-delta alpha, beta-gamma-butyrolactones and beta-substituted - beta - hydroxy-gamma-butyrolactones and methods of preparing them
US2359208A (en) * 1941-03-21 1944-09-26 Lilly Co Eli beta-substituted-delta alpha,beta-gamma-butyrolactones and beta-substituted-beta-hydroxy-gamma-butyrolactones and the methods of preparing them
EP0133376B1 (en) * 1983-08-03 1988-07-27 The Regents Of The University Of California Synthetic analgesic and/or anti-inflammatory derivatives of manoalide
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Also Published As

Publication number Publication date
WO1992019610A1 (en) 1992-11-12
JPH06507171A (ja) 1994-08-11
JP3181054B2 (ja) 2001-07-03
EP0579769A1 (en) 1994-01-26
ATE172459T1 (de) 1998-11-15
CA2109064A1 (en) 1992-10-31
DE69227366T2 (de) 1999-06-10
NO933918D0 (no) 1993-10-29
ES2124261T3 (es) 1999-02-01
DE69227366D1 (de) 1998-11-26
EP0579769B1 (en) 1998-10-21
AU1923892A (en) 1992-12-21
US5183906A (en) 1993-02-02

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