MX2011010647A - Analogos de isoxasol-3 (2h)-ona como agentes terapeuticos. - Google Patents

Analogos de isoxasol-3 (2h)-ona como agentes terapeuticos.

Info

Publication number
MX2011010647A
MX2011010647A MX2011010647A MX2011010647A MX2011010647A MX 2011010647 A MX2011010647 A MX 2011010647A MX 2011010647 A MX2011010647 A MX 2011010647A MX 2011010647 A MX2011010647 A MX 2011010647A MX 2011010647 A MX2011010647 A MX 2011010647A
Authority
MX
Mexico
Prior art keywords
alkyl
aryl
deuterium
optionally
optionally substituted
Prior art date
Application number
MX2011010647A
Other languages
English (en)
Inventor
Leifeng Cheng
Peter Schell
Jonas Bostrom
Tomas Fex
Michael Karle
Daniel Pettersen
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of MX2011010647A publication Critical patent/MX2011010647A/es

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Classifications

    • 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
    • C07D413/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4525Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
    • 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
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/08Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/04Drugs for skeletal disorders for non-specific disorders of the connective tissue
    • 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
    • A61P7/04Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • 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)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Epidemiology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Reproductive Health (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pregnancy & Childbirth (AREA)
  • Urology & Nephrology (AREA)
  • Endocrinology (AREA)
  • Biomedical Technology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

La invención se refiere a un compuesto representado por la fórmula I o una sal farmacéuticamente aceptable del mismo. En la fórmula, R1 y R2 representan independientemente un hidrógeno, un deuterio, un arilo, un heteroarilo, un alquilo de C1-C8 eventualmente substituido por uno o varios sustituyentes representados independientemente por R3, R3 que representa un arilo, un heteroarilo, uno o varios átomos de flúor, un alquilo de C1-C6 que contiene uno o varios átomos de flúor, un alquilo de C1-C6 que contiene uno o varios átomos de deuterio, un alquilo de C1-C6 que contiene un hidroxi, el arilo y el heteroarilo que son eventualmente sustituidos por uno o varios átomos de halógeno, un alcoxi fluorado, un alquilo fluorado, un sulfonilo, uno o varios átomos de deuterio, un alquilo de C1-6, un alcoxi de C1-6, un nitrilo, o R3 representa un alquilo de C1-6 eventualmente sustituido por uno o varios de los grupos siguientes: COOR4, OCQR4, CONR5R6, NR5COR6, CR4; R4 que representa un alquilo de C1-10 eventualmente sustituido por uno o varios átomos de flúor, un átomo de deuterio, un alcoxi, un arilcarboxilato, un carboxilato de alquilo; R5 y R6 se seleccionan independientemente entre un hidrogeno y un alquilo, o forman junto con un núcleo de carbono que tiene 4 a 8 miembros; o R1 y R2 forman un núcleo de carbono dotado con 3 a 10 miembros que comprenden eventualmente O o N, y son eventualmente sustituidos por un arilo o un alquilo de C1-10, un heteroarilo eventualmente sustituido por R3.
MX2011010647A 2009-04-07 2010-04-06 Analogos de isoxasol-3 (2h)-ona como agentes terapeuticos. MX2011010647A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US16722409P 2009-04-07 2009-04-07
US17195609P 2009-04-23 2009-04-23
PCT/SE2010/050375 WO2010117323A1 (en) 2009-04-07 2010-04-06 Method and apparatus for producing heat energy and carbon dioxide

Publications (1)

Publication Number Publication Date
MX2011010647A true MX2011010647A (es) 2012-02-21

Family

ID=42934883

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2011010647A MX2011010647A (es) 2009-04-07 2010-04-06 Analogos de isoxasol-3 (2h)-ona como agentes terapeuticos.

Country Status (21)

Country Link
US (1) US8415378B2 (es)
EP (1) EP2417131A4 (es)
JP (1) JP5711723B2 (es)
KR (1) KR101675607B1 (es)
CN (1) CN102459246B (es)
AR (1) AR076219A1 (es)
AU (1) AU2010235236B2 (es)
BR (1) BRPI1013984A2 (es)
CA (1) CA2757879C (es)
CO (1) CO6440580A2 (es)
CU (1) CU20110190A7 (es)
EA (1) EA020825B1 (es)
EC (1) ECSP11011385A (es)
IL (1) IL215336A0 (es)
MX (1) MX2011010647A (es)
NI (1) NI201100181A (es)
SG (1) SG174463A1 (es)
TW (1) TW201040166A (es)
UY (1) UY32543A (es)
WO (1) WO2010117323A1 (es)
ZA (1) ZA201108119B (es)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2011001349A (es) 2008-08-04 2011-08-17 Chidi Inc Ciertos inhibidores de quinurenin-3-monooxigenasa, composiciones farmaceuticas y metodos para su uso.
KR20120131161A (ko) 2010-01-25 2012-12-04 씨에이치디아이 파운데이션, 인코포레이티드 특정 키뉴레닌-3-모노옥시게나제 억제제, 그의 제약 조성물 및 사용 방법
WO2012047156A1 (en) * 2010-10-04 2012-04-12 Astrazeneca Ab Isoxazol-3(2h)-one analogs as plasminogen inhibitors and their use in the treatment of fibrinolysis related diseases
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
PT2750677T (pt) 2011-08-30 2017-07-03 Chdi Foundation Inc Inibidores de quinurenina-3-monooxigenase, composições farmacêuticas e métodos de utilização dos mesmos
BR112014004845A2 (pt) 2011-08-30 2017-04-04 Chdi Foundation Inc pelo menos uma entidade química; pelo menos um composto; composição farmacêutica; uso de uma quantidade terapeuticamente eficaz de pelo menos uma entidade química; composição farmacêutica embalada
US9073881B2 (en) 2011-09-23 2015-07-07 Hoffmann-La Roche Inc. Benzoic acid derivatives
ME03300B (me) 2012-06-13 2019-07-20 Incyte Holdings Corp Supsтituisana triciklična jedinjenja као inhibiтori fgfr
US9388185B2 (en) 2012-08-10 2016-07-12 Incyte Holdings Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
CN102977040B (zh) * 2012-11-20 2015-06-03 浙江工业大学 一种2-喹喔啉基二甲缩醛和2-喹喔啉基甲醛的合成方法
CN102977050B (zh) * 2012-11-20 2015-04-22 浙江工业大学 一种2-苯并噻唑二甲缩醛和2-苯并噻唑甲醛的合成方法
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
ES2657451T3 (es) 2013-04-19 2018-03-05 Incyte Holdings Corporation Heterocíclicos bicíclicos como inhibidores del FGFR
UY35809A (es) 2013-11-05 2015-05-29 Bayer Pharma AG (aza)piridopirazolopirimidinonas e indazolopirimidinonas y sus usos
UA120856C2 (uk) 2014-07-17 2020-02-25 Кхді Фаундейшн, Інк. Способи та композиції для лікування розладів, пов'язаних з віл
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
AU2015342021B2 (en) 2014-11-03 2020-02-27 Bayer Pharma Aktiengesellschaft Piperidinylpyrazolopyrimidinones and their use
US20170360766A1 (en) * 2014-12-19 2017-12-21 Emeriti Pharma Ab 3-(piperidin-4-yl)-isoxazol-3(oh)-ones for treatment of dermatologic disorders
US9580423B2 (en) 2015-02-20 2017-02-28 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
ES2751669T3 (es) 2015-02-20 2020-04-01 Incyte Corp Heterociclos bicíclicos como inhibidores FGFR
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
CN104725300A (zh) * 2015-02-28 2015-06-24 宁波九胜创新医药科技有限公司 一种1-(6-甲基吡啶-3-基)-2-(4-甲磺酰基苯基)乙酮的制备方法
WO2016173948A1 (en) 2015-04-30 2016-11-03 Bayer Pharma Aktiengesellschaft Indazolopyrimidinones as fibrinolysis inhibitors
CN107459514B (zh) * 2016-06-06 2020-10-23 南开大学 一类手性哌啶衍生物及其制备方法和用途
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
CN107857725A (zh) * 2017-12-19 2018-03-30 苏州艾缇克药物化学有限公司 一种2‑氨基吡啶‑4‑甲醇的合成方法
JP2021523118A (ja) 2018-05-04 2021-09-02 インサイト・コーポレイションIncyte Corporation Fgfr阻害剤の塩
CR20200590A (es) 2018-05-04 2021-04-26 Incyte Corp Formas sólidas de un inhibidor de fgfr y procesos para prepararlas
US11628162B2 (en) 2019-03-08 2023-04-18 Incyte Corporation Methods of treating cancer with an FGFR inhibitor
US11591329B2 (en) 2019-07-09 2023-02-28 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
IL291901A (en) 2019-10-14 2022-06-01 Incyte Corp Bicyclyl heterocycles as fgr suppressors
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
JP2023505257A (ja) 2019-12-04 2023-02-08 インサイト・コーポレイション Fgfr阻害剤の誘導体
JP2023505258A (ja) 2019-12-04 2023-02-08 インサイト・コーポレイション Fgfr阻害剤としての三環式複素環
US20240124443A1 (en) * 2021-02-05 2024-04-18 Scinnohub Pharmaceutical Co., Ltd Plasmin inhibitor, preparation method therefor, and application thereof
CA3220274A1 (en) 2021-06-09 2022-12-15 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69426604T2 (de) * 1993-11-24 2001-05-10 Du Pont Pharm Co Isoxazoline und isoxazole derivate als fibrinogen rezeptor antagonisten
AU1735200A (en) * 1998-11-18 2000-06-05 Du Pont Pharmaceuticals Company Novel isoxazoline fibrinogen receptor antagonists
US20030207873A1 (en) * 2002-04-10 2003-11-06 Edmund Harrington Inhibitors of Src and other protein kinases
KR20060003353A (ko) * 2003-04-15 2006-01-10 머크 앤드 캄파니 인코포레이티드 케모킨 수용체의벤족사지닐-아미도사이클로펜틸-헤테로사이클릭 조절제
US7598243B2 (en) * 2003-04-17 2009-10-06 Merck & Co., Inc. Heterocyclic cyclopentyl tetrahydroisoquinoline and tetrahydropyridopyridine modulators of chemokine receptor activity
CN101328173B (zh) * 2008-07-31 2010-12-15 石药集团欧意药业有限公司 一种制备6-氟-3-(4-哌啶基)-1,2-苯并异噁唑盐酸盐的方法

Also Published As

Publication number Publication date
ECSP11011385A (es) 2011-11-30
CA2757879C (en) 2017-06-06
AU2010235236B2 (en) 2013-10-24
CU20110190A7 (es) 2012-02-15
EP2417131A4 (en) 2014-08-27
WO2010117323A1 (en) 2010-10-14
IL215336A0 (en) 2011-12-29
US8415378B2 (en) 2013-04-09
US20100261755A1 (en) 2010-10-14
BRPI1013984A2 (pt) 2018-06-19
UY32543A (es) 2010-11-30
CN102459246A (zh) 2012-05-16
EA020825B1 (ru) 2015-02-27
CN102459246B (zh) 2014-05-07
WO2010117323A8 (en) 2010-11-18
AU2010235236A1 (en) 2011-10-20
CO6440580A2 (es) 2012-05-15
NI201100181A (es) 2012-06-14
EA201190237A1 (ru) 2012-04-30
KR101675607B1 (ko) 2016-11-11
ZA201108119B (en) 2012-07-25
AR076219A1 (es) 2011-05-26
JP2012522836A (ja) 2012-09-27
TW201040166A (en) 2010-11-16
KR20120034611A (ko) 2012-04-12
SG174463A1 (en) 2011-10-28
CA2757879A1 (en) 2010-10-14
JP5711723B2 (ja) 2015-05-07
EP2417131A1 (en) 2012-02-15

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