ATE414693T1 - Neuartige cis-imidazoline - Google Patents

Neuartige cis-imidazoline

Info

Publication number
ATE414693T1
ATE414693T1 AT05742255T AT05742255T ATE414693T1 AT E414693 T1 ATE414693 T1 AT E414693T1 AT 05742255 T AT05742255 T AT 05742255T AT 05742255 T AT05742255 T AT 05742255T AT E414693 T1 ATE414693 T1 AT E414693T1
Authority
AT
Austria
Prior art keywords
imidazolines
novel cis
cis
novel
Prior art date
Application number
AT05742255T
Other languages
English (en)
Inventor
Nader Fotouhi
Gregory Haley
Klaus Simonsen
Binh Vu
Stephen Webber
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Application granted granted Critical
Publication of ATE414693T1 publication Critical patent/ATE414693T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/20Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D233/22Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/20Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D233/26Radicals substituted by carbon atoms having three bonds to hetero atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
AT05742255T 2004-05-18 2005-05-10 Neuartige cis-imidazoline ATE414693T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US57227504P 2004-05-18 2004-05-18
US61553404P 2004-10-01 2004-10-01
US66877205P 2005-04-06 2005-04-06

Publications (1)

Publication Number Publication Date
ATE414693T1 true ATE414693T1 (de) 2008-12-15

Family

ID=35058746

Family Applications (1)

Application Number Title Priority Date Filing Date
AT05742255T ATE414693T1 (de) 2004-05-18 2005-05-10 Neuartige cis-imidazoline

Country Status (21)

Country Link
US (2) US7964724B2 (de)
EP (1) EP1753727B1 (de)
JP (1) JP4814228B2 (de)
KR (3) KR20110033964A (de)
CN (1) CN1953965B (de)
AR (1) AR049545A1 (de)
AT (1) ATE414693T1 (de)
AU (1) AU2005243465B2 (de)
BR (1) BRPI0511328A (de)
CA (1) CA2565189A1 (de)
DE (1) DE602005011132D1 (de)
ES (1) ES2314660T3 (de)
IL (1) IL178884A (de)
MX (1) MXPA06013246A (de)
MY (1) MY143800A (de)
NO (1) NO20065730L (de)
PE (1) PE20060679A1 (de)
RU (1) RU2006144811A (de)
TW (1) TW200600501A (de)
WO (1) WO2005110996A1 (de)
ZA (1) ZA200609595B (de)

Families Citing this family (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7893278B2 (en) * 2004-06-17 2011-02-22 Hoffman-La Roche Inc. CIS-imidazolines
TWI314552B (en) 2005-03-16 2009-09-11 Hoffmann La Roche Novel cis-2,4,5-triaryl-imidazolines,their use as anti-cancer medicaments and their manufacture process
KR20100129331A (ko) * 2005-12-01 2010-12-08 에프. 호프만-라 로슈 아게 항암제로서 사용하기 위한 p53 및 mdm2 단백질 간 상호작용의 저해제로서의 2,4,5-트리페닐 이미다졸린 유도체
AU2007207052B2 (en) 2006-01-18 2012-07-12 F. Hoffmann-La Roche Ag CIS-4, 5-biaryl-2-heterocyclic-imidazolines as MDM2 inhibitors
KR20090042779A (ko) 2006-06-30 2009-04-30 쉐링 코포레이션 P53 활성을 증가시키는 치환된 피페리딘 및 이의 사용
CA2670105A1 (en) * 2006-11-27 2008-06-05 Novartis Ag Substituted dihydroimidazoles and their use in the treatment of tumors
EP2103619A4 (de) 2006-12-14 2011-11-23 Daiichi Sankyo Co Ltd Imidazothiazolderivate
EP2118123B1 (de) * 2007-01-31 2015-10-14 Dana-Farber Cancer Institute, Inc. Stabilisierte p53-peptide und deren verwendungen
EP2508531B1 (de) 2007-03-28 2016-10-19 President and Fellows of Harvard College Geheftete Polypeptide
US7625895B2 (en) * 2007-04-12 2009-12-01 Hoffmann-Le Roche Inc. Diphenyl-dihydro-imidazopyridinones
BRPI0817850A2 (pt) 2007-10-09 2015-04-07 Hoffmann La Rouche Ag F Cis-imidazolinas quirais
JPWO2009151069A1 (ja) 2008-06-12 2011-11-17 第一三共株式会社 4,7−ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体
DE102008047128A1 (de) * 2008-09-15 2010-04-15 Johann Wolfgang Goethe-Universität Frankfurt am Main Verwendung von cis-Imidazolinen, insbesondere Nutlinen, zur Behandlung von chemoresistenten Krebserkrankungen
KR20110119641A (ko) 2009-01-16 2011-11-02 다이이찌 산쿄 가부시키가이샤 프롤린 고리 구조를 갖는 이미다조티아졸 유도체
AU2010307198B9 (en) 2009-10-14 2014-02-13 Merck Sharp & Dohme Corp. Substituted piperidines that increase p53 activity and the uses thereof
KR20120099462A (ko) 2009-11-12 2012-09-10 더 리젠츠 오브 더 유니버시티 오브 미시건 스피로-옥신돌 mdm2 길항제
US8440693B2 (en) 2009-12-22 2013-05-14 Novartis Ag Substituted isoquinolinones and quinazolinones
WO2011106650A2 (en) * 2010-02-27 2011-09-01 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Novel p53-mdm2/p53-mdm4 antagonists to treat proliferative disease
JO2998B1 (ar) 2010-06-04 2016-09-05 Amgen Inc مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان
MX355543B (es) 2010-08-13 2018-04-20 Aileron Therapeutics Inc Star Macrociclos peptidomiméticos.
EP2621275B1 (de) 2010-09-30 2018-03-28 St. Jude Children's Research Hospital Aryl-substituierte imidazole
AU2011326395B2 (en) 2010-11-12 2016-01-07 Ascenta Licensing Corporation Spiro-oxindole MDM2 antagonists
TR201807311T4 (tr) 2011-03-10 2018-06-21 Daiichi Sankyo Co Ltd Dispiropirolidin derivesi.
ES2624808T3 (es) 2011-05-11 2017-07-17 The Regents Of The University Of Michigan Antagonistas de MDM2 espirooxindólicos
WO2013049250A1 (en) 2011-09-27 2013-04-04 Amgen Inc. Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer
US20140328893A1 (en) 2011-10-11 2014-11-06 Institut National De La Sante Et De La Recherche Medicale (Inserm) Nutlin compounds for use in the treatment of pulmonary hypertension
MX358886B (es) 2011-10-18 2018-08-31 Aileron Therapeutics Inc Macrociclos peptidomimeticos.
EP2771008A4 (de) 2011-10-28 2015-04-08 Merck Sharp & Dohme Makrozyklen zur erhöhung einer p53-aktivität und verwendungen davon
US8969341B2 (en) 2011-11-29 2015-03-03 Novartis Ag Pyrazolopyrrolidine compounds
WO2013096150A1 (en) 2011-12-21 2013-06-27 Merck Sharp & Dohme Corp. Substituted piperidines as hdm2 inhibitors
US8815926B2 (en) 2012-01-26 2014-08-26 Novartis Ag Substituted pyrrolo[3,4-D]imidazoles for the treatment of MDM2/4 mediated diseases
CN107216380A (zh) 2012-02-15 2017-09-29 爱勒让治疗公司 拟肽大环化合物
CN104144695A (zh) 2012-02-15 2014-11-12 爱勒让治疗公司 三唑交联的和硫醚交联的拟肽大环化合物
JP6171003B2 (ja) 2012-05-24 2017-07-26 ノバルティス アーゲー ピロロピロリジノン化合物
TWI586668B (zh) 2012-09-06 2017-06-11 第一三共股份有限公司 二螺吡咯啶衍生物之結晶
JP6526563B2 (ja) 2012-11-01 2019-06-05 エイルロン セラピューティクス,インコーポレイテッド 二置換アミノ酸ならびにその調製および使用の方法
ES2707305T3 (es) 2012-12-20 2019-04-03 Merck Sharp & Dohme Imidazopiridinas sustituidas como inhibidores de HDM2
US9403827B2 (en) 2013-01-22 2016-08-02 Novartis Ag Substituted purinone compounds
WO2014115080A1 (en) 2013-01-22 2014-07-31 Novartis Ag Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction
US9540377B2 (en) 2013-01-30 2017-01-10 Merck Sharp & Dohme Corp. 2,6,7,8 substituted purines as HDM2 inhibitors
US11407721B2 (en) 2013-02-19 2022-08-09 Amgen Inc. CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer
CN105121407B (zh) 2013-02-28 2017-07-18 美国安进公司 用于治疗癌症的苯甲酸衍生物mdm2抑制剂
MX374513B (es) 2013-03-14 2025-03-06 Amgen Inc Compuestos de morfolinona de ácido heteroarilo como inhibidores mdm2 para el tratamiento de cáncer.
WO2014165816A1 (en) 2013-04-05 2014-10-09 North Carolina Central University Compounds useful for the treatment of metabolic disorders and synthesis of the same
US8975417B2 (en) 2013-05-27 2015-03-10 Novartis Ag Pyrazolopyrrolidine derivatives and their use in the treatment of disease
WO2014191894A1 (en) 2013-05-27 2014-12-04 Novartis Ag Imidazopyrrolidinone derivatives and their use in the treatment of disease
EA028175B1 (ru) 2013-05-28 2017-10-31 Новартис Аг Производные пиразолопирролидин-4-она в качестве ингибиторов вет и их применение при лечении заболевания
PL3004112T3 (pl) 2013-05-28 2018-02-28 Novartis Ag Pochodne pirazolo-pirolidyn-4-onu oraz ich zastosowanie w leczeniu choroby
CN104208066B (zh) * 2013-06-03 2016-06-15 中国科学院遗传与发育生物学研究所 哌嗪衍生物作为p53分子调节剂的用途
PE20160113A1 (es) 2013-06-10 2016-03-03 Amgen Inc Procesos de fabricacion y formas cristalinas de un inhibidor de mdm2
KR20160086930A (ko) 2013-11-21 2016-07-20 노파르티스 아게 피롤로피롤론 유도체 및 bet 억제제로서의 그의 용도
AU2015320549A1 (en) 2014-09-24 2017-04-13 Aileron Therapeutics, Inc. Peptidomimetic macrocycles and uses thereof
CN112972378A (zh) 2014-09-24 2021-06-18 艾瑞朗医疗公司 拟肽大环化合物及其制剂
EP3247699B1 (de) 2015-01-22 2019-05-15 Sanofi-Aventis Deutschland GmbH Verfahren zur herstellung von 2-[4-(cyclopropanecarbonyl)phenyl]-2-methyl-propanenitril
KR20170129879A (ko) 2015-03-20 2017-11-27 에일러론 테라퓨틱스 인코포레이티드 펩티드모방 거대고리 및 이의 용도
JP2018528217A (ja) 2015-09-10 2018-09-27 エルロン・セラピューティクス・インコーポレイテッドAileron Therapeutics,Inc. Mcl−1のモジュレーターとしてのペプチド模倣大環状分子
AU2017246453A1 (en) 2016-04-06 2018-11-08 The Regents Of The University Of Michigan Monofunctional intermediates for ligand-dependent target protein degradation
AU2017246452C1 (en) 2016-04-06 2021-06-03 The Regents Of The University Of Michigan MDM2 protein degraders
EP3458101B1 (de) 2016-05-20 2020-12-30 H. Hoffnabb-La Roche Ag Protac-antikörper-konjugate und verfahren zur verwendung
WO2019079677A1 (en) * 2017-10-20 2019-04-25 Corbus Pharmaceuticals, Inc. METHODS AND COMPOSITIONS RELATING TO 5- (1,1-DIMETHYLHEPTYL) -ORRESORCINOL ULTRAPUR
CA3112591A1 (en) 2018-10-08 2020-04-16 The Regents Of The University Of Michigan Small molecule mdm2 protein degraders
MX2022011602A (es) 2020-03-19 2023-01-04 Kymera Therapeutics Inc Degradadores de la proteína de homólogo de ratón de minuto 2 (mdm2) y usos de los mismos.
WO2023056069A1 (en) 2021-09-30 2023-04-06 Angiex, Inc. Degrader-antibody conjugates and methods of using same
US11548866B1 (en) 2021-11-22 2023-01-10 Ligature Therapeutics Pte. Ltd. Therapeutic compounds and methods of use thereof
US11504381B1 (en) * 2021-11-22 2022-11-22 Ligature Therapeutics Pte. Ltd. Therapeutic compounds and methods of use thereof
KR102868976B1 (ko) 2021-12-10 2025-11-03 (주)잇마플 생체이용율과 이미다졸 펩타이드가 증가된 수용성 닭가슴살 가수분해물 및 그 제조방법
WO2024240858A1 (en) 2023-05-23 2024-11-28 Valerio Therapeutics Protac molecules directed against dna damage repair system and uses thereof
CN116903457A (zh) * 2023-07-18 2023-10-20 上海添泽生物医药有限公司 一种2-羟基-5-异丙基苯甲酸的合成方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02101065A (ja) 1988-10-06 1990-04-12 Tanabe Seiyaku Co Ltd イミダゾリン誘導体及びその製法
DE4203547A1 (de) * 1992-02-07 1993-08-12 Knoll Ag Verfahren zur racemattrennung von verapamil
FR2756560A1 (fr) * 1996-12-04 1998-06-05 Adir Nouveaux derives de l'imidazoline, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
GB2351082A (en) 1999-06-18 2000-12-20 Lilly Forschung Gmbh Synthesis of Cyclic Substituted Amidines
US6653501B2 (en) * 2001-06-27 2003-11-25 Napro Biotherapeutics, Inc. Chiral resolution method for producing compounds useful in the synthesis of taxanes
AU2002366278B2 (en) * 2001-12-18 2007-07-19 F. Hoffmann-La Roche Ag CIS-2,4,5- triphenyl-imidazolines and their use in the treatment of tumors
JP4361798B2 (ja) * 2001-12-18 2009-11-11 エフ.ホフマン−ラ ロシュ アーゲー Mdm2インヒビターとしてのシス−イミダゾリン

Also Published As

Publication number Publication date
IL178884A (en) 2010-12-30
EP1753727B1 (de) 2008-11-19
RU2006144811A (ru) 2008-06-27
ZA200609595B (en) 2008-06-25
NO20065730L (no) 2007-01-19
AU2005243465A1 (en) 2005-11-24
JP2007538022A (ja) 2007-12-27
KR20070011516A (ko) 2007-01-24
US20090143364A1 (en) 2009-06-04
CN1953965A (zh) 2007-04-25
AU2005243465B2 (en) 2011-08-25
EP1753727A1 (de) 2007-02-21
MXPA06013246A (es) 2007-02-08
KR20110033964A (ko) 2011-04-01
IL178884A0 (en) 2007-03-08
DE602005011132D1 (de) 2009-01-02
KR100832277B1 (ko) 2008-05-26
JP4814228B2 (ja) 2011-11-16
WO2005110996A1 (en) 2005-11-24
US7964724B2 (en) 2011-06-21
CA2565189A1 (en) 2005-11-24
PE20060679A1 (es) 2006-08-11
US20050288287A1 (en) 2005-12-29
BRPI0511328A (pt) 2007-12-04
KR20080027969A (ko) 2008-03-28
TW200600501A (en) 2006-01-01
CN1953965B (zh) 2012-07-04
ES2314660T3 (es) 2009-03-16
AR049545A1 (es) 2006-08-16
MY143800A (en) 2011-07-15

Similar Documents

Publication Publication Date Title
NL301242I2 (nl) ublituximab
CY2019034I2 (el) 4-φαινυλαμινο-κιναζολιν-6-υλ-αμιδια
NL300881I2 (nl) bezlotoxumab
NO2017018I2 (no) umeklidiniumbromid
NO2017007I1 (no) Eluxadoline
ATE414693T1 (de) Neuartige cis-imidazoline
DE112005001624A5 (de) Brillengestell
ATE520680T1 (de) Hiv-hemmende 5-heterocyclylpyrimidine
ATE392425T1 (de) Thiazolyl-dihydro-indazole
DE602005023008D1 (de) Zugbetriebssteuersystem
ATE459633T1 (de) Makrolide
DE602005026084D1 (de) Tintenstrahlkopfanornung
DE112005000809A5 (de) Wankstabilisierungseinrichtung
DE202004017327U1 (de) Fitnessrad
NO20056129L (no) Spunstonne
DE502005004695D1 (de) Sicherheitsfangseil
NO20055101D0 (no) Sot-rensemiddel
AT500198B8 (de) Ladewagen
DE602005010518D1 (de) Reifenvulkanisierblase
DE112005000794T5 (de) Urethanspritzpistolenanordnung
ATE389633T1 (de) Omega-phenyloctanamide
DE602005020949D1 (de) Elastomerpolyolefinzusammensetzungen
FR2879412B1 (fr) Pedimetre
DE502005003159D1 (de) Kettenstichnähvorrichtung
AT500249A3 (de) Scheibenegge

Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification

Ref document number: 1753727

Country of ref document: EP