AR041467A1 - Indol-3-carboxamidas como activadores de glucoquinasa (gk) - Google Patents

Indol-3-carboxamidas como activadores de glucoquinasa (gk)

Info

Publication number
AR041467A1
AR041467A1 ARP030103589A ARP030103589A AR041467A1 AR 041467 A1 AR041467 A1 AR 041467A1 AR P030103589 A ARP030103589 A AR P030103589A AR P030103589 A ARP030103589 A AR P030103589A AR 041467 A1 AR041467 A1 AR 041467A1
Authority
AR
Argentina
Prior art keywords
carbon atom
ring
heteroaromatic ring
trifluoromethyl
cyano
Prior art date
Application number
ARP030103589A
Other languages
English (en)
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 AR041467A1 publication Critical patent/AR041467A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61P3/08Drugs 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/48Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D417/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Se proporciona compuestos de glucoquinasa que son útiles para incrementar la secreción de insulina en el tratamiento de diabetes de tipo II. También se reivindica proceso de obtención y composición farmacéutica. Reivindicación 1: Un compuesto de la fórmula (1), en donde: R1 es halógeno, nitro, amino, ciano, metilo, trifluorometilo, hidroxilo, metoxilo, trifluorometoxilo, metiltio, metilsulfinilo, o metilsulfonilo; R2 es alquilo inferior C2-5 o -CH2-R4 en donde R4 es cicloalquilo C3-6; y R3 es un anillo heteroaromático de cinco o seis miembros mono sustituido o no sustituido conectado por un átomo de carbono del anillo al grupo amina mostrado, cuyo anillo heteroaromático de cinco o seis miembros contiene de 1 a 3 heteroátomos seleccionados de azufre, oxígeno o nitrógeno, con un heteroátomo siendo nitrógeno que está adyacente al átomo de carbono del anillo enlanzante; dicho anillo heteroaromático mono sustituido siendo monosustituido en una posición en un átomo de carbono del anillo otro que el adyacente a dicho átomo de carbono enlazante con un sustituyente seleccionado del grupo que consiste en metilo, trifluorometilo, cloro, bromo, nitro, ciano, o un resto de grupo de fórmula (2); en donde n es 0 ó 1; y R5 es hidrógeno o alquilo inferior; o una sal aceptable farmacéuticamente de la misma.
ARP030103589A 2002-10-03 2003-10-01 Indol-3-carboxamidas como activadores de glucoquinasa (gk) AR041467A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US41573702P 2002-10-03 2002-10-03

Publications (1)

Publication Number Publication Date
AR041467A1 true AR041467A1 (es) 2005-05-18

Family

ID=32069904

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP030103589A AR041467A1 (es) 2002-10-03 2003-10-01 Indol-3-carboxamidas como activadores de glucoquinasa (gk)

Country Status (29)

Country Link
US (1) US6881844B2 (es)
EP (1) EP1549638B1 (es)
JP (1) JP4390704B2 (es)
KR (1) KR100646486B1 (es)
CN (1) CN100348596C (es)
AR (1) AR041467A1 (es)
AT (1) ATE374768T1 (es)
AU (1) AU2003270285B2 (es)
BR (1) BR0315047A (es)
CA (1) CA2499329C (es)
DE (1) DE60316709T2 (es)
DK (1) DK1549638T3 (es)
ES (1) ES2293005T3 (es)
HK (1) HK1083098A1 (es)
HR (1) HRP20050287A2 (es)
MX (1) MXPA05003391A (es)
MY (1) MY136764A (es)
NO (1) NO20051103L (es)
NZ (1) NZ538466A (es)
PA (1) PA8584001A1 (es)
PE (1) PE20050090A1 (es)
PL (1) PL375149A1 (es)
PT (1) PT1549638E (es)
RU (1) RU2309956C2 (es)
SI (1) SI1549638T1 (es)
TW (1) TW200413364A (es)
UY (1) UY28005A1 (es)
WO (1) WO2004031179A1 (es)
ZA (1) ZA200502619B (es)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE0102299D0 (sv) 2001-06-26 2001-06-26 Astrazeneca Ab Compounds
SE0102764D0 (sv) 2001-08-17 2001-08-17 Astrazeneca Ab Compounds
CA2498089A1 (en) * 2002-10-03 2004-06-17 Novartis Ag Substituted (thiazol-2-yl) -amide or sulfonamide as glycokinase activators useful in the treatment of type 2 diabetes
GB0226931D0 (en) 2002-11-19 2002-12-24 Astrazeneca Ab Chemical compounds
GB0226930D0 (en) * 2002-11-19 2002-12-24 Astrazeneca Ab Chemical compounds
EP1532980A1 (en) * 2003-11-24 2005-05-25 Novo Nordisk A/S N-heteroaryl indole carboxamides and analogues thereof, for use as glucokinase activators in the treatment of diabetes
ATE524479T1 (de) 2004-04-02 2011-09-15 Novartis Ag Sulfonamidthiazolpyridinderivate als zur behandlung von typ-2-diabetes geeignete glucokinaseaktivatoren
US7781451B2 (en) 2004-04-02 2010-08-24 Novartis Ag Thiazolopyridine derivatives, pharmaceut ical conditions containing them and methods of treating glucokinase mediated conditions
EP2308839B1 (en) 2005-04-20 2017-03-01 Takeda Pharmaceutical Company Limited Fused heterocyclic compounds
US7622492B2 (en) 2005-08-31 2009-11-24 Hoffmann-La Roche Inc. Pyrazolones as inhibitors of 11β-hydroxysteroid dehydrogenase
JP2007063225A (ja) 2005-09-01 2007-03-15 Takeda Chem Ind Ltd イミダゾピリジン化合物
WO2007039177A2 (en) 2005-09-29 2007-04-12 Sanofi-Aventis Phenyl- and pyridinyl- 1, 2 , 4 - oxadiazolone derivatives, processes for their preparation and their use as pharmaceuticals
GT200600429A (es) * 2005-09-30 2007-04-30 Compuestos organicos
GT200600428A (es) * 2005-09-30 2007-05-21 Compuestos organicos
US7799820B2 (en) 2005-09-30 2010-09-21 Banyu Pharmaceutical Co., Ltd. 2-Heterocycle-substituted indole derivatives for treating diabetes and associated conditions
JP2009013065A (ja) * 2005-10-14 2009-01-22 Astellas Pharma Inc 縮合へテロ環化合物
EP1948614A2 (en) * 2005-11-18 2008-07-30 Takeda San Diego, Inc. Glucokinase activators
US7351706B2 (en) * 2006-01-05 2008-04-01 Hoffmann-La Roche Inc. Indol-3-yl-carbonyl-spiro-piperidine derivatives
JP5302012B2 (ja) 2006-03-08 2013-10-02 タケダ カリフォルニア インコーポレイテッド グルコキナーゼ活性剤
EP1849785A1 (en) * 2006-04-28 2007-10-31 Neuropharma, S.A. N-(2-Thiazolyl)-amide derivatives as GSK-3 inhibitors
PE20110235A1 (es) 2006-05-04 2011-04-14 Boehringer Ingelheim Int Combinaciones farmaceuticas que comprenden linagliptina y metmorfina
WO2007143434A2 (en) * 2006-05-31 2007-12-13 Takeda San Diego, Inc. Indazole and isoindole derivatives as glucokinase activating agents
WO2008050821A1 (en) 2006-10-19 2008-05-02 Takeda Pharmaceutical Company Limited Indole compound
WO2008074694A1 (en) * 2006-12-20 2008-06-26 F. Hoffmann-La Roche Ag Crystallization of glucokinase activators
EP2091947A2 (en) 2006-12-20 2009-08-26 Takeda San Diego, Inc. Glucokinase activators
US8173645B2 (en) 2007-03-21 2012-05-08 Takeda San Diego, Inc. Glucokinase activators
EA020332B1 (ru) * 2007-08-10 2014-10-30 Х. Лундбекк А/С Аналоги гетероариламидов
MX2010012298A (es) 2008-05-16 2011-03-15 Takeda San Diego Inc Activadores de glucocinasa.
WO2010107736A2 (en) * 2009-03-20 2010-09-23 University Of Virginia Patent Foundation Broad spectrum benzothiophene-nitrothiazolide and other antimicrobials
JP2011006366A (ja) 2009-06-26 2011-01-13 Sanwa Kagaku Kenkyusho Co Ltd 新規チオフェンカルボキサミド誘導体及びその医薬用途
WO2012040170A2 (en) 2010-09-20 2012-03-29 University Of Virginia Patent Foundation Compositions and methods for treating tuberculosis
CN103044310B (zh) * 2013-01-18 2015-02-04 贵阳医学院 二氢吲哚-3-乙酸衍生物、其制备方法以及在药物中的应用
WO2023067628A1 (en) * 2021-10-20 2023-04-27 Council Of Scientific And Industrial Research An Indian Registered Body Incorporated Under The Regn. Of Soc. Act (Act Xxi Of 1860) A method for the preparation of indole-3-carboxylic acid derivatives

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2740686B1 (fr) 1995-11-03 1998-01-16 Sanofi Sa Formulation pharmaceutique lyophilisee stable
US6040321A (en) 1997-11-12 2000-03-21 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
US6262096B1 (en) 1997-11-12 2001-07-17 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
JP5278983B2 (ja) 1999-11-17 2013-09-04 塩野義製薬株式会社 アミド化合物の新規用途
US6433188B1 (en) 2000-12-06 2002-08-13 Wendy Lea Corbett Fused heteroaromatic glucokinase activators
BR0115999A (pt) 2000-12-06 2003-09-30 Hoffmann La Roche Composto, composição farmacêutica que compreende o mesmo, sua utilização, processo para o tratamento profilático ou terapêutico de diabetes do tipo ii e processo para a preparação do composto
US6482951B2 (en) 2000-12-13 2002-11-19 Hoffmann-La Roche Inc. Isoindolin-1-one glucokinase activators
JP4212358B2 (ja) 2000-12-28 2009-01-21 第一三共株式会社 Vla−4阻害薬
UA77303C2 (en) * 2002-06-14 2006-11-15 Pfizer Derivatives of thienopyridines substituted by benzocondensed heteroarylamide useful as therapeutic agents, pharmaceutical compositions and methods for their use

Also Published As

Publication number Publication date
CN1688574A (zh) 2005-10-26
DE60316709T2 (de) 2008-07-17
TW200413364A (en) 2004-08-01
SI1549638T1 (sl) 2008-02-29
AU2003270285A1 (en) 2004-04-23
MY136764A (en) 2008-11-28
KR20050046817A (ko) 2005-05-18
US20040067939A1 (en) 2004-04-08
NO20051103L (no) 2005-04-08
NZ538466A (en) 2007-05-31
CA2499329A1 (en) 2004-04-15
ZA200502619B (en) 2006-03-29
HK1083098A1 (en) 2006-06-23
DK1549638T3 (da) 2008-01-21
ATE374768T1 (de) 2007-10-15
JP2006504707A (ja) 2006-02-09
EP1549638A1 (en) 2005-07-06
PA8584001A1 (es) 2004-11-02
AU2003270285B2 (en) 2007-04-26
JP4390704B2 (ja) 2009-12-24
HRP20050287A2 (en) 2006-12-31
RU2309956C2 (ru) 2007-11-10
ES2293005T3 (es) 2008-03-16
PE20050090A1 (es) 2005-02-28
US6881844B2 (en) 2005-04-19
PL375149A1 (en) 2005-11-28
BR0315047A (pt) 2005-08-23
KR100646486B1 (ko) 2006-11-15
CA2499329C (en) 2009-04-21
MXPA05003391A (es) 2005-06-22
DE60316709D1 (de) 2007-11-15
WO2004031179A1 (en) 2004-04-15
UY28005A1 (es) 2004-04-30
CN100348596C (zh) 2007-11-14
RU2005113719A (ru) 2006-02-27
PT1549638E (pt) 2007-12-11
EP1549638B1 (en) 2007-10-03

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