MA35643B1 - Inhibiteur de cetp d'oxazolidinone bicyclique condensée - Google Patents

Inhibiteur de cetp d'oxazolidinone bicyclique condensée

Info

Publication number
MA35643B1
MA35643B1 MA37024A MA37024A MA35643B1 MA 35643 B1 MA35643 B1 MA 35643B1 MA 37024 A MA37024 A MA 37024A MA 37024 A MA37024 A MA 37024A MA 35643 B1 MA35643 B1 MA 35643B1
Authority
MA
Morocco
Prior art keywords
inhibitor
condensed bicyclic
cetp
bicyclic oxazolidinone
oxazolidinone cetp
Prior art date
Application number
MA37024A
Other languages
English (en)
Inventor
Pengcheng Patrick Shao
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
Application filed by Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of MA35643B1 publication Critical patent/MA35643B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic 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
    • C07D498/04Ortho-condensed systems
    • 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
    • A61K31/42Oxazoles
    • A61K31/424Oxazoles condensed with heterocyclic ring systems, e.g. clavulanic acid
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Vascular Medicine (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La présente invention concerne des composés ayant la structure de formule i, comprenant des sels pharmaceutiquement acceptables des composés, qui sont des inhibiteurs de cetp et sont utiles pour élever le cholestérol-hdl, abaisser le cholestérol-ldl, et pour traiter ou prévenir l'athérosclérose.
MA37024A 2011-10-28 2014-05-13 Inhibiteur de cetp d'oxazolidinone bicyclique condensée MA35643B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161552592P 2011-10-28 2011-10-28
PCT/US2012/061842 WO2013063217A1 (fr) 2011-10-28 2012-10-25 Inhibiteur de cetp d'oxazolidinone bicyclique condensée

Publications (1)

Publication Number Publication Date
MA35643B1 true MA35643B1 (fr) 2014-11-01

Family

ID=47143312

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37024A MA35643B1 (fr) 2011-10-28 2014-05-13 Inhibiteur de cetp d'oxazolidinone bicyclique condensée

Country Status (41)

Country Link
US (2) US8871738B2 (fr)
EP (1) EP2771345B1 (fr)
JP (1) JP5658427B2 (fr)
KR (1) KR101686308B1 (fr)
CN (1) CN103958524B (fr)
AR (1) AR088565A1 (fr)
AU (1) AU2012328759B2 (fr)
BR (1) BR112014010204A2 (fr)
CA (1) CA2852743C (fr)
CL (1) CL2014001090A1 (fr)
CO (1) CO6940419A2 (fr)
CR (1) CR20140256A (fr)
CY (1) CY1118464T1 (fr)
DK (1) DK2771345T3 (fr)
DO (1) DOP2014000086A (fr)
EA (1) EA026123B1 (fr)
EC (1) ECSP14002458A (fr)
ES (1) ES2604953T3 (fr)
GE (1) GEP20166434B (fr)
HR (1) HRP20161541T1 (fr)
HU (1) HUE030568T2 (fr)
IL (1) IL232130A (fr)
IN (1) IN2014CN03073A (fr)
JO (1) JO3210B1 (fr)
LT (1) LT2771345T (fr)
MA (1) MA35643B1 (fr)
ME (1) ME02557B (fr)
MX (1) MX345222B (fr)
NI (1) NI201400034A (fr)
PE (1) PE20141230A1 (fr)
PH (1) PH12014500890A1 (fr)
PL (1) PL2771345T3 (fr)
PT (1) PT2771345T (fr)
RS (1) RS55420B1 (fr)
SG (1) SG11201401884PA (fr)
SI (1) SI2771345T1 (fr)
TN (1) TN2014000158A1 (fr)
TW (1) TWI601731B (fr)
UA (1) UA114612C2 (fr)
WO (1) WO2013063217A1 (fr)
ZA (2) ZA201403091B (fr)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201007286D0 (en) 2010-04-30 2010-06-16 Astex Therapeutics Ltd New compounds
JP5852662B2 (ja) 2010-10-29 2016-02-03 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. 環状アミン置換されたオキサゾリジノン系cetp阻害薬
GB201020179D0 (en) 2010-11-29 2011-01-12 Astex Therapeutics Ltd New compounds
GB201118652D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
GB201118675D0 (en) 2011-10-28 2011-12-14 Astex Therapeutics Ltd New compounds
GB201118654D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
GB201118656D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
GB201209613D0 (en) 2012-05-30 2012-07-11 Astex Therapeutics Ltd New compounds
GB201209609D0 (en) 2012-05-30 2012-07-11 Astex Therapeutics Ltd New compounds
EP2934518B1 (fr) 2012-12-19 2020-02-19 Merck Sharp & Dohme Corp. Inhibiteurs de la cetp spirocycliques
US9376408B2 (en) 2012-12-20 2016-06-28 Merck Sharp & Dohme Corp. Therapeutic thiazolidinone compounds
CN105143193B (zh) * 2013-01-31 2017-12-15 株式会社钟根堂 作为cetp抑制剂的联芳基或杂环联芳基取代的环己烯衍生化合物
GB201307577D0 (en) 2013-04-26 2013-06-12 Astex Therapeutics Ltd New compounds
US9981970B2 (en) 2013-07-30 2018-05-29 Merck Sharp & Dohme Corp. Bicyclic ureas and thiadiazolidine-1, 1-dioxides as CETP inhibitors
US9937153B2 (en) * 2013-08-30 2018-04-10 Merck Sharp & Dohme Ltd. Oral pharmaceutical formulation of omarigliptin
EP3054945B1 (fr) 2013-10-10 2018-08-15 Merck Sharp & Dohme Corp. Indolines 3,3'-disubstituées utilisées comme inhibiteurs de la protéine de transfert du cholestérol estérifié
CN105814064A (zh) * 2013-12-17 2016-07-27 默沙东公司 作为胆固醇酯转运蛋白的抑制剂的稠合双环异噁唑啉类
LT3102212T (lt) 2014-02-05 2019-02-25 Dezima Pharma B.V. Cholesterilo esterio pernešimo baltymo (cetp) inhibitorius ir farmacinės kompozicijos, apimančios minėtą inhibitorių, skirtos panaudoti širdies ir kraujagyslių ligų gydymui arba prevencijai
JO3512B1 (ar) 2014-03-26 2020-07-05 Astex Therapeutics Ltd مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز
KR102479696B1 (ko) 2014-03-26 2022-12-22 아스텍스 테라퓨틱스 리미티드 Fgfr 억제제 및 igf1r 억제제의 조합물
HUE053654T2 (hu) 2014-03-26 2021-07-28 Astex Therapeutics Ltd FGFR- és CMET-inhibitorok kombinációi a rák kezelésére
EP3174537B1 (fr) 2014-07-29 2021-06-23 Merck Sharp & Dohme Corp. Isoxazolines monocycliques utilisées comme inhibiteurs de la protéine de transfert des esters de cholestérol
WO2016067194A1 (fr) * 2014-10-27 2016-05-06 Sun Pharmaceutical Industries Limited Procédé de préparation d'anacetrapib et d'un intermédiaire de celui-ci
US20170252338A1 (en) * 2014-11-28 2017-09-07 Kowa Company, Ltd. Medicine
JOP20200201A1 (ar) 2015-02-10 2017-06-16 Astex Therapeutics Ltd تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين
US10478494B2 (en) 2015-04-03 2019-11-19 Astex Therapeutics Ltd FGFR/PD-1 combination therapy for the treatment of cancer
CN109996757A (zh) * 2015-06-12 2019-07-09 罗地亚经营管理公司 含枝状体的混合纳米粒子、生产此类混合纳米粒子的方法以及它们的用途
US20180230166A1 (en) * 2015-07-13 2018-08-16 Merck Sharp & Dohme Corp. Bicyclic heterocycles as inhibitors of cholesterol ester transfer protein
CA2996857C (fr) 2015-09-23 2024-05-21 Janssen Pharmaceutica Nv Composes derives de la quinoxaline, de la quinoleine et de la quinazolin one pour le traitement du cancer
EP3353164B1 (fr) 2015-09-23 2021-11-03 Janssen Pharmaceutica, N.V. 1,4-benzodiazepines bi-heteroaryl substituees et leurs utilisations pour le traitement du cancer
CN106432053A (zh) * 2016-09-17 2017-02-22 青岛云天生物技术有限公司 一种尼拉帕布中间体4‑(3s‑哌啶‑3‑基)溴苯的制备方法
CN106432058A (zh) * 2016-09-17 2017-02-22 青岛云天生物技术有限公司 一种Niraparib中间体4‑(3S‑哌啶‑3‑基)苯胺的制备方法
CN111285894B (zh) * 2018-12-10 2021-03-05 北京天一绿甫医药科技有限公司 用于制备软海绵素类化合物的中间体及其制备方法
CN110639018B (zh) * 2019-11-14 2020-06-26 牡丹江医学院 一种防治老年性高血压的药物组合物及其用途

Family Cites Families (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4845079A (en) 1985-01-23 1989-07-04 Luly Jay R Peptidylaminodiols
US5066643A (en) 1985-02-19 1991-11-19 Sandoz Ltd. Fluorine and chlorine statine or statone containing peptides and method of use
US4894437A (en) 1985-11-15 1990-01-16 The Upjohn Company Novel renin inhibiting polypeptide analogs containing S-aryl-D- or L- or DL-cysteinyl, 3-(arylthio)lactic acid or 3-(arylthio)alkyl moieties
US4885292A (en) 1986-02-03 1989-12-05 E. R. Squibb & Sons, Inc. N-heterocyclic alcohol renin inhibitors
US4980283A (en) 1987-10-01 1990-12-25 Merck & Co., Inc. Renin-inhibitory pepstatin phenyl derivatives
US5089471A (en) 1987-10-01 1992-02-18 G. D. Searle & Co. Peptidyl beta-aminoacyl aminodiol carbamates as anti-hypertensive agents
US5034512A (en) 1987-10-22 1991-07-23 Warner-Lambert Company Branched backbone renin inhibitors
US5063207A (en) 1987-10-26 1991-11-05 Warner-Lambert Company Renin inhibitors, method for using them, and compositions containing them
US5055466A (en) 1987-11-23 1991-10-08 E. R. Squibb & Sons, Inc. N-morpholino derivatives and their use as anti-hypertensive agents
US5036054A (en) 1988-02-11 1991-07-30 Warner-Lambert Company Renin inhibitors containing alpha-heteroatom amino acids
US5036053A (en) 1988-05-27 1991-07-30 Warner-Lambert Company Diol-containing renin inhibitors
DE3841520A1 (de) 1988-12-09 1990-06-13 Hoechst Ag Enzymhemmende harnstoffderivate von dipeptiden, verfahren zu ihrer herstellung, diese enthaltende mittel und ihre verwendung
US5106835A (en) 1988-12-27 1992-04-21 American Cyanamid Company Renin inhibitors
US5063208A (en) 1989-07-26 1991-11-05 Abbott Laboratories Peptidyl aminodiol renin inhibitors
US5098924A (en) 1989-09-15 1992-03-24 E. R. Squibb & Sons, Inc. Diol sulfonamide and sulfinyl renin inhibitors
US5104869A (en) 1989-10-11 1992-04-14 American Cyanamid Company Renin inhibitors
US5114937A (en) 1989-11-28 1992-05-19 Warner-Lambert Company Renin inhibiting nonpeptides
US5064965A (en) 1990-03-08 1991-11-12 American Home Products Corporation Renin inhibitors
US5095119A (en) 1990-03-08 1992-03-10 American Home Products Corporation Renin inhibitors
US5075451A (en) 1990-03-08 1991-12-24 American Home Products Corporation Pyrrolimidazolones useful as renin inhibitors
US5071837A (en) 1990-11-28 1991-12-10 Warner-Lambert Company Novel renin inhibiting peptides
WO1997028149A1 (fr) 1996-02-02 1997-08-07 Merck & Co., Inc. Procede pour augmenter les niveaux de cholesterol hdl
CA2415742A1 (fr) 2000-07-25 2002-01-31 Merck & Co., Inc. Indoles n-substitues utiles pour le traitement du diabete
EP1357908A4 (fr) 2001-01-30 2009-07-15 Merck & Co Inc Acyl-sulfamides pour le traitement de l'obesite, du diabete et des troubles lipidiques
WO2003011824A1 (fr) 2001-07-31 2003-02-13 Bristol-Myers Squibb Company Modulateurs bicycliques de la fonction du recepteur androgene
US7393960B2 (en) 2002-08-29 2008-07-01 Merck & Co., Inc. Indoles having anti-diabetic activity
RU2328483C2 (ru) 2002-08-29 2008-07-10 Мерк Энд Ко., Инк. Индолы, обладающие противодиабетической активностью
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
WO2004112699A2 (fr) 2003-06-12 2004-12-29 Merck & Co., Inc. Inhibiteurs de kinesine mitotique
JP2007502279A (ja) 2003-08-13 2007-02-08 メルク エンド カムパニー インコーポレーテッド 有糸分裂キネシン阻害剤
ATE433984T1 (de) 2004-03-26 2009-07-15 Lilly Co Eli Verbindungen und verfahren zur behandlung von dyslipidämie
CN1938320A (zh) * 2004-03-26 2007-03-28 伊莱利利公司 用于治疗异常脂肪血症的化合物和方法
AU2005233160B2 (en) * 2004-04-13 2011-06-02 Merck Sharp & Dohme Corp. CETP inhibitors
DOP2005000123A (es) 2004-07-02 2011-07-15 Merck Sharp & Dohme Inhibidores de cetp
AR058400A1 (es) 2005-12-22 2008-01-30 Schering Corp Derivados de oxazoloisoquinolina como antagonistas del receptor de trombina
AU2006332681B2 (en) 2005-12-30 2011-04-07 Merck Sharp & Dohme Corp. 1, 3-oxazolidin-2-one derivatives useful as CETP inhibitors
AU2006335110B2 (en) * 2005-12-30 2011-04-14 Merck Sharp & Dohme Corp. CETP inhibitors
AU2006335108B2 (en) 2005-12-30 2011-04-07 Merck Sharp & Dohme Corp. CETP inhibitors
EP2348859B1 (fr) 2008-10-01 2013-12-04 Merck Sharp & Dohme Corp. Promédicaments d'inhibiteurs de cetp à base d'oxazolidinone
WO2011028395A1 (fr) 2009-08-24 2011-03-10 Merck Sharp & Dohme Corp. Inhibiteur de cetp à base de pyridyl oxazolidinone
JP5852662B2 (ja) 2010-10-29 2016-02-03 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. 環状アミン置換されたオキサゾリジノン系cetp阻害薬
US9353101B2 (en) 2012-05-02 2016-05-31 Merck Sharp & Dohme Corp. Cyclic amine substituted heterocyclic CETP inhibitors

Also Published As

Publication number Publication date
EP2771345A1 (fr) 2014-09-03
CA2852743C (fr) 2016-08-02
ECSP14002458A (es) 2015-11-30
IN2014CN03073A (fr) 2015-07-31
ME02557B (fr) 2017-02-20
KR101686308B1 (ko) 2016-12-13
CR20140256A (es) 2014-07-15
CA2852743A1 (fr) 2013-05-02
BR112014010204A2 (pt) 2017-05-09
MX2014005074A (es) 2014-08-01
AR088565A1 (es) 2014-06-18
CO6940419A2 (es) 2014-05-09
EA026123B1 (ru) 2017-03-31
HK1195558A1 (zh) 2014-11-14
WO2013063217A1 (fr) 2013-05-02
PT2771345T (pt) 2016-11-30
NI201400034A (es) 2014-10-10
ZA201403091B (en) 2015-04-29
PE20141230A1 (es) 2014-09-28
MX345222B (es) 2017-01-20
US9346825B2 (en) 2016-05-24
TW201321388A (zh) 2013-06-01
US20140378493A1 (en) 2014-12-25
US20130109649A1 (en) 2013-05-02
CN103958524A (zh) 2014-07-30
UA114612C2 (uk) 2017-07-10
EP2771345B1 (fr) 2016-09-21
NZ625435A (en) 2015-12-24
PH12014500890A1 (en) 2014-06-09
JO3210B1 (ar) 2018-03-08
DOP2014000086A (es) 2014-07-15
RS55420B1 (sr) 2017-04-28
EA201490889A1 (ru) 2015-05-29
CL2014001090A1 (es) 2014-08-01
TN2014000158A1 (en) 2015-09-30
GEP20166434B (en) 2016-02-10
SG11201401884PA (en) 2014-09-26
JP5658427B2 (ja) 2015-01-28
HRP20161541T1 (hr) 2016-12-30
DK2771345T3 (en) 2017-01-09
SI2771345T1 (sl) 2016-12-30
IL232130A (en) 2017-07-31
CY1118464T1 (el) 2017-07-12
IL232130A0 (en) 2014-05-28
CN103958524B (zh) 2016-04-06
HUE030568T2 (en) 2017-05-29
TWI601731B (zh) 2017-10-11
ES2604953T3 (es) 2017-03-10
ZA201406833B (en) 2016-02-24
JP2014532652A (ja) 2014-12-08
LT2771345T (lt) 2016-11-25
KR20140094571A (ko) 2014-07-30
US8871738B2 (en) 2014-10-28
AU2012328759B2 (en) 2015-09-10
AU2012328759A1 (en) 2014-05-01
PL2771345T3 (pl) 2017-04-28

Similar Documents

Publication Publication Date Title
MA35643B1 (fr) Inhibiteur de cetp d'oxazolidinone bicyclique condensée
PH12018500041A1 (en) Substituted aza compoounds as irak-4 inhibitors
EP2595482A4 (fr) Inhibiteurs de l'aldostérone synthase
EA200900152A1 (ru) Ингибиторы пирролотриазинкиназы
MA37712B1 (fr) Inhibiteurs macrocycliques de virus flaviviridae
TW200639166A (en) Amino-pyridines as inhibitors of β-secretase
MA33492B1 (fr) Inhibiteurs de bace
MA38050B1 (fr) Inhibiteurs de gdf-8
EA201500362A1 (ru) Ингибиторы rho-киназы
EA201200373A1 (ru) Соединения и композиции в качестве ингибиторов протеинкиназ
MX2009010057A (es) Compuesto de amino-5-[4-(difluorometoxi)fenil]-5-fenilimidazolona para la inhibicion de beta-secretasa.
MX2009009699A (es) Compuestos amino-5-[4-(difluorometoxi)fenil sustituidos]-5-fenilim idazolona como inhibidores de beta-secretasa.
TN2015000347A1 (fr) Azabenzimidazoles servant d'inhibiteurs d'isoenzymes pde4 pour le traitement de troubles du snc et d'autres troubles
UA108087C2 (uk) Тверді форми n-(4-(7-азабіцикло[2.2.1]гептан-7-іл)-2-(трифторметил)феніл)-4-оксо-5-(трифторметил)-1,4-дигідрохінолін-3-карбоксаміду
MA33304B1 (fr) Indazoles substitués par oxazole comme inhibiteurs de pi3-kinase
MX2013005826A (es) Benzoxazepinas como inhibidores de fosfatidilinositol 3-cinasa/objetivo de rapamicina en mamiferos (p13k/mtor) y metodos de uso y fabricacion.
EA201691759A1 (ru) Композиции и способы лечения легочной гипертензии
EA201290677A1 (ru) Соединения обратного амида в качестве ингибиторов протеиндеацетилазы и способы их применения
MX2015005015A (es) Inhibidores heteroarilo de pde4.
ECSP099755A (es) Derivados de pirrolopiridina y su uso como inhibidores de bace
EA201100580A1 (ru) Имидазопиридазинкарбонитрилы, используемые в качестве ингибиторов киназы
MX2012002752A (es) Compuestos de heteroarilo como inhibidores de cinasa.
MX2013012776A (es) Inhibidores de la tirosina cinasa de bazo que contienen aminopiridina.
EA201100391A1 (ru) Соединения, ингибирующие активность семикарбазид-чувствительной аминооксидазы
MX2012015098A (es) Compuestos heterociclicos fusionados como inhibidores de fosfodiesterasas (pdes).