CL2014002353A1 - Compuesto 2-[[5-cloro-2-[[(6s)-6-[4-(2-hidroxietil)piperazin-1-il]-1-metoxi-6,7,8,9-tetrahidro-5h-benzo[7]anulen-2-il]amino]pirimidin-4-il]amino]-n-metil-benzamida, inhibidor dual de alk y fak; sales del compuesto; composicion farmaceutica; y metodo de tratamiento de gliobalstoma, cancer de prostata y cancer de mama, entre otros. - Google Patents

Compuesto 2-[[5-cloro-2-[[(6s)-6-[4-(2-hidroxietil)piperazin-1-il]-1-metoxi-6,7,8,9-tetrahidro-5h-benzo[7]anulen-2-il]amino]pirimidin-4-il]amino]-n-metil-benzamida, inhibidor dual de alk y fak; sales del compuesto; composicion farmaceutica; y metodo de tratamiento de gliobalstoma, cancer de prostata y cancer de mama, entre otros.

Info

Publication number
CL2014002353A1
CL2014002353A1 CL2014002353A CL2014002353A CL2014002353A1 CL 2014002353 A1 CL2014002353 A1 CL 2014002353A1 CL 2014002353 A CL2014002353 A CL 2014002353A CL 2014002353 A CL2014002353 A CL 2014002353A CL 2014002353 A1 CL2014002353 A1 CL 2014002353A1
Authority
CL
Chile
Prior art keywords
amino
compound
anulen
gliobalstoma
piperazin
Prior art date
Application number
CL2014002353A
Other languages
English (en)
Spanish (es)
Inventor
P Allwein Shawn
J Jacobs Martin
R Ott Gregory
Courvoisier Laurent
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=CL2014002353(A1) "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 CL2014002353A1 publication Critical patent/CL2014002353A1/es

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)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (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)
CL2014002353A 2012-03-06 2014-09-05 Compuesto 2-[[5-cloro-2-[[(6s)-6-[4-(2-hidroxietil)piperazin-1-il]-1-metoxi-6,7,8,9-tetrahidro-5h-benzo[7]anulen-2-il]amino]pirimidin-4-il]amino]-n-metil-benzamida, inhibidor dual de alk y fak; sales del compuesto; composicion farmaceutica; y metodo de tratamiento de gliobalstoma, cancer de prostata y cancer de mama, entre otros. CL2014002353A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261607305P 2012-03-06 2012-03-06
PCT/US2013/029304 WO2013134353A1 (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
CL2014002353A1 true CL2014002353A1 (es) 2015-01-09

Family

ID=47892060

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2014002353A CL2014002353A1 (es) 2012-03-06 2014-09-05 Compuesto 2-[[5-cloro-2-[[(6s)-6-[4-(2-hidroxietil)piperazin-1-il]-1-metoxi-6,7,8,9-tetrahidro-5h-benzo[7]anulen-2-il]amino]pirimidin-4-il]amino]-n-metil-benzamida, inhibidor dual de alk y fak; sales del compuesto; composicion farmaceutica; y metodo de tratamiento de gliobalstoma, cancer de prostata y cancer de mama, entre otros.

Country Status (28)

Country Link
US (5) US9132128B2 (https=)
EP (2) EP2822939B1 (https=)
JP (2) JP6016953B2 (https=)
KR (1) KR102068374B1 (https=)
CN (2) CN106166155B (https=)
AU (1) AU2013229995B2 (https=)
CA (1) CA2865420C (https=)
CL (1) CL2014002353A1 (https=)
CY (1) CY1117565T1 (https=)
DK (1) DK2822939T3 (https=)
EA (2) EA033124B1 (https=)
ES (2) ES2681487T3 (https=)
HR (1) HRP20160387T1 (https=)
HU (1) HUE027976T2 (https=)
IL (2) IL234239A (https=)
ME (1) ME02460B (https=)
MX (2) MX372740B (https=)
MY (1) MY177290A (https=)
NZ (1) NZ630251A (https=)
PH (1) PH12014501979B1 (https=)
PL (1) PL2822939T3 (https=)
RS (1) RS54689B1 (https=)
SG (2) SG11201405371PA (https=)
SI (1) SI2822939T1 (https=)
SM (1) SMT201600134B (https=)
UA (1) UA115052C2 (https=)
WO (1) WO2013134353A1 (https=)
ZA (1) ZA201406147B (https=)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RS54689B1 (sr) * 2012-03-06 2016-08-31 Cephalon, Inc. Spojeni biciklični 2,4- diaminopirimidin derivat kao dualni alk i fak inhibitor
SG11201608303QA (en) 2014-04-04 2016-11-29 Del Mar Pharmaceuticals Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer
MX2017008430A (es) * 2014-12-23 2018-03-23 Cephalon Inc Métodos para preparar derivados de 2,4-diaminopirimidina bíclica fusionada.
CA3108236A1 (en) 2018-08-07 2020-02-13 In3Bio Ltd. Methods and compositions for inhibition of egf/egfr pathway in combination with anaplastic lymphoma kinase inhibitors
WO2024178339A2 (en) * 2023-02-23 2024-08-29 The Regents Of The University Of Michigan Methods for treating neuroblastoma with a dual anaplastic lymphoma kinase and focal adhesion kinase inhibitor
TW202508595A (zh) 2023-05-04 2025-03-01 美商銳新醫藥公司 用於ras相關疾病或病症之組合療法
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
AU2024360465A1 (en) 2023-10-12 2026-04-09 Revolution Medicines, Inc. Macrocyclic ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
TW202547461A (zh) 2024-05-17 2025-12-16 美商銳新醫藥公司 Ras抑制劑
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors
WO2026072904A2 (en) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions and methods for treating lung cancer

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1648455A4 (en) 2003-07-23 2009-03-04 Exelixis Inc MODULATORS OF ALK PROTEIN (ANAPLASTIC LYMPHOMA KINASE) AND METHODS OF USE
PT1660458E (pt) 2003-08-15 2012-04-27 Novartis Ag 2,4-pirimidinodiaminas úteis no tratamento de doenças neoplásicas, desordens inflamatórias e do sistema imunitário
CN1918158B (zh) * 2004-02-14 2011-03-02 Irm责任有限公司 作为蛋白激酶抑制剂的化合物和组合物
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
ES2622493T3 (es) * 2006-02-24 2017-07-06 Rigel Pharmaceuticals, Inc. Composiciones y métodos para la inhibición de la ruta de JAK
ES2555803T3 (es) 2006-10-23 2016-01-08 Cephalon, Inc. Fusión de derivados bicíclicos 2,4-diaminopirimidina como utilizar inhibidores ALK y c-Met
NZ577197A (en) * 2006-12-08 2011-02-25 Irm Llc Pyrimidine compounds especially 4-phenylamino-2-arylamino-pyrimidine derivatives and compositions as protein kinase inhibitors
CN101678215B (zh) * 2007-04-18 2014-10-01 辉瑞产品公司 用于治疗异常细胞生长的磺酰胺衍生物
ES2575084T3 (es) * 2009-06-10 2016-06-24 Chugai Seiyaku Kabushiki Kaisha Compuesto tetracíclico
RS54689B1 (sr) * 2012-03-06 2016-08-31 Cephalon, Inc. Spojeni biciklični 2,4- diaminopirimidin derivat kao dualni alk i fak inhibitor
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
MX2017008430A (es) * 2014-12-23 2018-03-23 Cephalon Inc Métodos para preparar derivados de 2,4-diaminopirimidina bíclica fusionada.

Also Published As

Publication number Publication date
US9339502B2 (en) 2016-05-17
SG11201405371PA (en) 2014-09-26
WO2013134353A1 (en) 2013-09-12
CN104159894B (zh) 2016-09-07
EP2822939B1 (en) 2016-02-17
AU2013229995A1 (en) 2014-09-25
US20190328735A1 (en) 2019-10-31
JP6016953B2 (ja) 2016-10-26
HRP20160387T1 (hr) 2016-05-20
CN106166155B (zh) 2019-01-18
US10111872B2 (en) 2018-10-30
SI2822939T1 (sl) 2016-04-29
SMT201600134B (it) 2016-07-01
RS54689B1 (sr) 2016-08-31
NZ630251A (en) 2016-02-26
US20150374693A1 (en) 2015-12-31
MX2014010613A (es) 2014-09-18
EP3056494B1 (en) 2018-05-02
EA201691574A1 (ru) 2017-03-31
HUE027976T2 (en) 2016-11-28
CN104159894A (zh) 2014-11-19
EA033124B1 (ru) 2019-08-30
US9132128B2 (en) 2015-09-15
AU2013229995B2 (en) 2017-04-13
DK2822939T3 (en) 2016-03-14
KR102068374B1 (ko) 2020-01-20
IL252364B (en) 2018-03-29
WO2013134353A8 (en) 2014-06-19
ME02460B (me) 2017-02-20
MX372740B (es) 2020-05-04
ES2681487T3 (es) 2018-09-13
ES2570976T3 (es) 2016-05-23
EP3056494A1 (en) 2016-08-17
IL252364A0 (en) 2017-07-31
CY1117565T1 (el) 2017-04-26
US20160243119A1 (en) 2016-08-25
US20170173017A1 (en) 2017-06-22
PH12014501979A1 (en) 2014-11-24
EP2822939A1 (en) 2015-01-14
MX347772B (es) 2017-05-12
PL2822939T3 (pl) 2016-08-31
US20150011561A1 (en) 2015-01-08
HK1226300A1 (zh) 2017-09-29
UA115052C2 (uk) 2017-09-11
JP2017039741A (ja) 2017-02-23
EA025859B1 (ru) 2017-02-28
ZA201406147B (en) 2015-12-23
HK1205119A1 (zh) 2015-12-11
US9623026B2 (en) 2017-04-18
US10632119B2 (en) 2020-04-28
EA201491641A1 (ru) 2015-04-30
MY177290A (en) 2020-09-10
IL234239A (en) 2017-06-29
KR20140138247A (ko) 2014-12-03
CA2865420C (en) 2020-06-02
CN106166155A (zh) 2016-11-30
PH12014501979B1 (en) 2014-11-24
CA2865420A1 (en) 2013-09-12
JP2015509540A (ja) 2015-03-30
SG10201507865QA (en) 2015-10-29

Similar Documents

Publication Publication Date Title
CL2014002353A1 (es) Compuesto 2-[[5-cloro-2-[[(6s)-6-[4-(2-hidroxietil)piperazin-1-il]-1-metoxi-6,7,8,9-tetrahidro-5h-benzo[7]anulen-2-il]amino]pirimidin-4-il]amino]-n-metil-benzamida, inhibidor dual de alk y fak; sales del compuesto; composicion farmaceutica; y metodo de tratamiento de gliobalstoma, cancer de prostata y cancer de mama, entre otros.
UY39630A (es) Inhibidores de bromodominios
MX383590B (es) Inhibidores de kdm1a para el tratamiento de enfermedades.
BR112013002375A2 (pt) composto, composição farmacêutica, métodos de tratar um indivíduo para um distúrbio proliferativo de induzir a apoptose das células cancerígenas, e de inibir a atividade de cinase em um mamífero, e, processo de preparação de composto
NI201800042A (es) Nuevos derivados de pirrolo[2,3-d]pirimidina como inhibidores duales de dyrk1/clk1
CU20120169A7 (es) Compuestos pirimidinílicos como inhibidores de la cinasa atr
PH12017501306A1 (en) Inhibitors of histone demethylases
CU24335B1 (es) Piridopirimidinas sustituidas como inhibidores de la quinasa mek y útiles para el tratamiento del cáncer
CL2014000175A1 (es) Compuesto 4,4,4-trifluoro-n-[(1s)-2-[[(7s)-5-(2-hidroxietil)-6-oxo-7h-pirido[2,3-d][3]benzazepin-7-il]amino]-1-metil-2-oxo-etil]butanamida, inhibidor de la señalizacion de la trayectoria notch; hidrato cristalino del compuesto; composicion farmaceutica; y su uso para el tratamiento de cancer tal como cancer de mama, entre otros.
BR112013029999A2 (pt) derivados de tiazol
UY35369A (es) Inhibidores quinazolínicos de formas mutadas activantes del receptor del factor de crecimiento epidérmico
CR20140187A (es) Compuestos de piperazina alquilados como inhibidores de la actividad btk
EA201391106A1 (ru) Новые гетероциклические производные
MY177344A (en) Compounds and their methods of use
BR112016000561B8 (pt) Compostos terapeuticamente ativos, uso dos mesmos, composição farmacêutica e uso da mesma
EA201490493A1 (ru) Пирано[3,2-d][1,3]тиазол в качестве ингибиторов гликозидазы
AR097455A1 (es) Composición farmacéutica que contiene compuesto de pirimidina como un ingrediente activo
EA201492125A1 (ru) НОВЫЕ 4-(ЗАМЕЩЕННЫЙ АМИНО)-7Н-ПИРРОЛО[2,3-d]ПИРИМИДИНЫ В КАЧЕСТВЕ ИНГИБИТОРОВ LRRK2
EA201490888A1 (ru) Новые производные пурина и их применение для лечения заболевания
CR20140399A (es) Pirrolidina-2-carboxamidas sustituidas
UA112795C2 (uk) Біциклічні піразинонові похідні
MX2014012477A (es) Inhibidores pirrolopirazona de tanquirasa.
EA201400771A1 (ru) Новые производные азетидина, фармацевтические композиции и их применение
UA113215C2 (xx) Похідні проліків (e)-n-метил-n-((3-метилбензофуран-2-іл)метил)-3-(7-оксо-5,6,7,8-тетрагідро-1,8-нафтиридин-3-іл)акриламіду
BR112013019160A2 (pt) novos compostos, composição farmacêutica, uso, processos e métodos