CY1117565T1 - Συνενωμενο δικυκλικο παραγωγο 2,4-διαμινοπυριδινης ως διπλος αναστολεας alk και fak - Google Patents

Συνενωμενο δικυκλικο παραγωγο 2,4-διαμινοπυριδινης ως διπλος αναστολεας alk και fak

Info

Publication number
CY1117565T1
CY1117565T1 CY20161100390T CY161100390T CY1117565T1 CY 1117565 T1 CY1117565 T1 CY 1117565T1 CY 20161100390 T CY20161100390 T CY 20161100390T CY 161100390 T CY161100390 T CY 161100390T CY 1117565 T1 CY1117565 T1 CY 1117565T1
Authority
CY
Cyprus
Prior art keywords
alk
fak
diaminopyridine
producer
double
Prior art date
Application number
CY20161100390T
Other languages
English (en)
Inventor
Martin J Jacobs
Gregory R Ott
Laurent Courvoisier
Shawn P Allwein
Original Assignee
Cephalon, Inc.
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=47892060&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CY1117565(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Cephalon, Inc. filed Critical Cephalon, Inc.
Publication of CY1117565T1 publication Critical patent/CY1117565T1/el

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D403/12Heterocyclic 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 chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicinal Preparation (AREA)
  • Saccharide Compounds (AREA)

Abstract

Η παρούσα εφεύρεση παρέχει μία ένωση τύπου (I) ή μία μορφή άλατος αυτής. Η ένωση τύπου (I) έχει δράση αναστολέα ALK και FAK και μπορεί να χρησιμοποιηθεί για αγωγή πολλαπλασιαστικών διαταραχών.
CY20161100390T 2012-03-06 2016-05-10 Συνενωμενο δικυκλικο παραγωγο 2,4-διαμινοπυριδινης ως διπλος αναστολεας alk και fak CY1117565T1 (el)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261607305P 2012-03-06 2012-03-06
EP13710258.8A EP2822939B1 (en) 2012-03-06 2013-03-06 Fused bicyclic 2,4-diaminopyrimidine derivative as a dual alk and fak inhibitor

Publications (1)

Publication Number Publication Date
CY1117565T1 true CY1117565T1 (el) 2017-04-26

Family

ID=47892060

Family Applications (1)

Application Number Title Priority Date Filing Date
CY20161100390T CY1117565T1 (el) 2012-03-06 2016-05-10 Συνενωμενο δικυκλικο παραγωγο 2,4-διαμινοπυριδινης ως διπλος αναστολεας alk και fak

Country Status (29)

Country Link
US (5) US9132128B2 (el)
EP (2) EP3056494B1 (el)
JP (2) JP6016953B2 (el)
KR (1) KR102068374B1 (el)
CN (2) CN104159894B (el)
AU (1) AU2013229995B2 (el)
CA (1) CA2865420C (el)
CL (1) CL2014002353A1 (el)
CY (1) CY1117565T1 (el)
DK (1) DK2822939T3 (el)
EA (2) EA025859B1 (el)
ES (2) ES2570976T3 (el)
HK (2) HK1205119A1 (el)
HR (1) HRP20160387T1 (el)
HU (1) HUE027976T2 (el)
IL (2) IL234239A (el)
ME (1) ME02460B (el)
MX (1) MX347772B (el)
MY (1) MY177290A (el)
NZ (1) NZ630251A (el)
PH (1) PH12014501979A1 (el)
PL (1) PL2822939T3 (el)
RS (1) RS54689B1 (el)
SG (2) SG10201507865QA (el)
SI (1) SI2822939T1 (el)
SM (1) SMT201600134B (el)
UA (1) UA115052C2 (el)
WO (1) WO2013134353A1 (el)
ZA (1) ZA201406147B (el)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL2822939T3 (pl) * 2012-03-06 2016-08-31 Cephalon Inc Skondensowane bicykliczne pochodne 2,4-diaminopirymidyny jako podwójne inhibitory ALK i FAK
CN106659765B (zh) 2014-04-04 2021-08-13 德玛医药 二脱水半乳糖醇及其类似物或衍生物用于治疗非小细胞肺癌和卵巢癌的用途
JP6849594B2 (ja) * 2014-12-23 2021-03-24 セファロン、インク. 縮合二環式2,4−ジアミノピリミジン誘導体を調整する方法
JP2021534094A (ja) 2018-08-07 2021-12-09 イン3バイオ・リミテッドIn3Bio Ltd. 未分化リンパ腫キナーゼ阻害剤と組み合わせてegf/egfr経路を抑制するための方法および組成物

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005009389A2 (en) 2003-07-23 2005-02-03 Exelixis, Inc. Anaplastic lymphoma kinase modulators and methods of use
PL2287156T3 (pl) 2003-08-15 2013-11-29 Novartis Ag 2,4-Di(fenyloamino)-pirymidyny stosowane w leczeniu chorób nowotworowych, chorób zapalnych i zaburzeń układu immunologicznego
CA2553785C (en) 2004-02-14 2011-02-08 Irm Llc Compounds and compositions as protein kinase inhibitors
JP2008502595A (ja) 2004-03-31 2008-01-31 エグゼリクシス, インコーポレイテッド 未分化リンパ腫キナーゼモジュレータおよびその使用方法
JP2009528295A (ja) * 2006-02-24 2009-08-06 ライジェル ファーマシューティカルズ, インコーポレイテッド Jak経路の阻害のための組成物および方法
MX2009004426A (es) 2006-10-23 2009-08-12 Cephalon Inc Derivados biciclicos fusionados de 2,4-diaminopirimidina como inhibidores alk y c-met.
EP2311807B1 (en) * 2006-12-08 2015-11-11 Novartis AG Compounds and composition as protein kinase inhibitors
GEP20125581B (en) * 2007-04-18 2012-07-25 Pfizer Prod Inc Sulfonyl amide derivatives for treatment of abnormal cell growth
HUE039167T2 (hu) * 2009-06-10 2018-12-28 Chugai Pharmaceutical Co Ltd Tetraciklikus vegyületek
PL2822939T3 (pl) * 2012-03-06 2016-08-31 Cephalon Inc Skondensowane bicykliczne pochodne 2,4-diaminopirymidyny jako podwójne inhibitory ALK i FAK
KR101446742B1 (ko) * 2012-08-10 2014-10-01 한국화학연구원 N2,n4-비스(4-(피페라진-1-일)페닐)피리미딘-2,4-디아민 유도체 또는 이의 약학적으로 허용가능한 염 및 이를 유효성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물
JP6849594B2 (ja) * 2014-12-23 2021-03-24 セファロン、インク. 縮合二環式2,4−ジアミノピリミジン誘導体を調整する方法

Also Published As

Publication number Publication date
EP2822939A1 (en) 2015-01-14
CN106166155B (zh) 2019-01-18
US20150011561A1 (en) 2015-01-08
SG11201405371PA (en) 2014-09-26
US20190328735A1 (en) 2019-10-31
KR102068374B1 (ko) 2020-01-20
US20150374693A1 (en) 2015-12-31
HK1205119A1 (zh) 2015-12-11
AU2013229995A1 (en) 2014-09-25
SMT201600134B (it) 2016-07-01
EP2822939B1 (en) 2016-02-17
CA2865420A1 (en) 2013-09-12
IL234239A (en) 2017-06-29
MX347772B (es) 2017-05-12
CN106166155A (zh) 2016-11-30
MY177290A (en) 2020-09-10
PH12014501979B1 (en) 2014-11-24
EA025859B1 (ru) 2017-02-28
US9623026B2 (en) 2017-04-18
SG10201507865QA (en) 2015-10-29
CN104159894A (zh) 2014-11-19
RS54689B1 (en) 2016-08-31
EA033124B1 (ru) 2019-08-30
IL252364A0 (en) 2017-07-31
NZ630251A (en) 2016-02-26
US20170173017A1 (en) 2017-06-22
WO2013134353A1 (en) 2013-09-12
PH12014501979A1 (en) 2014-11-24
EP3056494A1 (en) 2016-08-17
CN104159894B (zh) 2016-09-07
DK2822939T3 (en) 2016-03-14
EP3056494B1 (en) 2018-05-02
HRP20160387T1 (hr) 2016-05-20
JP2017039741A (ja) 2017-02-23
HUE027976T2 (en) 2016-11-28
MX2014010613A (es) 2014-09-18
PL2822939T3 (pl) 2016-08-31
CA2865420C (en) 2020-06-02
US20160243119A1 (en) 2016-08-25
HK1226300A1 (zh) 2017-09-29
EA201691574A1 (ru) 2017-03-31
ME02460B (me) 2017-02-20
SI2822939T1 (sl) 2016-04-29
JP6016953B2 (ja) 2016-10-26
US10632119B2 (en) 2020-04-28
US9132128B2 (en) 2015-09-15
CL2014002353A1 (es) 2015-01-09
US9339502B2 (en) 2016-05-17
KR20140138247A (ko) 2014-12-03
UA115052C2 (uk) 2017-09-11
IL252364B (en) 2018-03-29
WO2013134353A8 (en) 2014-06-19
AU2013229995B2 (en) 2017-04-13
ZA201406147B (en) 2015-12-23
ES2570976T3 (es) 2016-05-23
ES2681487T3 (es) 2018-09-13
US10111872B2 (en) 2018-10-30
JP2015509540A (ja) 2015-03-30
EA201491641A1 (ru) 2015-04-30

Similar Documents

Publication Publication Date Title
CR20150078A (es) Análogos de piridazina 1,4-disustituida y métodos para el tratamiento de condiciones relacionadas con la deficiencia de smn
PH12016500676A1 (en) Pyrimidine fgfr4 inhibitors
MY202022A (en) Pyrrolotriazine compounds as tam inhibitors
CR20150472A (es) USO DE DERIVADOS DE PIRAZOLOPIRIMIDINA PARA EL TRATAMIENTO DE TRANSTORNOS RELACIONADOS CON LA PI3Kd
EA201591455A1 (ru) Производные бензимидазолона в качестве ингибиторов бромодомена
EA201391390A1 (ru) Циклопропиламины в качестве ингибиторов lsd
EA201590224A1 (ru) Имидазотриазинкарбонитрилы, используемые в качестве ингибиторов киназы
CR20140468A (es) Inhibidores de diacilglicerol aciltransferasa 2
UA110338C2 (en) Chemical compounds
EA201401054A1 (ru) N-циклиламиды в качестве нематоцидов
NZ710444A (en) Compositions and methods for treating neurodegenerative diseases and cardiomyopathy
MX2016002794A (es) Compuestos antiproliferativos.
CR20130539A (es) Triazolopiridinas
EA201591360A1 (ru) Азабензимидазолы в качестве ингибиторов изозимов фдэ4 для лечения цнс и других расстройств
BR112016024533A2 (pt) derivados de amino pirazina como inibidores de fosfatidilinositol 3-cinase
EA201690844A1 (ru) Ингибиторы gsk-3
EA201590787A1 (ru) Замещенные пиридопиразины в качестве ингибиторов syk
PH12016500347A1 (en) Triazolopyridine compounds, compositions and methods of use thereof
EA201590250A1 (ru) Производные карбамат/мочевины
MX2015016332A (es) Inhibidores de alk biciclicos fusionados.
CY1117565T1 (el) Συνενωμενο δικυκλικο παραγωγο 2,4-διαμινοπυριδινης ως διπλος αναστολεας alk και fak
EA201491227A1 (ru) Новые производные морфолинила, подходящие для применения в качестве ингибиторов mogat-2
EA201591259A1 (ru) Твёрдые формы производного хиназолина и их применение в качестве ингибитора braf
DOP2019000021A (es) Derivado de triazolopirazinona útil como un inhibidor de pde1 humana
EA201590656A1 (ru) Азаиндолины