JP2011527345A - 新規な化合物、この化合物を含む医薬組成物、この化合物の使用方法、およびこの化合物の調製方法 - Google Patents

新規な化合物、この化合物を含む医薬組成物、この化合物の使用方法、およびこの化合物の調製方法 Download PDF

Info

Publication number
JP2011527345A
JP2011527345A JP2011517507A JP2011517507A JP2011527345A JP 2011527345 A JP2011527345 A JP 2011527345A JP 2011517507 A JP2011517507 A JP 2011517507A JP 2011517507 A JP2011517507 A JP 2011517507A JP 2011527345 A JP2011527345 A JP 2011527345A
Authority
JP
Japan
Prior art keywords
group
compound
aryl
alkyl
residue
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.)
Pending
Application number
JP2011517507A
Other languages
English (en)
Japanese (ja)
Other versions
JP2011527345A5 (enExample
Inventor
クレイグ エー. タウンゼンド,
フランシス クハイダ,
スーザン メドガールチ,
Original Assignee
ファスジェン, インコーポレイテッド
ザ・ジョンズ・ホプキンス・ユニバーシティー
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 ファスジェン, インコーポレイテッド, ザ・ジョンズ・ホプキンス・ユニバーシティー filed Critical ファスジェン, インコーポレイテッド
Publication of JP2011527345A publication Critical patent/JP2011527345A/ja
Publication of JP2011527345A5 publication Critical patent/JP2011527345A5/ja
Pending 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
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/08Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/18Sulfonamides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • 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
    • 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
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/03Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C311/06Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • 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
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/12Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
    • C07C311/13Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
    • 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
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • 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
    • C07D213/24Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/55Acids; Esters
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/24Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/3804Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
    • C07F9/3834Aromatic acids (P-C aromatic linkage)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/3804Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
    • C07F9/3882Arylalkanephosphonic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Biochemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Diabetes (AREA)
  • Epidemiology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Pyridine Compounds (AREA)
JP2011517507A 2008-07-07 2009-07-07 新規な化合物、この化合物を含む医薬組成物、この化合物の使用方法、およびこの化合物の調製方法 Pending JP2011527345A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US12957808P 2008-07-07 2008-07-07
US61/129,578 2008-07-07
PCT/US2009/049744 WO2010005922A1 (en) 2008-07-07 2009-07-07 Novel compounds, pharmaceutical compositions containing same, methods of use for same, and methods for preparing same

Publications (2)

Publication Number Publication Date
JP2011527345A true JP2011527345A (ja) 2011-10-27
JP2011527345A5 JP2011527345A5 (enExample) 2012-08-16

Family

ID=41507395

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011517507A Pending JP2011527345A (ja) 2008-07-07 2009-07-07 新規な化合物、この化合物を含む医薬組成物、この化合物の使用方法、およびこの化合物の調製方法

Country Status (7)

Country Link
US (1) US20120083471A1 (enExample)
EP (1) EP2303013A1 (enExample)
JP (1) JP2011527345A (enExample)
CN (1) CN102395270B (enExample)
CA (1) CA2729767A1 (enExample)
MX (1) MX2011000051A (enExample)
WO (1) WO2010005922A1 (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2012124744A1 (ja) * 2011-03-14 2014-07-24 大正製薬株式会社 含窒素縮合複素環化合物

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA103319C2 (en) 2008-05-06 2013-10-10 Глаксосмитклайн Ллк Thiazole- and oxazole-benzene sulfonamide compounds
EP2598481B1 (en) 2010-07-26 2016-08-31 Bristol-Myers Squibb Company Sulfonamide compounds useful as cyp17 inhibitors
CA2822039C (en) * 2010-12-16 2019-05-28 Allergan, Inc. Sulfur derivatives as chemokine receptor modulators
EP2567959B1 (en) 2011-09-12 2014-04-16 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013155528A2 (en) * 2012-04-13 2013-10-17 Fasgen, Inc. Methods for reducing brain inflammation, increasing insulin sensitivity, and reducing ceramide levels
KR102301867B1 (ko) 2013-12-18 2021-09-15 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 Nrf2 조절제
US9701627B2 (en) * 2014-06-16 2017-07-11 University Of Maryland, Baltimore LRRK2 GTP binding inhibitors for treatment of Parkinson's disease and neuroinflammatory disorders
WO2016172218A1 (en) * 2015-04-20 2016-10-27 The Regents Of The University Of Michigan Small molecule inhibitors of mcl-1 and uses thereof
ES2834490T3 (es) 2015-06-15 2021-06-17 Glaxosmithkline Ip Dev Ltd Reguladores de NRF2
US10604509B2 (en) 2015-06-15 2020-03-31 Glaxosmithkline Intellectual Property Development Limited Nrf2 regulators
US10364256B2 (en) 2015-10-06 2019-07-30 Glaxosmithkline Intellectual Property Development Limited Biaryl pyrazoles as NRF2 regulators
WO2019165232A1 (en) * 2018-02-23 2019-08-29 The Board Of Trustees Of The Leland Stanford Junior University Inhibitors of phospholipid synthesis and methods of use
WO2021035031A1 (en) * 2019-08-21 2021-02-25 The Board Of Trustees Of The Leland Stanford Junior University Inhibitors of phospholipid synthesis and methods of use
AR127055A1 (es) 2021-09-14 2023-12-13 Lilly Co Eli Sales agonistas de sstr4
WO2025140544A1 (zh) * 2023-12-28 2025-07-03 南京瑞初医药有限公司 Gsdmd抑制剂及其用途

Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2531367A (en) * 1947-07-15 1950-11-21 Sharp & Dohme Inc N-(substituted sulfonyl)-aminobenzoic acids
JPS52136146A (en) * 1976-03-18 1977-11-14 Richter Gedeon Vegyeszet Sulfonamide benzoic acid derivatives
JPS56100757A (en) * 1980-01-07 1981-08-12 Boehringer Mannheim Gmbh Novel sufonamide* its manfacture and blood platelet aggregation inhibiting and*or lipid lowering drug containing it
JPS5815967A (ja) * 1981-07-08 1983-01-29 サノフイ・ソシエテ・アノニム アミドベンズアミド化合物並びにその塩類、その製造法、及びそれ等を含んだ医薬組成物
US4595780A (en) * 1984-01-06 1986-06-17 Shionogi & Co., Ltd. Sulfonamido-benzamide derivatives
JPH04245257A (ja) * 1990-08-22 1992-09-01 Agfa Gevaert Nv 粒状トナー材料
JPH0532682A (ja) * 1990-02-02 1993-02-09 Hoechst Ag ウイルスによる病気を治療するためのベンジルホスホン酸誘導体の使用
JPH07290832A (ja) * 1994-04-26 1995-11-07 Mitsui Toatsu Chem Inc 感熱記録材料
US5981575A (en) * 1996-11-15 1999-11-09 Johns Hopkins University, The Inhibition of fatty acid synthase as a means to reduce adipocyte mass
JP2000006528A (ja) * 1998-06-25 2000-01-11 Fuji Photo Film Co Ltd 感熱記録材料
US6048680A (en) * 1998-12-09 2000-04-11 Eastman Kodak Company Photographic element containing pyrazoloazole coupler and a specific anti-fading combination
JP2000302793A (ja) * 1999-02-18 2000-10-31 Ono Pharmaceut Co Ltd ホスホン酸誘導体
WO2003043624A1 (en) * 2001-11-16 2003-05-30 Bristol-Myers Squibb Company Dual inhibitors of adipocyte fatty acid binding protein and keratinocyte fatty acid binding protein
WO2004022525A1 (en) * 2002-09-05 2004-03-18 Neurosearch A/S Amide derivatives and their use as chloride channel blockers
JP2004527557A (ja) * 2001-04-28 2004-09-09 アベンティス・ファーマ・ドイチユラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング アントラニル酸アミド、その製造方法、抗不整脈剤としてのその使用、およびその医薬調製物
JP2005514413A (ja) * 2001-12-26 2005-05-19 ジェンザイム コーポレーション リン酸塩輸送インヒビター
JP2005519924A (ja) * 2002-02-07 2005-07-07 ファルマシア・コーポレーション 粘膜送達のための医薬剤形
JP2006520756A (ja) * 2003-01-29 2006-09-14 パナコス ファーマシューティカルズ インコーポレーティッド ウイルスキャプシドスペーサーペプチド1タンパク質のプロセシングの破壊によるhiv−1複製の阻害
WO2007071443A1 (en) * 2005-12-22 2007-06-28 Novartis Ag Inhibitors of ccr9 activity
JP2008501634A (ja) * 2004-02-17 2008-01-24 ナステック ファーマスーティカル カンパニー インク. Y2受容体結合ペプチドの粘膜輸送強化組成物及び方法、及び肥満症の治療及び予防法
WO2008010934A2 (en) * 2006-07-14 2008-01-24 Chemocentryx, Inc. Triazolyl phenyl benzenesulfonamides
WO2008020037A1 (en) * 2006-08-16 2008-02-21 Action Medicines, S.L. Use of 2,5-dihydroxybenzene derivatives for treating obesity, hirsutism, hypertricosis and viral warts

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030124187A1 (en) * 1997-02-14 2003-07-03 Smithkline Beecham Laboratoires Pharmaceutiques, Pharmaceutical formulations comprising amoxycillin and clavulanate
DE602006003661D1 (de) * 2005-06-06 2008-12-24 Lilly Co Eli Ampa-rezeptoren-verstärker

Patent Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2531367A (en) * 1947-07-15 1950-11-21 Sharp & Dohme Inc N-(substituted sulfonyl)-aminobenzoic acids
JPS52136146A (en) * 1976-03-18 1977-11-14 Richter Gedeon Vegyeszet Sulfonamide benzoic acid derivatives
JPS56100757A (en) * 1980-01-07 1981-08-12 Boehringer Mannheim Gmbh Novel sufonamide* its manfacture and blood platelet aggregation inhibiting and*or lipid lowering drug containing it
JPS5815967A (ja) * 1981-07-08 1983-01-29 サノフイ・ソシエテ・アノニム アミドベンズアミド化合物並びにその塩類、その製造法、及びそれ等を含んだ医薬組成物
US4595780A (en) * 1984-01-06 1986-06-17 Shionogi & Co., Ltd. Sulfonamido-benzamide derivatives
JPH0532682A (ja) * 1990-02-02 1993-02-09 Hoechst Ag ウイルスによる病気を治療するためのベンジルホスホン酸誘導体の使用
JPH04245257A (ja) * 1990-08-22 1992-09-01 Agfa Gevaert Nv 粒状トナー材料
JPH07290832A (ja) * 1994-04-26 1995-11-07 Mitsui Toatsu Chem Inc 感熱記録材料
US5981575A (en) * 1996-11-15 1999-11-09 Johns Hopkins University, The Inhibition of fatty acid synthase as a means to reduce adipocyte mass
JP2000006528A (ja) * 1998-06-25 2000-01-11 Fuji Photo Film Co Ltd 感熱記録材料
US6048680A (en) * 1998-12-09 2000-04-11 Eastman Kodak Company Photographic element containing pyrazoloazole coupler and a specific anti-fading combination
JP2000302793A (ja) * 1999-02-18 2000-10-31 Ono Pharmaceut Co Ltd ホスホン酸誘導体
JP2004527557A (ja) * 2001-04-28 2004-09-09 アベンティス・ファーマ・ドイチユラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング アントラニル酸アミド、その製造方法、抗不整脈剤としてのその使用、およびその医薬調製物
WO2003043624A1 (en) * 2001-11-16 2003-05-30 Bristol-Myers Squibb Company Dual inhibitors of adipocyte fatty acid binding protein and keratinocyte fatty acid binding protein
JP2005514413A (ja) * 2001-12-26 2005-05-19 ジェンザイム コーポレーション リン酸塩輸送インヒビター
JP2005519924A (ja) * 2002-02-07 2005-07-07 ファルマシア・コーポレーション 粘膜送達のための医薬剤形
WO2004022525A1 (en) * 2002-09-05 2004-03-18 Neurosearch A/S Amide derivatives and their use as chloride channel blockers
JP2006520756A (ja) * 2003-01-29 2006-09-14 パナコス ファーマシューティカルズ インコーポレーティッド ウイルスキャプシドスペーサーペプチド1タンパク質のプロセシングの破壊によるhiv−1複製の阻害
JP2008501634A (ja) * 2004-02-17 2008-01-24 ナステック ファーマスーティカル カンパニー インク. Y2受容体結合ペプチドの粘膜輸送強化組成物及び方法、及び肥満症の治療及び予防法
WO2007071443A1 (en) * 2005-12-22 2007-06-28 Novartis Ag Inhibitors of ccr9 activity
WO2008010934A2 (en) * 2006-07-14 2008-01-24 Chemocentryx, Inc. Triazolyl phenyl benzenesulfonamides
WO2008020037A1 (en) * 2006-08-16 2008-02-21 Action Medicines, S.L. Use of 2,5-dihydroxybenzene derivatives for treating obesity, hirsutism, hypertricosis and viral warts

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
JPN6013058148; BORNE,RONALD F.,ET AL.: '"Antiinflammatory Activity of para-Substituted N-Benzenesulfonyl Derivatives of Anthranilic Acid"' JOURNAL OF PHARMACEUTICAL SCIENCES VOL.63,NO.4, 1974, PP.615-617 *
JPN6013058149; KAWAI,MEGUMI,ET AL.: '"Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with an' BIOORGANIC & MEDICINAL CHEMISTRY LETTERS VOL.16,NO.13, 2006, PP.3574-3577 *
JPN6013058150; LATIMER,P. H.,ET AL.: '"Sulfur studies. XV. The synthesis of alkanesulfonic acids and certain derivatives"' JOURNAL OF ORGANIC CHEMISTRY VOL.5, 1940, PP.24-28 *
JPN6013058152; SCOTT,ROBERT B.,JR.,ET AL.: '"A Study of aliphatic sulfonyl compounds. I. Octane-1- and -2-sulfonyl chlorides"' JOURNAL OF ORGANIC CHEMISTRY VOL.19, 1954, PP.830-839 *
JPN6013058153; WYDYSH,EDWARD A.,ET AL.: '"Design and Synthesis of Small Molecule Glycerol 3-Phosphate Acyltranferase Inhibitors"' JOURNAL OF MEDICINAL CHEMISTRY VOL.52,NO.10, 20090423, PP.3317-3327 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2012124744A1 (ja) * 2011-03-14 2014-07-24 大正製薬株式会社 含窒素縮合複素環化合物

Also Published As

Publication number Publication date
US20120083471A1 (en) 2012-04-05
CN102395270B (zh) 2014-11-12
CA2729767A1 (en) 2010-01-14
CN102395270A (zh) 2012-03-28
EP2303013A1 (en) 2011-04-06
MX2011000051A (es) 2011-07-28
WO2010005922A1 (en) 2010-01-14

Similar Documents

Publication Publication Date Title
JP2011527345A (ja) 新規な化合物、この化合物を含む医薬組成物、この化合物の使用方法、およびこの化合物の調製方法
CA2735478C (en) Malonyl-coa decarboxylase inhibitors useful as metabolic modulators
JP4503232B2 (ja) マロニル−CoA脱炭酸酵素阻害剤を用いた疾患の治療法
JP4855368B2 (ja) 代謝調節剤として有用なマロニル−CoA脱炭酸酵素阻害剤
JP6152149B2 (ja) 筋萎縮を阻害するための方法
BRPI0707957A2 (pt) composto, e, método para prevenção ou tratamento de uma condição ou sintoma patológico em um mamìfero
Festuccia et al. The PPARγ agonist rosiglitazone enhances rat brown adipose tissue lipogenesis from glucose without altering glucose uptake
JP4727578B2 (ja) マロニル−CoAデカルボキシラーゼ阻害剤として有用な複素環式化合物
JP2021073250A (ja) Ptp1b関連疾患の処置のためのアミノステロイド化合物
AU2017309751B2 (en) Sulfonamides as GPR40- and GPR120-agonists
Shiohara et al. Discovery of novel indane derivatives as liver-selective thyroid hormone receptor β (TRβ) agonists for the treatment of dyslipidemia
JP2013508327A (ja) シクロペンタンカルボキサミド誘導体、このような化合物を含む薬物及びそれらの使用
EP3564204A1 (en) 1,5-diphenyl-penta-1,4-dien-3-one compounds
WO2012112670A1 (en) Novel lipogenic inhibitors and uses thereof
CN103596570B (zh) 作为抗癌治疗的蛋白质靶的氧化鲨烯环化酶
ES2955462T3 (es) Nuevos tiromiméticos con un esqueleto de bifenilmetano y su uso
Shrestha et al. Derivatives of 1, 4-bis (3-hydroxycarbonyl-4-hydroxyl) styrylbenzene as PTP1B inhibitors with hypoglycemic activity
WO2019228994A1 (en) Oleic acid derivatives, pharmaceutical composition or food composition comprising said oleic acid derivatives, and their uses
WO2014114649A1 (en) Lipase inhibitors
US20110288176A1 (en) Ethacrynic acid-containing composition for prevention or treatment of transglutaminase-related diseases and method for prevention or treatment of transglutaminase-related diseases using the same
JP2018024645A (ja) プロテインホスファターゼ阻害剤
EP4602029A1 (en) Novel therapeutic molecule
US9340574B2 (en) Inhibitors of protein tyrosine phosphatases
HK40002404B (en) Sulfonamides as gpr40- and gpr120-agonists
HK40002404A (en) Sulfonamides as gpr40- and gpr120-agonists

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20120702

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20120702

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20140421