ES2514325T3 - Morfolinopirimidinas y su uso en terapia - Google Patents

Morfolinopirimidinas y su uso en terapia Download PDF

Info

Publication number
ES2514325T3
ES2514325T3 ES11725494.6T ES11725494T ES2514325T3 ES 2514325 T3 ES2514325 T3 ES 2514325T3 ES 11725494 T ES11725494 T ES 11725494T ES 2514325 T3 ES2514325 T3 ES 2514325T3
Authority
ES
Spain
Prior art keywords
methyl
pyrimidin
methylmorpholin
methylsulfonimidoyl
hydrogen
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
ES11725494.6T
Other languages
English (en)
Spanish (es)
Inventor
Kevin Michael Foote
Johannes Wilhelmus Maria Nissink
Paul Turner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AstraZeneca AB
Original Assignee
AstraZeneca AB
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 AstraZeneca AB filed Critical AstraZeneca AB
Application granted granted Critical
Publication of ES2514325T3 publication Critical patent/ES2514325T3/es
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • 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
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
ES11725494.6T 2010-06-11 2011-06-09 Morfolinopirimidinas y su uso en terapia Active ES2514325T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US35371310P 2010-06-11 2010-06-11
US353713P 2010-06-11
PCT/GB2011/051074 WO2011154737A1 (en) 2010-06-11 2011-06-09 Morpholino pyrimidines and their use in therapy

Publications (1)

Publication Number Publication Date
ES2514325T3 true ES2514325T3 (es) 2014-10-28

Family

ID=44168987

Family Applications (1)

Application Number Title Priority Date Filing Date
ES11725494.6T Active ES2514325T3 (es) 2010-06-11 2011-06-09 Morfolinopirimidinas y su uso en terapia

Country Status (38)

Country Link
US (5) US8252802B2 (US07794700-20100914-C00152.png)
EP (1) EP2579877B1 (US07794700-20100914-C00152.png)
JP (1) JP5721821B2 (US07794700-20100914-C00152.png)
KR (1) KR101820996B1 (US07794700-20100914-C00152.png)
CN (1) CN103068391B (US07794700-20100914-C00152.png)
AR (1) AR081859A1 (US07794700-20100914-C00152.png)
AU (1) AU2011263491B2 (US07794700-20100914-C00152.png)
BR (1) BR112012031561B1 (US07794700-20100914-C00152.png)
CA (1) CA2800203C (US07794700-20100914-C00152.png)
CL (1) CL2012003503A1 (US07794700-20100914-C00152.png)
CO (1) CO6640270A2 (US07794700-20100914-C00152.png)
CR (1) CR20120628A (US07794700-20100914-C00152.png)
CU (1) CU24109B1 (US07794700-20100914-C00152.png)
DK (1) DK2579877T3 (US07794700-20100914-C00152.png)
DO (1) DOP2012000310A (US07794700-20100914-C00152.png)
EA (1) EA022087B1 (US07794700-20100914-C00152.png)
EC (1) ECSP12012334A (US07794700-20100914-C00152.png)
ES (1) ES2514325T3 (US07794700-20100914-C00152.png)
GT (1) GT201200334A (US07794700-20100914-C00152.png)
HK (1) HK1182019A1 (US07794700-20100914-C00152.png)
HR (1) HRP20140953T1 (US07794700-20100914-C00152.png)
MX (1) MX2012014477A (US07794700-20100914-C00152.png)
MY (1) MY158193A (US07794700-20100914-C00152.png)
NI (1) NI201200184A (US07794700-20100914-C00152.png)
NZ (1) NZ604480A (US07794700-20100914-C00152.png)
PE (1) PE20130306A1 (US07794700-20100914-C00152.png)
PL (1) PL2579877T3 (US07794700-20100914-C00152.png)
PT (1) PT2579877E (US07794700-20100914-C00152.png)
RS (1) RS53566B1 (US07794700-20100914-C00152.png)
SA (1) SA111320519B1 (US07794700-20100914-C00152.png)
SG (1) SG185711A1 (US07794700-20100914-C00152.png)
SI (1) SI2579877T1 (US07794700-20100914-C00152.png)
SM (1) SMT201400146B (US07794700-20100914-C00152.png)
TW (1) TWI526208B (US07794700-20100914-C00152.png)
UA (1) UA109010C2 (US07794700-20100914-C00152.png)
UY (1) UY33440A (US07794700-20100914-C00152.png)
WO (1) WO2011154737A1 (US07794700-20100914-C00152.png)
ZA (1) ZA201300255B (US07794700-20100914-C00152.png)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SA111320519B1 (ar) 2010-06-11 2014-07-02 Astrazeneca Ab مركبات بيريميدينيل للاستخدام كمثبطات atr
PL3157566T3 (pl) 2014-06-17 2019-10-31 Vertex Pharma Metoda leczenia nowotworu przy użyciu kombinacji inhibitorów chk1 i atr
TWI656121B (zh) 2014-08-04 2019-04-11 德商拜耳製藥公司 2-(嗎啉-4-基)-1,7-萘啶
WO2017059357A1 (en) 2015-09-30 2017-04-06 Vertex Pharmaceuticals Incorporated Method for treating cancer using a combination of dna damaging agents and atr inhibitors
WO2018029117A1 (en) * 2016-08-10 2018-02-15 Rheinisch-Westfälische Technische Hochschule Aachen (RWTH) New atr inhibitors for the use in cancer therapy
CA3038657A1 (en) * 2016-09-27 2018-04-05 Vertex Pharmaceuticals Incorporated Method for treating cancer using a combination of dna-damaging agents and dna-pk inhibitors
AR110995A1 (es) 2017-02-24 2019-05-22 Bayer Ag Combinación de inhibidores de quinasa atr con sal de radio-223
WO2018153972A1 (en) 2017-02-24 2018-08-30 Bayer Pharma Aktiengesellschaft Combination of atr kinase inhibitors and antiandrogens
JOP20190197A1 (ar) 2017-02-24 2019-08-22 Bayer Pharma AG مثبط كيناز ايه تي آر للاستخدام في طريقة لعلاج مرض فرط التكاثر
WO2018206547A1 (en) 2017-05-12 2018-11-15 Bayer Pharma Aktiengesellschaft Combination of bub1 and atr inhibitors
WO2018218197A2 (en) 2017-05-26 2018-11-29 Board Of Regents, The University Of Texas System Tetrahydropyrido[4,3-d]pyrimidine inhibitors of atr kinase
CA3069693A1 (en) 2017-07-13 2019-01-17 Board Of Regents, University Of Texas System Heterocyclic inhibitors of atr kinase
EP3661560A1 (en) 2017-08-04 2020-06-10 Bayer Pharma Aktiengesellschaft Combination of atr kinase inhibitors and pd-1/pd-l1 inhibitors
EP3668839B1 (en) * 2017-08-17 2023-04-12 Board of Regents, The University of Texas System Heterocyclic inhibitors of atr kinase
EP3679041B1 (en) * 2017-09-08 2022-07-06 Newave Pharmaceutical Inc. Substituted pyrrolopyridines as atr inhibitors
EP3461480A1 (en) 2017-09-27 2019-04-03 Onxeo Combination of a dna damage response cell cycle checkpoint inhibitors and belinostat for treating cancer
US11712440B2 (en) 2017-12-08 2023-08-01 Bayer Aktiengesellschaft Predictive markers for ATR kinase inhibitors
GB201720989D0 (en) * 2017-12-15 2018-01-31 Glaxosmithkline Ip Dev Ltd Chemical compounds
BR112020016020A8 (pt) * 2018-02-07 2023-04-25 Shijiazhuang Sagacity New Drug Dev Company Ltd Inibidor de atr e aplicação do mesmo
US10894052B2 (en) 2018-03-16 2021-01-19 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of ATR kinase
US20210369724A1 (en) 2018-10-16 2021-12-02 Bayer Aktiengesellschaft Combination of atr kinase inhibitors with 2,3-dihydroimidazo[1,2-c]quinazoline compounds
MX2021007192A (es) * 2018-12-18 2021-07-21 Astrazeneca Ab Proceso farmaceutico e intermedios.
MX2021013774A (es) 2019-05-14 2021-12-10 Nuvation Bio Inc Compuestos anticancerigenos dirigidos a los receptores hormonales nucleares.
GB201908536D0 (en) * 2019-06-13 2019-07-31 Glaxosmithkline Ip Dev Ltd Compounds
CN112142744A (zh) * 2019-06-28 2020-12-29 上海瑛派药业有限公司 取代的稠合杂芳双环化合物作为激酶抑制剂及其应用
AU2020325416A1 (en) * 2019-08-06 2022-02-03 Wuxi Biocity Biopharmaceutics Co., Ltd. Crystalline form of ATR inhibitor and use thereof
US11952349B2 (en) 2019-11-13 2024-04-09 Nuvation Bio Inc. Anti-cancer nuclear hormone receptor-targeting compounds
WO2021098811A1 (zh) * 2019-11-21 2021-05-27 江苏恒瑞医药股份有限公司 吡唑并杂芳基类衍生物、其制备方法及其在医药上的应用
CN112939966B (zh) * 2019-12-10 2023-03-24 武汉光谷亚太医药研究院有限公司 嘧啶衍生物、其制备及应用
WO2021143821A1 (zh) * 2020-01-17 2021-07-22 江苏恒瑞医药股份有限公司 稠合杂芳基类衍生物、其制备方法及其在医药上的应用
WO2021189036A1 (en) * 2020-03-20 2021-09-23 H. Lee Moffitt Cancer Center And Research Institute, Inc. Taf1 inhibitors
US20230346791A1 (en) 2020-05-11 2023-11-02 Astrazeneca Ab Atr inhibitors for the treatment of cancer
EP4159734A4 (en) * 2020-05-29 2024-06-19 Wuxi Life Fountain Biotech Co., Ltd. FLUOROPYRROLOPYRIDINE COMPOUND AND APPLICATION THEREOF
CN111646985A (zh) * 2020-06-01 2020-09-11 江苏集萃分子工程研究院有限公司 一种含嘧啶杂环抗肿瘤药物分子azd6738的合成方法
CA3183867A1 (en) 2020-06-24 2021-12-30 Jerome Thomas Mettetal Ii Combination of antibody-drug conjugate and atr inhibitor
EP4166556A4 (en) * 2020-07-13 2024-06-26 Beijing Tide Pharmaceutical Co., Ltd. PYRAZOLOPYRIMIDINE COMPOUND USED AS ATR KINASE INHIBITOR
US20230399302A1 (en) * 2020-10-29 2023-12-14 H. Lee Moffitt Cancer Center And Research Institute, Inc. Process for the preparation of heteroaryl-substituted sulfur(vi) compounds
TW202304457A (zh) 2021-03-22 2023-02-01 瑞典商阿斯特捷利康公司 配製物
US11834458B2 (en) 2021-03-23 2023-12-05 Nuvation Bio Inc. Anti-cancer nuclear hormone receptor-targeting compounds
EP4313057A1 (en) 2021-03-26 2024-02-07 Astrazeneca AB Combination treatments for melanoma
JP2024516024A (ja) 2021-05-03 2024-04-11 ニューベイション・バイオ・インコーポレイテッド 抗がん核内ホルモン受容体標的化化合物
IT202100021863A1 (it) * 2021-08-13 2023-02-13 Univ Degli Studi Milano Morfolino pirimidine per l’uso nella prevenzione e/o nel trattamento di stati di ipereccitabilità neuronale
WO2023039573A1 (en) * 2021-09-10 2023-03-16 H. Lee Moffitt Cancer Center And Research Institute, Inc. Compounds for targeted degradation of taf1
CN116283960A (zh) 2021-12-21 2023-06-23 上海安诺达生物科技有限公司 取代的稠杂环化合物及其制备方法与应用
WO2023122723A1 (en) 2021-12-23 2023-06-29 The Broad Institute, Inc. Panels and methods for diagnosing and treating lung cancer
IL313929A (en) 2021-12-28 2024-08-01 Astrazeneca Uk Ltd Combining an antibody-drug conjugate and an ATR inhibitor
TW202348252A (zh) 2022-02-16 2023-12-16 英商梅迪繆思有限公司 用治療性結合分子治療癌症的組合療法
WO2023242302A1 (en) 2022-06-15 2023-12-21 Astrazeneca Ab Combination therapy for treating cancer
WO2024121753A1 (en) 2022-12-06 2024-06-13 Astrazeneca Ab Polq inhibitors

Family Cites Families (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3922735A1 (de) 1989-07-11 1991-01-24 Hoechst Ag Aminopyrimidin-derivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als fungizide
WO1998035985A1 (en) 1997-02-12 1998-08-20 The Regents Of The University Of Michigan Protein markers for lung cancer and use thereof
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
AU763618B2 (en) 1999-02-10 2003-07-31 Astrazeneca Ab Quinazoline derivatives as angiogenesis inhibitors
PT1244647E (pt) 1999-11-05 2006-10-31 Astrazeneca Ab Derivados de quinazolina como inibidores de vegf
DE122010000004I1 (de) 2000-02-15 2010-04-15 Sugen Inc Pyrrol substituierte indolin-2-on protein kinase inhibitoren
DE60144322D1 (de) 2000-04-27 2011-05-12 Astellas Pharma Inc Kondensierte heteroarylderivate
JP2003535078A (ja) 2000-05-31 2003-11-25 アストラゼネカ アクチボラグ 血管損傷活性のあるインドール誘導体
UA73993C2 (uk) 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
WO2002008213A1 (en) 2000-07-07 2002-01-31 Angiogene Pharmaceuticals Limited Colchinol derivatives as angiogenesis inhibitors
BR0112224A (pt) 2000-07-07 2003-06-10 Angiogene Pharm Ltd Composto, composição farmacêutica, uso de um composto ou de um sal, solvato ou pró-droga farmaceuticamente aceitável do mesmo, e, processo para preparar um composto
ATE340784T1 (de) 2000-11-10 2006-10-15 Hoffmann La Roche Pyrimidinderivate und deren verwendung als neuropeptid-y-rezeptorliganden
ES2375111T3 (es) 2002-11-21 2012-02-24 Novartis Ag Pirimidinas 2,4,6-trisustituidas como inhibidores de fosfotidilinositol (pi) 3-quinasa y su uso en el tratamiento de c�?ncer.
CA2527079A1 (en) 2003-05-29 2005-01-06 Synta Pharmaceuticals, Corp. Heterocyclic compounds for preventing and treating disorders associated with excessive bone loss
GB0415365D0 (en) 2004-07-09 2004-08-11 Astrazeneca Ab Pyrimidine derivatives
GB0415367D0 (en) 2004-07-09 2004-08-11 Astrazeneca Ab Pyrimidine derivatives
GB0415364D0 (en) 2004-07-09 2004-08-11 Astrazeneca Ab Pyrimidine derivatives
US7772271B2 (en) 2004-07-14 2010-08-10 Ptc Therapeutics, Inc. Methods for treating hepatitis C
WO2007084413A2 (en) 2004-07-14 2007-07-26 Ptc Therapeutics, Inc. Methods for treating hepatitis c
JP2008519850A (ja) 2004-11-10 2008-06-12 シンタ ファーマシューティカルズ コーポレーション Il−12調節化合物
WO2006124874A2 (en) 2005-05-12 2006-11-23 Kalypsys, Inc. Inhibitors of b-raf kinase
TW200720256A (en) 2005-05-13 2007-06-01 Synta Pharmaceuticals Corp IL-12 modulatory compounds
CN101248080B (zh) 2005-05-20 2012-09-05 梅特希尔基因公司 Vegf受体和hgf受体信号的抑制剂
DE102005024494A1 (de) 2005-05-27 2006-11-30 Bayer Healthcare Ag Verwendung von Cyanopyrimidinen
CN101213192B (zh) * 2005-07-01 2012-06-06 Irm责任有限公司 作为蛋白激酶抑制剂的嘧啶取代的苯并咪唑衍生物
EP1911753A1 (en) 2005-07-29 2008-04-16 Takeda Pharmaceutical Company Limited Spiro-cyclic compound
CN101305010A (zh) 2005-09-01 2008-11-12 阿雷生物药品公司 Raf抑制剂化合物及其用法
JP2007091649A (ja) 2005-09-29 2007-04-12 Taisho Pharmaceut Co Ltd ピリミジン誘導体及びその使用に関連する治療方法
JP4531027B2 (ja) 2005-09-29 2010-08-25 田辺三菱製薬株式会社 医薬組成物
KR20080063809A (ko) 2005-09-30 2008-07-07 버텍스 파마슈티칼스 인코포레이티드 야누스 키나아제의 억제제로서 유용한 데아자퓨린
ES2535854T3 (es) 2005-09-30 2015-05-18 Miikana Therapeutics, Inc. Compuestos de pirazol sustituidos
GB2431156A (en) 2005-10-11 2007-04-18 Piramed Ltd 1-cyclyl-3-substituted- -benzenes and -azines as inhibitors of phosphatidylinositol 3-kinase
GB0520657D0 (en) 2005-10-11 2005-11-16 Ludwig Inst Cancer Res Pharmaceutical compounds
AU2006307657B2 (en) 2005-10-28 2010-10-28 Astrazeneca Ab 4- (3-aminopyrazole) pyrimidine derivatives for use as tyrosine kinase inhibitors in the treatment of cancer
CA2636314A1 (en) 2005-11-29 2007-06-07 Toray Industries, Inc. Arylmethylene urea derivative and use thereof
GB0525083D0 (en) 2005-12-09 2006-01-18 Astrazeneca Ab Pyrimidine derivatives
GB0525081D0 (en) 2005-12-09 2006-01-18 Astrazeneca Ab Pyrimidine derivatives
GB0525080D0 (en) 2005-12-09 2006-01-18 Astrazeneca Ab Pyrimidine derivatives
NL2000323C2 (nl) 2005-12-20 2007-11-20 Pfizer Ltd Pyrimidine-derivaten.
AU2007204208A1 (en) * 2006-01-11 2007-07-19 Astrazeneca Ab Morpholino pyrimidine derivatives and their use in therapy
JO2660B1 (en) 2006-01-20 2012-06-17 نوفارتيس ايه جي Pi-3 inhibitors and methods of use
BRPI0706747A2 (pt) 2006-01-30 2011-04-05 Exelixis Inc 4-aril-2-amino-pirimidinas ou 4-aril-2-aminoalquil-pirimidinas como moduladores jak-2 e composições farmacêuticas que os contenham
CN101438288A (zh) 2006-03-15 2009-05-20 Csir公司 谷氨酰胺合成酶的磷酰基转移酶活性的调节
JP5243696B2 (ja) 2006-03-17 2013-07-24 田辺三菱製薬株式会社 ベンゼン誘導体
WO2007114323A1 (ja) 2006-04-04 2007-10-11 Taisho Pharmaceutical Co., Ltd. アミノピロリジン化合物
CN101472915A (zh) 2006-04-19 2009-07-01 诺瓦提斯公司 吲唑化合物和抑制cdc7的方法
WO2007126043A1 (ja) 2006-04-27 2007-11-08 Mitsubishi Tanabe Pharma Corporation チアゾール環を含むカルボン酸誘導体の医薬用途
GB0610909D0 (en) 2006-06-05 2006-07-12 Merck Sharp & Dohme Therapeutic treatment
CA2656290A1 (en) 2006-07-05 2008-01-10 Exelixis, Inc. Methods of using igf1r and abl kinase modulators
MX2009002046A (es) 2006-08-24 2009-03-06 Astrazeneca Ab Derivados de morfolino pirimidina utiles en el tratamiento de trastornos proliferativos.
WO2008023180A1 (en) 2006-08-24 2008-02-28 Astrazeneca Ab Morpholino pyrimidine derivatives useful in the treatment of proliferative disorders
EP2084159A1 (en) * 2006-10-16 2009-08-05 GPC Biotech Inc. Pyrido ý2, 3-d¨pyrimidines and their use as kinase inhibitors
EP2146981A1 (en) 2007-04-12 2010-01-27 F. Hoffmann-Roche AG Pharmaceutical compounds
US20100227858A1 (en) 2007-07-09 2010-09-09 Astrazeneca Ab Trisubstituted pyrimidine derivatives for the treatment of proliferative diseases
CN102282142A (zh) * 2008-11-14 2011-12-14 拜耳先灵制药股份公司 取代的芳族化合物和它们的用途
TW201028410A (en) * 2008-12-22 2010-08-01 Astrazeneca Ab Chemical compounds 610
SA111320519B1 (ar) 2010-06-11 2014-07-02 Astrazeneca Ab مركبات بيريميدينيل للاستخدام كمثبطات atr

Also Published As

Publication number Publication date
HK1182019A1 (en) 2013-11-22
US20160074412A1 (en) 2016-03-17
BR112012031561A2 (pt) 2016-12-06
KR101820996B1 (ko) 2018-01-22
US20140018364A1 (en) 2014-01-16
AU2011263491B2 (en) 2014-08-21
CN103068391A (zh) 2013-04-24
US9155742B2 (en) 2015-10-13
BR112012031561B1 (pt) 2019-12-03
SG185711A1 (en) 2012-12-28
SI2579877T1 (sl) 2014-11-28
NZ604480A (en) 2014-11-28
KR20130087008A (ko) 2013-08-05
SA111320519B1 (ar) 2014-07-02
CU24109B1 (es) 2015-07-30
ECSP12012334A (es) 2012-12-28
UA109010C2 (en) 2015-07-10
RS53566B1 (en) 2015-02-27
SMT201400146B (it) 2014-11-10
CN103068391B (zh) 2014-11-26
CA2800203A1 (en) 2011-12-15
PT2579877E (pt) 2014-10-14
US8999997B2 (en) 2015-04-07
CR20120628A (es) 2013-03-13
DK2579877T3 (da) 2014-10-13
MX2012014477A (es) 2013-06-13
US9421213B2 (en) 2016-08-23
US20150164908A1 (en) 2015-06-18
GT201200334A (es) 2014-12-22
US20110306613A1 (en) 2011-12-15
UY33440A (es) 2012-01-31
AU2011263491A1 (en) 2013-01-24
JP2013528204A (ja) 2013-07-08
US8552004B2 (en) 2013-10-08
ZA201300255B (en) 2013-09-25
TWI526208B (zh) 2016-03-21
EP2579877B1 (en) 2014-08-13
CO6640270A2 (es) 2013-03-22
WO2011154737A1 (en) 2011-12-15
HRP20140953T1 (hr) 2014-12-05
EP2579877A1 (en) 2013-04-17
US20130005725A1 (en) 2013-01-03
US8252802B2 (en) 2012-08-28
PL2579877T3 (pl) 2015-01-30
TW201201803A (en) 2012-01-16
NI201200184A (es) 2014-01-23
JP5721821B2 (ja) 2015-05-20
CA2800203C (en) 2019-01-22
EA201201680A1 (ru) 2013-11-29
MY158193A (en) 2016-09-15
CL2012003503A1 (es) 2013-03-08
DOP2012000310A (es) 2013-02-15
CU20120169A7 (es) 2014-02-28
PE20130306A1 (es) 2013-04-05
EA022087B1 (ru) 2015-10-30
AR081859A1 (es) 2012-10-24

Similar Documents

Publication Publication Date Title
ES2514325T3 (es) Morfolinopirimidinas y su uso en terapia
ES2876411T3 (es) Inhibidores de piridopirimdinona CDK2/4/6
ES2663605T3 (es) Dihidronaftiridinas y compuestos relacionados útiles como inhibidores de quinasas para el tratamiento de enfermedades proliferativas
ES2864839T3 (es) Macrociclos de diarilo quirales como moduladores de proteína quinasas
ES2483726T3 (es) Inhibidores de la P70 S6 quinasa
US10494376B2 (en) Tetrahydroisoquinoline derived PRMT5-inhibitors
ES2618637T3 (es) Compuestos, sus composiciones farmacéuticas y sus usos como inhibidores mutantes de IDH1 para el tratamiento de cánceres.
ES2718218T3 (es) Derivados de 4,5,6,7-tetrahidropirazolo[1,5-a]pirazina sustituidos como inhibidores de caseína cinasa 1 D/E
ES2742442T3 (es) Compuestos inhibidores
ES2643379T3 (es) Nuevas dihidropirimidinoisoquinolinonas y sus composiciones farmacéuticas para el tratamiento de trastornos inflamatorios
ES2426407T3 (es) Compuestos de pirrolo[2,3-d]pirimidina
ES2872003T3 (es) Inhibidores espirobicíclicos de la interacción de menina-MLL
ES2655882T3 (es) Compuestos anticancerígenos de aminopirimidina
ES2732897T3 (es) Derivados de pirazolopirimidina útiles como inhibidores de la tirosina cinasa de Bruton
ES2654288T3 (es) Moduladores de P2X7
ES2549879T3 (es) Inhibidores de péptido desformilasa
ES2620119T3 (es) Derivados heterocíclicos novedosos como moduladores de la actividad de quinasa
CN102711766B (zh) N-9-取代的嘌呤化合物、组合物和使用方法
ES2716165T3 (es) (5,6-Dihidro)pirimido[4,5-e]indolizinas
ES2816376T3 (es) Compuestos de 6-aril-4-(morfolin-4-il)-1H-piridin-2-ona útiles para el tratamiento del cáncer y la diabetes
RU2515541C2 (ru) N-7 замещенные пурины и пиразолопиримидины, их композиции и способы применения
ES2904645T3 (es) Derivados de pirrolopirazina como inhibidores de integrina alfa v
EA032081B1 (ru) ЗАМЕЩЕННЫЕ ПИПЕРИДИНОМ ПРОИЗВОДНЫЕ ПИРАЗОЛО[1,5-a]ПИРИМИДИНА С ИНГИБИРУЮЩЕЙ АКТИВНОСТЬЮ В ОТНОШЕНИИ РЕПЛИКАЦИИ РЕСПИРАТОРНО-СИНЦИТИАЛЬНОГО ВИРУСА (RSV)
US10787434B2 (en) Benzopiperdine derivatives and their use in the treatment of cancer and hemoglobinopathies
EP3426648A1 (en) Tetrahydroisoquinolines as prmt5 inhibitors