NO20006667L - Retinoid-relaterte reseptor funksjonsregulerende middel - Google Patents

Retinoid-relaterte reseptor funksjonsregulerende middel

Info

Publication number
NO20006667L
NO20006667L NO20006667A NO20006667A NO20006667L NO 20006667 L NO20006667 L NO 20006667L NO 20006667 A NO20006667 A NO 20006667A NO 20006667 A NO20006667 A NO 20006667A NO 20006667 L NO20006667 L NO 20006667L
Authority
NO
Norway
Prior art keywords
cachexia
hydrocarbon group
insulin
hydrogen
optionally substituted
Prior art date
Application number
NO20006667A
Other languages
English (en)
Other versions
NO20006667D0 (no
Inventor
Yasuo Sugiyama
Yu Momose
Hiroyuki Kimura
Junichi Sakamoto
Hiroyuki Odaka
Original Assignee
Takeda Chemical Industries Ltd
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 Takeda Chemical Industries Ltd filed Critical Takeda Chemical Industries Ltd
Publication of NO20006667D0 publication Critical patent/NO20006667D0/no
Publication of NO20006667L publication Critical patent/NO20006667L/no

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/32Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D277/30Radicals 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
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

En farmasøytisk sammensetning av oppfinnelsen som er en retionoid-relatert reseptorfunksjons- regulerende middel som omfatter en 1,3-azolderivat representert ved formelen (I): hvor R1 er en aromatisk hydrokarbongruppe eller en aromatisk heterosyklisk gruppe, som hver kan substitueres; R2 er hydrogen eller en eventuelt substituert hydrokarbon-gruppe; X ff O, S er en gruppe representert ved formelen: -NR4- hvori R4 er hydrogen eller en eventuelt substituert alkylgruppe; A er en aromatisk hydrokarbon gruppe eller en aromatisk heterosyklisk gruppe, som hver kan substitueres; R3 a en gruppe representert ved formelen: -OR5 hvori R3 er hydrogen eller en eventuelt substituert hydrokarbongruppe, eller -NR*R7 hvori R6 og R7 er den samme eller forskjellig og hver er hydrogen eller en eventuelt substituert hydrokarbongruppe, eller R6 og R7 kan sammen med tilliggende nitrogenatom danne en ring, forutsatt at forbindelsene er representert ved formelen: CH COOH COOH er ekskludert, eller dets salt, er lav i toksisitet, og kan anvendes, for eksempel som et middel for å forebygge eller behandle diabetes (for eksempel, insulinavhengig diabetes, ikke-insulinavhengig diabetes, gestasjonell diabetes), som et middel for å behandle eller hindre hyperlipidemi (for eksempel, hypertriglysemi, hyper-kolesterolemi, hypo-HD-lipoproteinemi), en insulinsensitivitetsforsterkende middel, et insulinresistens forbedrende middel, et middel for å hindre eller behandle svekket glukosetoleranse (IGT) og et middel for å hindre transisjon fra svekket glukose toleranse til diabetes. Videre kan en farmasøytisk sammensetning fra oppfinnelsen bli brukt, for eksempel, som et middel for å hindre eller behandle diabetiske komplikasjoner (for eksempel, neuropati, nefropati, retinopati, katarakt, makroangiopati, osteopeni), fedme, osteoporose, kakeksia, (for eksempel karsinomatøs kakeksia, tuberkulose kakeksia, diabetisk kakeksia, hemopatisk kakeksia, endokrinopatisk kakeksia, infektiøs kakeksia, eller kakeksia indusert ved ervervet immunosvikt syndrom), fettholdig lever, hypertensjon, polysystisk ovarie syndrom, nyresykdommer, for eksempel, diabetisk nefropati, glomulær nefritt, glomulær sklerose, nefrotisk syndrom, hypertensitiv nefrosklerose, terminal renal forstyrrelse (muskulær dystrofi, myokardial infarkt, angina pektoris), cerebral infarkt, insulin resistent syndrom, syndrom X, hyperinsulinemi-indusert sensorisk forstyrrelse, tumor (for eksempel leukemi, brystcancer, prostata cancer, hudcancer), arteriosklerose (for eksempel, aterosklerose) og som et farmasøytisk middel for å kontrollere appetitt og matinntak.
NO20006667A 1998-07-01 2000-12-27 Retinoid-relaterte reseptor funksjonsregulerende middel NO20006667L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP18669898 1998-07-01
PCT/JP1999/003520 WO2000001679A1 (en) 1998-07-01 1999-06-30 Retinoid-associated receptor regulators

Publications (2)

Publication Number Publication Date
NO20006667D0 NO20006667D0 (no) 2000-12-27
NO20006667L true NO20006667L (no) 2001-02-28

Family

ID=16193077

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20006667A NO20006667L (no) 1998-07-01 2000-12-27 Retinoid-relaterte reseptor funksjonsregulerende middel

Country Status (16)

Country Link
US (1) US6545009B1 (no)
EP (1) EP1092711A4 (no)
KR (1) KR20010053282A (no)
CN (1) CN1314899A (no)
AU (1) AU4394799A (no)
BR (1) BR9911752A (no)
CA (1) CA2332178A1 (no)
HU (1) HUP0102470A3 (no)
ID (1) ID29247A (no)
IL (1) IL140422A0 (no)
LV (1) LV12633B (no)
NO (1) NO20006667L (no)
PL (1) PL345247A1 (no)
SK (1) SK20182000A3 (no)
WO (1) WO2000001679A1 (no)
ZA (1) ZA200007635B (no)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6548529B1 (en) 1999-04-05 2003-04-15 Bristol-Myers Squibb Company Heterocyclic containing biphenyl aP2 inhibitors and method
AR035016A1 (es) 1999-08-25 2004-04-14 Takeda Chemical Industries Ltd Composicion de azol promotor de produccion/secrecion de neurotrofina, compuesto prodroga del mismo, composicion farmaceutica que lo comprende y uso del mismo para preparar esta ultima.
EP1394154A4 (en) 2001-03-23 2005-05-18 Takeda Pharmaceutical FIVE-GLASS HETEROCYCLIC ALKANIC ACID DERIVATIVE
WO2002085382A1 (en) * 2001-04-18 2002-10-31 Genzyme Corporation Methods of treating syndrome x with aliphatic polyamines
GB0112348D0 (en) * 2001-05-19 2001-07-11 Smithkline Beecham Plc Compounds
US20040248863A1 (en) * 2001-06-22 2004-12-09 Wright Samuel D. Combination of a ppar-alpha ligand and glucocorticoid for the treatment or prevention of inflamation
WO2003000249A1 (en) * 2001-06-26 2003-01-03 Takeda Chemical Industries, Ltd. Function regulator for retinoid relative receptor
JP2003081832A (ja) * 2001-06-26 2003-03-19 Takeda Chem Ind Ltd レチノイド関連受容体機能調節剤
JP2005516968A (ja) * 2001-12-29 2005-06-09 ノボ ノルディスク アクティーゼルスカブ Glp−1化合物と糖尿病後期合併症モジュレーターの組み合わせ使用
US7183276B2 (en) 2002-02-28 2007-02-27 Takeda Pharmaceutical Company Limited Azole compounds
CN1731994A (zh) 2002-11-01 2006-02-08 武田药品工业株式会社 预防或治疗神经病的药剂
GB0303503D0 (en) * 2003-02-14 2003-03-19 Novartis Ag Organic compounds
DE10308353A1 (de) * 2003-02-27 2004-12-02 Aventis Pharma Deutschland Gmbh Diarylcycloalkylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
JP5191744B2 (ja) * 2005-02-25 2013-05-08 ソウル ナショナル ユニバーシティー インダストリー ファンデーション ペルオキシソーム増殖子活性化受容体デルタリガンドのチアゾール誘導体及びその製造方法
WO2006091047A1 (en) * 2005-02-25 2006-08-31 Heonjoong Kang Thiazole derivatives as ppar delta ligands and their manufacturing process
CA2623327A1 (en) * 2005-10-07 2007-04-19 Kissei Pharmaceutical Co., Ltd. Nitrogenated heterocyclic compound and pharmaceutical composition comprising the same
WO2008064136A2 (en) * 2006-11-17 2008-05-29 Acadia Pharmaceuticals Inc. Compounds with activity at retinoic acid receptors
US8207196B2 (en) 2007-02-02 2012-06-26 Baylor College Of Medicine Compositions and methods for the treatment of metabolic disorders
US9233941B2 (en) 2007-02-02 2016-01-12 Baylor College Of Medicine Methods and compositions for the treatment of body weight related disorders
US9187485B2 (en) 2007-02-02 2015-11-17 Baylor College Of Medicine Methods and compositions for the treatment of cancer and related hyperproliferative disorders
US9212179B2 (en) 2007-02-02 2015-12-15 Baylor College Of Medicine Compositions and methods for the treatment of metabolic disorders
US9085566B2 (en) 2007-02-02 2015-07-21 Baylor College Of Medicine Compositions and methods for the treatment of metabolic and related disorders
EP2786993B1 (en) 2007-08-13 2017-11-15 Monsanto Technology LLC Compositions and methods for controlling nematodes
WO2011011105A2 (en) * 2009-05-07 2011-01-27 Baylor College Of Medicine Traceable retinoid acid for imaging, disease prevention and therapy
GB0915196D0 (en) 2009-09-01 2009-10-07 King S College London Therapeutic compounds and their use
WO2012028100A1 (en) * 2010-09-01 2012-03-08 Glaxo Group Limited Novel compounds
KR20170096181A (ko) 2014-12-19 2017-08-23 갈데르마 리써어치 앤드 디벨로프먼트 신규 화합물, 이의 합성 방법 및 의약 및 화장품에서의 이의 용도
WO2018002673A1 (en) 2016-07-01 2018-01-04 N4 Pharma Uk Limited Novel formulations of angiotensin ii receptor antagonists
US10865793B2 (en) 2016-12-06 2020-12-15 Air Squared, Inc. Scroll type device having liquid cooling through idler shafts
US20200025199A1 (en) 2018-07-17 2020-01-23 Air Squared, Inc. Dual drive co-rotating spinning scroll compressor or expander
US11530703B2 (en) 2018-07-18 2022-12-20 Air Squared, Inc. Orbiting scroll device lubrication
US11473572B2 (en) 2019-06-25 2022-10-18 Air Squared, Inc. Aftercooler for cooling compressed working fluid
US11898557B2 (en) 2020-11-30 2024-02-13 Air Squared, Inc. Liquid cooling of a scroll type compressor with liquid supply through the crankshaft
US11885328B2 (en) 2021-07-19 2024-01-30 Air Squared, Inc. Scroll device with an integrated cooling loop

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4001420A (en) 1968-12-12 1977-01-04 Science Union Et Cie, Societe Francaise De Recherche Medical Thiazolyl benzoic acid compounds
GB1308028A (en) 1970-06-12 1973-02-21 Science Union & Cie Thiazolylbenzoic acid derivatives and a process for their manufactur
JPS4932853A (no) 1972-07-27 1974-03-26
US3939115A (en) * 1974-10-02 1976-02-17 Eastman Kodak Company Polychromophoric ultraviolet stabilizers and their use in organic compositions
US4043973A (en) 1974-10-02 1977-08-23 Eastman Kodak Company Multichromophoric ultraviolet stabilizers for organic compositions
US4164480A (en) 1978-01-09 1979-08-14 Eastman Kodak Company Polychromophoric ultraviolet stabilizers and their use in organic compositions
SU1078859A1 (ru) 1982-03-31 1997-10-20 Б.М. Красовицкий 2-(5-фенилоксазолил-2)-5-(5-арилоксазолил-2)-бензойные кислоты в качестве органических люминофоров сине-зеленого свечения в органических растворителях и водной среде
JPH0725754B2 (ja) * 1986-01-30 1995-03-22 富山化学工業株式会社 新規なチアゾール化合物またはその塩
JP2524786B2 (ja) * 1987-12-15 1996-08-14 コニカ株式会社 直接ポジハロゲン化銀カラ―写真感光材料
DE3903993A1 (de) 1989-02-10 1990-08-16 Basf Ag Diarylsubstituierte heterocyclische verbindungen, ihre herstellung und arzneimittel daraus
JP2941937B2 (ja) 1990-01-25 1999-08-30 キヤノン株式会社 新規化合物、これを含む液晶組成物及びこれを使用した液晶素子並びに表示装置
JPH04154773A (ja) * 1990-10-15 1992-05-27 Green Cross Corp:The チアゾール誘導体
EP0513387B1 (en) 1990-11-30 2000-03-01 Otsuka Pharmaceutical Co., Ltd. Thiazole derivatives as active oxygen inhibitors
US5639770A (en) 1992-05-29 1997-06-17 Otsuka Pharmaceutical Co., Ltd. Thiazole derivatives
JP3385387B2 (ja) * 1992-05-29 2003-03-10 大塚製薬株式会社 チアゾール誘導体
US5342851A (en) 1992-10-07 1994-08-30 Mcneil-Ppc, Inc. Substituted thiazole derivatives useful as platelet aggregation inhibitors
DE4302051A1 (de) * 1993-01-26 1994-07-28 Thomae Gmbh Dr K 5-gliedrige Heterocyclen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
PL183233B1 (pl) 1995-02-24 2002-06-28 Basf Ag Nowe pochodne pirazol-4-ilo-benzoilu, sposób wytwarzania nowych pochodnych pirazol-4-ilo-benzoilu i środek chwastobójczy
JP3964478B2 (ja) 1995-06-30 2007-08-22 エーザイ・アール・アンド・ディー・マネジメント株式会社 ヘテロ環含有カルボン酸誘導体及びそれを含有する医薬
JP3865829B2 (ja) 1995-09-21 2007-01-10 株式会社医薬分子設計研究所 レチノイド作用増強性化合物
ES2124167B1 (es) 1996-06-04 1999-09-16 Espanola Prod Quimicos Nuevos derivados del bencimidazol con actividad antihistaminica.
WO1998008830A1 (de) * 1996-08-26 1998-03-05 Byk Gulden Lomberg Chemische Fabrik Gmbh Thiazol-derivate als selektive inhibitoren der pde-iv
JP4300373B2 (ja) * 1996-09-30 2009-07-22 大塚製薬株式会社 サイトカイン産生抑制剤及び接着抑制剤
AUPO691897A0 (en) * 1997-05-21 1997-06-12 Fujisawa Pharmaceutical Co., Ltd. New compound

Also Published As

Publication number Publication date
HUP0102470A3 (en) 2002-05-28
SK20182000A3 (sk) 2001-08-06
US6545009B1 (en) 2003-04-08
PL345247A1 (en) 2001-12-03
KR20010053282A (ko) 2001-06-25
CA2332178A1 (en) 2000-01-13
LV12633A (lv) 2001-03-20
LV12633B (en) 2001-07-20
ID29247A (id) 2001-08-16
ZA200007635B (en) 2002-01-02
EP1092711A4 (en) 2002-07-31
WO2000001679A1 (en) 2000-01-13
AU4394799A (en) 2000-01-24
CN1314899A (zh) 2001-09-26
NO20006667D0 (no) 2000-12-27
BR9911752A (pt) 2001-04-03
HUP0102470A2 (hu) 2002-04-29
EP1092711A1 (en) 2001-04-18
IL140422A0 (en) 2002-02-10

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