MA33342B1 - Inhibiteurs du canal potassique médullaire externe rénal - Google Patents

Inhibiteurs du canal potassique médullaire externe rénal

Info

Publication number
MA33342B1
MA33342B1 MA34422A MA34422A MA33342B1 MA 33342 B1 MA33342 B1 MA 33342B1 MA 34422 A MA34422 A MA 34422A MA 34422 A MA34422 A MA 34422A MA 33342 B1 MA33342 B1 MA 33342B1
Authority
MA
Morocco
Prior art keywords
renal
inhibitors
potassium channel
spinal canal
external potassium
Prior art date
Application number
MA34422A
Other languages
Arabic (ar)
English (en)
Inventor
Alexander Pasternak
Aurash Shahripour
Haifeng Tang
Nardos H Teumelsan
Lihu Yang
Yuping Zhu
Shawn P Walsh
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 MA33342B1 publication Critical patent/MA33342B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/87Benzo [c] furans; Hydrogenated benzo [c] furans
    • C07D307/88Benzo [c] furans; Hydrogenated benzo [c] furans with one oxygen atom directly attached in position 1 or 3
    • 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/16Otologicals
    • 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
    • A61P3/08Drugs 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
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/12Drugs for disorders of the metabolism for electrolyte homeostasis
    • 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
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10Antioedematous agents; Diuretics
    • 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
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • C07D295/135Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/155Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • 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
    • C07D405/08Heterocyclic 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 linked by a carbon chain containing alicyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/08Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/08Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing alicyclic rings
    • 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
    • C07D487/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Biomedical Technology (AREA)
  • Hospice & Palliative Care (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Psychiatry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Epidemiology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Furan Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pyrane Compounds (AREA)
  • Peptides Or Proteins (AREA)

Abstract

La présente invention a pour objet des composés ayant la formule structurelle I : et leurs sels pharmaceutiquement acceptables qui sont des inhibiteurs du canal potassique médullaire externe rénal (ROMK) (Kir1.1). Les composés de Formule I sont utiles en tant que diurétiques et natriurétiques et sont par conséquent utiles pour la thérapie et la prophylaxie des troubles résultant d'une rétention excessive de sel et d'eau, comprenant les maladies cardiovasculaires telles que l'hypertension et l'insuffisance cardiaque chronique et aiguë.
MA34422A 2009-05-06 2010-04-29 Inhibiteurs du canal potassique médullaire externe rénal MA33342B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US17584709P 2009-05-06 2009-05-06
PCT/US2010/032872 WO2010129379A1 (fr) 2009-05-06 2010-04-29 Inhibiteurs du canal potassique médullaire externe rénal

Publications (1)

Publication Number Publication Date
MA33342B1 true MA33342B1 (fr) 2012-06-01

Family

ID=42244955

Family Applications (1)

Application Number Title Priority Date Filing Date
MA34422A MA33342B1 (fr) 2009-05-06 2010-04-29 Inhibiteurs du canal potassique médullaire externe rénal

Country Status (31)

Country Link
US (2) US8673920B2 (fr)
EP (1) EP2427444B1 (fr)
JP (2) JP5092068B2 (fr)
KR (1) KR101373902B1 (fr)
CN (1) CN102459216B (fr)
AR (1) AR076836A1 (fr)
AU (1) AU2010246269C1 (fr)
BR (1) BRPI1014050A2 (fr)
CA (1) CA2759399C (fr)
CL (1) CL2011002761A1 (fr)
CO (1) CO6460758A2 (fr)
CR (1) CR20110578A (fr)
EA (1) EA021008B1 (fr)
EC (1) ECSP11011444A (fr)
ES (1) ES2561654T3 (fr)
GE (1) GEP20146055B (fr)
GT (1) GT201100278A (fr)
HN (1) HN2011002933A (fr)
IL (1) IL215836A0 (fr)
MA (1) MA33342B1 (fr)
MX (1) MX337570B (fr)
MY (1) MY157525A (fr)
NI (1) NI201100193A (fr)
NZ (1) NZ596229A (fr)
PE (1) PE20120346A1 (fr)
SG (1) SG175841A1 (fr)
TN (1) TN2011000540A1 (fr)
TW (1) TWI408135B (fr)
UA (1) UA106611C2 (fr)
WO (1) WO2010129379A1 (fr)
ZA (1) ZA201108070B (fr)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9073882B2 (en) 2010-10-27 2015-07-07 Merck Sharp & Dohme Corp. Inhibitors of the renal outer medullary potassium channel
US9056859B2 (en) 2010-10-29 2015-06-16 Merck Sharp & Dohme Corp. Inhibitors of the renal outer medullary potassium channel
JP2014513116A (ja) 2011-05-02 2014-05-29 ゾエティス・エルエルシー 抗菌剤として有用な新規セファロスポリン
BR112014003801A2 (pt) 2011-08-19 2017-03-07 Merck Sharp & Dohme composto, composição farmacêutica, e, métodos para a inibição de romk, para a provocação de diurese, natriurese ou ambas, e para o tratamento ou a profilaxia de um ou mais distúrbios
WO2013039802A1 (fr) * 2011-09-16 2013-03-21 Merck Sharp & Dohme Corp. Inhibiteurs du canal à potassium de la medulla externe du rein
WO2013062900A1 (fr) * 2011-10-25 2013-05-02 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
WO2013062892A1 (fr) * 2011-10-25 2013-05-02 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire extérieur rénal
US9493474B2 (en) 2011-10-31 2016-11-15 Merck Sharp & Dohme Corp. Inhibitors of the renal outer medullary potassium channel
EP2773199B1 (fr) * 2011-10-31 2019-04-10 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
US9108947B2 (en) 2011-10-31 2015-08-18 Merck Sharp & Dohme Corp. Inhibitors of the Renal Outer Medullary Potassium channel
EP2790511B1 (fr) * 2011-12-16 2016-09-14 Merck Sharp & Dohme Corp. Inhibiteurs du canal à potassium de la medulla externe du rein
WO2013102935A2 (fr) * 2012-01-03 2013-07-11 Council Of Scientific & Industrial Research Annélation médiée par le cuivre pour la synthèse efficace de phtalides substitués en position 3
AR092031A1 (es) * 2012-07-26 2015-03-18 Merck Sharp & Dohme Inhibidores del canal de potasio medular externo renal
WO2014015495A1 (fr) * 2012-07-26 2014-01-30 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
WO2014085210A1 (fr) 2012-11-29 2014-06-05 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire extérieur rénal
US9573961B2 (en) 2012-12-19 2017-02-21 Merck Sharp & Dohme Corp. Inhibitors of the renal outer medullary potassium channel
WO2014126944A2 (fr) * 2013-02-18 2014-08-21 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire extérieur rénal
EP2968288B1 (fr) 2013-03-15 2018-07-04 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire extérieur rénal
US9751881B2 (en) 2013-07-31 2017-09-05 Merck Sharp & Dohme Corp. Inhibitors of the renal outer medullary potassium channel
EP3063142B1 (fr) * 2013-10-31 2019-01-30 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
US10000484B2 (en) 2013-12-18 2018-06-19 Merck Sharp & Dohme Corp. Inhibitors of the renal outer medullary potassim channel
WO2015096035A1 (fr) 2013-12-24 2015-07-02 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
WO2015103756A1 (fr) 2014-01-09 2015-07-16 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
KR20160001316A (ko) 2014-06-27 2016-01-06 조선대학교산학협력단 3d 조영기술을 이용한 환자 맞춤형 임플란트 모형제작방법
WO2016008064A1 (fr) 2014-07-14 2016-01-21 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
WO2016091042A1 (fr) * 2014-12-08 2016-06-16 江苏恒瑞医药股份有限公司 Dérivés du pyridinecarboxamide, méthode de préparation de ces derniers, et utilisations pharmaceutiques de ce derniers
CN105693706B (zh) * 2014-12-10 2019-11-22 江苏恒瑞医药股份有限公司 异苯并呋喃酮类衍生物、其制备方法及其在医药上的应用
EP3250204B1 (fr) 2015-01-29 2019-10-30 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
WO2016127358A1 (fr) 2015-02-12 2016-08-18 Merck Sharp & Dohme Corp. Inhibiteurs du canal potassique médullaire externe rénal
EA037300B1 (ru) * 2016-04-20 2021-03-05 Бристол-Маерс Сквибб Компани Замещенные бициклические гетероциклические соединения
JP2019517494A (ja) * 2016-06-07 2019-06-24 江蘇恒瑞医薬股▲ふん▼有限公司 腎髄質外層カリウムチャネル阻害剤としての医薬的に許容される塩
MX2019000980A (es) 2016-07-29 2019-07-04 Sunovion Pharmaceuticals Inc Compuestos y composiciones y usos de los mismos.
CN106432214B (zh) * 2016-08-09 2019-05-07 成都拿盛科技有限公司 一种制备romk通道抑制剂中间体的方法
BR112019008824A2 (pt) * 2016-11-03 2019-07-09 Bristol-Myers Squibb Company derivados heterocíclicos bicíclicos substituídos úteis como inibidores de canal de romk
TWI791527B (zh) 2017-06-01 2023-02-11 美商必治妥美雅史谷比公司 經取代之含氮化合物
WO2019016115A1 (fr) * 2017-07-21 2019-01-24 BASF Agro B.V. Procédé de préparation de cétones d'aryle substituées
CN109879863B (zh) * 2017-12-06 2020-10-20 江苏恒瑞医药股份有限公司 一种肾外髓质分泌钾通道抑制剂的晶型及其制备方法
AU2018380171A1 (en) * 2017-12-06 2020-07-09 Jiangsu Hengrui Medicine Co., Ltd. Crystal form of renal outer medullary potassium channel inhibitor and preparation method thereof

Family Cites Families (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2988551A (en) 1954-07-30 1961-06-13 Union Chimique Belge Sa Piperazine derivatives
GB949088A (en) 1961-06-26 1964-02-12 Lepetit Spa Diazabicyclo-octane derivatives
US3435002A (en) 1967-05-15 1969-03-25 Gen Electric Polyamide acid resins and polyimides therefrom
GB1575310A (en) 1976-11-16 1980-09-17 Anphar Sa Piperidine derivatives
FR2522325B1 (fr) 1982-02-26 1985-08-09 Delalande Sa Nouveaux derives aryliques de la piperazine, de l'homopiperazine et de n,n'-dialkyl diamino-1,2 ethane, leur procede de preparation et leur application en therapeutique
NL8202636A (nl) 1982-06-29 1984-01-16 Gist Brocades Nv Piperazinederivaten, werkwijzen ter bereiding daarvan en farmaceutische preparaten die deze verbindingen bevatten.
DE3471486D1 (de) 1983-08-15 1988-06-30 Ciba Geigy Ag Photocurable compositions
US5145885A (en) 1983-08-15 1992-09-08 Ciba-Geigy Corporation Photopolymerizable compositions containing aminoaryl ketone photoinitiators
US4579863A (en) 1983-12-06 1986-04-01 Warner-Lambert Company Substituted trans-1,2-diaminocyclohexyl amide compounds
JPS6176476A (ja) * 1984-09-21 1986-04-18 Chugai Pharmaceut Co Ltd キサントン誘導体
US4661607A (en) 1984-09-21 1987-04-28 Chugai Seiyaku Kabushiki Kaisha Furoxanthone derivatives useful as diuretics
GB8603120D0 (en) 1986-02-07 1986-03-12 Pfizer Ltd Anti-dysrhythmia agents
JPH0745471B2 (ja) * 1986-12-04 1995-05-17 参天製薬株式会社 ピペラジン誘導体
US5215989A (en) 1989-12-08 1993-06-01 Merck & Co., Inc. Nitrogen-containing heterocyclic compounds as class III antiarrhythmic agents
US5032604A (en) * 1989-12-08 1991-07-16 Merck & Co., Inc. Class III antiarrhythmic agents
FR2673182A1 (fr) 1991-02-22 1992-08-28 Univ Caen Piperazines n,n'-disubstituees, leur procede de preparation et leur application en therapeutique.
KR100299734B1 (ko) 1993-07-28 2002-01-09 모리타 다카카즈 1,4-(디페닐알킬)피페라진유도체
KR960007560A (ko) * 1994-08-16 1996-03-22 김정규 신규한 아민 유도체, 그의 제조방법 및 항부정맥제로서의 용도
US5614526A (en) 1995-06-09 1997-03-25 Hoffmann-La Roche Inc. Use of phenoxy-piperzine derivatives
CA2256492C (fr) 1996-05-20 2006-04-04 Teijin Limited Derives de diamine cyclique de diarylaklyle utilises en tant qu'antagonistes des recepteurs de chimiokines
DE19637237A1 (de) 1996-09-13 1998-03-19 Merck Patent Gmbh Piperazin-Derivate
JPH10203986A (ja) 1997-01-22 1998-08-04 Mitsubishi Chem Corp 眼疾患用薬剤
JP2002540072A (ja) 1999-03-03 2002-11-26 メルク エンド カムパニー インコーポレーテッド プレニル蛋白トランスフェラーゼの阻害剤
EP1094063A1 (fr) 1999-10-18 2001-04-25 Applied Research Systems ARS Holding N.V. 9-(Pipérazinylalkyl)carbazoles comme modulateurs de Bax
DK1309591T3 (da) 2000-08-14 2007-03-26 Ortho Mcneil Pharm Inc Substituerede pyrazoler
US6693099B2 (en) 2000-10-17 2004-02-17 The Procter & Gamble Company Substituted piperazine compounds optionally containing a quinolyl moiety for treating multidrug resistance
SE0003795D0 (sv) * 2000-10-20 2000-10-20 Astrazeneca Ab Pharmaceutically useful compounds
GB0031088D0 (en) 2000-12-20 2001-01-31 Smithkline Beecham Plc Medicaments
CN1172919C (zh) * 2002-06-03 2004-10-27 上海医药工业研究院 芳烷醇哌嗪衍生物及其在制备抗抑郁症药物中的应用
GB0220214D0 (en) 2002-08-30 2002-10-09 Novo Pharmaceuticals De Ltd Compounds and their use
US20040204404A1 (en) 2002-09-30 2004-10-14 Robert Zelle Human N-type calcium channel blockers
AU2003275632A1 (en) 2002-10-25 2004-05-13 Mitsubishi Pharma Corporation N-oxide compounds
JPWO2004046110A1 (ja) 2002-11-15 2006-03-16 アステラス製薬株式会社 メラニン凝集ホルモン受容体拮抗剤
ATE430139T1 (de) 2003-04-03 2009-05-15 Merck Patent Gmbh Pyrrolidin-1,2-dicarbonsäure-1-(phenylamid)-2-( - (3-oxo-morpholin-4-yl)-phenylamid) derivate und verwandte verbindungen als inhibitoren des koagulationsfaktors xa zur behandlung von thromboembolischen erkrankungen
PL377864A1 (pl) 2003-04-03 2006-02-20 Merck Patent Gmbh Pochodne 1-N-(fenylo)-2-N-(fenylo)pirazolidyno-1,2-dikarboksyamidowe jako inhibitory czynnika koagulacyjnego Xa do leczenia zakrzepic
DE10329457A1 (de) 2003-04-03 2005-01-20 Merck Patent Gmbh Ethinylprolinderivate
JP5015593B2 (ja) 2003-06-18 2012-08-29 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング 血栓症の治療のための凝固因子XaおよびVIIaの阻害剤としての1−[(4−エチニルフェニル)]−2−[(フェニル)]−ピロリジン−1,2−ジカルボキサミド誘導体
AU2004266233A1 (en) 2003-08-13 2005-03-03 Amgen, Inc. Melanin concentrating hormone receptor antagonist
CN1897950A (zh) 2003-10-14 2007-01-17 惠氏公司 稠合芳基和杂芳基衍生物及其使用方法
GB0325956D0 (en) 2003-11-06 2003-12-10 Addex Pharmaceuticals Sa Novel compounds
EP1814551A2 (fr) 2004-09-20 2007-08-08 Xenon Pharmaceuticals Inc. Derives de pyridazine destines a l'inhibition du desaturase-coa-stearoyl de l'humain
DE102004045796A1 (de) 2004-09-22 2006-03-23 Merck Patent Gmbh Arzneimittel enthaltend Carbonylverbindungen sowie deren Verwendung
DE102004047254A1 (de) 2004-09-29 2006-04-13 Merck Patent Gmbh Carbonylverbindungen
WO2006098342A1 (fr) 2005-03-16 2006-09-21 Astellas Pharma Inc. Composes de la piperazinyle
GB0510139D0 (en) 2005-05-18 2005-06-22 Addex Pharmaceuticals Sa Novel compounds B1
US7754724B2 (en) 2005-06-30 2010-07-13 Dow Agrosciences Llc N-substituted piperazines
JP5114202B2 (ja) 2005-09-27 2013-01-09 塩野義製薬株式会社 Pgd2受容体アンタゴニスト活性を有するスルホンアミド誘導体
US7638531B2 (en) 2005-12-21 2009-12-29 Schering Corporation Phenoxypiperidines and analogs thereof useful as histamine H3 antagonists
WO2008147864A2 (fr) 2007-05-22 2008-12-04 Xenon Pharmaceuticals Inc. Procédés d'utilisaton de composés pipérazine dans le traitement de maladies ou états médiés par le canal sodium
WO2009149508A1 (fr) 2008-06-13 2009-12-17 Bionomics Limited Nouveaux bloqueurs du canal potassique et leurs utilisations

Also Published As

Publication number Publication date
MX2011011741A (es) 2011-11-29
US9018211B2 (en) 2015-04-28
PE20120346A1 (es) 2012-05-06
CO6460758A2 (es) 2012-06-15
TWI408135B (zh) 2013-09-11
CA2759399C (fr) 2013-11-26
AU2010246269B2 (en) 2013-09-26
AU2010246269A1 (en) 2011-11-24
CA2759399A1 (fr) 2010-11-11
TW201043615A (en) 2010-12-16
ES2561654T3 (es) 2016-02-29
MX337570B (es) 2016-03-10
KR101373902B1 (ko) 2014-03-18
US20100286123A1 (en) 2010-11-11
ECSP11011444A (es) 2011-12-30
AU2010246269C1 (en) 2014-02-20
IL215836A0 (en) 2012-01-31
TN2011000540A1 (en) 2013-05-24
EP2427444B1 (fr) 2015-12-16
AR076836A1 (es) 2011-07-13
GEP20146055B (en) 2014-03-10
JP5092068B2 (ja) 2012-12-05
NI201100193A (es) 2012-01-11
CN102459216A (zh) 2012-05-16
BRPI1014050A2 (pt) 2020-07-28
SG175841A1 (en) 2011-12-29
GT201100278A (es) 2015-05-20
ZA201108070B (en) 2015-06-24
UA106611C2 (uk) 2014-09-25
NZ596229A (en) 2013-12-20
EA021008B1 (ru) 2015-03-31
US20140142115A1 (en) 2014-05-22
JP2013014607A (ja) 2013-01-24
JP2012526118A (ja) 2012-10-25
CL2011002761A1 (es) 2012-04-09
CN102459216B (zh) 2015-01-28
KR20120011069A (ko) 2012-02-06
EA201171361A1 (ru) 2012-05-30
MY157525A (en) 2016-06-15
US8673920B2 (en) 2014-03-18
CR20110578A (es) 2012-01-09
JP5795755B2 (ja) 2015-10-14
HN2011002933A (es) 2014-09-08
WO2010129379A1 (fr) 2010-11-11
EP2427444A1 (fr) 2012-03-14

Similar Documents

Publication Publication Date Title
MA33342B1 (fr) Inhibiteurs du canal potassique médullaire externe rénal
WO2013066718A3 (fr) Inhibiteurs du canal potassique médullaire externe rénal
MX2014001946A (es) Inhibidores del canal de potasio medularmente externo renal.
MA42145A (fr) Triazoles agonistes du récepteur apj
MX365986B (es) Derivativos de piperidina fusionados con espiro para usarse como inhibidores del canal de potasio medular externo renal.
CR20210189A (es) Inhibidores de la proteina tirosina fosfatasa
WO2014126944A3 (fr) Inhibiteurs du canal potassique médullaire extérieur rénal
WO2014099633A3 (fr) Inhibiteurs du canal potassique médullaire externe rénal
MA43169B1 (fr) Composés héterocycliques en tant qu' inhibiteurs pi3k-gamma
TW200612911A (en) Compounds for the treatment of inflammatory disorders
TW200616620A (en) Compounds for the treatment of inflammatory disorders
UY31084A1 (es) Compuestos de azaindol para la inhibicion de b-secretasa
MA31084B1 (fr) Derives de piperidine agonistes de gpcr
MX2010006911A (es) Antagonistas del receptor mineralcorticoide no esteroidal derivado de 6h-dibenzo [b,e] oxepina.
BR0212477A (pt) 7-aza[2.2.1] bicicloheptanos substituìdos para o tratamento de doenças
MA32785B1 (fr) Procede de traitement ou de prevention de thrombose a l'aide d'etexilate de dabigatran ou d'un sel de celui-ci avec une efficacite accrue par rapport a une therapie classique par warfarine
MA39152B1 (fr) Cyclopentanes substitués en 1,2 utilisés comme antagonistes du récepteur d'orexine
MA34377B1 (fr) Composé de pipéridinyle en tant que modulateur de l'activité des récepteurs des chimiokines
PE20020351A1 (es) Composiciones farmaceuticas que comprenden acido 5-metil-2-(2'-cloro-6'-fluoroanilino)fenilacetico como inhibidor de la ciclooxigenasa-2
EA201100502A1 (ru) Гликозидные производные и их применения
MA38250B1 (fr) Nouveau dérivés d'hydantoïne pour leurs utilisations dans le traitement de maladies, comme l'osteoporose et la thrombocytopenie
MX2021001710A (es) Compuestos de fluoro ?-carbolina.
MA30567B1 (fr) Dérivés d'acide phénylacétique.
ECSP056055A (es) Nuevo compuesto intermedio para la preparación de imidazopiridinas terapéuticamente activas
EA201000119A1 (ru) Фармацевтические композиции, содержащие монохолиновые соли янтарной кислоты