TR201807411T4 - DNA-PK inhibitörleri. - Google Patents

DNA-PK inhibitörleri. Download PDF

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Publication number
TR201807411T4
TR201807411T4 TR2018/07411T TR201807411T TR201807411T4 TR 201807411 T4 TR201807411 T4 TR 201807411T4 TR 2018/07411 T TR2018/07411 T TR 2018/07411T TR 201807411 T TR201807411 T TR 201807411T TR 201807411 T4 TR201807411 T4 TR 201807411T4
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TR
Turkey
Prior art keywords
pharmaceutically acceptable
compound
acceptable salt
cancer
pharmaceutical composition
Prior art date
Application number
TR2018/07411T
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English (en)
Inventor
Paul Charifson S
Kevin Cottrell Michael
Deng Hongbo
John Duffy P
Gao Huai
Giroux Simon
Green Jeremy
Katrina Jackson Lee
Joseph Kennedy M
David Lauffer J
Mark Ledeboer Willem
Li Pan
John Maxwell Patrick
Mark Morris A
Albert Pierce Charles
Nathan Waal D
Xu Jinwang
Original Assignee
Vertex Pharma
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
Priority claimed from US14/056,560 external-priority patent/US9376448B2/en
Application filed by Vertex Pharma filed Critical Vertex Pharma
Publication of TR201807411T4 publication Critical patent/TR201807411T4/tr

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    • 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
    • C07D401/14Heterocyclic 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 three or more hetero 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
    • 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
    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems

Abstract

Mevcut buluş, DNA-PK'nin inhibitörleri olarak faydalı olan bileşikler ile ilgilidir. Buluş aynı zamanda söz konusu bileşikleri içeren farmasötik olarak kabul edilebilir bileşimleri ve çeşitli hastalıkların, durumların ve bozuklukların tedavisinde bileşimlerin kullanılmasına yönelik yöntemleri sağlar.

Claims (4)

ISTEMLER
1. Bir bilesik olup, özelligi bilesigin asagidakilerden olusan gruptan: ve bunun farmasötik olarak kabul edilebilir tuzundan seçilmesidir.
2. Istem 1'e göre bir bilesik olup, özelligi bilesigin asagidaki gibi veya bunun farmasötik olarak kabul edilebilir bir tuzu olmasidir.
3. istem 1`e göre bir bilesik olup, özelligi bilesigin asagidaki gibi 10 veya bunun farmasötik olarak kabul edilebilir bir tuzu olmasidir.
4. Istem 1'e göre bir bilesik olup, özelligi bilesigin asagidaki gibi veya bunun farmasötik olarak kabul edilebilir bir tuzu olmasidir. istem 1`e göre bir bilesik olup, özelligi bilesigin asagidaki gibi veya bunun farmasötik olarak kabul edilebilir bir tuzu olmasidir. Farmasötik bir bilesim olup, özelligi istemler 1-5'ten herhangi birine göre bir bilesik veya bunun farmasötik olarak kabul edilebilir bir tuzunu ve farmasötik olarak kabul edilebilir bir eksipiyani içermesidir. Istemler 1-5'ten herhangi birine göre bir bilesik veya bunun farmasötik olarak kabul edilebilir bir tuzu veya farmasötik bir bilesimi olup, özelligi bir hücrenin bir DNA lezyonunu indükleyen bir ajana karsi duyarli hale getirilmesinde kullanima yönelik söz konusu bilesigi veya bunun farmasötik olarak kabul edilebilir bir tuzunu içermesidir. Istemler 1-5'ten herhangi birine göre bir bilesik veya bunun farmasötik olarak kabul edilebilir bir tuzu veya farmasötik bir bilesimi olup, özelligi bir hastada kanserin tedavi edilmesine yönelik terapötik bir rejimin güçlendirilmesinde kullanima yönelik söz konusu bilesigi veya bunun farmasötik olarak kabul edilebilir bir tuzunu içermesidir. istem 8'e göre kullanima yönelik söz konusu bilesigi veya bunun farmasötik olarak kabul edilebilir bir tuzunu içeren bir bilesik veya bunun farmasötik olarak kabul edilebilir bir tuzu veya farmasötik bir bilesim olup, özelligi terapötik rejimin radyasyon terapisini içermesidir. Istem 8,e göre kullanima yönelik söz konusu bilesigi veya bunun farmasötik olarak kabul edilebilir bir tuzunu içeren bir bilesik veya bunun farmasötik olarak kabul edilebilir bir tuzu veya farmasötik bir bilesim olup, özelligi terapötik rejimin anti-kanser kemoterapötik ajani içermesidir. Istemler 1-5'ten herhangi birine göre bir bilesik veya bunun farmasötik olarak kabul edilebilir bir tuzu veya farmasötik bir bilesimi olup, özelligi bir hastada kanserin tedavi edilmesinde kullanima yönelik söz konusu bilesigi veya bunun farmasötik olarak kabul edilebilir bir tuzunu içermesidir. Istem 8 veya 11'e göre kullanima yönelik söz konusu bilesigi veya bunun farmasötik olarak kabul edilebilir bir tuzunu içeren istemler 1-5'ten herhangi birine göre bilesik veya bunun farmasötik olarak kabul edilebilir bir tuzu veya farmasötik bir bilesim olup, özelligi kanserin gögüs kanseri, kolorektal kanser, gastroözofajeal kanser, fibrosarkom, glioblastom, hepatoselüler kanser, bas ve boyun kanseri, melanom, akciger kanseri, pankreas kanseri veya prostat kanseri olmasidir.
TR2018/07411T 2013-10-17 2014-10-17 DNA-PK inhibitörleri. TR201807411T4 (tr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US14/056,560 US9376448B2 (en) 2012-04-24 2013-10-17 DNA-PK inhibitors

Publications (1)

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TR201807411T4 true TR201807411T4 (tr) 2018-06-21

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EP (1) EP3057959B1 (tr)
JP (1) JP6374959B2 (tr)
CN (1) CN105636958B (tr)
AU (1) AU2014337208B2 (tr)
BR (1) BR112016008423B1 (tr)
CA (1) CA2927392C (tr)
DK (1) DK3057959T3 (tr)
ES (1) ES2671354T3 (tr)
HR (1) HRP20180804T1 (tr)
HU (1) HUE037516T2 (tr)
LT (1) LT3057959T (tr)
PL (1) PL3057959T3 (tr)
PT (1) PT3057959T (tr)
RS (1) RS57306B1 (tr)
SI (1) SI3057959T1 (tr)
TR (1) TR201807411T4 (tr)
WO (1) WO2015058031A1 (tr)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL2861566T3 (pl) 2012-06-13 2017-06-30 F.Hoffmann-La Roche Ag Nowy diazaspirocykloalkan i azaspirocykloalkan
HUE045797T2 (hu) 2012-09-25 2020-01-28 Hoffmann La Roche Hexahidropirrolo[3,4-c]pirrol-származékok és rokonvegyületek mint autotaxin (ATX) inhibitorok, valamint a lizofoszfatidsav (LPA) termelés inhibitorai, például vesebetegségek kezelésére
AR095079A1 (es) 2013-03-12 2015-09-16 Hoffmann La Roche Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo
KR20160087900A (ko) 2013-11-26 2016-07-22 에프. 호프만-라 로슈 아게 신규한 옥타하이드로-사이클로부타[1,2-c;3,4-c'']다이피롤-2-일
EA032357B1 (ru) 2014-03-26 2019-05-31 Ф. Хоффманн-Ля Рош Аг Конденсированные [1,4]диазепиновые соединения в качестве ингибиторов продукции аутотаксина (atx) и лизофосфатидиловой кислоты (lpa)
CN106103446B (zh) 2014-03-26 2019-07-30 豪夫迈·罗氏有限公司 作为自分泌运动因子(atx)和溶血磷脂酸(lpa)生产抑制剂的二环化合物
MA41898A (fr) 2015-04-10 2018-02-13 Hoffmann La Roche Dérivés de quinazolinone bicyclique
AU2016316717B2 (en) 2015-09-04 2021-02-18 F. Hoffmann-La Roche Ag Phenoxymethyl derivatives
CA2991612A1 (en) 2015-09-24 2017-03-30 F. Hoffmann-La Roche Ag New bicyclic compounds as dual atx/ca inhibitors
CR20180072A (es) 2015-09-24 2018-02-26 Hoffmann La Roche Nuevos compuestos biciclicos como inhibidores de atx
AU2016328365B2 (en) 2015-09-24 2020-04-23 F. Hoffmann-La Roche Ag New bicyclic compounds as dual ATX/CA inhibitors
RU2018114289A (ru) 2015-09-24 2019-10-24 Ф. Хоффманн-Ля Рош Аг Бициклические соединения в качестве ингибиторов аутотаксина (atx)
CR20180323A (es) 2015-11-20 2018-08-06 Idorsia Pharmaceuticals Ltd Derivados de indol n-sustituídos como moduladores de los receptores de pge2
US11110108B2 (en) * 2016-09-27 2021-09-07 Vertex Pharmaceuticals Incorporated Method for treating cancer using a combination of DNA-damaging agents and DNA-PK inhibitors
SG11201908560SA (en) 2017-03-16 2019-10-30 Hoffmann La Roche Heterocyclic compounds useful as dual atx/ca inhibitors
JP7090099B2 (ja) 2017-03-16 2022-06-23 エフ.ホフマン-ラ ロシュ アーゲー Atxインヒビターとしての新規二環式化合物
ES2896476T3 (es) * 2017-05-18 2022-02-24 Idorsia Pharmaceuticals Ltd Derivados de pirimidina
AU2018268311B2 (en) 2017-05-18 2022-02-10 Idorsia Pharmaceuticals Ltd Pyrimidine derivatives as PGE2 receptor modulators
CA3060597A1 (en) 2017-05-18 2018-11-22 Idorsia Pharmaceuticals Ltd Phenyl derivatives as pge2 receptor modulators
EA039630B1 (ru) 2017-05-18 2022-02-18 Идорсия Фармасьютиклз Лтд N-замещенные индольные производные
ES2929309T3 (es) 2017-05-18 2022-11-28 Idorsia Pharmaceuticals Ltd Derivados de benzofurano y benzotiofeno como moduladores del receptor PGE2
JP2021503486A (ja) 2017-11-20 2021-02-12 アイカーン スクール オブ メディシン アット マウント サイナイ キナーゼ阻害剤化合物ならびに組成物および使用法
CA3086925A1 (en) 2018-01-05 2019-07-11 Ichan School Of Medicine At Mount Sinai Method of increasing proliferation of pancreatic beta cells, treatment method, and composition
CA3093340A1 (en) 2018-03-20 2019-09-26 Icahn School Of Medicine At Mount Sinai Kinase inhibitor compounds and compositions and methods of use
EP3906028A4 (en) * 2018-12-31 2022-10-12 Icahn School of Medicine at Mount Sinai KINA INHIBITOR COMPOUNDS AND COMPOSITIONS AND METHODS OF USE
CN112300126A (zh) * 2019-07-31 2021-02-02 山东轩竹医药科技有限公司 杂环类dna-pk抑制剂
CN112574211B (zh) * 2019-09-29 2022-06-14 山东轩竹医药科技有限公司 杂环类激酶抑制剂
CN112574179B (zh) * 2019-09-29 2022-05-10 山东轩竹医药科技有限公司 Dna-pk抑制剂
JP7428806B2 (ja) * 2019-12-31 2024-02-06 成都百裕制薬股▲ふん▼有限公司 プリン誘導体および医薬におけるその使用

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7179912B2 (en) * 2000-09-01 2007-02-20 Icos Corporation Materials and methods to potentiate cancer treatment
EP1678147B1 (en) * 2003-09-15 2012-08-08 Lead Discovery Center GmbH Pharmaceutically active 4,6-disubstituted aminopyrimidine derivatives as modulators of protein kinases
US20090221581A1 (en) * 2005-05-25 2009-09-03 Philipp Wabnitz Methods of treating pain
WO2008042639A1 (en) * 2006-10-02 2008-04-10 Irm Llc Compounds and compositions as protein kinase inhibitors
EA201201274A1 (ru) * 2010-03-10 2013-04-30 Инджениум Фармасьютиклз Гмбх Ингибиторы протеинкиназ
CN106986863B (zh) * 2012-04-24 2019-12-31 沃泰克斯药物股份有限公司 Dna-pk抑制剂

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SI3057959T1 (en) 2018-07-31
HUE037516T2 (hu) 2018-09-28
JP2016533366A (ja) 2016-10-27
EP3057959B1 (en) 2018-02-28
BR112016008423A2 (tr) 2017-08-01
RS57306B1 (sr) 2018-08-31
DK3057959T3 (en) 2018-06-06
CN105636958B (zh) 2018-01-05
PL3057959T3 (pl) 2018-08-31
ES2671354T3 (es) 2018-06-06
CA2927392C (en) 2021-11-09
CA2927392A1 (en) 2015-04-23
AU2014337208B2 (en) 2018-05-24
PT3057959T (pt) 2018-06-04
JP6374959B2 (ja) 2018-08-15
HRP20180804T1 (hr) 2018-08-10
EP3057959A1 (en) 2016-08-24
BR112016008423B1 (pt) 2022-02-22
WO2015058031A1 (en) 2015-04-23
CN105636958A (zh) 2016-06-01
LT3057959T (lt) 2018-06-11

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