MA31761B1 - Nouveaux inhibiteurs de seh et leur utilisation - Google Patents

Nouveaux inhibiteurs de seh et leur utilisation

Info

Publication number
MA31761B1
MA31761B1 MA32751A MA32751A MA31761B1 MA 31761 B1 MA31761 B1 MA 31761B1 MA 32751 A MA32751 A MA 32751A MA 32751 A MA32751 A MA 32751A MA 31761 B1 MA31761 B1 MA 31761B1
Authority
MA
Morocco
Prior art keywords
seh
relates
compounds
compound
treatment
Prior art date
Application number
MA32751A
Other languages
Arabic (ar)
English (en)
Inventor
Yun Ding
Reema K Thalji
Joseph Paul Marino Jr
Original Assignee
Glaxosmithkline Llc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Glaxosmithkline Llc filed Critical Glaxosmithkline Llc
Publication of MA31761B1 publication Critical patent/MA31761B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/46—Phenazines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/40—Nitrogen atoms
    • C07D251/48—Two nitrogen atoms
    • C07D251/52—Two nitrogen atoms with an oxygen or sulfur atom attached to the third ring carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

La présente invention concerne de nouveaux inhibiteurs de seh et leur utilisation dans le traitement de maladies médiées par l'enzyme seh. De façon spécifique, l'invention concerne des composés répondant à la formule i : r1, r2, r5, r6, a, b, y, z, n, et m étant définis ci-après, et des sels pharmaceutiquement acceptables de ces composés. Les composés de l'invention sont des inhibiteurs de seh et peuvent être utilisés dans le traitement de maladies médiées par l'enzyme seh, telles que l'hypertension. Par conséquent, l'invention concerne également des compositions pharmaceutiques contenant un composé de l'invention. L'invention concerne de plus des procédés d'inhibition de seh et le traitement de pathologies y étant associées au moyen d'un composé de l'invention ou d'une composition pharmaceutique contenant un composé de l'invention.
MA32751A 2007-10-11 2010-04-08 Nouveaux inhibiteurs de seh et leur utilisation MA31761B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US97915407P 2007-10-11 2007-10-11
PCT/US2008/079517 WO2009049157A1 (fr) 2007-10-11 2008-10-10 Nouveaux inhibiteurs de seh et leur utilisation

Publications (1)

Publication Number Publication Date
MA31761B1 true MA31761B1 (fr) 2010-10-01

Family

ID=40549589

Family Applications (1)

Application Number Title Priority Date Filing Date
MA32751A MA31761B1 (fr) 2007-10-11 2010-04-08 Nouveaux inhibiteurs de seh et leur utilisation

Country Status (29)

Country Link
US (2) US8173805B2 (fr)
EP (1) EP2214487B1 (fr)
JP (1) JP5372943B2 (fr)
KR (1) KR101546111B1 (fr)
CN (1) CN101896065B (fr)
AU (1) AU2008310732B2 (fr)
BR (1) BRPI0817542A2 (fr)
CA (1) CA2702265C (fr)
CO (1) CO6270285A2 (fr)
CR (1) CR11423A (fr)
CY (1) CY1114865T1 (fr)
DK (1) DK2214487T3 (fr)
DO (1) DOP2010000101A (fr)
EA (1) EA018414B1 (fr)
ES (1) ES2445444T3 (fr)
HK (1) HK1141211A1 (fr)
HR (1) HRP20140105T1 (fr)
IL (1) IL204889A (fr)
MA (1) MA31761B1 (fr)
MX (1) MX2010003942A (fr)
MY (1) MY157116A (fr)
NZ (1) NZ584471A (fr)
PL (1) PL2214487T3 (fr)
PT (1) PT2214487E (fr)
RS (1) RS53180B (fr)
SI (1) SI2214487T1 (fr)
UA (1) UA107444C2 (fr)
WO (1) WO2009049157A1 (fr)
ZA (1) ZA201002465B (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008105968A1 (fr) 2006-11-03 2008-09-04 Smithkline Beecham Corporation Nouveaux inhibiteurs de seh et utilisation de ces derniers
WO2009049165A1 (fr) 2007-10-11 2009-04-16 Smithkline Beecham Corporation Inhibiteurs inédits de la seh et leur utilisation
SI2214487T1 (sl) * 2007-10-11 2014-03-31 Glaxosmithkline Llc Novi sEH inhibitorji in njihova uporaba
FR2948027A1 (fr) 2009-07-17 2011-01-21 Merck Sante Sas Derives amines de dihydro-1,3,5-triazine pour leur utilisation dans le traitement des maladies associees a une ischemie et/ou une reperfusion
EP2567959B1 (fr) 2011-09-12 2014-04-16 Sanofi Dérivés d'amide d'acide 6-(4-hydroxy-phényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase
US8809552B2 (en) * 2011-11-01 2014-08-19 Hoffmann-La Roche Inc. Azetidine compounds, compositions and methods of use
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
WO2015003360A2 (fr) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs méthodes d'utilisation
WO2015104422A1 (fr) 2014-01-13 2015-07-16 Basf Se Composés dihydrothiophène dans la lutte contre des nuisibles invertébrés
WO2015155129A1 (fr) * 2014-04-07 2015-10-15 Basf Se Composé de diaminotriazine
US10308648B2 (en) 2014-10-16 2019-06-04 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5420283A (en) * 1993-08-02 1995-05-30 Pfizer Inc. Resolution of (R)-2-benzylsuccinic acid 4-[4-(N-t-butoxycarbonylmethylamino)-piperidine] amide
CA2348740A1 (fr) * 1998-12-23 2000-07-06 Ruth R. Wexler Inhibiteurs de la thrombine ou du facteur xa
US6630478B2 (en) * 2000-07-07 2003-10-07 Neotherapeutics, Inc. Methods for treatment of drug-induced peripheral neuropathy
US6451814B1 (en) * 2000-07-17 2002-09-17 Wyeth Heterocyclic β-3 adrenergic receptor agonists
KR100589032B1 (ko) 2000-10-20 2006-06-14 에자이 가부시키가이샤 질소 함유 방향환 유도체
WO2002058736A2 (fr) * 2000-12-12 2002-08-01 Neotherapetics, Inc. Utilisation d'analogues de purine a substitution en position 9 et d'autres molecules pour stimuler la neurogenese
PL210066B1 (pl) * 2000-12-21 2011-11-30 Vertex Pharma Związek pirazolowy, kompozycja zawierająca ten związek i jego zastosowania
MXPA03011681A (es) * 2001-06-29 2004-03-19 Boehringer Ingelheim Pharma Uso de inhibidores de epoxido hidrolasa soluble, para tratar enfermedades relacionadas con la enfermedad cardiovascular.
US20030055249A1 (en) 2001-07-17 2003-03-20 Fick David B. Synthesis and methods of use of pyrimidine analogues and derivatives
TWI329105B (en) * 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
PT1479397E (pt) * 2002-02-05 2011-09-01 Astellas Pharma Inc Derivados de 2,4,6-triamino-1,3,5-triazina
US20040087653A1 (en) 2002-05-16 2004-05-06 Manning Pamela T. Methods for the treatment of respiratory diseases and conditions with a selective iNOS inhibitor and a PDE inhibitor and compositions therefor
EP1464335A3 (fr) 2003-03-31 2007-05-09 Taisho Pharmaceutical Co. Ltd. Derivés de quinolines, tetrahydroquinolines et pyrimidines comme antagonistes du MCH
KR20060032190A (ko) * 2003-07-02 2006-04-14 버텍스 파마슈티칼스 인코포레이티드 전압 개폐 이온 채널의 조절제로서 유용한 피리미딘
WO2005028467A1 (fr) * 2003-09-15 2005-03-31 Anadys Pharmaceuticals, Inc. Composes heteroaromatiques et aromatiques a substitution 3,5-diaminopiperidine antibacteriens
WO2005028438A1 (fr) * 2003-09-22 2005-03-31 Banyu Pharmaceutical Co., Ltd. Nouveau derive de piperidine
GB0401269D0 (en) 2004-01-21 2004-02-25 Astrazeneca Ab Compounds
CA2580838A1 (fr) * 2004-09-27 2006-04-06 Amgen Inc. Composes heterocycliques substitues et procedes d'utilisation
WO2006053109A1 (fr) 2004-11-10 2006-05-18 Synta Pharmaceuticals Corp. Composes heteroaryle
US20060142572A1 (en) 2004-12-14 2006-06-29 Gabriel Martinez-Botella Inhibitors of ERK protein kinase and uses thereof
CA2608248A1 (fr) * 2005-05-06 2006-11-16 Boehringer Ingelheim International Gmbh Inhibiteurs de l'epoxyde hydrolase soluble et leurs methodes d'utilisation
CA2622754A1 (fr) * 2005-10-07 2007-04-19 Boehringer Ingelheim International Gmbh Composes de pyridinone ou pyrimidinone n-substitues utiles en tant qu'inhibiteurs d'epoxyde hydrolase soluble
EP1987004A2 (fr) * 2006-02-16 2008-11-05 Boehringer Ingelheim International GmbH Pyridineamides substitués pouvant être employés en tant qu'inhibiteurs d'époxyde hydrolase soluble
AR059826A1 (es) 2006-03-13 2008-04-30 Univ California Inhibidores de urea conformacionalmente restringidos de epoxido hidrolasa soluble
WO2008105968A1 (fr) * 2006-11-03 2008-09-04 Smithkline Beecham Corporation Nouveaux inhibiteurs de seh et utilisation de ces derniers
SI2214487T1 (sl) 2007-10-11 2014-03-31 Glaxosmithkline Llc Novi sEH inhibitorji in njihova uporaba
WO2009049165A1 (fr) 2007-10-11 2009-04-16 Smithkline Beecham Corporation Inhibiteurs inédits de la seh et leur utilisation
WO2009049154A1 (fr) 2007-10-11 2009-04-16 Smithkline Beecham Corporation Nouveaux inhibiteurs de seh et leur utilisation
WO2009048154A1 (fr) 2007-10-12 2009-04-16 Nec Corporation Dispositif à semi-conducteurs et son procédé de conception
WO2009070497A1 (fr) 2007-11-28 2009-06-04 Smithkline Beecham Corporation Inhibiteurs de ehs et de 11β-hsd1 et leur utilisation
WO2009073772A1 (fr) 2007-12-06 2009-06-11 Smithkline Beecham Corporation Nouveaux inhibiteurs de seh et leur utilisation
JP2011510998A (ja) * 2008-01-30 2011-04-07 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー 新規ｓＥＨ阻害剤およびその使用
US20100311775A1 (en) * 2008-01-30 2010-12-09 Smithkline Beecham Corporation Novel sEH Inhibitors and Their Use
JP2011510996A (ja) * 2008-01-30 2011-04-07 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー 新規ｓＥＨ阻害剤およびその使用
WO2010011917A1 (fr) 2008-07-25 2010-01-28 Glaxosmithkline Llc Inhibiteurs doubles de seh et 11β-hsd1

Also Published As

Publication number Publication date
CR11423A (es) 2010-06-28
EP2214487A1 (fr) 2010-08-11
KR20100075619A (ko) 2010-07-02
MY157116A (en) 2016-05-13
PT2214487E (pt) 2014-02-20
CA2702265A1 (fr) 2009-04-16
US20100210656A1 (en) 2010-08-19
AU2008310732A1 (en) 2009-04-16
US8173805B2 (en) 2012-05-08
EP2214487A4 (fr) 2011-12-21
CO6270285A2 (es) 2011-04-20
CA2702265C (fr) 2014-12-02
ES2445444T3 (es) 2014-03-03
CY1114865T1 (el) 2016-12-14
EA018414B1 (ru) 2013-07-30
IL204889A (en) 2014-08-31
US20100249137A1 (en) 2010-09-30
KR101546111B1 (ko) 2015-08-20
JP5372943B2 (ja) 2013-12-18
IL204889A0 (en) 2010-11-30
US8212032B2 (en) 2012-07-03
EP2214487B1 (fr) 2013-11-27
JP2011500594A (ja) 2011-01-06
EA201070442A1 (ru) 2010-10-29
DOP2010000101A (es) 2010-07-31
HK1141211A1 (en) 2010-11-05
NZ584471A (en) 2012-01-12
HRP20140105T1 (hr) 2014-03-14
MX2010003942A (es) 2010-04-30
CN101896065B (zh) 2013-12-18
CN101896065A (zh) 2010-11-24
ZA201002465B (en) 2010-12-29
DK2214487T3 (da) 2014-02-10
BRPI0817542A2 (pt) 2014-10-07
UA107444C2 (uk) 2015-01-12
RS53180B (en) 2014-06-30
WO2009049157A1 (fr) 2009-04-16
AU2008310732B2 (en) 2012-03-08
PL2214487T3 (pl) 2014-04-30
SI2214487T1 (sl) 2014-03-31

Similar Documents

Publication Publication Date Title
MA31761B1 (fr) Nouveaux inhibiteurs de seh et leur utilisation
MA30932B1 (fr) Spirocetones servant d'inhibiteurs d'acetyl-coa -carboxylase
TNSN07022A1 (fr) Derives de pyridine
TN2009000428A1 (fr) Derives de sulfonylamides destines au traitement d'une croissance cellulaire anormale
MA31419B1 (fr) Derives de pyridine
TN2009000138A1 (fr) Biaryl-ether-urees
MA32684B1 (fr) Dérivés de picolinamide en tant qu'inhibiteurs de kinase
TNSN05073A1 (fr) Quinazolinones spirocondensees nouvelles et leur utilisation comme inhibiteurs de phosphodiesterase
MA29926B1 (fr) Derives de pyrazine
MA33178B1 (fr) Pipéridines substituées comme antagonistes de ccr3
TNSN07275A1 (fr) Derives de triazole substitues, servant d'antagonistes d'ocytocine
MA27560A1 (fr) Nouveaux derives de fluorglycoside heterocycliques, produits pharmaceutiques contenant ces composes et leur utilisation
MA31373B1 (fr) Composes amino-heterocycliques
MA33836B1 (fr) Compositions pharmaceutiques contenant des ligands des récepteurs sigma
MA26697A1 (fr) Composes nouveaux inhibiteurs de gsk-3 et compositions pharmaceutiques les contenant
MA27389A1 (fr) Derives de benzimidazole nouveaux utiles comme agents antiproliferatifs.
MA32231B1 (fr) Composés organiques
MA30232B1 (fr) Inhibiteurs de kinase bases sur l'hydantoine
MA31894B1 (fr) Composes organiques
MA30333B1 (fr) Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete.
TNSN07349A1 (fr) Derives de n-(n-sulfonylaminomethyl) cyclopropanecarboxamide utiles pour le traitement de la douleur
MA31766B1 (fr) Composés organiques
MA30652B1 (fr) Composes organiques
MA31873B1 (fr) Inhibiteurs de la peptide déformylase
MA32887B1 (fr) Aminotetrahydropyranes en tant qu'inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete