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UY28778A1 - Derivados de pirrol como inhibidores del factor xa - Google Patents

Derivados de pirrol como inhibidores del factor xa

Info

Publication number
UY28778A1
UY28778A1 UY28778A UY28778A UY28778A1 UY 28778 A1 UY28778 A1 UY 28778A1 UY 28778 A UY28778 A UY 28778A UY 28778 A UY28778 A UY 28778A UY 28778 A1 UY28778 A1 UY 28778A1
Authority
UY
Uruguay
Prior art keywords
factor
compounds
formulas
factor viia
inhibitors
Prior art date
Application number
UY28778A
Other languages
English (en)
Inventor
Dr Marc Nazare
Dr Hans Matter
Dr Volkmar Wehner
Dr Michael Wagner
Dr Matthias Urmann
Dr Armin Bauer
Original Assignee
Sanofi Aventis Deutschland
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 Sanofi Aventis Deutschland filed Critical Sanofi Aventis Deutschland
Publication of UY28778A1 publication Critical patent/UY28778A1/es

Links

Classifications

    • 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
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • 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
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • 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
    • 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
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente invención se refiere a los compuestos de las fórmulas I y Ia, en las que R0; R1; R3; R4; R22; Q, V, G y M tienen los significados indicados más adelante. Los compuestos de las fórmulas I y Ia son compuestos valiosos farmacológicamente activos. Presentan un efecto antitrombótico fuerte y son adecuados, por ejemplo, para la terapia y la profilaxis de los trastornos cardiovasculares como enfermedades tromboembólicas o restenosis. Son inhibidores reversibles del factor Xa (FXa) y/o del factor VIIa (FVIIa) de las enzimas de coagulación de la sangre, y se pueden aplicar en general en condiciones en las que está presente una actividad no deseada del factor Xa y/o del factor VIIa o para la curación o prevención cuya inhibición del factor Xa y/o el factor VIIa se pretende. La invención se refiere además a los procedimientos para la preparación de compuestos de las fórmulas I Ia, a su utilización, en particular como ingredientes activos en productos farmacéuticos, y a las preparaciones farmacéuticas que los comprenden.
UY28778A 2004-02-27 2005-02-25 Derivados de pirrol como inhibidores del factor xa UY28778A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP04004503A EP1568698A1 (en) 2004-02-27 2004-02-27 Pyrrole-derivatives as factor Xa inhibitors

Publications (1)

Publication Number Publication Date
UY28778A1 true UY28778A1 (es) 2005-09-30

Family

ID=34745922

Family Applications (1)

Application Number Title Priority Date Filing Date
UY28778A UY28778A1 (es) 2004-02-27 2005-02-25 Derivados de pirrol como inhibidores del factor xa

Country Status (13)

Country Link
US (1) US7465806B2 (es)
EP (2) EP1568698A1 (es)
JP (1) JP4861306B2 (es)
KR (1) KR20070000487A (es)
CN (1) CN1926137A (es)
AU (1) AU2005219507A1 (es)
BR (1) BRPI0508048A (es)
CA (1) CA2557270A1 (es)
IL (1) IL177253A0 (es)
PE (1) PE20051170A1 (es)
TW (1) TW200538110A (es)
UY (1) UY28778A1 (es)
WO (1) WO2005085239A2 (es)

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MX358640B (es) 2008-01-04 2018-08-29 Intellikine Llc Isoquinolin-1 (2h) -onas y tieno [2,3-d]pirimidin-4(3h) -onas substituidas, y metodos de uso de las mismas.
WO2010137017A2 (en) 2009-05-27 2010-12-02 Yeda Research And Development Co. Ltd. Proteasome inhibitors and uses thereof
TWI546305B (zh) 2011-01-10 2016-08-21 英菲尼提製藥股份有限公司 製備異喹啉酮之方法及異喹啉酮之固體形式
US8828998B2 (en) 2012-06-25 2014-09-09 Infinity Pharmaceuticals, Inc. Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
CN105102000B (zh) 2012-11-01 2021-10-22 无限药品公司 使用pi3激酶亚型调节剂的癌症疗法
IL239682B (en) 2013-01-08 2018-10-31 Kalvista Pharmaceuticals Ltd History of benzylamine and 2-(aminomethyl)pyridine
GB201300304D0 (en) 2013-01-08 2013-02-20 Kalvista Pharmaceuticals Ltd Benzylamine derivatives
TWI636047B (zh) 2013-08-14 2018-09-21 英商卡爾維斯塔製藥有限公司 雜環衍生物
WO2015160975A2 (en) 2014-04-16 2015-10-22 Infinity Pharmaceuticals, Inc. Combination therapies
GB201421083D0 (en) 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd Enzyme inhibitors
GB201421085D0 (en) 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd New enzyme inhibitors
HRP20201131T1 (hr) 2016-05-31 2020-10-30 Kalvista Pharmaceuticals Limited Derivati pirazola kao inhibitori kalikreina plazme
GB201609607D0 (en) 2016-06-01 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of N-(3-Fluoro-4-methoxypyridin-2-yl)methyl)-3-(methoxymethyl)-1-({4-((2-oxopy ridin-1-yl)methyl)phenyl}methyl)pyrazole-4-carboxamide and salts
GB201609603D0 (en) 2016-06-01 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of N-[(6-cyano-2-fluoro-3-methoxyphenyl)Methyl]-3-(methoxymethyl)-1-({4-[(2-ox opyridin-1-YL)Methyl]phenyl}methyl)pyrazole-4-carboxamide
EP3474856B1 (en) 2016-06-24 2022-09-14 Infinity Pharmaceuticals, Inc. Combination therapies
DK3716952T3 (da) 2017-11-29 2022-03-14 Kalvista Pharmaceuticals Ltd Doseringsformer omfattende en plasmakallikrein-inhibitor
GB201719881D0 (en) 2017-11-29 2018-01-10 Kalvista Pharmaceuticals Ltd Solid forms of plasma kallikrein inhibitor and salts thereof
WO2021028645A1 (en) 2019-08-09 2021-02-18 Kalvista Pharmaceuticals Limited Plasma kallikrein inhibitors
CN113192004B (zh) * 2021-04-01 2022-01-18 温州医科大学附属第二医院（温州医科大学附属育英儿童医院） 一种基于冠脉多模影像裂纹形成和扩展的简化计算方法与斑块破裂风险量化的评估系统
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Also Published As

Publication number Publication date
CN1926137A (zh) 2007-03-07
EP1568698A1 (en) 2005-08-31
TW200538110A (en) 2005-12-01
IL177253A0 (en) 2006-12-10
JP2007523927A (ja) 2007-08-23
WO2005085239A3 (en) 2005-10-13
AU2005219507A1 (en) 2005-09-15
US7465806B2 (en) 2008-12-16
KR20070000487A (ko) 2007-01-02
PE20051170A1 (es) 2006-02-07
JP4861306B2 (ja) 2012-01-25
WO2005085239A2 (en) 2005-09-15
EP1725550A2 (en) 2006-11-29
US20070049573A1 (en) 2007-03-01
CA2557270A1 (en) 2005-09-15
BRPI0508048A (pt) 2007-07-17

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