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AU2001259589A1 - Sulfonyl aryl or heteroaryl hydroxamic acid compounds - Google Patents

Sulfonyl aryl or heteroaryl hydroxamic acid compounds

Info

Publication number
AU2001259589A1
AU2001259589A1 AU2001259589A AU5958901A AU2001259589A1 AU 2001259589 A1 AU2001259589 A1 AU 2001259589A1 AU 2001259589 A AU2001259589 A AU 2001259589A AU 5958901 A AU5958901 A AU 5958901A AU 2001259589 A1 AU2001259589 A1 AU 2001259589A1
Authority
AU
Australia
Prior art keywords
acid compounds
hydroxamic acid
sulfonyl aryl
heteroaryl hydroxamic
heteroaryl
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
AU2001259589A
Inventor
Thomas E Barta
Daniel P Becker
Louis J. Bedell
Gary A Decrescenzo
John N Freskos
Daniel P. Getman
Joseph Mcdonald
Brent V. Mischke
Shashidhar N Rao
Clara I Villamil
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.)
Pharmacia LLC
Original Assignee
Pharmacia LLC
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 Pharmacia LLC filed Critical Pharmacia LLC
Publication of AU2001259589A1 publication Critical patent/AU2001259589A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00—Sulfones; Sulfoxides
    • C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
    • C07D207/48—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/96—Sulfur atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/22—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
    • C07D295/26—Sulfur atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AU2001259589A 2000-05-11 2001-05-07 Sulfonyl aryl or heteroaryl hydroxamic acid compounds Abandoned AU2001259589A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US09/569,034 US7115632B1 (en) 1999-05-12 2000-05-11 Sulfonyl aryl or heteroaryl hydroxamic acid compounds
US09569034 2000-05-11
PCT/US2001/014706 WO2001085680A2 (en) 2000-05-11 2001-05-07 Sulfonyl aryl or heteroaryl hydroxamic acid compounds

Publications (1)

Publication Number Publication Date
AU2001259589A1 true AU2001259589A1 (en) 2001-11-20

Family

ID=24273821

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2001259589A Abandoned AU2001259589A1 (en) 2000-05-11 2001-05-07 Sulfonyl aryl or heteroaryl hydroxamic acid compounds

Country Status (3)

Country Link
US (1) US7115632B1 (en)
AU (1) AU2001259589A1 (en)
WO (1) WO2001085680A2 (en)

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US6683078B2 (en) * 2001-07-19 2004-01-27 Pharmacia Corporation Use of sulfonyl aryl or heteroaryl hydroxamic acids and derivatives thereof as aggrecanase inhibitors
NZ536116A (en) * 2002-04-03 2007-01-26 Topotarget Uk Ltd Carbamic acid compounds comprising a piperazine linkage as HDAC inhibitors
EP1583736A1 (en) 2003-01-17 2005-10-12 TopoTarget UK Limited Carbamic acid compounds comprising an ester or ketone linkage as hdac inhibitors
WO2009018233A1 (en) * 2007-07-30 2009-02-05 Ardea Biosciences, Inc. Derivatives of n-(arylamino) sulfonamides including polymorphs as inhibitors of mek as well as compositions, methods of use and methods for preparing the same
US8101799B2 (en) * 2005-07-21 2012-01-24 Ardea Biosciences Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK
EP1908751A1 (en) * 2006-10-03 2008-04-09 EOS S.p.A. N-hydroxy benzamides with antitumour activity
JP5479337B2 (en) * 2007-07-30 2014-04-23 アルディア バイオサイエンス，インク． Combination of MEK inhibitor and RAF kinase inhibitor and use thereof
US8044240B2 (en) 2008-03-06 2011-10-25 Ardea Biosciences Inc. Polymorphic form of N-(S)-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide and uses thereof
ES2437100T3 (en) 2009-06-04 2014-01-08 Merck Sharp & Dohme Corp. Active metabolite of a thrombin receptor antagonist
KR20120083905A (en) 2009-10-09 2012-07-26 자프겐 코포레이션 Sulphone compounds for use in the treatment of obesity
CN103249735B (en) 2010-07-22 2016-04-06 扎夫根股份有限公司 Tricyclic compounds and methods for their preparation and use
EP2668169B1 (en) 2011-01-26 2017-11-15 Zafgen, Inc. Tetrazole compounds and methods of making and using same
BR112013028534A2 (en) 2011-05-06 2016-09-06 Zafgen Inc partially saturated tricyclic compounds and methods for their production and use
AU2012253759B2 (en) 2011-05-06 2016-01-21 Zafgen Inc. Tricyclic sulfonamide compounds and methods of making and using same
US9242997B2 (en) 2011-05-06 2016-01-26 Zafgen, Inc. Tricyclic pyrazole sulphonamide compunds and methods of making and using same
CA2861390A1 (en) 2012-01-18 2013-07-25 Zafgen, Inc. Tricyclic sulfonamide compounds and methods of making and using same
JP2015509102A (en) 2012-01-18 2015-03-26 ザフゲン，インコーポレイテッド Tricyclic sulfone compounds and methods for making and using the same
JP6169716B2 (en) 2012-11-05 2017-07-26 ザフゲン，インコーポレイテッド How to treat liver disease
BR112015010225A2 (en) 2012-11-05 2017-07-11 Zafgen Inc tricyclic compounds and their methods of production and use
BR112015010223A2 (en) 2012-11-05 2017-07-11 Zafgen Inc tricyclic compounds for use in the treatment and / or control of obesity
EP3116509B1 (en) * 2014-03-12 2022-06-22 The Trustees of Columbia University in the City of New York A new class of mu-opioid receptor agonists
CN108135866A (en) 2015-09-16 2018-06-08 哥伦比亚大学董事会 Carboxyl diaryl sulphur azepine amine is as μ-opioid receptor agonist
CA3115038A1 (en) 2018-10-04 2020-04-09 Inserm (Institut National De La Sante Et De La Recherche Medicale) Egfr inhibitors for treating keratodermas

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US4595700A (en) 1984-12-21 1986-06-17 G. D. Searle & Co. Thiol based collagenase inhibitors
US5103014A (en) 1987-09-30 1992-04-07 American Home Products Corporation Certain 3,3'-[[[(2-phenyl-4-thiazolyl)methoxy]phenyl]methylene]dithiobis-propanoic acid derivatives
GB2212153B (en) 1987-11-16 1992-01-15 Squibb & Sons Inc Phenyl hydroxamic acids
GB8827305D0 (en) 1988-11-23 1988-12-29 British Bio Technology Compounds
DK0493925T3 (en) 1990-12-17 1998-07-27 Sankyo Co Pyrazole derivatives with herbicidal activity, their preparation and use
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US5376664A (en) 1992-07-27 1994-12-27 The Du Pont Merck Pharmaceutical Company Unsymmetrical mono-3-nitro bis-naphthalimides as anticancer agents
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Also Published As

Publication number Publication date
WO2001085680A2 (en) 2001-11-15
US7115632B1 (en) 2006-10-03
WO2001085680A3 (en) 2002-03-07

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