WO2009037394A3 - DERIVES DE 6-CYCLOAMINO-S-(PYRIDAZIN-YL)IMIDAZO[1,2-b]-PYRIDAZINE, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE. - Google Patents

DERIVES DE 6-CYCLOAMINO-S-(PYRIDAZIN-YL)IMIDAZO[1,2-b]-PYRIDAZINE, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE. Download PDF

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Publication number
WO2009037394A3
WO2009037394A3 PCT/FR2008/001057 FR2008001057W WO2009037394A3 WO 2009037394 A3 WO2009037394 A3 WO 2009037394A3 FR 2008001057 W FR2008001057 W FR 2008001057W WO 2009037394 A3 WO2009037394 A3 WO 2009037394A3
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WO
WIPO (PCT)
Prior art keywords
optionally substituted
cycloamino
pyridazin
imidazo
pyridazine
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.)
Ceased
Application number
PCT/FR2008/001057
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English (en)
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WO2009037394A2 (fr
Inventor
Philippe Burnier
Yulin Chiang
Sylvain Cote-Des-Combes
Adrien-Tak Li
Frederic Puech
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Sanofi Aventis France
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Sanofi Aventis France
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Filing date
Publication date
Priority to EP08831515.5A priority Critical patent/EP2178879B1/fr
Priority to NZ582683A priority patent/NZ582683A/en
Priority to ES08831515T priority patent/ES2429765T3/es
Priority to AU2008300449A priority patent/AU2008300449A1/en
Priority to JP2010516539A priority patent/JP5431319B2/ja
Priority to CA2693116A priority patent/CA2693116A1/fr
Priority to CN200880103986A priority patent/CN101784552A/zh
Priority to BRPI0814510-5A2A priority patent/BRPI0814510A2/pt
Application filed by Sanofi Aventis France filed Critical Sanofi Aventis France
Priority to EA201070161A priority patent/EA016376B1/ru
Publication of WO2009037394A2 publication Critical patent/WO2009037394A2/fr
Publication of WO2009037394A3 publication Critical patent/WO2009037394A3/fr
Priority to US12/685,030 priority patent/US8455491B2/en
Anticipated expiration legal-status Critical
Priority to US13/887,845 priority patent/US9108971B2/en
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychology (AREA)
  • Pain & Pain Management (AREA)
  • Anesthesiology (AREA)
  • Addiction (AREA)
  • Hematology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

L'invention concerne les dérivés de 6-cycloamino-3-(pyridazin-4-yl)imidazo[1,2- bjpyridazine, de formule générale (I) dans laquelle Ffe représente un groupe aryle éventuellement substitué; A représente u groupe C1-7-alkylène éventuellement substitué; B représente un groupe C1-7-alkylèn éventuellement substitué; L représente soit un atome d'azote éventuellement substitué pa un groupe Rc ou Rd, soit un atome de carbone substitué par un groupe Re1 et un groupe Rd ou deux groupes Re2; les atomes de carbone de A et de B étant éventuellemen substitués par un ou plusieurs, groupes Rf identiques ou différents l'un de l'autre; R7 et R8 représentent, indépendamment l'un de l'autre, un atome d'hydrogène ou un groupe un groupe C1-6-alkyle. L'invention concerne également leur procédé de préparation et leur application en thérapeutique comme inhibiteurs de la phosphorylation de la caséine pour le traitement des troubles du sommeil, des troubles du rythme circadien, des maladies liées à la dépendance ou de la prolifération cellulaire.
PCT/FR2008/001057 2007-07-19 2008-07-18 DERIVES DE 6-CYCLOAMINO-S-(PYRIDAZIN-YL)IMIDAZO[1,2-b]-PYRIDAZINE, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE. Ceased WO2009037394A2 (fr)

Priority Applications (11)

Application Number Priority Date Filing Date Title
CN200880103986A CN101784552A (zh) 2007-07-19 2008-07-18 6-环氨基-3-(哒嗪-4-基)咪唑并[1,2-b]哒嗪的衍生物、其制备和其治疗学用途
ES08831515T ES2429765T3 (es) 2007-07-19 2008-07-18 6-Cicloamino-S-(piridazin-il)imidazo[1,2-B]-piridazina y sus derivados, su preparación y su aplicación en terapéutica
AU2008300449A AU2008300449A1 (en) 2007-07-19 2008-07-18 6-cycloamino-s-(pyridazin-4-yl)imidazo[1,2-b]-pyridazine and derivatives thereof preparation and therapeutic application thereof
JP2010516539A JP5431319B2 (ja) 2007-07-19 2008-07-18 ６−シクロアミノ−３−（ピリダジン−４−イル）イミダゾ［１，２−ｂ］−ピリダジンおよびこれらの誘導体、これらの調製および治療上の用途
CA2693116A CA2693116A1 (fr) 2007-07-19 2008-07-18 Derives de 6-cycloamino-3-(pyridazin-4-yl)imidazo[1,2-b]-pyridazine, leur preparation et leur application en therapeutique
BRPI0814510-5A2A BRPI0814510A2 (pt) 2007-07-19 2008-07-18 Derivados de 6-cicloamino-3-(piridazin-4-il)imidazol[1,2-b]-piridazina, sua preparação e sua aplicação em terapêutica
EA201070161A EA016376B1 (ru) 2007-07-19 2008-07-18 ПРОИЗВОДНЫЕ 6-ЦИКЛОАМИНО-3-(ПИРИДАЗИН-4-ИЛ)ИМИДАЗО[1,2-b]ПИРИДАЗИНА, ИХ ПОЛУЧЕНИЕ И ИХ ПРИМЕНЕНИЕ В ТЕРАПИИ
EP08831515.5A EP2178879B1 (fr) 2007-07-19 2008-07-18 DERIVES DE 6-CYCLOAMINO-S-(PYRIDAZIN-YL)IMIDAZO[1,2-b]-PYRIDAZINE, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE.
NZ582683A NZ582683A (en) 2007-07-19 2008-07-18 6-cycloamino-s-(pyridazin-4-yl)imidazo[1,2-b]-pyridazine and derivatives thereof preparation and therapeutic application thereof
US12/685,030 US8455491B2 (en) 2007-07-19 2010-01-11 6-cycloamino-3-(pyridazin-4-yl)imidazo[1,2-b]pyridazine and derivatives and pharmaceutical compositions comprising the same
US13/887,845 US9108971B2 (en) 2007-07-19 2013-05-06 6-cycloamino-3-(pyridazin-4-yl)imidazo[1,2-b]-pyridazine and derivatives thereof preparation and therapeutic application thereof

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US95071107P 2007-07-19 2007-07-19
FR0705224A FR2918986B1 (fr) 2007-07-19 2007-07-19 Derives de 6-cycloamino-3-(pyridazin-4-yl)imidazo[1,2-b]- pyridazine, leur preparation et leur application en therapeutique
FR0705224 2007-07-19
US60/950,711 2007-07-19

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US12/685,030 Continuation US8455491B2 (en) 2007-07-19 2010-01-11 6-cycloamino-3-(pyridazin-4-yl)imidazo[1,2-b]pyridazine and derivatives and pharmaceutical compositions comprising the same

Publications (2)

Publication Number Publication Date
WO2009037394A2 WO2009037394A2 (fr) 2009-03-26
WO2009037394A3 true WO2009037394A3 (fr) 2009-06-18

Family

ID=39183122

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/FR2008/001057 Ceased WO2009037394A2 (fr) 2007-07-19 2008-07-18 DERIVES DE 6-CYCLOAMINO-S-(PYRIDAZIN-YL)IMIDAZO[1,2-b]-PYRIDAZINE, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE.

Country Status (22)

Country Link
US (2) US8455491B2 (fr)
EP (1) EP2178879B1 (fr)
JP (1) JP5431319B2 (fr)
KR (1) KR20100041771A (fr)
CN (1) CN101784552A (fr)
AR (1) AR069272A1 (fr)
AU (1) AU2008300449A1 (fr)
BR (1) BRPI0814510A2 (fr)
CA (1) CA2693116A1 (fr)
CL (1) CL2008002138A1 (fr)
CO (1) CO6290690A2 (fr)
EA (1) EA016376B1 (fr)
ES (1) ES2429765T3 (fr)
FR (1) FR2918986B1 (fr)
MA (1) MA31616B1 (fr)
NZ (1) NZ582683A (fr)
PA (1) PA8789901A1 (fr)
PE (1) PE20090493A1 (fr)
TW (1) TW200914456A (fr)
UY (1) UY31236A1 (fr)
WO (1) WO2009037394A2 (fr)
ZA (1) ZA201001214B (fr)

Cited By (4)

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Publication number Priority date Publication date Assignee Title
US8846675B2 (en) 2007-07-19 2014-09-30 Cymabay Therapeutics, Inc. N-linked heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders
US8921350B2 (en) 2006-12-28 2014-12-30 Cymabay Therapeutics, Inc. Heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders
US9150567B2 (en) 2009-10-01 2015-10-06 Cymabay Therapeutics, Inc. Substituted tetrazol-1-yl-phenoxymethyl-thiazol-2-yl-piperidinyl-pyrimidine salts
US9241924B2 (en) 2010-06-23 2016-01-26 Cymabay Therapeutics, Inc. Compositions of 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine

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US7868001B2 (en) * 2007-11-02 2011-01-11 Hutchison Medipharma Enterprises Limited Cytokine inhibitors
FR2939134A1 (fr) * 2008-12-01 2010-06-04 Sanofi Aventis Derives de 6-cycloamino-3-(1h-pyrrolo°2,3-b!pyridin-4-yl) imidazo°1,2-b!-pyridazine, leur preparation et leur application en therapeutique
FR2940284B1 (fr) * 2008-12-19 2011-02-18 Sanofi Aventis Derives de 6-cycloamino-2,3-di-pyridinyl-imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique
FR2940285A1 (fr) * 2008-12-19 2010-06-25 Sanofi Aventis Derives de 6-cycloamino-2-thienyl-3-(pyridin-4-yl)imidazo °1,2-b!-pyridazine et 6-cycloamino-2-furanyl-3- (pyridin-4-yl)imidazo°1,2-b!-pyridazine, leur preparation et leur application en therapeutique
WO2011050202A1 (fr) 2009-10-23 2011-04-28 Janssen Pharmaceutica Nv Composés hétérocycliques condensés en tant que modulateurs de récepteur d'orexine
ES2585806T3 (es) * 2009-10-23 2016-10-10 Janssen Pharmaceutica N.V. Octahidropirrolo [3,4-c] pirroles disustituidos como moduladores de receptores de orexina
WO2011050200A1 (fr) 2009-10-23 2011-04-28 Janssen Pharmaceutica Nv Composés hétérocycliques condensés en tant que modulateurs de récepteur d'orexine
PH12012500778A1 (en) 2009-10-30 2012-11-26 Janssen Pharmaceutica Nv IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS
AR080754A1 (es) 2010-03-09 2012-05-09 Janssen Pharmaceutica Nv Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10
AU2011290238B8 (en) * 2010-08-09 2015-09-03 Nb Health Laboratory Co. Ltd. Inhibitor of casein kinase 1delta and casein kinase 1E
EP2651405A2 (fr) * 2010-12-14 2013-10-23 Electrophoretics Limited Inhibiteurs de caséine kinase 1 (ck1 )
US9586962B2 (en) 2011-04-20 2017-03-07 Janssen Pharmaceutica Nv Disubstituted octahydropyrrolo [3,4-C] pyrroles as orexin receptor modulators
BR112013033375B1 (pt) 2011-06-27 2022-05-10 Janssen Pharmaceutica N.V Derivados de 1-aril-4-metil-[1,2,4]triazolo[4,3-a]quinoxa-lina, seu uso, composição farmacêutica que os compreende, processo de preparação dos mesmos, solução estéril e composto intermediário
HK1206250A1 (en) 2012-06-26 2016-01-08 Janssen Pharmaceutica Nv Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl-[1,2,4] triazolo [4,3-a] quinoxaline compounds and ped 10 inhibitors for use in the treatment of neurological or metabolic disorders
WO2014009305A1 (fr) 2012-07-09 2014-01-16 Janssen Pharmaceutica Nv Inhibiteurs de l'enzyme phosphodiestérase 10
JP6267231B2 (ja) * 2012-12-21 2018-01-24 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ カゼインキナーゼ１δ／ε阻害剤としての新規な置換イミダゾール
EP2935272B1 (fr) * 2012-12-21 2017-02-22 Bristol-Myers Squibb Company Pyrazole imidazopyrazines substitues par pyrazole comme inhibiteurs de casein kinase 1 d/e
GB201321734D0 (en) * 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic Agents
RU2016132574A (ru) * 2014-01-09 2018-02-12 Интра-Селлулар Терапиз, Инк. Органические соединения
US10828302B2 (en) 2016-03-10 2020-11-10 Janssen Pharmaceutica Nv Methods of treating depression using orexin-2 receptor antagonists
AU2017305392A1 (en) 2016-08-03 2019-02-21 Cymabay Therapeutics, Inc. Oxymethylene aryl compounds for treating inflammatory gastrointestinal diseases or gastrointestinal conditions
ES2747768T3 (es) 2017-03-20 2020-03-11 Forma Therapeutics Inc Composiciones de pirrolopirrol como activadores de quinasa de piruvato (PKR)
SG11202007422QA (en) 2018-02-05 2020-09-29 Alkermes Inc Compounds for the treatment of pain
ES2989438T3 (es) 2018-09-19 2024-11-26 Novo Nordisk Healthcare Ag Activación de la piruvato cinasa R
US12053458B2 (en) 2018-09-19 2024-08-06 Novo Nordisk Health Care Ag Treating sickle cell disease with a pyruvate kinase R activating compound
TW202112368A (zh) 2019-06-13 2021-04-01 荷蘭商法西歐知識產權股份有限公司 用於治療有關dux4表現之疾病的抑制劑組合
US20220378756A1 (en) 2019-09-19 2022-12-01 Forma Therapeutics, Inc. Activating pyruvate kinase r
CN115335057A (zh) * 2020-03-27 2022-11-11 北京原基华毅生物科技有限公司 抑制酪蛋白激酶的方法
EP4126878A4 (fr) * 2020-03-27 2024-07-10 Gritscience Biopharmaceuticals Co., Ltd. Composés utilisés en tant qu'inhibiteurs de la caséine kinase
US12128035B2 (en) 2021-03-19 2024-10-29 Novo Nordisk Health Care Ag Activating pyruvate kinase R
WO2023064857A1 (fr) 2021-10-14 2023-04-20 Incyte Corporation Composés de quinoléine utiles en tant qu'inhibiteurs de kras

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WO2005080355A1 (fr) * 2004-02-12 2005-09-01 Neurogen Corporation Imidazo-pyridazines, triazolo-pyridazines et ligands associes des recepteurs de benzodiazepine
WO2007009773A1 (fr) * 2005-07-21 2007-01-25 Novartis Ag Derives de pyrazolo[1,5a]pyrimidin-7-yl-amine utilises en tant qu'inhibiteurs des proteines kinases
WO2007013673A1 (fr) * 2005-07-29 2007-02-01 Astellas Pharma Inc. Hétérocycles fusionnés en tant qu’inhibiteurs de lck
WO2007025540A2 (fr) * 2005-09-02 2007-03-08 Bayer Schering Pharma Aktiengesellschaft Imidazo[1,2b]pyridazines substituees constituant des inhibiteurs de kinases, leur production et leur utilisation comme medicaments

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DE60026998T2 (de) 1999-06-08 2007-04-05 Aventis Pharmaceuticals Inc. Screeningsverfahren zur änderung zirkadiane-rhythmus-eiweisse
DE602004020685D1 (de) * 2003-12-11 2009-05-28 Aventis Pharma Inc Substituierte 1h-pyrroloä3,2-b, 3,2-c und 2,3-cüpyridin-2-carbonsäureamide und verwandte analoga als inhibitoren von caseinkinase-i-epsilon

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WO1989001333A1 (fr) * 1987-08-07 1989-02-23 The Australian National University IMIDAZO[1,2-b]PYRIDAZINES
WO2005080355A1 (fr) * 2004-02-12 2005-09-01 Neurogen Corporation Imidazo-pyridazines, triazolo-pyridazines et ligands associes des recepteurs de benzodiazepine
WO2007009773A1 (fr) * 2005-07-21 2007-01-25 Novartis Ag Derives de pyrazolo[1,5a]pyrimidin-7-yl-amine utilises en tant qu'inhibiteurs des proteines kinases
WO2007013673A1 (fr) * 2005-07-29 2007-02-01 Astellas Pharma Inc. Hétérocycles fusionnés en tant qu’inhibiteurs de lck
WO2007025540A2 (fr) * 2005-09-02 2007-03-08 Bayer Schering Pharma Aktiengesellschaft Imidazo[1,2b]pyridazines substituees constituant des inhibiteurs de kinases, leur production et leur utilisation comme medicaments

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8921350B2 (en) 2006-12-28 2014-12-30 Cymabay Therapeutics, Inc. Heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders
US8975258B2 (en) 2006-12-28 2015-03-10 Cymabay Therapeutics, Inc. Heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders
US8846675B2 (en) 2007-07-19 2014-09-30 Cymabay Therapeutics, Inc. N-linked heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders
US9150567B2 (en) 2009-10-01 2015-10-06 Cymabay Therapeutics, Inc. Substituted tetrazol-1-yl-phenoxymethyl-thiazol-2-yl-piperidinyl-pyrimidine salts
US9241924B2 (en) 2010-06-23 2016-01-26 Cymabay Therapeutics, Inc. Compositions of 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine

Also Published As

Publication number Publication date
AU2008300449A1 (en) 2009-03-26
FR2918986A1 (fr) 2009-01-23
CO6290690A2 (es) 2011-06-20
KR20100041771A (ko) 2010-04-22
ES2429765T3 (es) 2013-11-15
EP2178879A2 (fr) 2010-04-28
EA016376B1 (ru) 2012-04-30
US20130245023A1 (en) 2013-09-19
BRPI0814510A2 (pt) 2015-02-03
NZ582683A (en) 2011-07-29
JP5431319B2 (ja) 2014-03-05
PE20090493A1 (es) 2009-05-27
CA2693116A1 (fr) 2009-03-26
FR2918986B1 (fr) 2009-09-04
AR069272A1 (es) 2010-01-13
EA201070161A1 (ru) 2010-08-30
WO2009037394A2 (fr) 2009-03-26
CN101784552A (zh) 2010-07-21
US8455491B2 (en) 2013-06-04
CL2008002138A1 (es) 2009-10-23
US20100152157A1 (en) 2010-06-17
ZA201001214B (en) 2011-05-25
UY31236A1 (es) 2009-03-02
EP2178879B1 (fr) 2013-07-03
US9108971B2 (en) 2015-08-18
TW200914456A (en) 2009-04-01
PA8789901A1 (es) 2009-02-09
MA31616B1 (fr) 2010-08-02
JP2010533686A (ja) 2010-10-28

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