MA38654B1 - Dérivés de type promédicament de triazolopyridines substituées - Google Patents

Dérivés de type promédicament de triazolopyridines substituées

Info

Publication number
MA38654B1
MA38654B1 MA38654A MA38654A MA38654B1 MA 38654 B1 MA38654 B1 MA 38654B1 MA 38654 A MA38654 A MA 38654A MA 38654 A MA38654 A MA 38654A MA 38654 B1 MA38654 B1 MA 38654B1
Authority
MA
Morocco
Prior art keywords
derivatives
prodrug type
substituted triazolopyridines
triazolopyridines
substituted
Prior art date
Application number
MA38654A
Other languages
English (en)
Inventor
Gerhard Siemeister
Antje Margret Wengner
Volker Schulze
Philip Lienau
Hans-Georg Lerchen
Ulrich Lücking
Dirk Kosemund
Michael Brüning
Detlef Stöckigt
Donald Bierer
Ursula Krenz
Ildikó Terebesi
Original Assignee
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 Pharma AG filed Critical Bayer Pharma AG
Publication of MA38654B1 publication Critical patent/MA38654B1/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
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06008—Dipeptides with the first amino acid being neutral
    • C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06034—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
    • C07K5/06052—Val-amino acid
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06086—Dipeptides with the first amino acid being basic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Cette invention concerne des dérivés de type promédicament d'inhibiteurs de kinases mps-1, des procédés pour les préparer et leur utilisation pour traiter et/ou prévenir des maladies.
MA38654A 2013-06-11 2014-06-06 Dérivés de type promédicament de triazolopyridines substituées MA38654B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP13171508 2013-06-11
PCT/EP2014/061779 WO2014198647A2 (fr) 2013-06-11 2014-06-06 Dérivés de type promédicament de triazolopyridines substituées

Publications (1)

Publication Number Publication Date
MA38654B1 true MA38654B1 (fr) 2018-11-30

Family

ID=48576905

Family Applications (1)

Application Number Title Priority Date Filing Date
MA38654A MA38654B1 (fr) 2013-06-11 2014-06-06 Dérivés de type promédicament de triazolopyridines substituées

Country Status (35)

Country Link
US (1) US9586958B2 (fr)
EP (1) EP3008062B1 (fr)
JP (1) JP2016526534A (fr)
KR (1) KR20160019492A (fr)
CN (1) CN105377848A (fr)
AP (1) AP2015008898A0 (fr)
AR (1) AR096585A1 (fr)
AU (1) AU2014280356A1 (fr)
CA (1) CA2914745A1 (fr)
CL (1) CL2015003605A1 (fr)
CR (1) CR20150659A (fr)
CU (1) CU20150176A7 (fr)
DK (1) DK3008062T3 (fr)
DO (1) DOP2015000299A (fr)
EA (1) EA201600002A1 (fr)
ES (1) ES2626790T3 (fr)
HK (1) HK1221955A1 (fr)
HR (1) HRP20170717T1 (fr)
HU (1) HUE033131T2 (fr)
IL (1) IL242847A0 (fr)
LT (1) LT3008062T (fr)
MA (1) MA38654B1 (fr)
MX (1) MX2015017119A (fr)
NI (1) NI201500176A (fr)
PE (1) PE20160156A1 (fr)
PH (1) PH12015502746A1 (fr)
PL (1) PL3008062T3 (fr)
PT (1) PT3008062T (fr)
RS (1) RS56034B1 (fr)
SG (1) SG11201509858QA (fr)
SI (1) SI3008062T1 (fr)
TN (1) TN2015000545A1 (fr)
UY (1) UY35610A (fr)
WO (1) WO2014198647A2 (fr)
ZA (1) ZA201508868B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA41136A (fr) * 2014-12-09 2017-10-17 Bayer Pharma AG Composés pour le traitement d'un cancer
FI3283642T3 (fi) 2015-04-17 2024-01-11 Crossfire Oncology Holding B V Prognostisia biomarkkereita ttk-inhibiittorikemoterapiaan
AU2017246228B2 (en) * 2016-04-04 2021-04-15 Chemocentryx, Inc. Soluble C5aR antagonists
AU2022408915A1 (en) * 2021-12-15 2024-06-27 Sillajen, Inc. Methods of treating neoplastic diseases

Family Cites Families (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL127566A0 (en) 1996-08-28 1999-10-28 Pfizer Substituted 6,5-hetero- bicyclic derivatives
DE69828607T2 (de) 1997-05-28 2006-01-05 Aventis Pharmaceuticals Inc. CHINOLIN- UND CHINOXALIN-VERBINDUNGEN DIE DEN VON BLUTPLÄTTCHEN ABSTAMMMENDEN WACHSTUMSFAKTOR UND/ODER PDGF- UND P56lck-TYROSIN-KINASE HEMMEN
US6514989B1 (en) 2001-07-20 2003-02-04 Hoffmann-La Roche Inc. Aromatic and heteroaromatic substituted 1,2,4-triazolo pyridine derivatives
JP2004346016A (ja) 2003-05-22 2004-12-09 Otsuka Chemical Co Ltd トリフルオロメチルキノキサリン化合物、その製造方法、及び有害生物防除剤
AU2004275694B2 (en) 2003-06-30 2008-03-06 Bizbiotech Co., Ltd. Compounds, compositions and methods
WO2006038116A2 (fr) 2004-10-07 2006-04-13 Warner-Lambert Company Llc Agents antibacteriens
WO2007025090A2 (fr) 2005-08-25 2007-03-01 Kalypsys, Inc. Inhibiteurs de kinase mapk/erk
US7723336B2 (en) 2005-09-22 2010-05-25 Bristol-Myers Squibb Company Fused heterocyclic compounds useful as kinase modulators
US20070078136A1 (en) 2005-09-22 2007-04-05 Bristol-Myers Squibb Company Fused heterocyclic compounds useful as kinase modulators
WO2007065010A2 (fr) 2005-12-02 2007-06-07 Hif Bio, Inc. Composes anti-angiogenese
PT2029602E (pt) 2006-05-31 2010-07-08 Galapagos Nv Compostos de triazolopirazina uteis para o tratamento de doenãas degenerativas e inflamatërias
CN101528231A (zh) 2006-08-16 2009-09-09 埃克塞利希斯股份有限公司 在癌症的治疗中使用pi3k和mek调控剂
JP5336375B2 (ja) 2006-08-30 2013-11-06 セルゾーム リミテッド キナーゼ阻害剤としてのトリアゾール誘導体
PE20090288A1 (es) 2007-05-10 2009-04-03 Smithkline Beecham Corp Derivados de quinoxalina como inhibidores de la pi3 quinasa
US8053574B2 (en) 2007-07-18 2011-11-08 Novartis Ag Organic compounds
WO2009021083A1 (fr) 2007-08-09 2009-02-12 Smithkline Beecham Corporation Dérivés des quinoxalines utilisés comme inhibiteurs des pi3-kinases
MX2010002115A (es) 2007-08-23 2010-06-01 Aztrazeneca Ab 2-anilinopurin-8-onas como inhibidores de ttk/mps1 para el tratamiento de trastornos .proliferativos.
CA2691448A1 (fr) 2007-08-31 2009-03-05 Dominique Swinnen Composes de triazolopyridine et leur utilisation comme inhibiteurs de ask
GB0719803D0 (en) 2007-10-10 2007-11-21 Cancer Rec Tech Ltd Therapeutic compounds and their use
MX2010005700A (es) 2007-11-27 2010-06-11 Cellzome Ltd Amino triazoles como inhibidores pi3k.
JP5599783B2 (ja) 2008-05-30 2014-10-01 アムジエン・インコーポレーテツド Ｐｉ３キナーゼの阻害薬
TWI491610B (zh) 2008-10-09 2015-07-11 必治妥美雅史谷比公司 作為激酶抑制劑之咪唑并嗒腈
WO2010092015A1 (fr) 2009-02-10 2010-08-19 Cellzome Limited Dérivés d'urée-triazolo[1,5-a]pyridine en tant qu'inhibiteurs de pi3k
SG173610A1 (en) 2009-02-13 2011-09-29 Fovea Pharmaceuticals Sa [1, 2, 4] triazolo [1, 5 -a] pyridines as kinase inhibitors
CN102413831B (zh) 2009-04-29 2014-06-04 拜耳知识产权有限责任公司 取代的咪唑并喹喔啉
TW201107329A (en) 2009-07-30 2011-03-01 Oncotherapy Science Inc Fused imidazole derivative having ttk inhibitory action
CA2772790C (fr) 2009-09-04 2017-06-27 Benjamin Bader Aminoquinoxalines substituees servant d'inhibiteurs de tyrosine-threonine kinases
EP2343294A1 (fr) 2009-11-30 2011-07-13 Bayer Schering Pharma AG Triazolopyridines substituées
EP2343295A1 (fr) * 2009-11-30 2011-07-13 Bayer Schering Pharma AG Dérivés de triazolopyridine
EP2343297A1 (fr) * 2009-11-30 2011-07-13 Bayer Schering Pharma AG Triazolopyridines
BR112012017310A2 (pt) 2010-01-15 2016-04-19 Janssen Pharmaceuticals Inc derivados de triazol substituídos como moduladores de gama secretase
US20110190269A1 (en) 2010-02-01 2011-08-04 Karlheinz Baumann Gamma secretase modulators
UY33452A (es) * 2010-06-16 2012-01-31 Bayer Schering Pharma Ag Triazolopiridinas sustituidas
TWI541243B (zh) 2010-09-10 2016-07-11 拜耳知識產權公司 經取代咪唑并嗒
HRP20150517T1 (hr) * 2011-04-21 2015-06-19 Bayer Intellectual Property Gmbh Triazolopiridini
UA112096C2 (uk) * 2011-12-12 2016-07-25 Байєр Інтеллектуал Проперті Гмбх Заміщені триазолопіридини та їх застосування як інгібіторів ttk
CN104284896B (zh) 2012-03-14 2016-06-01 拜耳知识产权有限责任公司 取代的咪唑并哒嗪
CA2878481A1 (fr) * 2012-07-10 2014-01-16 Bayer Pharma Aktiengesellschaft Procede de preparation de triazolopyridines substituees
AR096469A1 (es) * 2013-06-06 2015-12-30 Bayer Pharma AG Composiciones farmacéuticas que comprenden compuestos del tipo triazolpiridinas
JP2016527193A (ja) * 2013-06-07 2016-09-08 バイエル・ファルマ・アクティエンゲゼルシャフト 置換トリアゾロピリジン
SG11201509351UA (en) * 2013-06-10 2015-12-30 Bayer Pharma AG Novel compounds for the treatment of cancer
HK1219879A1 (zh) * 2013-06-11 2017-04-21 Bayer Pharma Aktiengesellschaft 用於治疗癌症的包含mps-1激酶抑制剂和有丝分裂抑制剂的组合

Also Published As

Publication number Publication date
NI201500176A (es) 2016-01-06
IL242847A0 (en) 2016-02-01
EA201600002A1 (ru) 2016-06-30
PH12015502746A1 (en) 2016-03-21
WO2014198647A2 (fr) 2014-12-18
AP2015008898A0 (en) 2015-12-31
MX2015017119A (es) 2016-04-06
CN105377848A (zh) 2016-03-02
CU20150176A7 (es) 2016-05-30
TN2015000545A1 (en) 2017-04-06
CL2015003605A1 (es) 2016-06-24
PL3008062T3 (pl) 2017-08-31
EP3008062B1 (fr) 2017-04-05
JP2016526534A (ja) 2016-09-05
UY35610A (es) 2015-01-30
AR096585A1 (es) 2016-01-20
CA2914745A1 (fr) 2014-12-18
AU2014280356A1 (en) 2015-12-24
US20160207915A1 (en) 2016-07-21
HRP20170717T1 (hr) 2017-07-28
WO2014198647A3 (fr) 2015-02-05
EP3008062A2 (fr) 2016-04-20
PT3008062T (pt) 2017-06-07
US9586958B2 (en) 2017-03-07
DOP2015000299A (es) 2016-03-15
DK3008062T3 (en) 2017-06-12
HK1221955A1 (zh) 2017-06-16
SI3008062T1 (sl) 2017-06-30
CR20150659A (es) 2016-01-29
ZA201508868B (en) 2017-08-30
PE20160156A1 (es) 2016-04-20
HUE033131T2 (en) 2017-11-28
LT3008062T (lt) 2017-06-12
SG11201509858QA (en) 2015-12-30
RS56034B1 (sr) 2017-09-29
KR20160019492A (ko) 2016-02-19
ES2626790T3 (es) 2017-07-26

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