MA30333B1 - Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete. - Google Patents
Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete.Info
- Publication number
- MA30333B1 MA30333B1 MA31288A MA31288A MA30333B1 MA 30333 B1 MA30333 B1 MA 30333B1 MA 31288 A MA31288 A MA 31288A MA 31288 A MA31288 A MA 31288A MA 30333 B1 MA30333 B1 MA 30333B1
- Authority
- MA
- Morocco
- Prior art keywords
- prevention
- treatment
- inhibitors
- useful
- dipeptidyl peptidase
- Prior art date
Links
Classifications
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/351—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Diabetes (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Epidemiology (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 développée I qui sont des inhibiteurs de l'enzyme dipeptidyl-peptidase-IV et qui sont utiles dans le traitement ou la prévention de maladies dans lesquelles l'enzyme dipeptidyl-peptidase-IV est impliquée, telles que le diabète et en particulier le diabète type 2. L'invention concerne aussi des compositions pharmaceutiques comprenant ces composés et l'usage de ces composés et compositions dans la prévention ou le traitement de ces maladies dans lesquelles l'enzyme dipeptidyl-peptidase-IV est impliquée.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78651806P | 2006-03-28 | 2006-03-28 | |
US83812206P | 2006-08-16 | 2006-08-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA30333B1 true MA30333B1 (fr) | 2009-04-01 |
Family
ID=38521359
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA31288A MA30333B1 (fr) | 2006-03-28 | 2008-10-14 | Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete. |
Country Status (22)
Country | Link |
---|---|
US (1) | US7678905B2 (fr) |
EP (1) | EP2001883B1 (fr) |
JP (1) | JP5229706B2 (fr) |
KR (1) | KR20090005306A (fr) |
AR (1) | AR059984A1 (fr) |
AT (1) | ATE554091T1 (fr) |
AU (1) | AU2007243631B2 (fr) |
BR (1) | BRPI0709141A2 (fr) |
CA (1) | CA2646962C (fr) |
CR (1) | CR10343A (fr) |
DO (1) | DOP2007000051A (fr) |
EA (1) | EA200870380A1 (fr) |
EC (1) | ECSP088765A (fr) |
GT (1) | GT200800184A (fr) |
MA (1) | MA30333B1 (fr) |
MX (1) | MX2008012490A (fr) |
NO (1) | NO20084508L (fr) |
PE (1) | PE20071104A1 (fr) |
SV (1) | SV2008003045A (fr) |
TN (1) | TNSN08367A1 (fr) |
TW (1) | TW200806669A (fr) |
WO (1) | WO2007126745A2 (fr) |
Families Citing this family (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2007218053B2 (en) | 2006-02-15 | 2010-05-27 | Merck Sharp & Dohme Corp. | Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
US7812027B2 (en) | 2006-05-16 | 2010-10-12 | Merck Sharp & Dohme Corp. | Substitued [1,2,4]triazolo[1,5-a]pyrazines as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
US7855206B2 (en) | 2006-11-14 | 2010-12-21 | Merck Sharp & Dohme Corp. | Tricyclic heteroaromatic compounds as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
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 |
EP2025674A1 (fr) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Tetrahydronaphthaline substituée, son procédé de fabrication et son utilisation en tant que médicament |
EP2190428A4 (fr) | 2007-08-21 | 2012-02-29 | Merck Sharp & Dohme | Composés hétérocycliques en tant qu'inhibiteurs de dipeptidylpeptidase-iv pour le traitement ou la prévention des diabètes |
US7902376B2 (en) | 2008-01-23 | 2011-03-08 | Merck Sharp & Dohme Corp. | Process for preparing chiral dipeptidyl peptidase-IV inhibitor intermediates |
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 |
AU2010289871B2 (en) * | 2009-09-02 | 2014-07-10 | Merck Sharp & Dohme Corp. | Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
US20130072427A1 (en) * | 2009-09-23 | 2013-03-21 | Pfizer Inc. | Gpr 119 modulators |
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 |
WO2011107494A1 (fr) | 2010-03-03 | 2011-09-09 | Sanofi | Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation |
EP2571876B1 (fr) * | 2010-05-21 | 2016-09-07 | Merck Sharp & Dohme Corp. | Composés hétérocycliques substitués à sept chaînons en tant qu'inhibiteurs de la dipeptidyl-peptidase iv pour le traitement du diabète |
US8933024B2 (en) | 2010-06-18 | 2015-01-13 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and 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 |
TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
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 |
US8691832B2 (en) | 2010-12-06 | 2014-04-08 | Merck Sharp & Dohme Corp. | Tricyclic heterocycles useful as dipeptidyl peptidase-IV inhibitors |
US8871758B2 (en) | 2011-03-08 | 2014-10-28 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
EP2683704B1 (fr) | 2011-03-08 | 2014-12-17 | Sanofi | Dérivés oxathiazine ramifiés, procédé pour leur préparation, utilisation en tant que médicament, agents pharmaceutiques contenant ces dérivés et leur utilisation |
US8901114B2 (en) | 2011-03-08 | 2014-12-02 | Sanofi | Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof |
WO2012120055A1 (fr) | 2011-03-08 | 2012-09-13 | Sanofi | Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
WO2012120054A1 (fr) | 2011-03-08 | 2012-09-13 | Sanofi | Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
EP2726075A4 (fr) | 2011-06-29 | 2014-11-19 | Merck Sharp & Dohme | Nouvelles formes cristallines d'un inhibiteur de peptidase-iv |
WO2013006526A2 (fr) | 2011-07-05 | 2013-01-10 | Merck Sharp & Dohme Corp. | Hétérocycles tricycliques utiles comme inhibiteurs de la dipeptidyl peptidase-iv |
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 |
WO2013045413A1 (fr) | 2011-09-27 | 2013-04-04 | Sanofi | Dérivés d'amide d'acide 6-(4-hydroxyphényl)-3-alkyl-1h-pyrazolo[3,4-b] pyridine-4-carboxylique utilisés comme inhibiteurs de kinase |
EP2814485A4 (fr) | 2012-02-17 | 2015-08-26 | Merck Sharp & Dohme | Inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prévention du diabète |
US9156848B2 (en) | 2012-07-23 | 2015-10-13 | Merck Sharp & Dohme Corp. | Treating diabetes with dipeptidyl peptidase-IV inhibitors |
EP2874622A4 (fr) | 2012-07-23 | 2015-12-30 | Merck Sharp & Dohme | Traitement du diabète par administration d'inhibiteurs de dipeptidyl peptidase-iv |
TWI500613B (zh) * | 2012-10-17 | 2015-09-21 | Cadila Healthcare Ltd | 新穎之雜環化合物 |
WO2014064215A1 (fr) | 2012-10-24 | 2014-05-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Inhibiteurs de la kinase tpl2 pour prévenir ou traiter le diabète et favoriser la survie de cellules β |
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 |
WO2015192701A1 (fr) * | 2014-06-17 | 2015-12-23 | 四川海思科制药有限公司 | Dérivé de cycle aminopyranoïde, composition contenant ledit dérivé et son utilisation |
JP6574474B2 (ja) | 2014-07-21 | 2019-09-11 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | キラルジペプチジルペプチダーゼ−iv阻害剤の製造方法 |
EP3214079B1 (fr) | 2014-10-31 | 2020-06-24 | East China University Of Science And Technology | Dérivés benzo à cycle à six chaînons en tant qu'inhibiteur de la dpp-4 et son utilisation |
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 |
EP3273981B1 (fr) | 2015-03-24 | 2020-04-29 | INSERM - Institut National de la Santé et de la Recherche Médicale | Procédé et composition pharmaceutique pour une utilisation dans le traitement du diabète |
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 |
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 |
CN108699068B (zh) * | 2016-05-25 | 2021-01-08 | 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制备方法 |
PL3483164T3 (pl) | 2017-03-20 | 2020-08-24 | Forma Therapeutics, Inc. | Kompozycje pirolopirolu jako aktywatory kinazy pirogronianowej (PKR) |
WO2020061378A1 (fr) | 2018-09-19 | 2020-03-26 | Forma Therapeutics, Inc. | Traitement de la drépanocytose avec un composé activant la pyruvate kinase r |
US11001588B2 (en) | 2018-09-19 | 2021-05-11 | Forma Therapeutics, Inc. | Activating pyruvate kinase R and mutants thereof |
JP7525380B2 (ja) | 2020-11-27 | 2024-07-30 | 株式会社ダイヘン | 巻線装置 |
US12128035B2 (en) | 2021-03-19 | 2024-10-29 | Novo Nordisk Health Care Ag | Activating pyruvate kinase R |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5114961A (en) * | 1989-06-08 | 1992-05-19 | Merck & Co., Inc. | 2,5-diaryl tetrahydrofurans and analogs thereof as PAF antagonists |
ATE370943T1 (de) * | 2001-06-27 | 2007-09-15 | Smithkline Beecham Corp | Fluoropyrrolidine als dipeptidyl-peptidase inhibitoren |
WO2005030751A2 (fr) * | 2003-09-08 | 2005-04-07 | Takeda Pharmaceutical Company Limited | Inhibiteurs de dipeptidyle peptidase |
JP4963671B2 (ja) * | 2004-06-21 | 2012-06-27 | 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 |
EP1796669B1 (fr) | 2004-10-01 | 2010-09-22 | Merck Sharp & Dohme Corp. | Aminopiperidines utilisees comme inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete |
AU2005309606B2 (en) | 2004-11-29 | 2011-01-06 | Merck Sharp & Dohme Corp. | Fused aminopiperidines as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
CN101500573A (zh) | 2005-05-25 | 2009-08-05 | 默克公司 | 用于糖尿病治疗或者预防的作为二肽基肽酶-ⅳ抑制剂的氨基环己烷 |
JP5075125B2 (ja) | 2005-08-26 | 2012-11-14 | 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用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 |
AU2007218053B2 (en) * | 2006-02-15 | 2010-05-27 | Merck Sharp & Dohme Corp. | Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
US7812027B2 (en) * | 2006-05-16 | 2010-10-12 | Merck Sharp & Dohme Corp. | Substitued [1,2,4]triazolo[1,5-a]pyrazines as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
US7855206B2 (en) * | 2006-11-14 | 2010-12-21 | Merck Sharp & Dohme Corp. | Tricyclic heteroaromatic compounds as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
-
2007
- 2007-03-19 TW TW096109375A patent/TW200806669A/zh unknown
- 2007-03-20 DO DO2007000051A patent/DOP2007000051A/es unknown
- 2007-03-20 AR ARP070101127A patent/AR059984A1/es not_active Application Discontinuation
- 2007-03-23 PE PE2007000315A patent/PE20071104A1/es not_active Application Discontinuation
- 2007-03-26 MX MX2008012490A patent/MX2008012490A/es unknown
- 2007-03-26 EP EP07754011A patent/EP2001883B1/fr active Active
- 2007-03-26 BR BRPI0709141-9A patent/BRPI0709141A2/pt not_active IP Right Cessation
- 2007-03-26 JP JP2009502918A patent/JP5229706B2/ja not_active Expired - Fee Related
- 2007-03-26 EA EA200870380A patent/EA200870380A1/ru unknown
- 2007-03-26 AT AT07754011T patent/ATE554091T1/de active
- 2007-03-26 KR KR1020087023571A patent/KR20090005306A/ko not_active Application Discontinuation
- 2007-03-26 CA CA2646962A patent/CA2646962C/fr not_active Expired - Fee Related
- 2007-03-26 WO PCT/US2007/007434 patent/WO2007126745A2/fr active Application Filing
- 2007-03-26 AU AU2007243631A patent/AU2007243631B2/en not_active Ceased
- 2007-03-27 US US11/728,673 patent/US7678905B2/en active Active
-
2008
- 2008-09-17 GT GT200800184A patent/GT200800184A/es unknown
- 2008-09-22 TN TNP2008000367A patent/TNSN08367A1/en unknown
- 2008-09-24 EC EC2008008765A patent/ECSP088765A/es unknown
- 2008-09-26 SV SV2008003045A patent/SV2008003045A/es not_active Application Discontinuation
- 2008-10-06 CR CR10343A patent/CR10343A/es unknown
- 2008-10-14 MA MA31288A patent/MA30333B1/fr unknown
- 2008-10-27 NO NO20084508A patent/NO20084508L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP2001883A2 (fr) | 2008-12-17 |
JP5229706B2 (ja) | 2013-07-03 |
KR20090005306A (ko) | 2009-01-13 |
CA2646962C (fr) | 2011-06-21 |
JP2009531437A (ja) | 2009-09-03 |
DOP2007000051A (es) | 2007-12-15 |
MX2008012490A (es) | 2008-10-10 |
ATE554091T1 (de) | 2012-05-15 |
EA200870380A1 (ru) | 2009-02-27 |
TW200806669A (en) | 2008-02-01 |
AR059984A1 (es) | 2008-05-14 |
CA2646962A1 (fr) | 2007-11-08 |
AU2007243631A1 (en) | 2007-11-08 |
TNSN08367A1 (en) | 2009-12-29 |
EP2001883B1 (fr) | 2012-04-18 |
BRPI0709141A2 (pt) | 2011-06-28 |
NO20084508L (no) | 2008-10-27 |
US7678905B2 (en) | 2010-03-16 |
WO2007126745A2 (fr) | 2007-11-08 |
CR10343A (es) | 2008-10-29 |
ECSP088765A (es) | 2008-10-31 |
GT200800184A (es) | 2011-09-05 |
US20070232676A1 (en) | 2007-10-04 |
PE20071104A1 (es) | 2007-12-29 |
AU2007243631B2 (en) | 2011-11-24 |
WO2007126745A3 (fr) | 2007-12-21 |
SV2008003045A (es) | 2009-11-09 |
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