MA35016B1 - Imidazopyridazines en gtant qu'inhibiteurs de la kinase akt - Google Patents

Imidazopyridazines en gtant qu'inhibiteurs de la kinase akt

Info

Publication number
MA35016B1
MA35016B1 MA36290A MA36290A MA35016B1 MA 35016 B1 MA35016 B1 MA 35016B1 MA 36290 A MA36290 A MA 36290A MA 36290 A MA36290 A MA 36290A MA 35016 B1 MA35016 B1 MA 35016B1
Authority
MA
Morocco
Prior art keywords
imidazopyridazines
akt inhibitors
kinase akt
kinase
inhibitors
Prior art date
Application number
MA36290A
Other languages
English (en)
Inventor
Lars Bärfacker
William Johnston Scott
Andrea Hägebarth
Stuart Ince
Hartmut Rehwinkel
Oliver Politz
Roland Neuhaus
Hans Briem
Ulf Bömer
Original Assignee
Bayer Ip Gmbh
Bayer Pharma AG
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 Bayer Ip Gmbh, Bayer Pharma AG filed Critical Bayer Ip Gmbh
Publication of MA35016B1 publication Critical patent/MA35016B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/14—Drugs for genital or sexual disorders; Contraceptives for lactation disorders, e.g. galactorrhoea
    • 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

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Endocrinology (AREA)
  • Pregnancy & Childbirth (AREA)
  • Reproductive Health (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Cosmetics (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

L'invention concerne des imidazopyridazines de la formule (I) et un procédé pour leur fabrication et leur utilisation.
MA36290A 2011-04-07 2012-04-05 Imidazopyridazines en gtant qu'inhibiteurs de la kinase akt MA35016B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161472732P 2011-04-07 2011-04-07
PCT/EP2012/056300 WO2012136776A1 (fr) 2011-04-07 2012-04-05 Imidazopyridazines en tant qu'inhibiteurs de la kinase akt

Publications (1)

Publication Number Publication Date
MA35016B1 true MA35016B1 (fr) 2014-04-03

Family

ID=45953129

Family Applications (1)

Application Number Title Priority Date Filing Date
MA36290A MA35016B1 (fr) 2011-04-07 2012-04-05 Imidazopyridazines en gtant qu'inhibiteurs de la kinase akt

Country Status (43)

Country Link
US (2) US9206185B2 (fr)
EP (1) EP2694510B1 (fr)
JP (1) JP5906303B2 (fr)
KR (1) KR20140022057A (fr)
CN (1) CN103596957B (fr)
AP (1) AP3597A (fr)
AR (1) AR087148A1 (fr)
AU (1) AU2012238589B2 (fr)
BR (1) BR112013025777A2 (fr)
CA (1) CA2832374A1 (fr)
CL (1) CL2013002878A1 (fr)
CO (1) CO6862145A2 (fr)
CR (1) CR20130515A (fr)
CU (1) CU24263B1 (fr)
CY (1) CY1117163T1 (fr)
DK (1) DK2694510T3 (fr)
DO (1) DOP2013000226A (fr)
EA (1) EA024890B1 (fr)
EC (1) ECSP13013008A (fr)
ES (1) ES2558780T3 (fr)
GT (1) GT201300238A (fr)
HR (1) HRP20160011T1 (fr)
HU (1) HUE026323T2 (fr)
IL (1) IL228567A0 (fr)
JO (1) JO3068B1 (fr)
MA (1) MA35016B1 (fr)
ME (1) ME02316B (fr)
MX (1) MX336865B (fr)
NI (1) NI201300105A (fr)
PE (1) PE20141380A1 (fr)
PH (1) PH12013502073A1 (fr)
PL (1) PL2694510T3 (fr)
PT (1) PT2694510E (fr)
RS (1) RS54480B1 (fr)
SG (1) SG193631A1 (fr)
SI (1) SI2694510T1 (fr)
SM (1) SMT201600001B (fr)
TN (1) TN2013000400A1 (fr)
TW (1) TWI535719B (fr)
UA (1) UA111739C2 (fr)
UY (1) UY34006A (fr)
WO (1) WO2012136776A1 (fr)
ZA (1) ZA201307223B (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9447049B2 (en) 2010-03-01 2016-09-20 University Of Tennessee Research Foundation Compounds for treatment of cancer
US9029408B2 (en) 2008-06-16 2015-05-12 Gtx, Inc. Compounds for treatment of cancer
DK2303021T3 (en) 2008-06-16 2019-04-08 Univ Tennessee Res Found RELATIONSHIPS FOR TREATING CANCER
US11084811B2 (en) 2010-03-01 2021-08-10 Oncternal Therapeutics, Inc. Compounds for treatment of cancer
KR101939704B1 (ko) 2010-03-01 2019-01-17 지티엑스, 인코포레이티드 암 치료용 화합물
EA024890B1 (ru) * 2011-04-07 2016-10-31 Байер Интеллектчуал Проперти Гмбх Имидазопиридазины в качестве ингибиторов akt киназы
WO2013104610A1 (fr) * 2012-01-10 2013-07-18 Bayer Intellectual Property Gmbh Imidazopyrazines substituées utilisées comme inhibiteurs de l'akt kinase
CN104066736B (zh) * 2012-01-10 2017-03-08 拜耳知识产权有限责任公司 作为akt激酶抑制剂的取代的吡唑并嘧啶
MA38121A1 (fr) * 2012-11-30 2016-10-31 Glaxosmithkline Llc Nouvelle composition pharmaceutique
CN105163584B (zh) * 2013-03-05 2019-06-04 田纳西大学研究基金会 用于治疗癌症的化合物
WO2014158467A1 (fr) * 2013-03-12 2014-10-02 Glaxosmithkline Llc Combinaison
JP2016517434A (ja) * 2013-03-14 2016-06-16 エピザイム，インコーポレイティド 癌を処置するための併用療法
US10214545B2 (en) * 2014-01-09 2019-02-26 Bayer Pharma Aktiengesellschaft Amido-substituted imidazopyridazines useful in the treatment of hyper-proliferative and/or angiogenesis disorders
CN110225912B (zh) * 2016-11-28 2022-10-21 百时美施贵宝公司 Gsk-3抑制剂
EP3453706A1 (fr) 2017-09-08 2019-03-13 Basf Se Composés pesticides de l'imizazole
GB2600384A (en) 2020-09-30 2022-05-04 Vaderis Therapeutics Ag Allosteric AKT inhibitors for use in the treatment of hereditary hemorrhagic telangiectasia

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6649629B2 (en) 1999-12-23 2003-11-18 Nitromed, Inc. Nitrosated and nitrosylated cyclooxygenase-2 inhibitors, compositions and methods of use
EP1268478B1 (fr) 2000-03-31 2007-05-02 Ortho-McNeil Pharmaceutical, Inc. Imidazopyridines phenyle-substituees
AU2001252609A1 (en) 2000-04-27 2001-11-12 Imperial Cancer Research Technology Ltd. Imidazopyridine derivatives
KR20050122210A (ko) 2003-03-17 2005-12-28 다케다 샌디에고, 인코포레이티드 히스톤 탈아세틸화 효소 억제제
WO2004096131A2 (fr) 2003-04-24 2004-11-11 Merck & Co., Inc. Inhibiteurs de l'activite akt
WO2005014598A1 (fr) 2003-07-30 2005-02-17 Laboratorios S.A.L.V.A.T., S.A. Imidazopyrimidines substituees pour la prevention et le traitement du cancer
EP1737843B1 (fr) 2004-04-09 2011-02-23 Merck Sharp & Dohme Corp. Inhibiteurs de l'activite d'akt
AU2005290081B2 (en) 2004-08-23 2010-12-02 Merck Sharp & Dohme Corp. Inhibitors of Akt activity
JP2008510741A (ja) 2004-08-24 2008-04-10 ビーエーエスエフ ソシエタス・ヨーロピア イオン液体を製造するための出発化合物としてのイミダゾリウム−メチルスルファイト
WO2006065601A2 (fr) 2004-12-15 2006-06-22 Merck & Co., Inc. Inhibiteurs d'activite akt
RU2007147382A (ru) 2005-05-20 2009-06-27 Эррэй Биофарма Инк. (Us) Соединения, являющиеся ингибиторами raf, и способы их применения
AU2006258124B8 (en) 2005-06-10 2010-01-07 Merck Sharp & Dohme Corp. Inhibitors of Akt activity
US20070049591A1 (en) 2005-08-25 2007-03-01 Kalypsys, Inc. Inhibitors of MAPK/Erk Kinase
PE20070978A1 (es) 2006-02-14 2007-11-15 Novartis Ag COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks)
US7530313B2 (en) 2006-05-12 2009-05-12 Day & Zimmerman, Inc. Self-destruct fuze delay mechanism
AR064010A1 (es) 2006-12-06 2009-03-04 Merck & Co Inc Inhibidores de la actividad de la akt
BRPI0811065A2 (pt) * 2007-06-08 2014-12-02 Abbott Lab Indazóis 5-heteroaril substituídos como inibidores de quinase
UY31293A1 (es) 2007-08-14 2009-03-31 Pirimidinas biciclicas fusionadas
DE602008005894D1 (de) * 2007-08-14 2011-05-12 Bayer Schering Pharma Ag Kondensierte imidazole zur krebsbehandlung
WO2009086130A1 (fr) 2007-12-21 2009-07-09 Wyeth Composés d'imidazo-[1,2-b]-pyridazine comme modulateurs des récepteurs x du foie
AU2009255358A1 (en) 2008-06-03 2009-12-10 Msd K.K. Inhibitors of Akt activity
CA2726358A1 (fr) 2008-06-03 2009-12-10 Merck Sharp & Dohme Corp. Inhibiteurs de l'activite akt
AR074072A1 (es) 2008-11-11 2010-12-22 Lilly Co Eli Compuesto de imidazol -piperidin -pirrol-pirimidin-6-ona, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para tratar el glioblastoma multiforme
PA8854101A1 (es) 2008-12-18 2010-07-27 Ortho Mcneil Janssen Pharm Derivados de imidazol bicíclicos sustituidos como moduladores de gamma secretasa
WO2010088177A1 (fr) 2009-02-02 2010-08-05 Merck Sharp & Dohme Corp. Inhibiteurs de l'activité d'akt
KR20110114663A (ko) * 2009-02-13 2011-10-19 바이엘 파마 악티엔게젤샤프트 융합된 피리미딘
WO2010104933A1 (fr) 2009-03-11 2010-09-16 Merck Sharp & Dohme Corp. Inhibiteurs de l'activité akt
WO2010114780A1 (fr) * 2009-04-01 2010-10-07 Merck Sharp & Dohme Corp. Inhibiteurs de l'activité akt
AR076936A1 (es) 2009-06-02 2011-07-20 Vitae Pharmaceuticals Inc Inhibidores de carbamato y urea de la 11 beta hidroxiesteroide deshidrogenasa 1
EP2473495A1 (fr) 2009-09-18 2012-07-11 Almac Discovery Limited Composés pharmaceutiques
JP5830094B2 (ja) * 2010-07-12 2015-12-09 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ 置換イミダゾ［１，２−ａ］ピリミジンおよび−ピリジン
ES2539257T3 (es) * 2010-07-28 2015-06-29 Bayer Intellectual Property Gmbh Imidazo[1,2-b]piridazinas sustituidas
EA024890B1 (ru) * 2011-04-07 2016-10-31 Байер Интеллектчуал Проперти Гмбх Имидазопиридазины в качестве ингибиторов akt киназы

Also Published As

Publication number Publication date
WO2012136776A1 (fr) 2012-10-11
UA111739C2 (uk) 2016-06-10
HUE026323T2 (en) 2016-05-30
CN103596957A (zh) 2014-02-19
TN2013000400A1 (en) 2015-03-30
TWI535719B (zh) 2016-06-01
EA201301130A1 (ru) 2014-07-30
US9604989B2 (en) 2017-03-28
NI201300105A (es) 2014-07-14
US9206185B2 (en) 2015-12-08
ES2558780T3 (es) 2016-02-08
IL228567A0 (en) 2013-12-31
EP2694510A1 (fr) 2014-02-12
AU2012238589B2 (en) 2017-02-16
CL2013002878A1 (es) 2014-05-02
MX2013011699A (es) 2014-01-31
CR20130515A (es) 2013-12-04
RS54480B1 (sr) 2016-06-30
AR087148A1 (es) 2014-02-26
ZA201307223B (en) 2014-12-23
SG193631A1 (en) 2013-11-29
AP3597A (en) 2016-02-19
US20150368250A1 (en) 2015-12-24
CA2832374A1 (fr) 2012-10-11
KR20140022057A (ko) 2014-02-21
PH12013502073A1 (en) 2014-01-13
SMT201600001B (it) 2016-02-25
ME02316B (me) 2016-06-20
PT2694510E (pt) 2016-02-08
HRP20160011T1 (hr) 2016-02-12
AP2013007215A0 (en) 2013-10-31
CN103596957B (zh) 2016-12-07
JO3068B1 (ar) 2017-03-15
CY1117163T1 (el) 2017-04-05
ECSP13013008A (es) 2013-12-31
DK2694510T3 (en) 2016-01-18
US20140113901A1 (en) 2014-04-24
AU2012238589A1 (en) 2013-11-07
BR112013025777A2 (pt) 2016-12-20
JP2014510127A (ja) 2014-04-24
JP5906303B2 (ja) 2016-04-20
MX336865B (es) 2016-02-04
TW201245204A (en) 2012-11-16
CU20130135A7 (es) 2014-02-28
CO6862145A2 (es) 2014-02-10
SI2694510T1 (sl) 2016-02-29
UY34006A (es) 2012-10-31
DOP2013000226A (es) 2013-11-15
EA024890B1 (ru) 2016-10-31
PE20141380A1 (es) 2014-10-18
GT201300238A (es) 2015-04-06
CU24263B1 (es) 2017-07-04
NZ616270A (en) 2015-09-25
EP2694510B1 (fr) 2015-10-14
PL2694510T3 (pl) 2016-03-31

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