MA32887B1 - Aminotetrahydropyranes en tant qu'inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete - Google Patents

Aminotetrahydropyranes en tant qu'inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete

Info

Publication number
MA32887B1
MA32887B1 MA33925A MA33925A MA32887B1 MA 32887 B1 MA32887 B1 MA 32887B1 MA 33925 A MA33925 A MA 33925A MA 33925 A MA33925 A MA 33925A MA 32887 B1 MA32887 B1 MA 32887B1
Authority
MA
Morocco
Prior art keywords
dipeptidyl peptidase
diabetes
prevention
treatment
aminotetrahydroperan
Prior art date
Application number
MA33925A
Other languages
Arabic (ar)
English (en)
Inventor
Tesfaye Biftu
Ping Chen
Jason M Cox
Ann E Weber
Original Assignee
Merck Sharp & Dohme
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=41559521&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA32887(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of MA32887B1 publication Critical patent/MA32887B1/fr

Links

Classifications

    • 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
    • C07D309/16Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D309/28Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D309/30Oxygen atoms, e.g. delta-lactones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/4151,2-Diazoles
    • A61K31/41621,2-Diazoles condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/1703Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • A61K38/1709Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22Hormones
    • A61K38/26Glucagons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • 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
    • A61P3/06Antihyperlipidemics
    • 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
    • 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
    • C07D405/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Zoology (AREA)
  • Immunology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Endocrinology (AREA)
  • Marine Sciences & Fisheries (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention concerne de nouveaux aminotétrahydropyranes substitués de formule structurale I qui sont des inhibiteurs de l'enzyme dipeptidyle peptidase-IV et qui sont utiles dans le traitement ou la prévention de maladies dans lesquelles l'enzyme dipeptidyle peptidase-IV est impliquée, telles que le diabète et particulièrement le diabète de type 2. L'invention concerne en outre des compositions pharmaceutiques comprenant ces composés et l'utilisation de ces composés et compositions dans la prévention ou le traitement de maladies dans lesquelles l'enzyme dipeptidyle peptidase-IV est impliquée.
MA33925A 2008-11-13 2011-06-08 Aminotetrahydropyranes en tant qu'inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete MA32887B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US19917908P 2008-11-13 2008-11-13
PCT/US2009/063976 WO2010056708A1 (fr) 2008-11-13 2009-11-11 Aminotétrahydropyranes en tant qu’inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prévention du diabète

Publications (1)

Publication Number Publication Date
MA32887B1 true MA32887B1 (fr) 2011-12-01

Family

ID=41559521

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33925A MA32887B1 (fr) 2008-11-13 2011-06-08 Aminotetrahydropyranes en tant qu'inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete

Country Status (39)

Country Link
US (8) US8143289B2 (fr)
EP (4) EP2676961B1 (fr)
JP (2) JP4854825B1 (fr)
KR (2) KR101260162B1 (fr)
CN (1) CN102272136B (fr)
AR (1) AR074306A1 (fr)
AU (1) AU2009314191B2 (fr)
BR (1) BRPI0921375B8 (fr)
CA (1) CA2742783C (fr)
CL (1) CL2011001082A1 (fr)
CO (1) CO6382129A2 (fr)
CR (1) CR20110257A (fr)
CY (1) CY1114617T1 (fr)
DK (1) DK2358717T3 (fr)
DO (1) DOP2011000128A (fr)
EA (1) EA018613B1 (fr)
EC (1) ECSP11011044A (fr)
ES (1) ES2432191T3 (fr)
GE (1) GEP20135724B (fr)
HN (1) HN2011001256A (fr)
HR (1) HRP20130924T1 (fr)
IL (2) IL212485A (fr)
JO (1) JO2870B1 (fr)
MA (1) MA32887B1 (fr)
MX (1) MX2011005044A (fr)
MY (1) MY150787A (fr)
NI (1) NI201100081A (fr)
NZ (1) NZ592826A (fr)
PA (1) PA8848201A1 (fr)
PE (1) PE20120027A1 (fr)
PL (1) PL2358717T3 (fr)
PT (1) PT2358717E (fr)
RS (1) RS52946B (fr)
SI (1) SI2358717T1 (fr)
SV (1) SV2011003903A (fr)
TN (1) TN2011000201A1 (fr)
TW (1) TWI398443B (fr)
UA (1) UA101414C2 (fr)
WO (1) WO2010056708A1 (fr)

Families Citing this family (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0915720A2 (pt) 2008-06-12 2015-08-04 Janssen Pharmaceutica Nv Moduladores de diaminopiridina, pirimidina, e piridazina do receptor de histamina h4
JO2870B1 (en) 2008-11-13 2015-03-15 ميرك شارب اند دوهم كورب Amino Tetra Hydro Pirans as Inhibitors of Peptide Dipeptide IV for the Treatment or Prevention of Diabetes
CA2771352A1 (fr) 2009-09-02 2011-03-10 Merck Sharp & Dohme Corp. Aminotetrahydropanes utilises comme inhibiteurs de la dipeptyl peptidase-iv pour traiter ou prevenir le diabete
WO2011037793A1 (fr) 2009-09-25 2011-03-31 Merck Sharp & Dohme Corp. Aminopipéridines substituées utilisées en tant qu'inhibiteurs de la dipeptidyl peptidase-iv dans le cadre du traitement du diabète
US8853212B2 (en) 2010-02-22 2014-10-07 Merck Sharp & Dohme Corp Substituted aminotetrahydrothiopyrans and derivatives thereof as dipeptidyl peptidase-IV inhibitors for the treatment of diabetes
WO2011146358A1 (fr) 2010-05-21 2011-11-24 Merck Sharp & Dohme Corp. Composés hétérocycliques substitués à sept chaînons en tant qu'inhibiteurs de la dipeptidyl-peptidase iv pour le traitement du diabète
WO2012078448A1 (fr) 2010-12-06 2012-06-14 Schering Corporation Hétérocycles tricycliques utiles comme inhibiteurs de la dipeptidyl peptidase iv
JP2014521594A (ja) * 2011-05-25 2014-08-28 アミリン・ファーマシューティカルズ,リミテッド・ライアビリティ・カンパニー 長持続期間デュアルホルモンコンジュゲート
CA2838738A1 (fr) * 2011-06-29 2013-01-03 Merck Sharp & Dohme Corp. Nouvelles formes cristallines d'un inhibiteur de peptidase-iv
EP2729468A4 (fr) 2011-07-05 2015-03-18 Merck Sharp & Dohme Hétérocycles tricycliques utiles comme inhibiteurs de la dipeptidyl peptidase-iv
WO2013122920A1 (fr) 2012-02-17 2013-08-22 Merck Sharp & Dohme Corp. Inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prévention du diabète
EP2874622A4 (fr) 2012-07-23 2015-12-30 Merck Sharp & Dohme Traitement du diabète par administration d'inhibiteurs de dipeptidyl peptidase-iv
US9156848B2 (en) 2012-07-23 2015-10-13 Merck Sharp & Dohme Corp. Treating diabetes with dipeptidyl peptidase-IV inhibitors
TWI500613B (zh) 2012-10-17 2015-09-21 Cadila Healthcare Ltd 新穎之雜環化合物
EP3038465B1 (fr) * 2013-08-30 2021-10-06 Merck Sharp & Dohme Corp. Formulation pharmaceutique orale d'omarigliptine
ES2587585T3 (es) 2014-03-20 2016-10-25 F.I.S.- Fabbrica Italiana Sintetici S.P.A. Procedimiento para la preparación de intermedios clave de omarigliptina
CN105037367A (zh) * 2014-04-18 2015-11-11 四川海思科制药有限公司 氨基六元环类衍生物及其在医药上的应用
CN105085528A (zh) * 2014-05-15 2015-11-25 成都贝斯凯瑞生物科技有限公司 作为二肽基肽酶-iv抑制剂的氨基四氢吡喃衍生物
CN105085530B (zh) * 2014-05-23 2019-01-04 四川海思科制药有限公司 三元稠合环取代的氨基六元环类衍生物及其在医药上的应用
MY181641A (en) * 2014-06-17 2020-12-30 Sichuan Haisco Pharmaceutical Co Ltd Amino pyran ring derivative and composition and use thereof
CN105294694B (zh) * 2014-06-18 2019-01-04 四川海思科制药有限公司 氨基六元环类衍生物及其在医药上的应用
US9862725B2 (en) 2014-07-21 2018-01-09 Merck Sharp & Dohme Corp. Process for preparing chiral dipeptidyl peptidase-IV inhibitors
CN105985357A (zh) * 2015-02-12 2016-10-05 北京赛林泰医药技术有限公司 取代的氨基六元饱和杂脂环类长效dpp-iv抑制剂
CN107250135B (zh) * 2015-08-24 2020-05-26 四川科伦博泰生物医药股份有限公司 长效二肽基肽酶-ⅳ抑制剂、用途及其中间体的制备方法
CN106478631B (zh) * 2015-08-24 2019-04-05 四川科伦药物研究院有限公司 长效二肽基肽酶-iv抑制剂、用途及其中间体的制备方法
WO2017032705A1 (fr) 2015-08-25 2017-03-02 Sandoz Ag Forme cristalline d'omarigliptine
TWI681962B (zh) * 2015-08-26 2020-01-11 大陸商四川海思科製藥有限公司 胺基六員環類衍生物及其在醫藥上的應用
TWI640524B (zh) * 2015-08-27 2018-11-11 四川海思科製藥有限公司 Aminopyran ring derivatives and compositions and uses thereof
CN105198847B (zh) * 2015-10-28 2017-05-17 四川凯科医药科技有限公司 一种化合物的制备方法
JP6475368B2 (ja) * 2015-12-03 2019-02-27 エッフェ・イ・エッセ − ファッブリカ・イタリアーナ・シンテテイチ・ソチエタ・ペル・アツィオーニF.I.S. − Fabbrica Italiana Sintetici S.p.A. アミノテトラヒドロピラン類の製造方法
CN105399744B (zh) * 2015-12-17 2017-07-18 黄燕鸽 一种奥格列汀的合成方法
EP3181565A1 (fr) 2015-12-18 2017-06-21 Sandoz Ag Sels cristallins d'omarigliptin
CN106916158A (zh) * 2015-12-25 2017-07-04 四川海思科制药有限公司 一种吡喃衍生物盐酸盐水合物及其中间体的制备方法
CN106916157A (zh) * 2015-12-25 2017-07-04 四川海思科制药有限公司 取代的氨基吡喃衍生物的晶型
CN106928228B (zh) * 2015-12-29 2019-08-30 杭州普晒医药科技有限公司 奥格列汀盐及其晶型、它们的制备方法和药物组合物
CN107337674B (zh) * 2016-04-29 2019-09-20 江苏吉贝尔药业股份有限公司 用于dpp-iv抑制剂的四氢吡喃胺衍生物、其药物组合物和制剂以及用途
CN109071551B (zh) * 2016-05-25 2020-12-08 四川海思科制药有限公司 一种三氟甲基取代的吡喃衍生物的制备方法
WO2017202365A1 (fr) * 2016-05-25 2017-11-30 四川海思科制药有限公司 Procédé de préparation d'un dérivé de pyranne substitué par un trifluorométhyle
CN107652291B (zh) * 2016-07-26 2020-07-14 中国科学院上海药物研究所 一种制备手性四氢吡喃衍生物的方法
WO2018028666A1 (fr) * 2016-08-12 2018-02-15 正大天晴药业集团股份有限公司 Cristal d'inhibiteur de dpp-iv à action prolongée et son sel
CN106674227B (zh) * 2016-12-06 2019-03-19 上海博志研新药物技术有限公司 一种奥格列汀及其中间体的制备方法
EP3335702A1 (fr) 2016-12-16 2018-06-20 Hexal AG Compositions pharmaceutiques comprenant de l'omarigliptine
EP3335701A1 (fr) 2016-12-16 2018-06-20 Hexal AG Composition pharmaceutique contenant de l'omarigliptine
EP3335703A1 (fr) 2016-12-16 2018-06-20 Hexal AG Composition pharmaceutique contenant de l'omarigliptine
EP3335704A1 (fr) 2016-12-16 2018-06-20 Hexal AG Composition pharmaceutique comprenant de l'omarigliptine
CN107024590A (zh) * 2017-03-13 2017-08-08 新疆医科大学 一种诊断1型和2型糖尿病的血清蛋白标志物组
WO2018167589A1 (fr) 2017-03-16 2018-09-20 Inventia Healthcare Private Limited Composition pharmaceutique comprenant de la dapagliflozine
ES2747768T3 (es) 2017-03-20 2020-03-11 Forma Therapeutics Inc Composiciones de pirrolopirrol como activadores de quinasa de piruvato (PKR)
CN109796455B (zh) * 2017-11-17 2021-02-26 四川海思科制药有限公司 一种氨基吡喃衍生物的盐、其晶型及其制备方法和用途
CN116919952A (zh) * 2018-02-06 2023-10-24 四川海思科制药有限公司 一种氨基吡喃衍生物的组合物
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
US12421269B2 (en) 2019-07-26 2025-09-23 Cgenetech (Suzhou, China) Co., Ltd. SGLT2/DPP4 inhibitor and application thereof
CN110568100B (zh) * 2019-09-12 2022-05-31 江西金水宝制药有限公司 一种米格列奈钙r-异构体的检测方法
US20220378756A1 (en) 2019-09-19 2022-12-01 Forma Therapeutics, Inc. Activating pyruvate kinase r
CN111793071B (zh) * 2020-07-06 2021-06-04 四川凯科医药科技有限公司 奥格列汀的合成工艺
US12128035B2 (en) 2021-03-19 2024-10-29 Novo Nordisk Health Care Ag Activating pyruvate kinase R
CN119504764B (zh) * 2024-11-26 2025-09-23 斯坦德药典标准物质研发(湖北)有限公司 一种Omarigliptin的制备方法

Family Cites Families (70)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4166452A (en) 1976-05-03 1979-09-04 Generales Constantine D J Jr Apparatus for testing human responses to stimuli
US4256108A (en) 1977-04-07 1981-03-17 Alza Corporation Microporous-semipermeable laminated osmotic system
US4265874A (en) 1980-04-25 1981-05-05 Alza Corporation Method of delivering drug with aid of effervescent activity generated in environment of use
US5232929A (en) 1990-11-28 1993-08-03 Pfizer Inc. 3-aminopiperidine derivatives and related nitrogen containing heterocycles and pharmaceutical compositions and use
US5545618A (en) 1990-01-24 1996-08-13 Buckley; Douglas I. GLP-1 analogs useful for diabetes treatment
IL111785A0 (en) 1993-12-03 1995-01-24 Ferring Bv Dp-iv inhibitors and pharmaceutical compositions containing them
DE19616486C5 (de) 1996-04-25 2016-06-30 Royalty Pharma Collection Trust Verfahren zur Senkung des Blutglukosespiegels in Säugern
AR008789A1 (es) 1996-07-31 2000-02-23 Bayer Corp Piridinas y bifenilos substituidos
UA65549C2 (uk) 1996-11-05 2004-04-15 Елі Ліллі Енд Компані Спосіб регулювання ожиріння шляхом периферійного введення аналогів та похідних glp-1 (варіанти) та фармацевтична композиція
TW492957B (en) 1996-11-07 2002-07-01 Novartis Ag N-substituted 2-cyanopyrrolidnes
US6054587A (en) 1997-03-07 2000-04-25 Metabasis Therapeutics, Inc. Indole and azaindole inhibitors of fructose-1,6-bisphosphatase
AU6452098A (en) 1997-03-07 1998-09-22 Metabasis Therapeutics, Inc. Novel purine inhibitors of fructose-1,6-bisphosphatase
DE69819311T2 (de) 1997-03-07 2004-07-29 Metabasis Therapeutics Inc., San Diego Neue benzimidazol inhibitoren der fructose-1,6-bisphosphatase
AU749271B2 (en) 1997-07-01 2002-06-20 Agouron Pharmaceuticals, Inc. Glucagon antagonists/inverse agonists
US6613942B1 (en) 1997-07-01 2003-09-02 Novo Nordisk A/S Glucagon antagonists/inverse agonists
PA8469501A1 (es) * 1998-04-10 2000-09-29 Pfizer Prod Inc Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico
CA2331122A1 (fr) 1998-05-04 1999-11-11 Point Therapeutics, Inc. Stimulation hematopoietique
ATE246197T1 (de) 1998-09-09 2003-08-15 Metabasis Therapeutics Inc Neue heteroaromatische fructose 1,6- bisphosphatase inhibitoren
CO5150173A1 (es) 1998-12-10 2002-04-29 Novartis Ag Compuestos n-(glicilo sustituido)-2-cianopirrolidinas inhibidores de peptidasa de dipeptidilo-iv (dpp-iv) los cuales son efectivos en el tratamiento de condiciones mediadas por la inhibicion de dpp-iv
GB9906715D0 (en) 1999-03-23 1999-05-19 Ferring Bv Compositions for promoting growth
WO2000069810A1 (fr) 1999-05-17 2000-11-23 Novo Nordisk A/S Antagonistes/agonistes inverses de glucagon
WO2002008188A1 (fr) 2000-07-25 2002-01-31 Merck & Co., Inc. Indoles n-substitues utiles pour le traitement du diabete
KR20030096227A (ko) 2000-10-27 2003-12-24 프로비오드룩 아게 신경 및 신경정신 질환의 치료방법
WO2002060388A2 (fr) 2001-01-30 2002-08-08 Merck & Co., Inc. Acyl-sulfamides pour le traitement de l'obesite, du diabete et des troubles lipidiques
DE60221983T2 (de) 2001-06-27 2008-05-15 Smithkline Beecham Corp. Fluorpyrrolidine als dipeptidyl-peptidase inhibitoren
UA74912C2 (en) 2001-07-06 2006-02-15 Merck & Co Inc Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes
GB0121709D0 (en) 2001-09-07 2001-10-31 Imp College Innovations Ltd Food inhibition agent
AR040241A1 (es) 2002-06-10 2005-03-23 Merck & Co Inc Inhibidores de la 11-beta-hidroxiesteroide deshidrogrenasa 1 para el tratamiento de la diabetes obesidad y dislipidemia
WO2004020408A1 (fr) 2002-08-29 2004-03-11 Merck & Co., Inc. Indoles a activite antidiabetique
WO2004019869A2 (fr) 2002-08-29 2004-03-11 Merck & Co., Inc. Indoles presentant un effet antidiabetique
WO2004037159A2 (fr) 2002-10-23 2004-05-06 Obetherapy Biotechnology Composes, compositions et methodes permettant de moduler le metabolisme des graisses
US7192922B2 (en) 2002-11-19 2007-03-20 Allegheny-Singer Research Institute Method of treating left ventricular dysfunction
JO2397B1 (en) 2002-12-20 2007-06-17 ميرك شارب اند دوم كوربوريشن Terazol derivatives as beta-hydroxy steroid dihydrogenase-1 inhibitors
JP2007504285A (ja) 2003-01-17 2007-03-01 メルク エンド カムパニー インコーポレーテッド N−シクロヘキシルアミノカルボニルベンゼンスルホンアミド誘導体
WO2004091499A2 (fr) 2003-04-09 2004-10-28 Neose Technologies, Inc. Formation intracellulaire de conjugues de peptides
US7145012B2 (en) * 2003-04-23 2006-12-05 Pfizer Inc. Cannabinoid receptor ligands and uses thereof
US20040214856A1 (en) * 2003-04-23 2004-10-28 Pfizer Inc Cannabinoid receptor ligands and uses thereof
WO2005030751A2 (fr) * 2003-09-08 2005-04-07 Takeda Pharmaceutical Company Limited Inhibiteurs de dipeptidyle peptidase
WO2005061523A1 (fr) 2003-12-23 2005-07-07 Progen Industries Limited Composes mimetiques du glycosaminoglycane (gag)
AU2005265148B2 (en) * 2004-06-21 2011-01-20 Merck Sharp & Dohme Corp. Aminocyclohexanes as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes
WO2006020372A2 (fr) 2004-07-23 2006-02-23 Neose Technologies, Inc. Modification enzymatique de glycopeptides
US7718667B2 (en) * 2004-09-28 2010-05-18 Merck Sharp & Dohme Corp. Fused aminopiperidines as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes
AU2005292134B2 (en) 2004-10-01 2010-12-23 Merck Sharp & Dohme Corp. Aminopiperidines as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes
US20090253752A1 (en) 2004-10-25 2009-10-08 Bryan Burkey Combination of dpp-iv inhibitor, ppar antidiabetic and metmorfin
JP4999698B2 (ja) 2004-11-29 2012-08-15 メルク・シャープ・エンド・ドーム・コーポレイション 糖尿病の治療または予防用のジペプチジルペプチダーゼ−iv阻害剤としての縮合アミノピペリジン
CN101090888A (zh) 2004-12-20 2007-12-19 霍夫曼-拉罗奇有限公司 4-氨基哌啶衍生物
US7411093B2 (en) 2004-12-20 2008-08-12 Hoffman-La Roche Inc. Aminocycloalkanes as DPP-IV inhibitors
EP1702916A1 (fr) 2005-03-18 2006-09-20 Santhera Pharmaceuticals (Schweiz) GmbH Inhibiteurs de DPP-IV
TWI357902B (en) * 2005-04-01 2012-02-11 Lg Life Science Ltd Dipeptidyl peptidase-iv inhibiting compounds, meth
JP5069678B2 (ja) 2005-05-25 2012-11-07 メルク・シャープ・エンド・ドーム・コーポレイション 糖尿病の治療又は予防のためのジペプチジルペプチダーゼiv阻害剤としてのアミノシクロヘキサン
RU2485135C2 (ru) 2005-06-13 2013-06-20 Импиэриэл Инноувейшнс Лимитид Соединения оксинтомодулина (варианты), фармацевтическая композиция на их основе, способы лечения и профилактики ожирения и сопутствующих заболеваний (варианты) и лекарственное средство (варианты)
CA2619111C (fr) 2005-08-26 2013-04-09 Merck & Co., Inc. Aminopiperidines fusionnees utilisees comme inhibiteurs de dipeptidyl-peptidase-iv pour le traitement ou la prevention du diabete
US7943615B2 (en) 2005-12-14 2011-05-17 Merck Sharp & Dohme Corp. Fused aminopiperidines as dipeptidyl peptidase-4 inhibitors for the treatment or prevention of diabetes
CA2636757A1 (fr) * 2006-01-25 2007-08-02 Tesfaye Biftu Aminocyclohexanes utiles en tant qu'inhibiteurs de la dipeptidyl peptidase-iv pour traiter ou prevenir le diabete
WO2007097931A2 (fr) 2006-02-15 2007-08-30 Merck & Co., Inc. Aminotétrahydropyrannes en tant qu'inhibiteurs de dipeptidylpeptidase-iv dans le traitement prophylactique ou thérapeutique du diabète
CN101389648B (zh) 2006-02-22 2013-07-17 默沙东公司 肽胃泌酸调节素衍生物
KR20090005329A (ko) 2006-03-20 2009-01-13 머크 앤드 캄파니 인코포레이티드 뉴로메딘 u 수용체 효능제 및 이의 용도
TW200806669A (en) * 2006-03-28 2008-02-01 Merck & Co Inc Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes
AU2007254357B2 (en) 2006-05-16 2011-07-21 Merck Sharp & Dohme Corp. Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes
AU2007275294A1 (en) 2006-07-18 2008-01-24 Centocor, Inc. Human GLP-1 mimetibodies, compositions, methods and uses
CA2668662A1 (fr) * 2006-11-14 2008-05-22 Merck & Co., Inc. Composes heteroaromatiques tricycliques en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention de diabetes
AU2008216265B2 (en) 2007-02-15 2014-04-03 Indiana University Research And Technology Corporation Glucagon/GLP-1 receptor co-agonists
AU2008267724A1 (en) 2007-06-28 2008-12-31 Merck Frosst Canada Ltd Substituted fused pyrimidines as antagonists of GPR105 activity
EP2178537A4 (fr) 2007-07-19 2011-08-17 Merck Sharp & Dohme Dérivés de bêta-carboline en tant que composés antidiabétiques
WO2009014676A1 (fr) * 2007-07-23 2009-01-29 Merck & Co., Inc. Nouvelle forme cristalline d'un sel de dichlorhydrate d'un inhibiteur de la dipeptidyle peptidase iv
CA2696211C (fr) 2007-08-21 2015-05-26 Merck Sharp & Dohme Corp. Composes heterocycliques en tant qu'inhibiteurs de dipeptidylpeptidase-iv pour le traitement ou la prevention des diabetes
WO2009042053A2 (fr) 2007-09-21 2009-04-02 Merck & Co., Inc. Agonistes du récepteur de la neuromédine u et leurs utilisations
US7902376B2 (en) * 2008-01-23 2011-03-08 Merck Sharp & Dohme Corp. Process for preparing chiral dipeptidyl peptidase-IV inhibitor intermediates
CN102272135A (zh) 2008-10-08 2011-12-07 百时美施贵宝公司 唑并吡咯酮黑色素浓集激素受体-1拮抗剂
JO2870B1 (en) 2008-11-13 2015-03-15 ميرك شارب اند دوهم كورب Amino Tetra Hydro Pirans as Inhibitors of Peptide Dipeptide IV for the Treatment or Prevention of Diabetes

Also Published As

Publication number Publication date
CO6382129A2 (es) 2012-02-15
NZ592826A (en) 2012-06-29
CN102272136B (zh) 2015-01-14
EP2358717B1 (fr) 2013-08-21
WO2010056708A1 (fr) 2010-05-20
HRP20130924T1 (hr) 2013-11-08
IL212485A0 (en) 2011-06-30
KR101260162B1 (ko) 2013-05-09
KR20120107133A (ko) 2012-09-28
MY150787A (en) 2014-02-28
AU2009314191A1 (en) 2010-05-20
GEP20135724B (en) 2013-01-10
AR074306A1 (es) 2011-01-05
TN2011000201A1 (en) 2012-12-17
DK2358717T3 (da) 2013-11-18
EP2676960B1 (fr) 2017-04-19
PE20120027A1 (es) 2012-02-05
EP2676960A1 (fr) 2013-12-25
US8772328B2 (en) 2014-07-08
BRPI0921375B1 (pt) 2020-11-03
US20150126443A1 (en) 2015-05-07
US8592371B2 (en) 2013-11-26
US8415297B2 (en) 2013-04-09
ECSP11011044A (es) 2011-06-30
KR101454093B1 (ko) 2014-10-27
RS52946B (sr) 2014-02-28
US20150344487A1 (en) 2015-12-03
DOP2011000128A (es) 2011-06-30
JP5537507B2 (ja) 2014-07-02
IL212485A (en) 2013-08-29
TW201024299A (en) 2010-07-01
EP2676961B1 (fr) 2017-04-19
JP4854825B1 (ja) 2012-01-18
PT2358717E (pt) 2013-11-26
BRPI0921375B8 (pt) 2021-05-25
TWI398443B (zh) 2013-06-11
CR20110257A (es) 2011-07-01
AU2009314191B2 (en) 2012-02-16
US20120149637A1 (en) 2012-06-14
EP2676959A1 (fr) 2013-12-25
UA101414C2 (uk) 2013-03-25
BRPI0921375A2 (pt) 2015-12-29
US20100120863A1 (en) 2010-05-13
ES2432191T3 (es) 2013-12-02
US8143289B2 (en) 2012-03-27
US9278976B2 (en) 2016-03-08
US20130157940A1 (en) 2013-06-20
KR20110074581A (ko) 2011-06-30
US8951965B2 (en) 2015-02-10
SV2011003903A (es) 2011-10-13
CL2011001082A1 (es) 2012-02-24
US20160137622A1 (en) 2016-05-19
US9138426B2 (en) 2015-09-22
PA8848201A1 (es) 2010-06-28
NI201100081A (es) 2011-11-03
EP2358717A1 (fr) 2011-08-24
JP2011251973A (ja) 2011-12-15
JO2870B1 (en) 2015-03-15
EA201170670A1 (ru) 2011-12-30
CA2742783A1 (fr) 2010-05-20
CA2742783C (fr) 2013-01-08
CY1114617T1 (el) 2016-10-05
EA018613B1 (ru) 2013-09-30
EP2676961A1 (fr) 2013-12-25
US9403790B2 (en) 2016-08-02
IL225198A (en) 2016-02-29
SI2358717T1 (sl) 2014-02-28
MX2011005044A (es) 2011-06-17
US20140051740A1 (en) 2014-02-20
CN102272136A (zh) 2011-12-07
PL2358717T3 (pl) 2014-01-31
US20140287993A1 (en) 2014-09-25
HK1154849A1 (en) 2012-05-04
HN2011001256A (es) 2013-10-14
JP2012508746A (ja) 2012-04-12

Similar Documents

Publication Publication Date Title
MA32887B1 (fr) Aminotetrahydropyranes en tant qu'inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete
MA30333B1 (fr) Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete.
EP1796669A4 (fr) Aminopiperidines utilisees comme inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete
EP1888066A4 (fr) Aminocyclohexanes en tant qu'inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete
DE602004023932D1 (de) 3-amino-4-phenylbutansäurederivate als dipeptidylpeptidase-hemmer zur behandlung oder vorbeugung von diabetes
WO2007087231A3 (fr) Aminocyclohexanes utiles en tant qu'inhibiteurs de la dipeptidyl peptidase-iv pour traiter ou prévenir le diabète
WO2007097931A3 (fr) Aminotétrahydropyrannes en tant qu'inhibiteurs de dipeptidylpeptidase-iv dans le traitement prophylactique ou thérapeutique du diabète
WO2007136603A3 (fr) Aminotétrahydropyranes en tant qu'inhibiteurs de la dipeptidyl peptidase-iv pour le traitement ou la prévention du diabète
EA200870019A1 (ru) Лактамовые соединения и способы их применения
EP1490335A4 (fr) Inhibiteurs de la dipeptidyl peptidase beta-amino heterocycliques pour le traitement ou la prevention du diabete
EP1921917A4 (fr) Aminopiperidines fusionnees utilisees comme inhibiteurs de dipeptidyl-peptidase-iv pour le traitement ou la prevention du diabete
ATE451369T1 (de) Piperidinopyrimidindipeptidylpeptidaseinhibitor n zur behandlung von diabetes
MA32903B1 (fr) Inhibiteurs de proteine-kinases
ATE527259T1 (de) Kondensierte aminopiperidine als dipeptidylpeptidase-iv-inhibitoren zur behandlung oder prävention von diabetes
MA32727B1 (fr) Pyrazolylaminopyridines au titre d'inhibiteurs de fak
MA31919B1 (fr) Composés inhibiteurs de la dipeptidyl peptidase-iv, leurs procédés de préparation, et compositions pharmaceutiques contenant ces composés comme agent actif
DK1556362T3 (da) Heterocykliske beta-aminodipeptidylpeptidaseinhibitorer til behandling eller forebyggelse af diabetes
EP1784188A4 (fr) Derives de triazole accoles inhibiteurs de la dipeptidyl peptidase-iv utilises dans le traitement ou la prevention du diabete
MA32471B1 (fr) Composés de borates esters et compositions pharmaceutiques contenant des composés
WO2007070434A3 (fr) Amino-piperidines fusionnees en tant qu'inhibiteurs de la dipeptidyl peptidase-4 pour le traitement ou la prevention du diabete
IS7817A (is) Fenýlalanín afleiður sem dípeptidýl peptíðasa hindrar til að meðhöndla eða fyrirbyggja sykursýki.
IN2012DN00721A (fr)
EP1554280A4 (fr) Inhibiteurs de la dipeptidyl peptidase heterocyclique beta-amino antidiabetiques
MA32929B1 (fr) Lactames en tant qu'inhibiteurs de bêta-sécrétase
EP2077719A4 (fr) Inhibiteurs pipéridines et pyrrolidines de la bêta-secrétase utilisés dans le traitement de la maladie d'alzheimer