NO20084830L - C-fenylglycitolforbindelse for behandling av diabetes - Google Patents

C-fenylglycitolforbindelse for behandling av diabetes

Info

Publication number
NO20084830L
NO20084830L NO20084830A NO20084830A NO20084830L NO 20084830 L NO20084830 L NO 20084830L NO 20084830 A NO20084830 A NO 20084830A NO 20084830 A NO20084830 A NO 20084830A NO 20084830 L NO20084830 L NO 20084830L
Authority
NO
Norway
Prior art keywords
group
phenylglycitol
formula
compound
diabetes
Prior art date
Application number
NO20084830A
Other languages
English (en)
Inventor
Hiroyuki Kakinuma
Hideaki Amada
Yuko Hashimoto
Takahiro Ol
Hitomi Takahashi
Yohei Kobashi
Yuki Iwata
Original Assignee
Taisho Pharmaceutical Co 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 Taisho Pharmaceutical Co Ltd filed Critical Taisho Pharmaceutical Co Ltd
Publication of NO20084830L publication Critical patent/NO20084830L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/351Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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
    • C07D309/10Oxygen atoms
    • C07D309/12Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Emergency Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrane Compounds (AREA)

Abstract

Det er tilveiebrakt en ny C-fenylglycitolforbindelse som kan tjene som et profylaktisk eller terapeutisk middel for diabetes ved å inhibere både SGLTl aktivitet og SGLT2 aktivitet og derved utvise en glukoseabsorpsjonsundertrykkende virkning og en virkning på uringlukoseutskillelse. En C-fenylglycitolforbindelse representert ved formel (I) nedenfor eller et farmasøytisk aksepterbart salt derav eller et hydrat derav hvori R1 og R2 er like eller forskjellige og representerer et hydrogenatom, en hydroksylgruppe, en C1-6-alkylgruppe, en C1-6-alkoksygruppe eller et halogenatom, R3 er et hydrogenatom, en C1-6-alkylgruppe, en C1-6-alkoksy-gruppe eller et halogenatom, Y er en C1-6-alkylengruppe, -0-(CH2)n- (n er et helt tall fra 1 til 4) eller en C2-6-alkenylengruppe, med den betingelse at når Z er -NHC (=NH) NH2 eller -NHCON (RB) Rc, da er ikke n lik 1, Z is -CONHRA, -NHC (=NH) NH2 eller -NHCON (RB) Rc, formel (A) eller formel (B).S
NO20084830A 2006-05-19 2008-11-17 C-fenylglycitolforbindelse for behandling av diabetes NO20084830L (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2006139891 2006-05-19
JP2006200033 2006-07-21
PCT/JP2007/060653 WO2007136116A2 (en) 2006-05-19 2007-05-18 C-phenyl glycitol compound for the treatment of diabetes

Publications (1)

Publication Number Publication Date
NO20084830L true NO20084830L (no) 2009-02-19

Family

ID=38617514

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20084830A NO20084830L (no) 2006-05-19 2008-11-17 C-fenylglycitolforbindelse for behandling av diabetes

Country Status (15)

Country Link
US (1) US7973012B2 (no)
EP (1) EP2076503B1 (no)
JP (1) JP5067644B2 (no)
KR (1) KR20090016456A (no)
CN (1) CN101490028B (no)
AR (1) AR061026A1 (no)
AU (1) AU2007252432B2 (no)
BR (1) BRPI0711949A2 (no)
CA (1) CA2652707A1 (no)
MX (1) MX2008014512A (no)
NO (1) NO20084830L (no)
NZ (1) NZ573687A (no)
RU (1) RU2437876C2 (no)
TW (1) TW200812995A (no)
WO (1) WO2007136116A2 (no)

Families Citing this family (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8198464B2 (en) 2006-12-21 2012-06-12 Astellas Pharma Inc. Method for producing C-glycoside derivative and intermediate for synthesis thereof
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
KR101107425B1 (ko) 2007-08-23 2012-01-19 테라코스, 인코포레이티드 벤질벤젠 유도체 및 사용 방법
CN102026970B (zh) 2007-11-21 2013-07-31 解码遗传Ehf公司 用于治疗肺部和心血管病症的联芳基pde4抑制剂
UA101004C2 (en) 2007-12-13 2013-02-25 Теракос, Инк. Derivatives of benzylphenylcyclohexane and use thereof
KR101516677B1 (ko) * 2008-01-31 2015-05-04 고토부키 세이야쿠 가부시키가이샤 지방성 간 질환의 치료용 의약 조성물
EP2668953A1 (en) * 2008-05-22 2013-12-04 Bristol-Myers Squibb Company Pharmaceutical compositions comprising an SGLT2 inhibitor with a supply of carbohydrate and/or an inhibitor of uric acid synthesis
US9061060B2 (en) 2008-07-15 2015-06-23 Theracos Inc. Deuterated benzylbenzene derivatives and methods of use
WO2010022313A2 (en) 2008-08-22 2010-02-25 Theracos, Inc. Processes for the preparation of sglt2 inhibitors
SG173587A1 (en) * 2009-02-13 2011-09-29 Boehringer Ingelheim Int Sglt-2 inhibitor for treating type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance or hyperglycemia
JP5505741B2 (ja) 2009-02-23 2014-05-28 大正製薬株式会社 Sglt1阻害剤としての4−イソプロピルフェニルグルシトール化合物
US10610489B2 (en) 2009-10-02 2020-04-07 Boehringer Ingelheim International Gmbh Pharmaceutical composition, pharmaceutical dosage form, process for their preparation, methods for treating and uses thereof
PT2496583E (pt) 2009-11-02 2015-01-14 Pfizer Derivados de dioxa-biciclo[3.2.1]octano-2,3,4-triol
AR079438A1 (es) 2009-12-09 2012-01-25 Panacea Biotec Ltd Derivados de azucar, composiciones farmaceuticas y sus usos
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
US8575114B2 (en) 2010-03-23 2013-11-05 Albany Molecular Research, Inc. SGLT-2 inhibitors, methods of making them, and uses thereof
WO2011153712A1 (en) 2010-06-12 2011-12-15 Theracos, Inc. Crystalline form of benzylbenzene sglt2 inhibitor
WO2011157827A1 (de) 2010-06-18 2011-12-22 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
JP2013224263A (ja) * 2010-08-19 2013-10-31 Taisho Pharmaceutical Co Ltd 4−イソプロピルフェニルグルシトール化合物
JP5817317B2 (ja) * 2010-08-20 2015-11-18 大正製薬株式会社 4−イソプロピルフェニルグルシトール化合物を有効成分として含有することを特徴とする糖尿病の予防又は治療剤
TW201219414A (en) 2010-08-20 2012-05-16 Taisho Pharmaceutical Co Ltd Crystal form of 4-isopropylphenyl glucitol compound and process for production thereof
WO2012023600A1 (ja) 2010-08-20 2012-02-23 大正製薬株式会社 4-イソプロピル-6-メトキシフェニル グルシトール化合物
CN102453026A (zh) * 2010-10-27 2012-05-16 上海艾力斯医药科技有限公司 C-芳基葡糖苷衍生物、制备方法及其应用
EP2683705B1 (de) 2011-03-08 2015-04-22 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
US8710050B2 (en) 2011-03-08 2014-04-29 Sanofi Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
WO2012120056A1 (de) 2011-03-08 2012-09-13 Sanofi Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
WO2012120052A1 (de) 2011-03-08 2012-09-13 Sanofi Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung
EP2683704B1 (de) 2011-03-08 2014-12-17 Sanofi Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
JP6117186B2 (ja) * 2011-05-20 2017-04-19 ヤンセン ファーマシューティカ エヌ.ベー. Sglt−2の阻害物質として有用な化合物の製造方法
KR101719758B1 (ko) 2011-06-25 2017-03-24 수안주 파마 코포레이션 리미티드 씨 글루코사이드 유도체
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
EP2755722B1 (en) 2011-09-13 2017-05-24 Panacea Biotec Ltd. Novel sglt inhibitors
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
US9193751B2 (en) 2012-04-10 2015-11-24 Theracos, Inc. Process for the preparation of benzylbenzene SGLT2 inhibitors
UA113086C2 (xx) 2012-05-10 2016-12-12 Піразольні сполуки як інгібітори sglt1
TW201425326A (zh) 2012-10-05 2014-07-01 Lilly Co Eli 新穎脲化合物
FR2998202B1 (fr) * 2012-11-19 2015-04-17 Centre Nat Rech Scient Soudage heterogene aluminium/cuivre
DK3489226T3 (da) 2012-11-20 2021-04-26 Lexicon Pharmaceuticals Inc Hæmmere for natriumglucose-cotransporter 1
AU2014213251B2 (en) 2013-02-04 2017-07-20 Taisho Pharmaceutical Co., Ltd. Prophylactic or therapeutic drug for constipation
US20140303097A1 (en) 2013-04-05 2014-10-09 Boehringer Ingelheim International Gmbh Pharmaceutical composition, methods for treating and uses thereof
US11813275B2 (en) 2013-04-05 2023-11-14 Boehringer Ingelheim International Gmbh Pharmaceutical composition, methods for treating and uses thereof
PT2981271T (pt) 2013-04-05 2019-02-19 Boehringer Ingelheim Int Utilizações terapêuticas de empagliflozina
CN105377266A (zh) 2013-04-18 2016-03-02 勃林格殷格翰国际有限公司 药物组合物、治疗方法及其用途
CN105611920B (zh) 2013-10-12 2021-07-16 泰拉科斯萨普有限责任公司 羟基-二苯甲烷衍生物的制备
AR098670A1 (es) * 2013-11-08 2016-06-08 Lilly Co Eli Inhibidor de sglt1
US9315438B2 (en) 2014-01-03 2016-04-19 Xuanzhu Pharma Co., Ltd Optically pure benzyl-4-chlorophenyl-C-glucoside derivative
WO2017141202A1 (en) 2016-02-17 2017-08-24 Lupin Limited Complex of sglt2 inhibitor and process for preparation thereof
CN107540706A (zh) * 2016-06-28 2018-01-05 山东诚创医药技术开发有限公司 伊格列净中间体的制备方法
CN106632223B (zh) * 2016-08-24 2019-04-23 浙江美诺华药物化学有限公司 2-(3-溴-4-(3-氟苄氧基)苯基)-1,3-二氧戊环及其制备方法
CN108033876A (zh) * 2017-12-20 2018-05-15 江汉大学 一种5-溴-2-氯苯甲醛的制备方法
CN110066302B (zh) 2018-01-23 2022-12-27 广东东阳光药业有限公司 吡喃葡萄糖基衍生物及其用途
US11186602B2 (en) 2018-01-31 2021-11-30 Sunshine Lake Pharma Co., Ltd. Glucopyranosyl derivative and use thereof
CN108610385A (zh) * 2018-04-23 2018-10-02 中国科学院成都生物研究所 一种钠-葡萄糖协同转运蛋白1抑制剂的药物用途
US20230086354A1 (en) * 2019-07-10 2023-03-23 Sunshine Lake Pharma Co., Ltd. Glucopyranosyl derivatives and their uses
JP2023526699A (ja) * 2020-05-15 2023-06-22 上▲海▼▲哲▼▲イェ▼生物科技有限公司 アリールグルコシド誘導体及び薬物におけるその使用

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE216704T1 (de) 1996-12-26 2002-05-15 Tanabe Seiyaku Co Propiophenonderivate und verfahren zu ihrer herstellung
AU6024998A (en) 1997-01-15 1998-08-07 Glycomed Incorporated Aryl c-glycoside compounds and sulfated esters thereof
PH12000002657B1 (en) * 1999-10-12 2006-02-21 Bristol Myers Squibb Co C-aryl glucoside SGLT2 inhibitors
TR200202200T2 (tr) 2000-03-17 2002-12-23 Kissei Pharmaceutical Co., Ltd. Glükopiranosiloksibenzilbenzen türevleri, bu türevleri ihtiva eden tıbbi bileşimler ve türevlerin hazırlanması için ara-maddeler.
US6683056B2 (en) * 2000-03-30 2004-01-27 Bristol-Myers Squibb Company O-aryl glucoside SGLT2 inhibitors and method
JP4399251B2 (ja) * 2001-05-30 2010-01-13 キッセイ薬品工業株式会社 グルコピラノシルオキシピラゾール誘導体、それを含有する医薬組成物、その医薬用途およびその製造中間体
ATE469161T1 (de) 2002-08-08 2010-06-15 Kissei Pharmaceutical Pyrazolderivat, dieses enthaltende medizinische zusammensetzung, medizinische verwendung davon, und zwischenprodukt für dessen herstellung
JP2004137245A (ja) 2002-08-23 2004-05-13 Kissei Pharmaceut Co Ltd ピラゾール誘導体、それを含有する医薬組成物、その医薬用途及びその製造中間体
JP4606876B2 (ja) 2002-08-27 2011-01-05 キッセイ薬品工業株式会社 ピラゾール誘導体、それを含有する医薬組成物及びその医薬用途
AU2003289156A1 (en) 2002-12-04 2004-06-23 Kissei Pharmaceutical Co., Ltd. Preventive or remedy for diseases caused by hyperglycemia
SI1730131T1 (sl) * 2004-03-16 2012-08-31 Boehringer Ingelheim Int Glukopiranozil-substituirani benzenski derivati, zdravila, ki vsebujejo te spojine, njihova uporaba in postopek za njihovo pripravo
DE102004028241B4 (de) 2004-06-11 2007-09-13 Sanofi-Aventis Deutschland Gmbh Neue Fluorglykosidderivate von Pyrazolen, diese Verbindungen enthaltende Arzneimittel und Herstellung dieser Arzneimittel
TW200637839A (en) * 2005-01-07 2006-11-01 Taisho Pharmaceutical Co Ltd 1-thio-d-glucitol derivatives

Also Published As

Publication number Publication date
NZ573687A (en) 2010-10-29
BRPI0711949A2 (pt) 2012-01-17
AU2007252432A1 (en) 2007-11-29
AR061026A1 (es) 2008-07-30
JP2009537509A (ja) 2009-10-29
EP2076503A2 (en) 2009-07-08
TW200812995A (en) 2008-03-16
CN101490028A (zh) 2009-07-22
CA2652707A1 (en) 2007-11-29
MX2008014512A (es) 2008-11-27
RU2437876C2 (ru) 2011-12-27
EP2076503B1 (en) 2013-07-17
AU2007252432B2 (en) 2011-11-17
WO2007136116A3 (en) 2008-03-13
WO2007136116A2 (en) 2007-11-29
CN101490028B (zh) 2013-02-06
RU2008150383A (ru) 2010-06-27
JP5067644B2 (ja) 2012-11-07
US20100022460A1 (en) 2010-01-28
US7973012B2 (en) 2011-07-05
KR20090016456A (ko) 2009-02-13

Similar Documents

Publication Publication Date Title
NO20084830L (no) C-fenylglycitolforbindelse for behandling av diabetes
NO20085240L (no) C-fenyl-1-tioglucitolforbindelse
NO20084127L (no) Benzylfenylglukopyranosidderivat
NO20062583L (no) Difenylazetidinonderivater med kolesterolabsorpsjonsinhiberende aktivitet
NO20084968L (no) Dihydropyrazolpyrimidinonderivater
NO20081315L (no) Benzokinazolinderivater og deres anvendelse ved behandling av benlidelser
NO20092286L (no) Nitrogenhaldige heterosykliske forbindelser og anvendelse derav
MY129023A (en) Glucopyranosyloxybenzylbenzene derivatives and medicinal compositions containing the same
NO20060823L (no) Benzimidazol, benztiazol og benzoksazol derivater og deres anvendelse som LTA4H modulatorer
NO20083207L (no) Inhibitorer av IAP
EA200800172A1 (ru) 2,4-диаминопиримидины как ингибиторы aurora
NO20080675L (no) P38-Map kinaseinhibitorer og metoder for deres anvendelse
NO20082090L (no) Pyridopyrimidinoninhibitorer av P13K alfa
NO20085176L (no) Fenyl substituerte heteroaryl-derivater og andvendelse som anti-tumor agenter
NO20084845L (no) 2-pyrazinonderivater for behandling av sykdom eller tilstander der inhibiering av neutrofil elastaseaktivitetet er gunstig
NO20070323L (no) Organiske forbindelser
NO20056192L (no) Kapaseinhibitorer og anvendelse derav
NO20081217L (no) Nye benzotiazolonderivater
NO20083845L (no) 2,4-diaminopyrimidiner som celle-cyklus kinase inhibitorer
NO20072608L (no) Biaryloksymetylarenkarboksylsyrer
MX2009008756A (es) Compuesto macrociclico.
UA83057C2 (ru) Замещенные производные диоксида тиазолбензоизотиазола и их применение
NO20075617L (no) 4-fenyl-5-okso-1,4,5,6,7,8-heksahydrokinolinderivater for behandling av infertilitet
ATE415395T1 (de) Benzofuran- und benzothiophenderivate, die sich für die behandlung von herzkreislauferkrankungen eignen
NO20072089L (no) Benzimidazolderivater, sammensetninger som inneholder dem, fremstilling derav og anvendelse derav

Legal Events

Date Code Title Description
FC2A Withdrawal, rejection or dismissal of laid open patent application