SG178990A1 - Fluoro-substituted 3,5-dicyano-4-(1h-indazol-5-yl)-2,6-dimethyl-1,4-dihydropyridine derivatives and methods of use thereof - Google Patents

Fluoro-substituted 3,5-dicyano-4-(1h-indazol-5-yl)-2,6-dimethyl-1,4-dihydropyridine derivatives and methods of use thereof

Info

Publication number
SG178990A1
SG178990A1 SG2012015400A SG2012015400A SG178990A1 SG 178990 A1 SG178990 A1 SG 178990A1 SG 2012015400 A SG2012015400 A SG 2012015400A SG 2012015400 A SG2012015400 A SG 2012015400A SG 178990 A1 SG178990 A1 SG 178990A1
Authority
SG
Singapore
Prior art keywords
indazol
dicyano
dimethyl
substituted
fluoro
Prior art date
Application number
SG2012015400A
Other languages
English (en)
Inventor
Martin Michels
Markus Follmann
Alexandros Vakalopoulos
Katja Zimmermann
Nicole Teusch
Mario Lobell
Donald Bierer
Karen Engel
Maria Kissel
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 SG178990A1 publication Critical patent/SG178990A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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 two hetero rings
    • C07D401/04Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/4151,2-Diazoles
    • A61K31/4161,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
SG2012015400A 2009-10-06 2010-10-01 Fluoro-substituted 3,5-dicyano-4-(1h-indazol-5-yl)-2,6-dimethyl-1,4-dihydropyridine derivatives and methods of use thereof SG178990A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP09172304 2009-10-06
PCT/EP2010/064648 WO2011042368A1 (en) 2009-10-06 2010-10-01 Fluoro-substituted 3,5-dicyano-4-(1h-indazol-5-yl)-2,6-dimethyl-1,4-dihydropyridine derivatives and methods of use thereof

Publications (1)

Publication Number Publication Date
SG178990A1 true SG178990A1 (en) 2012-04-27

Family

ID=43357944

Family Applications (1)

Application Number Title Priority Date Filing Date
SG2012015400A SG178990A1 (en) 2009-10-06 2010-10-01 Fluoro-substituted 3,5-dicyano-4-(1h-indazol-5-yl)-2,6-dimethyl-1,4-dihydropyridine derivatives and methods of use thereof

Country Status (27)

Country Link
US (1) US9422263B2 (enExample)
EP (1) EP2485726B1 (enExample)
JP (1) JP5753175B2 (enExample)
KR (1) KR20120091005A (enExample)
CN (1) CN102573838B (enExample)
AR (1) AR078486A1 (enExample)
AU (1) AU2010305550A1 (enExample)
BR (1) BR112012006842A2 (enExample)
CA (1) CA2773676C (enExample)
CL (1) CL2012000753A1 (enExample)
CR (1) CR20120150A (enExample)
CU (1) CU20120051A7 (enExample)
DO (1) DOP2012000085A (enExample)
EC (1) ECSP12011748A (enExample)
ES (1) ES2458117T3 (enExample)
IL (1) IL218415A0 (enExample)
IN (1) IN2012DN02675A (enExample)
MX (1) MX2012003603A (enExample)
NZ (1) NZ599006A (enExample)
PE (1) PE20121392A1 (enExample)
PH (1) PH12012500640A1 (enExample)
RU (1) RU2012111695A (enExample)
SG (1) SG178990A1 (enExample)
TW (1) TW201124396A (enExample)
UY (1) UY32922A (enExample)
WO (1) WO2011042368A1 (enExample)
ZA (1) ZA201201524B (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0650179Y2 (ja) 1989-06-01 1994-12-21 株式会社プラコー ブロー成形機用のダイヘッド
JPH0756186Y2 (ja) 1989-07-24 1995-12-25 株式会社日本製鋼所 パリソンの押出成形装置
JP2781376B2 (ja) 1996-06-17 1998-07-30 エクセル株式会社 中空成形品
DE102009056886A1 (de) * 2009-12-03 2011-06-09 Bayer Schering Pharma Aktiengesellschaft cMet-Inhibitoren zur Behandlung der Endometriose
HUE070387T2 (hu) 2019-02-11 2025-06-28 Merck Patent Gmbh Indazolil-izoxazol származékok betegségek, mint például rák kezelésére

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3635977A (en) 1969-11-03 1972-01-18 American Cyanamid Co Certain 6-trifluoromethylcytosines and thiocytosines their synthesis and their use in the synthesis of uracisls and thiouracil
ATE126207T1 (de) 1989-01-26 1995-08-15 Bayer Ag Optisch aktive (meth)acrylsäure-derivate, ihre herstellung, ihre polymerisation zu optisch aktiven polymeren und deren verwendung.
DE19546136A1 (de) 1995-12-11 1997-06-12 Bayer Ag Chirale stationäre Phasen für die chromatographische Trennung von optischen Isomeren
TW200406385A (en) 2002-05-31 2004-05-01 Eisai Co Ltd Pyrazole compound and pharmaceutical composition containing the same
WO2005085227A1 (en) 2004-03-02 2005-09-15 Smithkline Beecham Corporation Inhibitors of akt activity
WO2005084672A1 (de) 2004-03-03 2005-09-15 Boehringer Ingelheim International Gmbh Ausgewählte cgrp-antagonisten, verfahren zu deren herstellung sowie deren verwendung als arzneimittel
EP1828135A4 (en) 2004-12-13 2009-08-12 Irm Llc COMPOUNDS AND COMPOSITIONS AS MODULATORS OF STEROIDAL RECEPTORS AND CALCIUM CHANNEL ACTIVITIES
EP1858325A4 (en) 2005-01-07 2010-06-30 Roskamp Res Llc COMPOUNDS FOR INHIBITING BETA-AMYLOID PRODUCTION AND METHODS FOR IDENTIFYING THESE COMPOUNDS
EP1855664A4 (en) * 2005-01-19 2009-12-23 Merck & Co Inc INHIBITORS OF MITOTIC KINESINE
ES2396160T3 (es) * 2006-12-14 2013-02-19 Bayer Intellectual Property Gmbh Derivados de DIHIDROPIRIDINA que utiliza como inhibidores de la proteina quinasa

Also Published As

Publication number Publication date
UY32922A (es) 2011-04-29
BR112012006842A2 (pt) 2016-06-07
ZA201201524B (en) 2013-05-29
CA2773676A1 (en) 2011-04-14
MX2012003603A (es) 2012-04-20
CR20120150A (es) 2012-08-03
CA2773676C (en) 2017-07-04
NZ599006A (en) 2013-11-29
ECSP12011748A (es) 2012-05-30
PH12012500640A1 (en) 2012-11-12
PE20121392A1 (es) 2012-10-14
HK1172835A1 (en) 2013-05-03
DOP2012000085A (es) 2012-07-15
US20120264785A1 (en) 2012-10-18
CL2012000753A1 (es) 2012-09-14
RU2012111695A (ru) 2013-10-10
CN102573838A (zh) 2012-07-11
IL218415A0 (en) 2012-04-30
TW201124396A (en) 2011-07-16
US9422263B2 (en) 2016-08-23
KR20120091005A (ko) 2012-08-17
ES2458117T3 (es) 2014-04-30
WO2011042368A1 (en) 2011-04-14
JP5753175B2 (ja) 2015-07-22
JP2013506699A (ja) 2013-02-28
CU20120051A7 (es) 2012-06-29
EP2485726A1 (en) 2012-08-15
AR078486A1 (es) 2011-11-09
AU2010305550A1 (en) 2012-03-29
EP2485726B1 (en) 2014-03-12
IN2012DN02675A (enExample) 2015-09-04
CN102573838B (zh) 2014-09-24

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