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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

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides 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
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16Sulfonamides 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides 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
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/21Sulfonamides 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00Sulfones; Sulfoxides
    • C07C317/44Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/46Heterocyclic 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
    • C07D207/48Sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/96Sulfur atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic 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
    • C07D295/22Heterocyclic 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
    • C07D295/26Sulfur 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
US09569034 2000-05-11
US09/569,034 US7115632B1 (en) 1999-05-12 2000-05-11 Sulfonyl aryl or heteroaryl hydroxamic acid compounds
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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DE60321775D1 (en) * 2002-04-03 2008-08-07 Topotarget Uk Ltd CARBOXIC ACID DERIVATIVES CONTAIN A PIPERAZINE COMPOUND AS HDAC INHIBITORS
JP4612621B2 (en) 2003-01-17 2011-01-12 トポターゲット ユーケー リミテッド Carbamate compounds containing ester or ketone linkages as HDAC inhibitors
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
CA2924436A1 (en) * 2007-07-30 2009-02-05 Ardea Biosciences, Inc. Pharmaceutical combinations of n-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide as inhibitors of mek and methods of use
AP2817A (en) * 2007-07-30 2013-12-31 Ardea Biosciences Inc Derivatives of n-(arylamino)sulfonamides includingpolymorphs as inhibitors of mek as well as compos itions, methods of use and methods for preparing the same
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
CA2777108A1 (en) 2009-10-09 2011-04-14 Zafgen Corporation Sulphone compounds and methods of making and using same
EP2595988B1 (en) 2010-07-22 2014-12-17 Zafgen, Inc. Tricyclic compounds and methds of making and using same
BR112013018771A2 (en) 2011-01-26 2019-09-17 Zafgen Inc tetrazole compounds and methods for making and using them
CA2835209A1 (en) 2011-05-06 2012-11-15 Zafgen, Inc. Tricyclic pyrazole sulfonamide compounds and methods of making and using same
EA025526B1 (en) 2011-05-06 2017-01-30 Зафджен Инк. Partially saturated tricyclic compounds and methods of making and using same
KR20140053013A (en) 2011-05-06 2014-05-07 자프겐 인크. 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
WO2013109739A1 (en) 2012-01-18 2013-07-25 Zafgen, Inc. Tricyclic sulfonamide compounds and methods of making and using same
MX2015005733A (en) 2012-11-05 2016-02-10 Zafgen Inc Tricyclic compounds for use in the treatment and/or control of obesity.
CN104870433A (en) 2012-11-05 2015-08-26 扎夫根股份有限公司 Tricyclic compounds and methods of making and using 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
CA2942522A1 (en) * 2014-03-12 2015-09-17 The Trustees Of Columbia University In The City Of New York 5,5-dioxo-11h-benzo[c][2,1]benzothiazepine derivatives and their use as 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
US20210393632A1 (en) 2018-10-04 2021-12-23 INSERM (Institut National de la Santé et de la Recherche Médicale) Egfr inhibitors for treating keratodermas

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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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