CL2014001131A1 - Compuestos derivados de 6-(aril)pirido[2,3-d]pirimidina-7(8h)-ona, o una sal o n-oxido de los mismos, como inhibidores de pak; composicion farmaceutica que los comprende, util para tratar un trastorno de proliferacion celular, tal como cancer de mama, colorrectal, de piel, del snc y de higado. - Google Patents

Compuestos derivados de 6-(aril)pirido[2,3-d]pirimidina-7(8h)-ona, o una sal o n-oxido de los mismos, como inhibidores de pak; composicion farmaceutica que los comprende, util para tratar un trastorno de proliferacion celular, tal como cancer de mama, colorrectal, de piel, del snc y de higado.

Info

Publication number
CL2014001131A1
CL2014001131A1 CL2014001131A CL2014001131A CL2014001131A1 CL 2014001131 A1 CL2014001131 A1 CL 2014001131A1 CL 2014001131 A CL2014001131 A CL 2014001131A CL 2014001131 A CL2014001131 A CL 2014001131A CL 2014001131 A1 CL2014001131 A1 CL 2014001131A1
Authority
CL
Chile
Prior art keywords
snc
pyrido
colorectal
pyrimidine
breast
Prior art date
Application number
CL2014001131A
Other languages
English (en)
Inventor
David Campell
Sergio G Duron
Original Assignee
Afraxis Holdings Inc
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 Afraxis Holdings Inc filed Critical Afraxis Holdings Inc
Publication of CL2014001131A1 publication Critical patent/CL2014001131A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • 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
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
CL2014001131A 2011-11-04 2014-04-30 Compuestos derivados de 6-(aril)pirido[2,3-d]pirimidina-7(8h)-ona, o una sal o n-oxido de los mismos, como inhibidores de pak; composicion farmaceutica que los comprende, util para tratar un trastorno de proliferacion celular, tal como cancer de mama, colorrectal, de piel, del snc y de higado. CL2014001131A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161555902P 2011-11-04 2011-11-04

Publications (1)

Publication Number Publication Date
CL2014001131A1 true CL2014001131A1 (es) 2014-08-22

Family

ID=48192852

Family Applications (2)

Application Number Title Priority Date Filing Date
CL2014001132A CL2014001132A1 (es) 2011-11-04 2014-04-30 Compuestos derivados de 6-(aril)pirido[2,3-d]pirimidina-7(8h)-ona, o una sal o n-oxido de los mismos, como inhibidores de pak; composicion farmaceutica que los comprende, util para tratar el sindrome del x fragil.
CL2014001131A CL2014001131A1 (es) 2011-11-04 2014-04-30 Compuestos derivados de 6-(aril)pirido[2,3-d]pirimidina-7(8h)-ona, o una sal o n-oxido de los mismos, como inhibidores de pak; composicion farmaceutica que los comprende, util para tratar un trastorno de proliferacion celular, tal como cancer de mama, colorrectal, de piel, del snc y de higado.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
CL2014001132A CL2014001132A1 (es) 2011-11-04 2014-04-30 Compuestos derivados de 6-(aril)pirido[2,3-d]pirimidina-7(8h)-ona, o una sal o n-oxido de los mismos, como inhibidores de pak; composicion farmaceutica que los comprende, util para tratar el sindrome del x fragil.

Country Status (20)

Country Link
US (2) US20150031693A1 (es)
EP (2) EP2773642A1 (es)
JP (2) JP2015501786A (es)
KR (2) KR20140096098A (es)
CN (2) CN104039786A (es)
AR (1) AR089175A1 (es)
AU (2) AU2012327183A1 (es)
BR (2) BR112014010631A2 (es)
CA (2) CA2854462A1 (es)
CL (2) CL2014001132A1 (es)
CO (1) CO7030960A2 (es)
CR (2) CR20140250A (es)
EA (2) EA201490927A1 (es)
IL (2) IL232154A0 (es)
MA (2) MA35660B1 (es)
MX (2) MX2014005296A (es)
PH (2) PH12014500956A1 (es)
SG (2) SG11201401996TA (es)
TW (1) TW201326169A (es)
WO (2) WO2013067434A1 (es)

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WO2011156780A2 (en) * 2010-06-10 2011-12-15 Afraxis, Inc. 8-(sulfonylbenzyl)pyrido[2,3-d]pyrimidin-7(8h)-ones for the treatment of cns disorders
SG11201401937YA (en) 2011-11-04 2014-05-29 Hoffmann La Roche New aryl-quinoline derivatives
TWI647220B (zh) 2013-03-15 2019-01-11 美商西建卡爾有限責任公司 雜芳基化合物及其用途
MY181020A (en) 2013-03-15 2020-12-16 Sanofi Sa Heteroaryl compounds and uses thereof
WO2015011252A1 (en) * 2013-07-26 2015-01-29 F. Hoffmann-La Roche Ag Pyrimidine-pyridinone serine/threonine kinase inhibitors
DK3102577T3 (en) * 2014-02-07 2018-11-12 Principia Biopharma Inc QUINOLONDERIVATIVES AS FIBROBLAST GROWTH FACTOR RECEPTOR INHIBITORS
MA38393B1 (fr) 2014-03-13 2018-11-30 Sanofi Sa Composés hétéroaryle et utilisations associées
WO2016015597A1 (en) 2014-07-26 2016-02-04 Sunshine Lake Pharma Co., Ltd. Compounds as cdk small-molecule inhibitors and uses thereof
US20170042806A1 (en) 2015-04-29 2017-02-16 Dexcel Pharma Technologies Ltd. Orally disintegrating compositions
CA3013959C (en) * 2016-02-17 2024-05-28 Nuralogix Corporation System and method for detecting physiological state
US10076494B2 (en) 2016-06-16 2018-09-18 Dexcel Pharma Technologies Ltd. Stable orally disintegrating pharmaceutical compositions
JP7090037B2 (ja) * 2016-06-23 2022-06-23 エフ.ホフマン-ラ ロシュ アーゲー 新規な[1,2,3]トリアゾロ[4,5-d]ピリミジン誘導体
US11685954B2 (en) * 2016-07-15 2023-06-27 Dana-Farber Cancer Institute, Inc. Biomarkers predictive of endocrine resistance in breast cancer
CN106818805A (zh) * 2016-12-27 2017-06-13 东莞市联洲知识产权运营管理有限公司 一种天然乙酰胆碱酯酶抑制剂及其杀虫应用
CN107083428B (zh) * 2017-04-10 2020-09-25 徐州医科大学 Pak5在癌症诊断预后治疗及药物筛选中的应用
TWI831829B (zh) 2018-09-12 2024-02-11 美商建南德克公司 苯氧基-吡啶基-嘧啶化合物及使用方法
US20220002429A1 (en) * 2018-10-24 2022-01-06 Northwestern University Tumor cell aggregation inhibitors' for treating cancer
WO2020142612A1 (en) * 2019-01-03 2020-07-09 Genentech, Inc. Pyrido-pyrimidinone and pteridinone compounds as inhibitors of endoribonuclease inositol requiring enzyme i (ire i alpha) for the treatment of cancer diseases.
CN112213400B (zh) * 2019-07-09 2022-06-07 四川弘合生物科技有限公司 一种β-榄香烯及其有关物质的检测方法
CN110496128B (zh) * 2019-09-23 2022-09-30 吉林大学 利培酮或帕潘立酮在制备治疗弥漫性大b细胞淋巴瘤的药物中的应用
PE20231311A1 (es) 2020-11-18 2023-08-24 Deciphera Pharmaceuticals Llc Inhibidores de gcn2 y perk quinasas y metodos de uso de los mismos
CN117858879A (zh) * 2021-01-15 2024-04-09 南京再明医药有限公司 Cdk2/4/6抑制剂及其制备方法和应用
CN113046323A (zh) * 2021-04-02 2021-06-29 四川农业大学 一种基于miR-532-5p及其靶基因调控卵巢颗粒细胞的方法
MX2024006627A (es) 2021-12-03 2024-08-22 Deciphera Pharmaceuticals Llc Inhibidores de gcn2 y perk quinasa y metodos de uso de los mismos.
WO2025257301A1 (en) * 2024-06-13 2025-12-18 Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts Treatment of neurofibromatosis type 2 by inhibitors of g6pd, acsl3 and/or oxsm

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1201765A3 (en) * 2000-10-16 2003-08-27 Axxima Pharmaceuticals Aktiengesellschaft Cellular kinases involved in cytomegalovirus infection and their inhibition
WO2008055842A1 (en) * 2006-11-09 2008-05-15 F. Hoffmann-La Roche Ag Substituted 6-phenyl-pyrido [2,3-d] pyrimidin-7-one derivatives as kinase inhibitors and methods for using the same
EP2112150B1 (en) * 2008-04-22 2013-10-16 Forma Therapeutics, Inc. Improved raf inhibitors
WO2010071846A2 (en) * 2008-12-19 2010-06-24 Afraxis, Inc. Compounds for treating neuropsychiatric conditions
CN102648200A (zh) * 2009-10-09 2012-08-22 亚弗克希斯公司 用于治疗cns病症的8-乙基-6-(芳基)吡啶并[2,3-d]嘧啶-7(8h)-酮
EP2580214A4 (en) * 2010-06-09 2013-12-04 Afraxis Holdings Inc 8- (SULFONYLARYL) PYRIDO [2,3-D] PYRIMIDIN-7 (8H) -ONES FOR THE TREATMENT OF CNS DISORDERS
WO2011156780A2 (en) * 2010-06-10 2011-12-15 Afraxis, Inc. 8-(sulfonylbenzyl)pyrido[2,3-d]pyrimidin-7(8h)-ones for the treatment of cns disorders

Also Published As

Publication number Publication date
EP2773642A1 (en) 2014-09-10
IL232215A0 (en) 2014-06-30
TW201326169A (zh) 2013-07-01
MX2014005296A (es) 2014-08-27
EA201490925A1 (ru) 2014-09-30
WO2013067434A1 (en) 2013-05-10
US20130116263A1 (en) 2013-05-09
US20150031693A1 (en) 2015-01-29
BR112014010420A2 (pt) 2017-04-25
SG11201401914WA (en) 2014-05-29
AU2012327183A8 (en) 2013-07-18
CA2854471A1 (en) 2013-05-10
BR112014010631A2 (pt) 2017-04-25
EA201490927A1 (ru) 2014-10-30
CA2854462A1 (en) 2013-05-10
MX2014005292A (es) 2014-09-11
MA35660B1 (fr) 2014-11-01
CO7030960A2 (es) 2014-08-21
CN104093717A (zh) 2014-10-08
CR20140250A (es) 2014-08-20
EP2773643A4 (en) 2015-07-29
MA35661B1 (fr) 2014-11-01
PH12014500995A1 (en) 2014-08-04
AU2012327183A1 (en) 2013-05-30
IL232154A0 (en) 2014-05-28
KR20140096098A (ko) 2014-08-04
CN104039786A (zh) 2014-09-10
SG11201401996TA (en) 2014-05-29
JP2014532724A (ja) 2014-12-08
WO2013067423A1 (en) 2013-05-10
AU2012327187A8 (en) 2013-07-25
PH12014500956A1 (en) 2014-06-30
CL2014001132A1 (es) 2014-08-22
JP2015501786A (ja) 2015-01-19
EP2773643A1 (en) 2014-09-10
CR20140251A (es) 2014-08-20
AR089175A1 (es) 2014-08-06
KR20140105451A (ko) 2014-09-01
AU2012327187A1 (en) 2013-05-23

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