MA35660B1 - Inhibiteurs de la protéine pak pour le traitement du syndrome de l'x fragile - Google Patents

Inhibiteurs de la protéine pak pour le traitement du syndrome de l'x fragile

Info

Publication number
MA35660B1
MA35660B1 MA37064A MA37064A MA35660B1 MA 35660 B1 MA35660 B1 MA 35660B1 MA 37064 A MA37064 A MA 37064A MA 37064 A MA37064 A MA 37064A MA 35660 B1 MA35660 B1 MA 35660B1
Authority
MA
Morocco
Prior art keywords
fragile
syndrome
treatment
inhibitors
pak protein
Prior art date
Application number
MA37064A
Other languages
English (en)
Inventor
John C Mckew
Wenwei Huang
David Campbell
Sergio G Duron
Mark Behnke
Min Shen
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 MA35660B1 publication Critical patent/MA35660B1/fr

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)

Abstract

Cette invention concerne des inhibiteurs de la protéine pak et des méthodes d'utilisation d'inhibiteurs de la protéine pak pour le traitement du syndrome de l'x fragile.
MA37064A 2011-11-04 2014-05-26 Inhibiteurs de la protéine pak pour le traitement du syndrome de l'x fragile MA35660B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161555902P 2011-11-04 2011-11-04
PCT/US2012/063426 WO2013067434A1 (fr) 2011-11-04 2012-11-02 Inhibiteurs de la protéine pak pour le traitement du syndrome de l'x fragile

Publications (1)

Publication Number Publication Date
MA35660B1 true MA35660B1 (fr) 2014-11-01

Family

ID=48192852

Family Applications (2)

Application Number Title Priority Date Filing Date
MA37064A MA35660B1 (fr) 2011-11-04 2014-05-26 Inhibiteurs de la protéine pak pour le traitement du syndrome de l'x fragile
MA37065A MA35661B1 (fr) 2011-11-04 2014-05-26 Inhibiteurs de pak pour le traitement de troubles de prolifération cellulaire

Family Applications After (1)

Application Number Title Priority Date Filing Date
MA37065A MA35661B1 (fr) 2011-11-04 2014-05-26 Inhibiteurs de pak pour le traitement de troubles de prolifération cellulaire

Country Status (20)

Country Link
US (2) US20150031693A1 (fr)
EP (2) EP2773643A4 (fr)
JP (2) JP2015501786A (fr)
KR (2) KR20140105451A (fr)
CN (2) CN104093717A (fr)
AR (1) AR089175A1 (fr)
AU (2) AU2012327183A1 (fr)
BR (2) BR112014010631A2 (fr)
CA (2) CA2854471A1 (fr)
CL (2) CL2014001131A1 (fr)
CO (1) CO7030960A2 (fr)
CR (2) CR20140250A (fr)
EA (2) EA201490927A1 (fr)
IL (2) IL232154A0 (fr)
MA (2) MA35660B1 (fr)
MX (2) MX2014005292A (fr)
PH (2) PH12014500956A1 (fr)
SG (2) SG11201401996TA (fr)
TW (1) TW201326169A (fr)
WO (2) WO2013067423A1 (fr)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130252967A1 (en) * 2010-06-10 2013-09-26 Afraxis, Inc. 8-(sulfonylbenzyl)pyrido[2,3-d]pyrimidin-7(8h)-ones for the treatment of cns disorders
CN103906735B (zh) 2011-11-04 2016-12-07 霍夫曼-拉罗奇有限公司 新芳基-喹啉衍生物
CN105307657B (zh) 2013-03-15 2020-07-10 西建卡尔有限责任公司 杂芳基化合物和其用途
EP3943087A1 (fr) 2013-03-15 2022-01-26 Celgene CAR LLC Composés hétéroaryle et utilisations associées
US9321786B2 (en) 2013-03-15 2016-04-26 Celgene Avilomics Research, Inc. Heteroaryl compounds and uses thereof
WO2015011252A1 (fr) * 2013-07-26 2015-01-29 F. Hoffmann-La Roche Ag Inhibiteurs pyrimidine-pyridinone de sérine/thréonine kinase
PT3102577T (pt) * 2014-02-07 2018-10-23 Principia Biopharma Inc Derivados de quinolona como inibidores do recetor do fator de crescimento de fibroblastos
CN105294682B (zh) 2014-07-26 2017-07-07 广东东阳光药业有限公司 Cdk类小分子抑制剂的化合物及其用途
US20170042806A1 (en) 2015-04-29 2017-02-16 Dexcel Pharma Technologies Ltd. Orally disintegrating compositions
US10694988B2 (en) * 2016-02-17 2020-06-30 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
WO2017220516A1 (fr) * 2016-06-23 2017-12-28 F. Hoffmann-La Roche Ag Dérivés de triazolo[4,5-d]pyrimidine
WO2018013466A2 (fr) * 2016-07-15 2018-01-18 Dana-Farber Cancer Institute, Inc. Biomarqueurs prédictifs de la résistance endocrinienne dans le cancer du sein
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
WO2020086882A1 (fr) * 2018-10-24 2020-04-30 Northwestern University Inhibiteurs d'agrégation de cellules tumorales pour le traitement du cancer
WO2020142612A1 (fr) 2019-01-03 2020-07-09 Genentech, Inc. Composés de pyrido-pyrimidinone et de ptéridinone utilisés en tant qu'inhibiteurs de l'enzyme nécessitant l'inositol i (ire i alpha) à activité endoribonucléase pour le traitement de maladies cancéreuses
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
IL302807A (en) 2020-11-18 2023-07-01 Deciphera Pharmaceuticals Llc Gcn2 and perk kinase inhibitors and methods of use thereof
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
PE20250609A1 (es) 2021-12-03 2025-02-26 Deciphera Pharmaceuticals Llc Inhibidores de gcn2 y perk quinasa y metodos de uso de los mismos
WO2025257301A1 (fr) * 2024-06-13 2025-12-18 Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts Traitement de la neurofibromatose de type 2 par des inhibiteurs de g6pd, acsl3 et/ou oxsm

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1201765A3 (fr) * 2000-10-16 2003-08-27 Axxima Pharmaceuticals Aktiengesellschaft Kinases cellulaires impliqués dans l'infection par cytomégalovirus et leur inhibition
WO2008055842A1 (fr) * 2006-11-09 2008-05-15 F. Hoffmann-La Roche Ag Dérivés de 6-phényl-pyrido [2,3-d] pyrimidine-7-one substitués utilisés comme inhibiteurs de la kinase et méthodes d'utilisation de ceux-ci
EP2112150B1 (fr) * 2008-04-22 2013-10-16 Forma Therapeutics, Inc. Inhibiteurs Raf améliorés
WO2010071846A2 (fr) * 2008-12-19 2010-06-24 Afraxis, Inc. Composés pour traiter des états neuropsychiatriques
US8372970B2 (en) * 2009-10-09 2013-02-12 Afraxis, Inc. 8-ethyl-6-(aryl)pyrido[2,3-D]pyrimidin-7(8H)-ones for the treatment of CNS disorders
EP2580214A4 (fr) * 2010-06-09 2013-12-04 Afraxis Holdings Inc 8-(sulfonylaryl)pyrido[2,3-d]pyrimidin-7(8h)-ones pour le traitement de troubles du snc
US20130252967A1 (en) * 2010-06-10 2013-09-26 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
WO2013067434A1 (fr) 2013-05-10
CR20140250A (es) 2014-08-20
EA201490925A1 (ru) 2014-09-30
PH12014500956A1 (en) 2014-06-30
MA35661B1 (fr) 2014-11-01
PH12014500995A1 (en) 2014-08-04
BR112014010631A2 (pt) 2017-04-25
EA201490927A1 (ru) 2014-10-30
AU2012327187A1 (en) 2013-05-23
AR089175A1 (es) 2014-08-06
TW201326169A (zh) 2013-07-01
CL2014001132A1 (es) 2014-08-22
AU2012327183A1 (en) 2013-05-30
CL2014001131A1 (es) 2014-08-22
MX2014005296A (es) 2014-08-27
US20130116263A1 (en) 2013-05-09
SG11201401996TA (en) 2014-05-29
WO2013067423A1 (fr) 2013-05-10
EP2773643A4 (fr) 2015-07-29
IL232215A0 (en) 2014-06-30
EP2773642A1 (fr) 2014-09-10
AU2012327183A8 (en) 2013-07-18
CA2854462A1 (fr) 2013-05-10
CA2854471A1 (fr) 2013-05-10
MX2014005292A (es) 2014-09-11
BR112014010420A2 (pt) 2017-04-25
AU2012327187A8 (en) 2013-07-25
CR20140251A (es) 2014-08-20
IL232154A0 (en) 2014-05-28
JP2014532724A (ja) 2014-12-08
CN104093717A (zh) 2014-10-08
US20150031693A1 (en) 2015-01-29
EP2773643A1 (fr) 2014-09-10
KR20140096098A (ko) 2014-08-04
SG11201401914WA (en) 2014-05-29
JP2015501786A (ja) 2015-01-19
KR20140105451A (ko) 2014-09-01
CO7030960A2 (es) 2014-08-21
CN104039786A (zh) 2014-09-10

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