ATE470665T1 - Cycloalkylaminderivate als inhibitoren der wechselwirkung zwischen mdm2 und p53 - Google Patents

Cycloalkylaminderivate als inhibitoren der wechselwirkung zwischen mdm2 und p53

Info

Publication number
ATE470665T1
ATE470665T1 AT07727060T AT07727060T ATE470665T1 AT E470665 T1 ATE470665 T1 AT E470665T1 AT 07727060 T AT07727060 T AT 07727060T AT 07727060 T AT07727060 T AT 07727060T AT E470665 T1 ATE470665 T1 AT E470665T1
Authority
AT
Austria
Prior art keywords
mdm2
interaction
cycloalkylamin
inhibitors
derivatives
Prior art date
Application number
AT07727060T
Other languages
English (en)
Inventor
Jean Lacrampe
Christophe Meyer
Bruno Schoentjes
Alain Poncelet
Camille Wermuth
Bruno Giethlen
Jean-Marie Contreras
Muriel Joubert
Hijfte Luc Van
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Application granted granted Critical
Publication of ATE470665T1 publication Critical patent/ATE470665T1/de

Links

Classifications

    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
AT07727060T 2006-03-22 2007-03-19 Cycloalkylaminderivate als inhibitoren der wechselwirkung zwischen mdm2 und p53 ATE470665T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP06111529 2006-03-22
US78512006P 2006-03-23 2006-03-23
PCT/EP2007/052582 WO2007107545A1 (en) 2006-03-22 2007-03-19 Cyclic-alkylaminederivatives as inhibitors of the interaction between mdm2 and p53

Publications (1)

Publication Number Publication Date
ATE470665T1 true ATE470665T1 (de) 2010-06-15

Family

ID=38110050

Family Applications (1)

Application Number Title Priority Date Filing Date
AT07727060T ATE470665T1 (de) 2006-03-22 2007-03-19 Cycloalkylaminderivate als inhibitoren der wechselwirkung zwischen mdm2 und p53

Country Status (8)

Country Link
US (2) US8088795B2 (de)
EP (1) EP1999126B1 (de)
JP (1) JP5162574B2 (de)
AT (1) ATE470665T1 (de)
AU (1) AU2007228784B2 (de)
CA (1) CA2644649C (de)
DE (1) DE602007007065D1 (de)
WO (1) WO2007107545A1 (de)

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ATE547415T1 (de) 2007-09-21 2012-03-15 Janssen Pharmaceutica Nv Inhibitoren der wechselwirkung zwischen mdm2 und p53
JP5627574B2 (ja) 2008-06-03 2014-11-19 インターミューン， インコーポレイテッド 炎症性および線維性疾患を治療するための化合物および方法
MX2011008195A (es) 2009-02-04 2011-09-06 Janssen Pharmaceutica Nv Derivados de indol como agentes anticancer.
US8658170B2 (en) 2010-01-06 2014-02-25 Joseph P. Errico Combination therapy with MDM2 and EFGR inhibitors
US20130149314A1 (en) 2010-02-09 2013-06-13 Jörn Bullerdiek p19Arf, HMGA2 and MDM2 For Use in the Diagnosis and Treatment of Aberrant Cell Growth
EP2596366A4 (de) * 2010-07-21 2014-04-16 Joseph P Errico Kombinationstherapie mit mdm2 und efgr-hemmern
FR2967072B1 (fr) 2010-11-05 2013-03-29 Univ Dundee Procede pour ameliorer la production de virus et semences vaccinales influenza
US10016414B2 (en) * 2010-11-12 2018-07-10 University Of Massachusetts Modulation of ubiquitination of synaptic proteins for the treatment of neurodegenerative and psychiatric disorders
CN103221094B (zh) * 2010-11-19 2016-04-20 诺华有限公司 Mdm2/4及p53相互作用抑制剂的结晶型
AR092742A1 (es) 2012-10-02 2015-04-29 Intermune Inc Piridinonas antifibroticas
WO2014085486A2 (en) 2012-11-30 2014-06-05 Waters Technologies Corporation Methods and apparatus for the analysis of vitamin d metabolites
EP2935263B1 (de) 2012-12-20 2018-12-05 Merck Sharp & Dohme Corp. Substituierte imidazopyridine als hdm2 inhibitoren
EP2983674A4 (de) 2013-04-08 2017-05-10 Dennis M. Brown Therapeutischer nutzen suboptimal verabreichter chemischer verbindungen
EP3527569B1 (de) 2014-02-03 2021-08-25 Vitae Pharmaceuticals, LLC Dihydropyrrolopyridininhibitoren von ror-gamma zur behandlung von augentrockenheit
US10233195B2 (en) 2014-04-02 2019-03-19 Intermune, Inc. Anti-fibrotic pyridinones
CR20170076A (es) 2014-08-04 2017-06-26 Nuevolution As Derivados de pirimidima sustituidos con heterociclilo opcionalmente condensados útiles para el tratamiento de enfermedades inflamatorias, metabólicas, oncológicas y autoinmunitarias
TWI675032B (zh) 2014-10-14 2019-10-21 美商維它藥物公司 ＲＯＲ-γ之二氫吡咯并吡啶抑制劑
US9845308B2 (en) 2014-11-05 2017-12-19 Vitae Pharmaceuticals, Inc. Isoindoline inhibitors of ROR-gamma
US9663515B2 (en) 2014-11-05 2017-05-30 Vitae Pharmaceuticals, Inc. Dihydropyrrolopyridine inhibitors of ROR-gamma
WO2016181414A1 (en) * 2015-05-12 2016-11-17 Council Of Scientific & Industrial Research Process for the synthesis of ivacaftor and related compounds
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TW202332444A (zh) * 2015-10-23 2023-08-16 日商第一三共股份有限公司 用於治療癌症之醫藥組成物
EP3868750A1 (de) 2015-11-20 2021-08-25 Vitae Pharmaceuticals, LLC Modulatoren von ror-gamma
US9630968B1 (en) 2015-12-23 2017-04-25 Arqule, Inc. Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof
TW202220968A (zh) 2016-01-29 2022-06-01 美商維它藥物有限責任公司 ＲＯＲ－γ調節劑
CN118436801A (zh) 2016-05-20 2024-08-06 豪夫迈·罗氏有限公司 Protac抗体缀合物及其使用方法
US9481674B1 (en) 2016-06-10 2016-11-01 Vitae Pharmaceuticals, Inc. Dihydropyrrolopyridine inhibitors of ROR-gamma
SG11201901197PA (en) 2016-08-24 2019-03-28 Arqule Inc Amino-pyrrolopyrimidinone compounds and methods of use thereof
MA49685A (fr) 2017-07-24 2021-04-14 Vitae Pharmaceuticals Llc INHIBITEURS DE ROR gamma
WO2019018975A1 (en) 2017-07-24 2019-01-31 Vitae Pharmaceuticals, Inc. INHIBITORS OF ROR GAMMA
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EP4126874A1 (de) 2020-03-31 2023-02-08 Nuevolution A/S Gegen nukleare rezeptoren aktive verbindungen
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US20030149038A1 (en) * 2001-11-09 2003-08-07 The Regents Of The University Of California Alpha-helix mimicry by a class of organic molecules
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Also Published As

Publication number Publication date
WO2007107545A1 (en) 2007-09-27
CA2644649C (en) 2014-06-17
CA2644649A1 (en) 2007-09-27
US20100168163A1 (en) 2010-07-01
EP1999126A1 (de) 2008-12-10
AU2007228784B2 (en) 2012-03-08
AU2007228784A1 (en) 2007-09-27
JP5162574B2 (ja) 2013-03-13
US8377961B2 (en) 2013-02-19
JP2009530345A (ja) 2009-08-27
EP1999126B1 (de) 2010-06-09
DE602007007065D1 (de) 2010-07-22
US20120071508A1 (en) 2012-03-22
US8088795B2 (en) 2012-01-03

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