MA30890B1 - Compose indole - Google Patents

Compose indole

Info

Publication number
MA30890B1
MA30890B1 MA31871A MA31871A MA30890B1 MA 30890 B1 MA30890 B1 MA 30890B1 MA 31871 A MA31871 A MA 31871A MA 31871 A MA31871 A MA 31871A MA 30890 B1 MA30890 B1 MA 30890B1
Authority
MA
Morocco
Prior art keywords
indole compound
agent
prodruce
gluckkinase
prophylaxis
Prior art date
Application number
MA31871A
Other languages
English (en)
Inventor
Tsuneo Yasuma
Osamu Ujikawa
Masahiro Itoh
Kazuko Aoki
Original Assignee
Takeda Pharmaceutical
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39010108&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA30890(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Takeda Pharmaceutical filed Critical Takeda Pharmaceutical
Publication of MA30890B1 publication Critical patent/MA30890B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/14—Heterocyclic 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 three or more hetero rings
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/433—Thidiazoles
    • 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
    • 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
    • A61P3/04—Anorexiants; Antiobesity agents
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Diabetes (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Epidemiology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

LA PRÉSENTE INVENTION CONCERNE UN ACTIVATEUR DE GLUCOKINASE UTILE EN TANT QU'AGENT PHARMACEUTIQUE TEL QU'UN AGENT POUR LA PROPHYLAXIE OU LE TRAITEMENT DU DIABÈTE, DE L'OBÉSITÉ ET AUTRES CONDITIONS SIMILAIRES. LA PRÉSENTE INVENTION PROPOSE UN ACTIVATEUR DE GLUCOKINASE CONTENANT UN COMPOSÉ REPRÉSENTÉ PAR LA FORMULE (I) : DANS LAQUELLE R1 EST UN ATOME D'HYDROGÈNE OU UN ATOME D'HALOGÈNE; R2 EST UN GROUPE REPRÉSENTÉ PAR DANS LAQUELLE CHAQUE SYMBOLE EST DÉFINI DANS LA DESCRIPTION, OU UN SEL DE CELUI-CI OU UN PROMÉDICAMENT DE CELUI-CI.
MA31871A 2006-10-19 2009-05-13 Compose indole MA30890B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006285551 2006-10-19

Publications (1)

Publication Number Publication Date
MA30890B1 true MA30890B1 (fr) 2009-11-02

Family

ID=39010108

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31871A MA30890B1 (fr) 2006-10-19 2009-05-13 Compose indole

Country Status (26)

Country Link
US (4) US7652133B2 (fr)
EP (2) EP2508524A3 (fr)
JP (1) JP5260507B2 (fr)
KR (1) KR101444486B1 (fr)
CN (1) CN101573357B (fr)
AU (1) AU2007310064B2 (fr)
BR (1) BRPI0717722A2 (fr)
CA (1) CA2666973C (fr)
CL (1) CL2008001017A1 (fr)
CR (1) CR10748A (fr)
EC (1) ECSP099330A (fr)
GE (1) GEP20115241B (fr)
IL (1) IL198154A (fr)
MA (1) MA30890B1 (fr)
ME (1) MEP11809A (fr)
MX (1) MX2009003972A (fr)
MY (1) MY158052A (fr)
NO (1) NO20091948L (fr)
NZ (1) NZ576570A (fr)
PE (1) PE20090884A1 (fr)
RU (1) RU2454415C9 (fr)
TN (1) TN2009000129A1 (fr)
TW (1) TWI460176B (fr)
UA (1) UA97257C2 (fr)
WO (1) WO2008050821A1 (fr)
ZA (1) ZA200902585B (fr)

Families Citing this family (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101511074B1 (ko) * 2007-04-16 2015-04-13 애브비 인코포레이티드 7-치환된 인돌 Ｍｃｌ-1 억제제
JPWO2008136428A1 (ja) 2007-04-27 2010-07-29 武田薬品工業株式会社 含窒素５員複素環化合物
EP2025674A1 (fr) 2007-08-15 2009-02-18 sanofi-aventis Tetrahydronaphthaline substituée, son procédé de fabrication et son utilisation en tant que médicament
EP2178870B1 (fr) * 2007-08-17 2018-09-19 LG Chem, Ltd. Composés d'indole et d'indazole en tant qu'inhibiteurs de nécrose cellulaire
RU2450001C2 (ru) * 2007-12-20 2012-05-10 Эл Джи Лайф Сайенсиз Лтд. Активаторы глюкокиназы и фармацевтические композиции, содержащие их в качестве активного ингредиента
KR101098583B1 (ko) * 2008-01-04 2011-12-26 주식회사 엘지생명과학 세포, 조직 및 장기 보존 효과를 갖는 인돌 및 인다졸 유도체
WO2009097995A1 (fr) * 2008-02-07 2009-08-13 Sanofi-Aventis Nouvelles imidazolidines substituées par un phényle, procédé de production, médicaments contenant ces composés et leur utilisation
CA2720686A1 (fr) 2008-04-10 2009-10-15 Takeda Pharmaceutical Company Limited Composes cycliques condenses et utilisation de ceux-ci
WO2009128481A1 (fr) * 2008-04-16 2009-10-22 武田薬品工業株式会社 Composé hétérocyclique azoté à cinq chaînons
AR072297A1 (es) * 2008-06-27 2010-08-18 Novartis Ag Derivados de indol-2-il-piridin-3-ilo, composicion farmaceutica que los comprende y su uso en medicamentos para el tratamiento de enfermedades mediadas por la sintasa aldosterona.
WO2010021686A1 (fr) * 2008-08-18 2010-02-25 Promega Corporation Composés luminogènes et procédés de détection des enzymes 3a du cytochrome p450
TW201014850A (en) 2008-09-25 2010-04-16 Takeda Pharmaceutical Solid pharmaceutical composition
JP5535931B2 (ja) 2008-10-27 2014-07-02 武田薬品工業株式会社 二環性化合物
US8557805B2 (en) 2008-12-29 2013-10-15 Takeda Pharmaceutical Company Limited Fused ring compound and use thereof
WO2010117085A1 (fr) * 2009-04-09 2010-10-14 Banyu Pharmaceutical Co.,Ltd. Dérivés d'aryl-indole
US20120172351A1 (en) 2009-06-09 2012-07-05 Nobuyuki Negoro Novel fused cyclic compound and use thereof
CN102548556A (zh) 2009-07-28 2012-07-04 武田药品工业株式会社 片剂
WO2011107494A1 (fr) 2010-03-03 2011-09-09 Sanofi Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation
UY33354A (es) 2010-04-27 2011-12-01 Takeda Pharmaceutical Compuesto biciclico como inhibidor acc
CN103068816B (zh) 2010-06-16 2015-01-07 武田药品工业株式会社 酰胺化合物的结晶
WO2011159781A2 (fr) * 2010-06-17 2011-12-22 Senomyx, Inc. Modulateurs de goût amer
EP2582709B1 (fr) 2010-06-18 2018-01-24 Sanofi Dérivés d'azolopyridin-3-one en tant qu'inhibiteurs de lipases et de phospholipases
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
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
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
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
WO2012036293A1 (fr) 2010-09-17 2012-03-22 武田薬品工業株式会社 Agent thérapeutique du diabète
US8729102B2 (en) 2010-11-30 2014-05-20 Takeda Pharmaceutical Company Limited Bicyclic compound
UY33913A (es) 2011-02-17 2012-09-28 Takeda Pharmaceutical Método de producción de derivado de dihidrobenzofurano ópticamente activo
WO2013037390A1 (fr) 2011-09-12 2013-03-21 Sanofi Dérivés amides d'acide 6-(4-hydroxyphényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase
EP2760862B1 (fr) 2011-09-27 2015-10-21 Sanofi Dérivés d'amide d'acide 6-(4-hydroxyphényl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique utilisés comme inhibiteurs de kinase
US8921576B2 (en) * 2011-10-19 2014-12-30 Kowa Company, Ltd. Spiroindoline compound, and medicinal agent comprising same
JPWO2013061962A1 (ja) 2011-10-24 2015-04-02 武田薬品工業株式会社 二環性化合物
US9365540B2 (en) 2012-01-12 2016-06-14 Takeda Pharmaceutical Company Limited Benzimidazole derivatives as MCH receptor antagonists
WO2013122029A1 (fr) 2012-02-13 2013-08-22 武田薬品工業株式会社 Composé à noyaux aromatiques
EP2816023A4 (fr) 2012-02-13 2015-09-09 Takeda Pharmaceutical Composé à noyaux aromatiques
EP2814466B1 (fr) 2012-02-15 2018-12-26 Takeda Pharmaceutical Company Limited Comprimé comprenant 1-(4-methoxybutyl)-n-(2-methylpropyl)-n-[(3s,5r)-5-(morpholin-4-ylcarbonyl)piperidin-3-yl]-1h-benzimidazole-2-carboxamide ou son sel
JP6106179B2 (ja) 2012-02-24 2017-03-29 武田薬品工業株式会社 芳香環化合物
CN104350040B (zh) 2012-03-29 2016-06-01 武田药品工业株式会社 芳环化合物
WO2013155223A1 (fr) 2012-04-10 2013-10-17 The Regents Of The University Of California Compositions et méthodes pour le traitement du cancer
WO2013168759A1 (fr) 2012-05-10 2013-11-14 武田薬品工業株式会社 Composé cyclique aromatique
US9505772B2 (en) 2012-05-10 2016-11-29 Takeda Pharmaceutical Company Limited Aromatic ring compound
JP6122879B2 (ja) 2012-06-05 2017-04-26 武田薬品工業株式会社 固形製剤
JP2015127299A (ja) 2012-07-19 2015-07-09 武田薬品工業株式会社 固形製剤
US9719970B2 (en) 2012-11-30 2017-08-01 Waters Technologies Corporation Methods and apparatus for the analysis of vitamin D metabolites
US9605000B2 (en) 2013-03-14 2017-03-28 Takeda Pharmaceutical Company Limited Spiro azetidine isoxazole derivatives and their use as SSTR antagonists
US10005720B2 (en) 2013-04-05 2018-06-26 North Carolina Central University Compounds useful for the treatment of metabolic disorders and synthesis of the same
UY35650A (es) 2013-07-09 2015-02-27 Takeda Pharmaceutical Compuesto heterocíclico
ES2672992T3 (es) 2013-08-09 2018-06-19 Takeda Pharmaceutical Company Limited Compuesto aromático
EP3037412B1 (fr) * 2013-08-22 2020-09-30 LG Chem, Ltd. Composé indole-amide en tant qu'inhibiteur de la nécrose
JO3442B1 (ar) 2013-10-07 2019-10-20 Takeda Pharmaceuticals Co مضادات ذات نوع فرعي من مستقبل سوماتوستاتين 5 (sstr5)
US9346776B2 (en) 2014-02-13 2016-05-24 Takeda Pharmaceutical Company Limited Fused heterocyclic compound
US9428470B2 (en) 2014-02-13 2016-08-30 Takeda Pharmaceutical Company Limited Heterocyclic compound
CN104098498A (zh) * 2014-07-30 2014-10-15 天津市斯芬克司药物研发有限公司 一种吲唑类化合物及其制备方法
AR111307A1 (es) 2017-03-30 2019-06-26 Takeda Pharmaceuticals Co Derivados de 1’,2’-dihidroespiro[ciclohexan-1,3’-indol] o 1’,2’-dihidroespiro[ciclohexan-1,3’-pirrolo[3,2-b]piridina] como inhibidores de hexakisfosfato quinasa
US11186565B2 (en) 2017-03-31 2021-11-30 Takeda Pharmaceutical Company Limited Aromatic compound
AR111199A1 (es) 2017-03-31 2019-06-12 Takeda Pharmaceuticals Co Compuesto aromático agonista de gpr40
JOP20190211A1 (ar) 2017-03-31 2019-09-15 Takeda Pharmaceuticals Co ببتيد منشط لمستقبل gip
MX2020009950A (es) 2018-03-23 2021-04-28 Carmot Therapeutics Inc Moduladores de receptores acoplados a proteina g.
EP3650440A4 (fr) 2018-08-27 2020-11-25 Scohia Pharma, Inc. Composé d'ester benzoïque
EP3856768A2 (fr) 2018-09-24 2021-08-04 Takeda Pharmaceutical Company Limited Composés peptidiques agonistes du récepteur du gip et leurs utilisations
US20220016215A1 (en) 2018-09-24 2022-01-20 Takeda Phaarmaceutical Company Limited Gip receptor agonist peptide compounds and uses thereof
CN109250963B (zh) * 2018-09-29 2021-07-16 福建省昊立建设工程有限公司 一种复合增韧混凝土及其制备方法
PT4097099T (pt) 2020-02-07 2024-07-19 Gasherbrum Bio Inc Agonistas heterocíclicos de glp-1
IL296592A (en) 2020-03-25 2022-11-01 Takeda Pharmaceuticals Co Qd dosing of gip receptor agonist peptide compounds and uses thereof
IL296219A (en) 2020-03-25 2022-11-01 Takeda Pharmaceuticals Co Qw dosing of gip receptor agonist peptide compounds and uses thereof
CN113563306B (zh) * 2020-04-28 2022-07-01 新发药业有限公司 一种2-(4-苯氧基苯基)-6-(哌啶-4-)基烟酰胺的制备方法
WO2021219019A1 (fr) 2020-04-29 2021-11-04 Gasherbrum Bio, Inc. Agonistes hétérocycliques du glp -1
KR20240007251A (ko) 2021-05-13 2024-01-16 카모트 테라퓨틱스, 인크. G-단백질 결합 수용체의 조절제
EP4490155A1 (fr) 2022-03-09 2025-01-15 Gasherbrum Bio, Inc. Agonistes hétérocycliques de glp-1
JP2025510741A (ja) 2022-03-21 2025-04-15 ガシャーブラム・バイオ・インコーポレイテッド ヘテロ環式ｇｌｐ－１アゴニスト
US20250250269A1 (en) 2022-04-14 2025-08-07 Gasherbrum Bio, Inc. Heterocyclic glp-1 agonists
CN121002014A (zh) 2022-12-15 2025-11-21 加舒布鲁姆生物公司 具有glp-1激动剂活性的化合物的盐和固体形式
EP4638455A1 (fr) 2022-12-22 2025-10-29 Gasherbrum Bio, Inc. Agonistes de glp-1 hétérocycliques
JP2026501285A (ja) 2022-12-22 2026-01-14 ガシャーブラム・バイオ・インコーポレイテッド ヘテロ環式ｇｌｐ－１アゴニスト
KR20250168210A (ko) 2023-02-16 2025-12-02 가셔브룸 바이오, 인크. 헤테로시클릭 glp-1 효능제
US20250019389A1 (en) 2023-06-30 2025-01-16 Gasherbrum Bio, Inc. Heterocyclic agonists
EP4743174A1 (fr) 2023-07-13 2026-05-20 Aconcagua Bio, Inc. Modulateurs de l'activité du récepteur de la calcitonine et/ou du récepteur de l'amyline
JP2026526054A (ja) 2023-07-13 2026-08-04 アコンカグア・バイオ・インコーポレイテッド 化合物、組成物、および方法
EP4771001A1 (fr) 2023-08-31 2026-07-08 Gasherbrum Bio, Inc. Agonistes de glp-1 à base de hétéroaryl-hétérocycloalkyl
US20250188081A1 (en) * 2023-12-08 2025-06-12 Shaman Pharma, LLC Method for Production of Spiro-Oxindole and Indoxyl Derivatives of Mitragynine
WO2025137307A1 (fr) 2023-12-20 2025-06-26 Gasherbrum Bio, Inc. Agonistes hétérocycliques de glp-1
WO2025154021A1 (fr) 2024-01-19 2025-07-24 Takeda Pharmaceutical Company Limited Composés peptidiques agonistes du récepteur de gip améliorés et leurs utilisations
WO2025154020A1 (fr) 2024-01-19 2025-07-24 Takeda Pharmaceutical Company Limited Composés peptidiques agonistes du récepteur gip améliorés et leurs utilisations
WO2025171340A1 (fr) 2024-02-08 2025-08-14 Aconcagua Bio, Inc. Traitement d'états associés au récepteur de la calcitonine et/ou de l'amyline
WO2026041075A1 (fr) 2024-08-21 2026-02-26 Gasherbrum Bio, Inc. Agonistes de gpl-1
WO2026051998A1 (fr) 2024-09-04 2026-03-12 Aconcagua Bio, Inc. Composés, compositions et procédés
WO2026096926A1 (fr) 2024-11-01 2026-05-07 Aconcagua Bio, Inc. Composés, compositions et méthodes
WO2026156091A1 (fr) 2025-01-15 2026-07-23 Aconcagua Bio, Inc. Composés et compositions pour traiter des états associés à l'activité du récepteur de la calcitonine et/ou du récepteur de l'amyline

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2656610B1 (fr) 1989-12-29 1992-05-07 Sanofi Sa Derives d'amino-2 phenyl-4 thiazole, leur procede de preparation et leur application therapeutique.
JP3545461B2 (ja) * 1993-09-10 2004-07-21 エーザイ株式会社 二環式ヘテロ環含有スルホンアミド誘導体
RU2121997C1 (ru) 1993-09-10 1998-11-20 Эйсай Ко., ЛТД Производные 7-амино-1н-индола
CN1072649C (zh) 1995-09-13 2001-10-10 武田药品工业株式会社 苯并氧杂吖庚因化合物,其生产方法和用途
GEP20032920B (en) * 1998-02-25 2003-03-25 Genetics Inst Inhibitors of Phospholipase Enzymes
JP4007743B2 (ja) 1999-02-26 2007-11-14 エーザイ・アール・アンド・ディー・マネジメント株式会社 血管新生阻害剤
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.
GB0003636D0 (en) * 2000-02-16 2000-04-05 Smithkline Beecham Plc Novel compounds
PT1285651E (pt) 2000-04-28 2010-10-21 Takeda Pharmaceutical Antagonistas da hormona concentradora da melanina
EP1283199A4 (fr) 2000-05-16 2003-12-17 Takeda Chemical Industries Ltd Antagoniste de l'hormone de concentration de la melanine
ES2293005T3 (es) * 2002-10-03 2008-03-16 F. Hoffmann-La Roche Ag Indol-3-carboxamidas como activadores de la glucocinasa.
EP1532980A1 (fr) * 2003-11-24 2005-05-25 Novo Nordisk A/S Carboxamides d'indole n-heteroarylé et leurs analogues, utiles comme des activateurs de glucokinase pour le traitement de diabetes
US7498445B2 (en) * 2004-05-05 2009-03-03 Renopharm Ltd. Thiazole-based nitric oxide donors capable of releasing two or more nitric oxide molecules and uses thereof
EP1632491A1 (fr) * 2004-08-30 2006-03-08 Laboratorios Del Dr. Esteve, S.A. composes indole substitues et leur utilisation comme modulateurs du recepteur 5-ht6
US8957070B2 (en) * 2005-04-20 2015-02-17 Takeda Pharmaceutical Company Limited Glucokinase activator compounds, methods of activating glucokinase and methods of treating diabetes and obesity
WO2007037543A1 (fr) 2005-09-29 2007-04-05 Banyu Pharmaceutical Co., Ltd. Dérivé de biarylamide
JP4990783B2 (ja) 2005-09-30 2012-08-01 Ｍｓｄ株式会社 ２−ヘテロアリール置換インドール誘導体
CA2694058C (fr) 2007-08-14 2016-06-07 Bayer Schering Pharma Aktiengesellschaft Pyrimidines bicycliques condensees
CA2695251C (fr) 2007-08-14 2016-06-21 Bayer Schering Pharma Aktiengesellschaft Imidazoles fusionnes pour le traitement du cancer
JP2011500625A (ja) 2007-10-18 2011-01-06 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ トリ置換された１，２，４−トリアゾール
JO2784B1 (en) 2007-10-18 2014-03-15 شركة جانسين فارماسوتيكا ان. في 5,3,1 - Triazole substitute derivative

Also Published As

Publication number Publication date
BRPI0717722A2 (pt) 2013-10-29
CN101573357B (zh) 2013-01-23
GEP20115241B (en) 2011-06-10
US7718798B2 (en) 2010-05-18
RU2454415C2 (ru) 2012-06-27
UA97257C2 (en) 2012-01-25
US20100137610A1 (en) 2010-06-03
WO2008050821A1 (fr) 2008-05-02
IL198154A (en) 2014-08-31
ME00681B (fr) 2011-12-20
US20080096877A1 (en) 2008-04-24
MX2009003972A (es) 2009-04-27
US7652133B2 (en) 2010-01-26
EP2508524A2 (fr) 2012-10-10
ECSP099330A (es) 2009-06-30
NZ576570A (en) 2010-11-26
JP5260507B2 (ja) 2013-08-14
JP2010506825A (ja) 2010-03-04
PE20090884A1 (es) 2009-08-05
CR10748A (es) 2009-05-20
US8410087B2 (en) 2013-04-02
AU2007310064A2 (en) 2009-06-04
TN2009000129A1 (en) 2010-10-18
EP2074119A1 (fr) 2009-07-01
AU2007310064B2 (en) 2013-03-28
US7777047B2 (en) 2010-08-17
EP2508524A3 (fr) 2012-10-24
RU2009118602A (ru) 2010-11-27
RU2454415C9 (ru) 2013-02-27
CA2666973C (fr) 2015-03-31
MY158052A (en) 2016-08-30
MEP11809A (en) 2011-12-20
ZA200902585B (en) 2010-09-29
CL2008001017A1 (es) 2009-04-24
US20100144702A1 (en) 2010-06-10
KR20090068292A (ko) 2009-06-25
KR101444486B1 (ko) 2014-09-24
CN101573357A (zh) 2009-11-04
CA2666973A1 (fr) 2008-05-02
TW200825071A (en) 2008-06-16
TWI460176B (zh) 2014-11-11
US20090286975A1 (en) 2009-11-19
NO20091948L (no) 2009-07-13
IL198154A0 (en) 2009-12-24
AU2007310064A1 (en) 2008-05-02

Similar Documents

Publication Publication Date Title
MA32283B1 (fr) Composes cycliques condenses et utilisation de ceux-ci
MA29323B1 (fr) Composes de l'acide pyridylacetique
MA65131B1 (fr) Utilisation d'un inhibiteur d'ezh2 dans la préparation d'un médicament pour le traitement d'un lymphome à cellules t
MA33581B1 (fr) Composition pharmaceutique contenant un dérivé de quinoléine
MA31169B1 (fr) Preparation solide comprenant de l'alogliptine et de la pioglitazone
MA30228B1 (fr) Pipéridinoylpyrrolidines agonistes du récepteur de mélanocortine de type 4
MA30911B1 (fr) Nouveaux derives de sulfonamide en tant qu'antagonistes de bradykinine
MA32171B1 (fr) Compose heterocyclique
MA29250B1 (fr) Cyclohexylamides servant d'antagonistes des recepteurs de dopamine d3, d2 et de 5ht1a
TN2009000204A1 (fr) Spirocetones servant d'inhibiteurs d'acetyl-coa-carboxylase
MA30456B1 (fr) Nouveau dérivé de coumarine présentant une activité anti-tumorale.
MA32965B1 (fr) Derives de sulfonamides
UA97257C2 (en) Indole derivatives
MA31710B1 (fr) (carboxylalkylenephenyl)phényloxamides, procédés pour la production de ceux-ci et utilisation de ceux-ci en tant que medicament
MA31419B1 (fr) Derives de pyridine
MA29926B1 (fr) Derives de pyrazine
MA32164B1 (fr) Derive heterocyclique fusionne et son utilisation
MA30355B1 (fr) Derives d'azabicyclo [3. 1. 0] hexyle utilises comme modulateurs des recepteurs de la dopamine d3
TNSN06358A1 (fr) Methyl-aryl-ou-heteroaryl-amides substitues
TNSN07022A1 (fr) Derives de pyridine
MA30999B1 (fr) Composés.
MA30428B1 (fr) Derives de dihydropyrazolopyrimidinones
MA34713B1 (fr) Compose bicyclique
MA30142B1 (fr) Agonistes du recepteur de neuropeptide-2
MA30916B1 (fr) Nouveaux derives de benzamide en tant qu'antagonistes de bradykinine