MA26855A1 - Activateurs de glucokinases transolefiniques - Google Patents

Activateurs de glucokinases transolefiniques

Info

Publication number
MA26855A1
MA26855A1 MA26690A MA26690A MA26855A1 MA 26855 A1 MA26855 A1 MA 26855A1 MA 26690 A MA26690 A MA 26690A MA 26690 A MA26690 A MA 26690A MA 26855 A1 MA26855 A1 MA 26855A1
Authority
MA
Morocco
Prior art keywords
transolefinic
glucokinases
activators
transolefinic glucokinases
Prior art date
Application number
MA26690A
Other languages
English (en)
Inventor
Ramakanth Sarabu
Achyutharao Sidduri
Wendy Lea Corbett
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA26855A1 publication Critical patent/MA26855A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic 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
    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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 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
    • C07D213/72—Nitrogen atoms
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
    • C07C275/48—Y being a hydrogen or a carbon atom
    • C07C275/50—Y being a hydrogen or an acyclic carbon atom
    • 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
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic 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
    • C07D277/32—Heterocyclic 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 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
    • C07D277/38—Nitrogen atoms
    • C07D277/44—Acylated amino or imino radicals
    • C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Detergent Compositions (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
MA26690A 1999-12-15 2002-06-14 Activateurs de glucokinases transolefiniques MA26855A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US17078399P 1999-12-15 1999-12-15

Publications (1)

Publication Number Publication Date
MA26855A1 true MA26855A1 (fr) 2004-12-20

Family

ID=22621235

Family Applications (1)

Application Number Title Priority Date Filing Date
MA26690A MA26855A1 (fr) 1999-12-15 2002-06-14 Activateurs de glucokinases transolefiniques

Country Status (33)

Country Link
US (1) US6353111B1 (fr)
EP (1) EP1242397B1 (fr)
JP (1) JP3824936B2 (fr)
KR (1) KR100502032B1 (fr)
CN (1) CN1185219C (fr)
AR (1) AR032752A1 (fr)
AT (1) ATE305461T1 (fr)
AU (1) AU781029B2 (fr)
CA (1) CA2392903C (fr)
CO (1) CO5050295A1 (fr)
CZ (1) CZ20022412A3 (fr)
DE (1) DE60022903T2 (fr)
DK (1) DK1242397T3 (fr)
ES (1) ES2249322T3 (fr)
GC (1) GC0000264A (fr)
HK (1) HK1054383B (fr)
HR (1) HRP20020514A2 (fr)
HU (1) HUP0203753A3 (fr)
IL (2) IL150083A0 (fr)
JO (1) JO2180B1 (fr)
MA (1) MA26855A1 (fr)
MX (1) MXPA02005874A (fr)
MY (1) MY125484A (fr)
NO (1) NO323142B1 (fr)
NZ (1) NZ518974A (fr)
PE (1) PE20011022A1 (fr)
PL (1) PL355815A1 (fr)
RU (1) RU2245332C2 (fr)
TW (1) TWI262916B (fr)
UY (1) UY26483A1 (fr)
WO (1) WO2001044216A1 (fr)
YU (1) YU41402A (fr)
ZA (1) ZA200203829B (fr)

Families Citing this family (67)

* Cited by examiner, † Cited by third party
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SE0102299D0 (sv) 2001-06-26 2001-06-26 Astrazeneca Ab Compounds
SE0102764D0 (sv) * 2001-08-17 2001-08-17 Astrazeneca Ab Compounds
RU2374236C2 (ru) 2001-12-21 2009-11-27 Ново Нордиск А/С Амидные производные в качестве активаторов gk
US7410956B2 (en) 2002-02-11 2008-08-12 Vertex Pharmaceuticals Incorporated Caspase inhibitor prodrugs
EP1496052B1 (fr) * 2002-03-26 2009-08-05 Banyu Pharmaceutical Co., Ltd. Nouveau derive aminobenzamide
KR101124245B1 (ko) 2002-06-27 2012-07-02 노보 노르디스크 에이/에스 치료제로서 아릴 카르보닐 유도체
AU2003243921B2 (en) 2002-06-27 2009-05-07 Novo Nordisk A/S Aryl carbonyl derivatives as therapeutic agents
JP2006509774A (ja) * 2002-10-03 2006-03-23 ノバルティス アクチエンゲゼルシャフト ２型糖尿病の処置において有用なグルコキナーゼアクチベーターとしての置換（チアゾール−２−イル）−アミドまたはスルホンアミド
GB0226930D0 (en) * 2002-11-19 2002-12-24 Astrazeneca Ab Chemical compounds
GB0226931D0 (en) 2002-11-19 2002-12-24 Astrazeneca Ab Chemical compounds
US7132425B2 (en) 2002-12-12 2006-11-07 Hoffmann-La Roche Inc. 5-substituted-six-membered heteroaromatic glucokinase activators
WO2004063194A1 (fr) * 2003-01-06 2004-07-29 Eli Lilly And Company Composes heteroaryle
PL378117A1 (pl) * 2003-02-11 2006-03-06 Prosidion Limited Tricyklopodstawione związki amidowe
JP4621198B2 (ja) * 2003-02-11 2011-01-26 プロシディオン・リミテッド トリ（シクロ）置換アミドグルコキナーゼ活性化化合物
WO2005066145A1 (fr) 2004-01-06 2005-07-21 Novo Nordisk A/S Heteroaryl-urees et leur utilisation en tant qu'activateurs de glucokinase
ATE426597T1 (de) 2004-02-18 2009-04-15 Astrazeneca Ab Benzamidderivate und deren verwendung als glucokinaseaktivierende mittel
CN1960995B (zh) * 2004-04-02 2010-12-08 诺瓦提斯公司 作为葡糖激酶活化剂、可用于治疗ⅱ型糖尿病的磺酰胺-噻唑并吡啶衍生物
EP1737870A1 (fr) * 2004-04-02 2007-01-03 Novartis AG Derives thiazolopyridine, compositions pharmaceutiques les contenant et procedes de traitement de troubles a mediation par glucokinase
AU2005235798A1 (en) * 2004-04-21 2005-11-03 Prosidion Limited Tri(cyclo) substituted amide compounds
CN100567276C (zh) * 2004-04-21 2009-12-09 普罗西迪恩有限公司 三（环）取代的酰胺类化合物
TW200600086A (en) 2004-06-05 2006-01-01 Astrazeneca Ab Chemical compound
US20080026987A1 (en) * 2004-06-17 2008-01-31 Novo Nordisk A/S Use of Liver-Selective Glucokinase Activators
MX2007001650A (es) * 2004-08-12 2007-07-13 Prosidion Ltd Fenilacetamidas substituidas y su uso como activadores de glucocinasa.
CA2614518A1 (fr) 2005-07-08 2007-01-18 Novo-Nordisk A/S Activateurs de dicycloalkyluree glucokinase
US7642259B2 (en) 2005-07-09 2010-01-05 Astrazeneca Ab Heteroaryl benzamide derivatives for use as GLK activators in the treatment of diabetes
WO2007015805A1 (fr) 2005-07-20 2007-02-08 Eli Lilly And Company Composés joints en position 1-amino
JP2007063225A (ja) * 2005-09-01 2007-03-15 Takeda Chem Ind Ltd イミダゾピリジン化合物
JP2009509988A (ja) 2005-09-29 2009-03-12 サノフィ−アベンティス フェニル−及びピリジニル−１，２，４−オキサジアゾロン誘導体、その製造方法、及び医薬品としてのその使用
GT200600428A (es) * 2005-09-30 2007-05-21 Compuestos organicos
GT200600429A (es) * 2005-09-30 2007-04-30 Compuestos organicos
CA2626475A1 (fr) * 2005-11-03 2007-05-10 Prosidion Limited Amides a substitution tricyclo
WO2007123581A1 (fr) 2005-11-17 2007-11-01 Eli Lilly And Company Antagonistes des récepteurs du glucagon, leur préparation et leurs utilisations thérapeutiques
WO2007061923A2 (fr) * 2005-11-18 2007-05-31 Takeda San Diego, Inc. Activateurs de la glucokinase
US8034822B2 (en) 2006-03-08 2011-10-11 Takeda San Diego, Inc. Glucokinase activators
PE20110235A1 (es) 2006-05-04 2011-04-14 Boehringer Ingelheim Int Combinaciones farmaceuticas que comprenden linagliptina y metmorfina
US8008332B2 (en) * 2006-05-31 2011-08-30 Takeda San Diego, Inc. Substituted indazoles as glucokinase activators
CA2660570C (fr) 2006-08-24 2016-08-09 University Of Tennessee Research Foundation Acylanilides substitues et procedes d'utilisation de ceux-ci
SA07280576B1 (ar) 2006-10-26 2011-06-22 استرازينيكا ايه بي مركبات بنزويل أمينو سيكليل غير متجانسة بأعتبارها عوامل منشطة للجلوكوكيناز
US7902248B2 (en) * 2006-12-14 2011-03-08 Hoffmann-La Roche Inc. Oxime glucokinase activators
WO2008079787A2 (fr) 2006-12-20 2008-07-03 Takeda San Diego, Inc. Activateurs de glucokinase
TW200831081A (en) * 2006-12-25 2008-08-01 Kyorin Seiyaku Kk Glucokinase activator
US8940900B2 (en) 2007-02-28 2015-01-27 Advinus Therapeutics Private Limited 2,2,2-tri-substituted acetamide derivatives as glucokinase activators, their process and pharmaceutical application
CN101687800B (zh) * 2007-03-07 2012-03-21 杏林制药株式会社 葡糖激酶活化物质
US8173645B2 (en) * 2007-03-21 2012-05-08 Takeda San Diego, Inc. Glucokinase activators
EP2203448B1 (fr) * 2007-09-21 2011-06-22 Sanofi-Aventis Dérivés de phénothiazine à liaison double, procédé pour les produire et leur utilisation comme médicaments
CL2009000004A1 (es) * 2008-01-15 2010-02-19 Lilly Co Eli Forma cristalina de r-2-(4-ciclopropansulfonil-fenil)-n-pirazin-2-il-3-(tetrahidropiran-4-il)-propionamida; composicion farmaceutica que comprende a dicha forma cristalina; y uso para el tratamiento de diabetes o hiperglicemia.
AU2009205070A1 (en) 2008-01-18 2009-07-23 Astellas Pharma Inc. Phenyl acetamide derivative
MY163114A (en) 2008-04-28 2017-08-15 Kyorin Seiyaku Kk Cyclopentylacrylamide derivative
TWI445707B (zh) 2008-05-16 2014-07-21 Takeda California Inc 葡萄糖激酶活化劑
US8450494B2 (en) 2009-06-22 2013-05-28 Cadila Healthcare Limited Disubstituted benzamide derivatives as glucokinase (GK) activators
EA201270217A1 (ru) 2009-07-31 2012-09-28 Кадила Хелзкэр Лимитед Замещенные бензамидные производные в качестве активаторов глюкокиназы (гк)
KR100970871B1 (ko) * 2009-11-30 2010-07-20 케이제이알디 (주) 바닥재 어셈블리 및 바닥재의 시공방법
JP5750050B2 (ja) 2009-12-04 2015-07-15 大正製薬株式会社 ２−ピリドン化合物
JP5909482B2 (ja) 2010-03-31 2016-04-26 ザ スクリプス リサーチ インスティテュート 細胞の再プログラム
US9622992B2 (en) 2012-07-13 2017-04-18 Gtx, Inc. Method of treating androgen receptor (AR)-positive breast cancers with selective androgen receptor modulator (SARMs)
US10314807B2 (en) 2012-07-13 2019-06-11 Gtx, Inc. Method of treating HER2-positive breast cancers with selective androgen receptor modulators (SARMS)
US9744149B2 (en) 2012-07-13 2017-08-29 Gtx, Inc. Method of treating androgen receptor (AR)-positive breast cancers with selective androgen receptor modulator (SARMs)
US9969683B2 (en) 2012-07-13 2018-05-15 Gtx, Inc. Method of treating estrogen receptor (ER)-positive breast cancers with selective androgen receptor modulator (SARMS)
US10258596B2 (en) 2012-07-13 2019-04-16 Gtx, Inc. Method of treating HER2-positive breast cancers with selective androgen receptor modulators (SARMS)
MX375256B (es) 2012-07-13 2025-03-06 Gtx Inc Metodo para tratar canceres de mama positivos a receptor de androgeno (ar) con modulador de receptor de androgeno selectivo (sarms).
US10987334B2 (en) 2012-07-13 2021-04-27 University Of Tennessee Research Foundation Method of treating ER mutant expressing breast cancers with selective androgen receptor modulators (SARMs)
ES2641469T3 (es) 2012-11-13 2017-11-10 Nissan Chemical Industries, Ltd. Compuesto de 2-piridona
GB201714777D0 (en) 2017-09-14 2017-11-01 Univ London Queen Mary Agent
KR20210020866A (ko) 2018-06-12 2021-02-24 브이티브이 테라퓨틱스 엘엘씨 인슐린 또는 인슐린 유사체와 조합된 글루코키나제 활성제의 치료적 용도
WO2021167840A1 (fr) 2020-02-18 2021-08-26 Vtv Therapeutics Llc Activateurs de glucokinase sulfone et sulfoxyde et leurs procédés d'utilisation
EP4161640A4 (fr) 2020-06-08 2024-01-17 vTv Therapeutics LLC Sels ou co-cristaux de {2-[3-cyclohéxyl-3-(trans-4-propoxy-cyclohéxyl)-uréido]-thiazol-5-ylsulfanyl}-acide acétique et leurs utilisations

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US5169951A (en) 1990-04-23 1992-12-08 Ciba-Geigy Corporation Process for preparing nematicidal compositions
US5510478A (en) * 1994-11-30 1996-04-23 American Home Products Corporation 2-arylamidothiazole derivatives with CNS activity
HRP20010688B1 (en) * 1999-03-29 2008-10-31 F. Hoffmann - La Roche Ag Glucokinase activators

Also Published As

Publication number Publication date
MXPA02005874A (es) 2002-10-23
YU41402A (sh) 2005-07-19
CA2392903A1 (fr) 2001-06-21
IL150083A (en) 2010-04-15
IL150083A0 (en) 2002-12-01
DK1242397T3 (da) 2006-02-13
JO2180B1 (en) 2003-04-23
HRP20020514A2 (en) 2004-06-30
KR100502032B1 (ko) 2005-07-25
HUP0203753A2 (hu) 2003-03-28
CA2392903C (fr) 2008-08-05
CZ20022412A3 (cs) 2002-10-16
CN1411453A (zh) 2003-04-16
MY125484A (en) 2006-08-30
GC0000264A (en) 2006-11-01
RU2245332C2 (ru) 2005-01-27
HK1054383A1 (en) 2003-11-28
TWI262916B (en) 2006-10-01
AU2365201A (en) 2001-06-25
ATE305461T1 (de) 2005-10-15
AU781029B2 (en) 2005-04-28
KR20020067555A (ko) 2002-08-22
WO2001044216A1 (fr) 2001-06-21
HUP0203753A3 (en) 2004-12-28
UY26483A1 (es) 2001-06-29
NZ518974A (en) 2004-04-30
EP1242397A1 (fr) 2002-09-25
DE60022903D1 (de) 2006-02-09
US6353111B1 (en) 2002-03-05
JP3824936B2 (ja) 2006-09-20
ES2249322T3 (es) 2006-04-01
DE60022903T2 (de) 2006-07-06
ZA200203829B (en) 2003-08-14
NO323142B1 (no) 2007-01-08
NO20022863D0 (no) 2002-06-14
AR032752A1 (es) 2003-11-26
JP2003516980A (ja) 2003-05-20
CN1185219C (zh) 2005-01-19
HK1054383B (zh) 2005-04-22
PL355815A1 (en) 2004-05-17
PE20011022A1 (es) 2001-10-11
EP1242397B1 (fr) 2005-09-28
CO5050295A1 (es) 2001-06-27
NO20022863L (no) 2002-06-14

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