MA40523A - 2-(morpholin-4-yl)-1,7-naphthyridines - Google Patents

2-(morpholin-4-yl)-1,7-naphthyridines

Info

Publication number
MA40523A
MA40523A MA040523A MA40523A MA40523A MA 40523 A MA40523 A MA 40523A MA 040523 A MA040523 A MA 040523A MA 40523 A MA40523 A MA 40523A MA 40523 A MA40523 A MA 40523A
Authority
MA
Morocco
Prior art keywords
compounds
morpholin
preparation
naphthyridines
disease
Prior art date
Application number
MA040523A
Other languages
English (en)
Other versions
MA40523B1 (fr
Inventor
Benjamin Bader
Wilhelm Bone
Hans Briem
Uwe Eberspächer
Knut Eis
Joanna Grudzinska-Goebel
Marcus Koppitz
Julien Lefranc
Philip Lienau
Ulrich Lücking
Dieter Moosmayer
Hans Schick
Gerhard Siemeister
Nussbaum Franz Von
Antje Margret Wengner
Lars Wortmann
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 MA40523A publication Critical patent/MA40523A/fr
Publication of MA40523B1 publication Critical patent/MA40523B1/fr

Links

Classifications

    • 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
    • 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
    • A61K31/535Heterocyclic 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
    • A61K31/53861,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
    • 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
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/675Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/22Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention porte sur des composés 2-(morpholin-4-yl)-l,7-naphtyridine substitués représentés par la formule générale (i) ou (ib), sur des procédés de préparation desdits composés, sur des composés intermédiaires utiles pour la préparation desdits composés, sur des combinaisons et des compositions pharmaceutiques comprenant lesdits composés et sur l'utilisation desdits composés pour la fabrication d'une composition pharmaceutique utile pour le traitement ou la prophylaxie d'une maladie, en particulier d'une maladie hyperproliférative en tant qu'agent unique ou en combinaison avec d'autres principes actifs.
MA40523A 2014-08-04 2015-08-03 2-(morpholin-4-yl)-1,7-naphthyridines MA40523B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP14179692 2014-08-04
EP15159342 2015-03-17
EP15744596.6A EP3177619B1 (fr) 2014-08-04 2015-08-03 2-(morpholin-4-yl)-1,7-naphthyridines
PCT/EP2015/067804 WO2016020320A1 (fr) 2014-08-04 2015-08-03 2- (morpholin -4-yl)-l,7-naphtyridines

Publications (2)

Publication Number Publication Date
MA40523A true MA40523A (fr) 2017-06-14
MA40523B1 MA40523B1 (fr) 2018-09-28

Family

ID=53762196

Family Applications (1)

Application Number Title Priority Date Filing Date
MA40523A MA40523B1 (fr) 2014-08-04 2015-08-03 2-(morpholin-4-yl)-1,7-naphthyridines

Country Status (42)

Country Link
US (4) US9993484B2 (fr)
EP (2) EP3395818B1 (fr)
JP (2) JP6266839B2 (fr)
KR (2) KR102180006B1 (fr)
CN (3) CN110204544B (fr)
AP (1) AP2017009702A0 (fr)
AU (2) AU2015299173B2 (fr)
BR (1) BR112017002221B1 (fr)
CA (1) CA2956992C (fr)
CL (1) CL2017000287A1 (fr)
CO (1) CO2017001035A2 (fr)
CR (1) CR20170034A (fr)
CU (1) CU24419B1 (fr)
CY (2) CY1120673T1 (fr)
DK (2) DK3395818T3 (fr)
DO (1) DOP2017000038A (fr)
EA (2) EA031678B1 (fr)
EC (1) ECSP17007538A (fr)
ES (2) ES2900599T3 (fr)
HR (2) HRP20211770T1 (fr)
HU (2) HUE038533T2 (fr)
IL (2) IL250220B (fr)
JO (1) JO3447B1 (fr)
LT (2) LT3177619T (fr)
MA (1) MA40523B1 (fr)
MX (2) MX376270B (fr)
MY (1) MY192883A (fr)
NI (1) NI201700011A (fr)
PE (1) PE20170666A1 (fr)
PH (2) PH12017500204B1 (fr)
PL (2) PL3395818T3 (fr)
PT (1) PT3177619T (fr)
RS (2) RS62609B1 (fr)
SA (1) SA517380830B1 (fr)
SG (1) SG11201700750UA (fr)
SI (2) SI3177619T1 (fr)
TN (1) TN2017000027A1 (fr)
TW (2) TWI700283B (fr)
UA (2) UA123928C2 (fr)
UY (1) UY36254A (fr)
WO (1) WO2016020320A1 (fr)
ZA (1) ZA202101003B (fr)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CR20170076A (es) 2014-08-04 2017-06-26 Nuevolution As Derivados de pirimidima sustituidos con heterociclilo opcionalmente condensados útiles para el tratamiento de enfermedades inflamatorias, metabólicas, oncológicas y autoinmunitarias
TWI700283B (zh) 2014-08-04 2020-08-01 德商拜耳製藥公司 2-(嗎啉-4-基)-1,7-萘啶
CA3011189C (fr) * 2016-01-14 2024-02-20 Bayer Pharma Aktiengesellschaft 2-(morpholin-4-yl)-1,7-naphthyridines substituees en 5
TWI794171B (zh) 2016-05-11 2023-03-01 美商滬亞生物國際有限公司 Hdac抑制劑與pd-l1抑制劑之組合治療
TWI808055B (zh) 2016-05-11 2023-07-11 美商滬亞生物國際有限公司 Hdac 抑制劑與 pd-1 抑制劑之組合治療
EP3585365B1 (fr) 2017-02-24 2021-08-25 Bayer Pharma Aktiengesellschaft Combinaison de atr kinase inhibiteurs avec parp inhibiteurs
TW201840319A (zh) 2017-02-24 2018-11-16 德商拜耳廠股份有限公司 Atr激酶抑制劑與鐳-223鹽之組合
WO2018153971A1 (fr) 2017-02-24 2018-08-30 Bayer Pharma Aktiengesellschaft Combinaison d'inhibiteurs de kinase atr
CA3054248A1 (fr) 2017-02-24 2018-08-30 Bayer As Polytherapie comprenant un agent radiopharmaceutique et un inhibiteur de reparation d'adn
JOP20190197A1 (ar) 2017-02-24 2019-08-22 Bayer Pharma AG مثبط كيناز ايه تي آر للاستخدام في طريقة لعلاج مرض فرط التكاثر
WO2018153970A1 (fr) 2017-02-24 2018-08-30 Bayer Pharma Aktiengesellschaft Formes solides de 2-[(3r)-3-méthylmorpholin-4-yl]-4-(1-méthyl-1h-pyrazol-5-yl)-8-(1h-pyrazol-5-yl)-1,7-naphtyridine
WO2018153972A1 (fr) 2017-02-24 2018-08-30 Bayer Pharma Aktiengesellschaft Combinaison d'inhibiteurs de kinase atr et d'anti-androgènes
WO2018206547A1 (fr) 2017-05-12 2018-11-15 Bayer Pharma Aktiengesellschaft Combinaison d'inhibiteurs de bub1 et d'atr
WO2018218197A2 (fr) 2017-05-26 2018-11-29 Board Of Regents, The University Of Texas System Inhibiteurs de la kinase atr à base de tétrahydropyrido[4,3-d]pyrimidine
US10377591B2 (en) 2017-07-07 2019-08-13 Zebra Technologies Corporation Input handling for media processing devices
CN111867590B (zh) * 2017-07-13 2023-11-17 德州大学系统董事会 Atr激酶的杂环抑制剂
WO2019025440A1 (fr) 2017-08-04 2019-02-07 Bayer Pharma Aktiengesellschaft Combinaison d'inhibiteurs de kinase atr et d'inhibiteurs de pd-1/pd-l1
CA3071795A1 (fr) 2017-08-04 2019-02-07 Bayer Aktiengesellschaft Derives de 6-phenyl-4,5-dihydropyridazin-3(2h)-one utilises en tant qu'inhibiteurs de pde3a et pde3b pour le traitement du cancer
JOP20200024A1 (ar) 2017-08-04 2020-02-02 Bayer Ag مركبات ثنائي هيدروكساديازينون
CN111886224B (zh) 2017-08-17 2024-07-23 德州大学系统董事会 Atr激酶的杂环抑制剂
WO2019057852A1 (fr) 2017-09-22 2019-03-28 Bayer Aktiengesellschaft Utilisation de kap1 en tant que biomarqueur pour la détection ou la surveillance de l'inhibition d'atr chez un sujet
EP3461480A1 (fr) 2017-09-27 2019-04-03 Onxeo Combinaison d'inhibiteurs de point de contrôle du cycle cellulaire de réponse à un dommage à l'adn et de belinostat pour traiter le cancer
CA3084863A1 (fr) 2017-12-08 2019-06-13 Bayer Aktiengesellschaft Marqueurs predictifs pour inhibiteurs d'atr kinase
EP3753937B1 (fr) * 2018-02-07 2024-01-10 Wuxi Biocity Biopharmaceutics Co., Ltd. Inhibiteur d'atr et son application
EP3765008B1 (fr) * 2018-03-16 2023-06-07 Board of Regents, The University of Texas System Inhibiteurs hétérocycliques de la kinase atr
SG11202101011RA (en) 2018-08-24 2021-02-25 Bayer Ag Method for preparing 2-[(3r)-3-methylmorpholin-4-yl]-4-[1-methyl-1h-pyrazol-5-yl)-8-(1h-pyrazol-5-yl)-1,7-naphthyridine
EP3866805A1 (fr) * 2018-10-16 2021-08-25 Bayer Aktiengesellschaft Combinaison d'inhibiteurs de kinase atr avec des composés de 2,3-dihydro-imidazo[1,2-c]quinazoline
JP2022510501A (ja) * 2018-10-30 2022-01-26 リペア セラピューティクス インコーポレイテッド 化合物、医薬組成物、ならびに化合物の調製方法及びatrキナーゼ阻害剤としてのその使用方法
AR117929A1 (es) 2019-02-01 2021-09-01 Bayer Ag Compuestos de 1,2,4-triazin-3(2h)-ona
JP7677897B2 (ja) * 2019-02-11 2025-05-15 バイエル アクチェンゲゼルシャフト 過剰増殖性疾患の治療における使用のためのatrキナーゼ阻害剤bay1895344
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
AU2020317381A1 (en) * 2019-07-22 2022-02-10 Repare Therapeutics Inc. Substituted 2-morpholinopyridine derivatives as ATR kinase inhibitors
KR20220103987A (ko) * 2019-11-21 2022-07-25 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 피라졸로-헤테로아릴 유도체, 그것의 제조 방법, 및 그것의 의학적 용도
BR112022011426A2 (pt) * 2019-12-11 2022-08-30 Repare Therapeutics Inc Uso de inibidores de atr em combinação com inibidores de parp
AU2020405446A1 (en) 2019-12-20 2022-05-26 Nuevolution A/S Compounds active towards nuclear receptors
AU2020408107B2 (en) 2019-12-20 2026-04-23 Nuevolution A/S Compounds active towards nuclear receptors
EP4126874A1 (fr) 2020-03-31 2023-02-08 Nuevolution A/S Composés actifs vis-à-vis des récepteurs nucléaires
US11613532B2 (en) 2020-03-31 2023-03-28 Nuevolution A/S Compounds active towards nuclear receptors
TW202216701A (zh) * 2020-07-03 2022-05-01 香港商德琪研發有限公司 Atr抑制劑及其用途
KR20230039675A (ko) * 2020-07-13 2023-03-21 베이징 타이드 파마슈티컬 코퍼레이션 리미티드 Atr 키나제 억제제로 사용되는 피라졸로피리미딘 화합물
CN112110934B (zh) * 2020-09-23 2021-12-07 上海应用技术大学 一种基于azd9291的生物标记物及其制备方法与应用
CN116234551A (zh) * 2020-09-27 2023-06-06 南京明德新药研发有限公司 一类1,7-萘啶类化合物及其应用
ES3054165T3 (en) 2020-10-16 2026-01-30 Shanghai De Novo Pharmatech Co Ltd Triheterocyclic derivative, and pharmaceutical composition and application thereof
US20240059695A1 (en) * 2020-12-25 2024-02-22 Impact Therapeutics (Shanghai), Inc SUBSTITUTED IMIDAZO[1,5-b]PYRIDAZINE COMPOUNDS AS KINASE INHIBITORS AND USE THEREOF
AU2022271549A1 (en) * 2021-05-12 2023-11-16 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Sulfoximine-containing atr inhibitor compound
KR20240012471A (ko) * 2021-05-21 2024-01-29 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 피라졸로헤테로아릴계 유도체의 약학적으로 허용 가능한 염 및 이의 결정형
AU2022316931A1 (en) * 2021-07-27 2024-03-14 Littdd Medicines Ltd 8-oxo-3-azabicyclo[3.2.1]octane compound or salt thereof, and preparation method therefor and use thereof
CA3227336A1 (fr) * 2021-08-11 2023-02-16 Yuli Xie Derive de naphtyridine utile comme inhibiteur de l'atr et son procede de preparation
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
CN116731011A (zh) * 2022-03-01 2023-09-12 武汉众诚康健生物医药科技有限公司 一种萘啶衍生物及其应用
CN116925070B (zh) * 2022-04-24 2026-03-17 扬子江药业集团有限公司 取代的氮杂稠环化合物及其医药用途
US20250352539A1 (en) 2022-06-15 2025-11-20 Astrazeneca Ab Combination therapy for treating cancer
WO2024188937A1 (fr) 2023-03-13 2024-09-19 Bayer Aktiengesellschaft Associations d'inhibiteurs de kinase atr et d'inhibiteurs de parp pour traiter des affections hyper-prolifératives, par exemple un cancer
WO2025015238A2 (fr) * 2023-07-12 2025-01-16 Kansas State University Research Foundation N-oxydes de n-méthylmorpholine substitués chiraux et leurs procédés de fabrication et d'utilisation
WO2025181153A1 (fr) 2024-03-01 2025-09-04 F. Hoffmann-La Roche Ag Utilisation d'inhibiteurs d'atr en combinaison avec des inhibiteurs de pi3k alpha
WO2025229051A1 (fr) 2024-05-03 2025-11-06 F. Hoffmann-La Roche Ag Utilisation d'inhibiteurs d'atr en combinaison avec un agent anti-androgène
WO2025233224A1 (fr) 2024-05-09 2025-11-13 F. Hoffmann-La Roche Ag Utilisation d'inhibiteurs d'atr en combinaison avec une thérapie anti-pd(l)1

Family Cites Families (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1307271A (en) 1970-06-25 1973-02-14 Shell Int Research Sulphoximine derivatives and their use in herbicidal compositions
US4008068A (en) * 1976-03-08 1977-02-15 Velsicol Chemical Corporation 1-Thiadiazolyl-5-morpholinoimidazolidinones
JP2002540206A (ja) 1999-03-11 2002-11-26 ニューロゲン コーポレイション アリールの縮合した2,4−二置換ピリジン:nk3受容体リガンド
DE10349423A1 (de) 2003-10-16 2005-06-16 Schering Ag Sulfoximinsubstituierte Parimidine als CDK- und/oder VEGF-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel
US20070054916A1 (en) 2004-10-01 2007-03-08 Amgen Inc. Aryl nitrogen-containing bicyclic compounds and methods of use
WO2007000445A1 (fr) 2005-06-29 2007-01-04 Boehringer Ingelheim International Gmbh Derives de benzyle-benzene a substitution glucopyranosyle, medicaments contenant de tels composes, utilisation et production de ces derniers
KR101464384B1 (ko) * 2005-11-22 2014-11-21 쿠도스 파마슈티칼스 리미티드 mTOR 억제제로서 피리도피리미딘, 피라조피리미딘 및피리미도피리미딘 유도체
DE102005062742A1 (de) 2005-12-22 2007-06-28 Bayer Schering Pharma Ag Sulfoximin substituierte Pyrimidine, Verfahren zu deren Herstellung und ihre Verwendung als Arzneimittel
EP1803723A1 (fr) 2006-01-03 2007-07-04 Bayer Schering Pharma Aktiengesellschaft Dérivés (2,4,9-triaza-1(2,4)-pyrimidina-3(1,3)-benzenacyclononaphan-3^4-yl)-sulfoximide en tant qu'inhibiteurs de la kinase aurora pour le traitement de cancer
US7910747B2 (en) 2006-07-06 2011-03-22 Bristol-Myers Squibb Company Phosphonate and phosphinate pyrazolylamide glucokinase activators
ES2301380B1 (es) 2006-08-09 2009-06-08 Laboratorios Almirall S.A. Nuevos derivados de 1,7-naftiridina.
PT2057156T (pt) * 2006-08-23 2017-05-04 Kudos Pharm Ltd Derivados de 2-metilmorfolina pirido-, pirazo- e pirimidopirimidina como inibidores de mtor
JP5564045B2 (ja) * 2008-09-02 2014-07-30 ノバルティス アーゲー 二環式キナーゼ阻害剤
CA2742550A1 (fr) * 2008-10-03 2010-04-08 Merck Serono S.A. 4-morpholino-pyrido[3,2-d]pyrimidines
JP5702293B2 (ja) 2008-11-10 2015-04-15 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated Atrキナーゼの阻害剤として有用な化合物
US20100144345A1 (en) 2008-12-09 2010-06-10 Microsoft Corporation Using called party mobile presence and movement in communication application
BRPI0924084B1 (pt) 2008-12-19 2021-12-21 Vertex Pharmaceuticals Incorporated Derivados de pirazina e composição farmacêutica que os compreende
US20110053923A1 (en) * 2008-12-22 2011-03-03 Astrazeneca Chemical compounds 610
TW201111378A (en) 2009-09-11 2011-04-01 Bayer Schering Pharma Ag Substituted (heteroarylmethyl) thiohydantoins
US8962631B2 (en) 2010-05-12 2015-02-24 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of ATR kinase
US9062008B2 (en) 2010-05-12 2015-06-23 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of ATR kinase
EP2569287B1 (fr) 2010-05-12 2014-07-09 Vertex Pharmaceuticals Inc. Composés utilisables en tant qu'inhibiteurs de la kinase atr
JP2013526538A (ja) 2010-05-12 2013-06-24 バーテックス ファーマシューティカルズ インコーポレイテッド Atrキナーゼ阻害剤として有用な化合物
WO2011143422A1 (fr) 2010-05-12 2011-11-17 Vertex Pharmaceuticals Incorporated Dérivés de 2-aminopyridine utiles en tant qu'inhibiteurs de la kinase atr
AU2011253025A1 (en) 2010-05-12 2012-11-29 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of ATR kinase
SA111320519B1 (ar) 2010-06-11 2014-07-02 Astrazeneca Ab مركبات بيريميدينيل للاستخدام كمثبطات atr
WO2011163527A1 (fr) * 2010-06-23 2011-12-29 Vertex Pharmaceuticals Incorporated Dérivés de pyrrolo-pyrazine utiles en tant qu'inhibiteurs de l'atr kinase
WO2012003283A1 (fr) * 2010-06-30 2012-01-05 Amgen Inc. Composés hétérocycliques et leur emploi en tant qu'inhibiteurs de l'activité de pi3k
WO2012138938A1 (fr) 2011-04-05 2012-10-11 Vertex Pharmaceuticals Incorporated Composés aminopyrazines utiles en tant qu'inhibiteurs de la kinase atr
JP2014517079A (ja) 2011-06-22 2014-07-17 バーテックス ファーマシューティカルズ インコーポレイテッド Atrキナーゼ阻害剤として有用な化合物
JP2014522818A (ja) 2011-06-22 2014-09-08 バーテックス ファーマシューティカルズ インコーポレイテッド Atrキナーゼ阻害剤として有用な化合物
EP2723745A1 (fr) 2011-06-22 2014-04-30 Vertex Pharmaceuticals Inc. Composés utiles comme inhibiteurs de la kinase atr
US8846656B2 (en) * 2011-07-22 2014-09-30 Novartis Ag Tetrahydropyrido-pyridine and tetrahydropyrido-pyrimidine compounds and use thereof as C5a receptor modulators
MX2014003796A (es) 2011-09-30 2015-01-16 Vertex Pharma Compuestos utiles como inhibidores de la cinasa ataxia telangiectasia mutada y rad3 relacionados (atr).
WO2013049719A1 (fr) 2011-09-30 2013-04-04 Vertex Pharmaceuticals Incorporated Composés utiles en tant qu'inhibiteurs de kinase atr
IN2014CN02501A (fr) 2011-09-30 2015-06-26 Vertex Pharma
WO2013049720A1 (fr) 2011-09-30 2013-04-04 Vertex Pharmaceuticals Incorporated Composés utiles en tant qu'inhibiteurs de kinase atr
EP2776422A1 (fr) 2011-11-09 2014-09-17 Vertex Pharmaceuticals Incorporated Composés utiles en tant qu'inhibiteurs de la kinase atr
US8841449B2 (en) 2011-11-09 2014-09-23 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of ATR kinase
WO2013071093A1 (fr) 2011-11-09 2013-05-16 Vertex Pharmaceuticals Incorporated Composés de pyrazine utiles comme inhibiteurs de kinase atr
EP2776429A1 (fr) 2011-11-09 2014-09-17 Vertex Pharmaceuticals Incorporated Composés utiles comme inhibiteurs de kinase atr
EP2776421A1 (fr) 2011-11-09 2014-09-17 Vertex Pharmaceuticals Incorporated Composés utiles comme inhibiteurs de kinase atr
US20140044802A1 (en) 2012-04-05 2014-02-13 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of atr kinase and combination therapies thereof
US8912198B2 (en) 2012-10-16 2014-12-16 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of ATR kinase
SMT202000713T1 (it) 2012-12-07 2021-03-15 Vertex Pharma Pirazolo [1,5-a] pirimidine utili come inibitori dell'atr chinasi per il trattamento di malattie del cancro
WO2014109414A1 (fr) * 2013-01-11 2014-07-17 富士フイルム株式会社 Composé hétérocyclique contenant de l'azote ou sel de celui-ci
JP2016512815A (ja) 2013-03-15 2016-05-09 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated Atrキナーゼの阻害剤として有用な縮合ピラゾロピリミジン誘導体
TWI700283B (zh) * 2014-08-04 2020-08-01 德商拜耳製藥公司 2-(嗎啉-4-基)-1,7-萘啶
CA3011189C (fr) * 2016-01-14 2024-02-20 Bayer Pharma Aktiengesellschaft 2-(morpholin-4-yl)-1,7-naphthyridines substituees en 5
WO2018153972A1 (fr) 2017-02-24 2018-08-30 Bayer Pharma Aktiengesellschaft Combinaison d'inhibiteurs de kinase atr et d'anti-androgènes
TW201840319A (zh) 2017-02-24 2018-11-16 德商拜耳廠股份有限公司 Atr激酶抑制劑與鐳-223鹽之組合
EP3585365B1 (fr) 2017-02-24 2021-08-25 Bayer Pharma Aktiengesellschaft Combinaison de atr kinase inhibiteurs avec parp inhibiteurs
WO2018153971A1 (fr) 2017-02-24 2018-08-30 Bayer Pharma Aktiengesellschaft Combinaison d'inhibiteurs de kinase atr
CA3054248A1 (fr) 2017-02-24 2018-08-30 Bayer As Polytherapie comprenant un agent radiopharmaceutique et un inhibiteur de reparation d'adn
JOP20190197A1 (ar) 2017-02-24 2019-08-22 Bayer Pharma AG مثبط كيناز ايه تي آر للاستخدام في طريقة لعلاج مرض فرط التكاثر
WO2018153970A1 (fr) 2017-02-24 2018-08-30 Bayer Pharma Aktiengesellschaft Formes solides de 2-[(3r)-3-méthylmorpholin-4-yl]-4-(1-méthyl-1h-pyrazol-5-yl)-8-(1h-pyrazol-5-yl)-1,7-naphtyridine
WO2018206547A1 (fr) 2017-05-12 2018-11-15 Bayer Pharma Aktiengesellschaft Combinaison d'inhibiteurs de bub1 et d'atr
CN111065946B (zh) 2017-06-28 2023-08-18 康宁研究与开发公司 具有键接连接端口和固定特征的多端口件和其他装置及其制造方法
WO2019025440A1 (fr) 2017-08-04 2019-02-07 Bayer Pharma Aktiengesellschaft Combinaison d'inhibiteurs de kinase atr et d'inhibiteurs de pd-1/pd-l1
CA3084863A1 (fr) 2017-12-08 2019-06-13 Bayer Aktiengesellschaft Marqueurs predictifs pour inhibiteurs d'atr kinase
SG11202101011RA (en) 2018-08-24 2021-02-25 Bayer Ag Method for preparing 2-[(3r)-3-methylmorpholin-4-yl]-4-[1-methyl-1h-pyrazol-5-yl)-8-(1h-pyrazol-5-yl)-1,7-naphthyridine
US12098291B2 (en) 2018-10-05 2024-09-24 Isp Investments Llc Smooth high solids film coating composition comprising water soluble cellulose ether, process for preparing the same and method of use thereof
EP3866805A1 (fr) 2018-10-16 2021-08-25 Bayer Aktiengesellschaft Combinaison d'inhibiteurs de kinase atr avec des composés de 2,3-dihydro-imidazo[1,2-c]quinazoline
JP7677897B2 (ja) 2019-02-11 2025-05-15 バイエル アクチェンゲゼルシャフト 過剰増殖性疾患の治療における使用のためのatrキナーゼ阻害剤bay1895344

Also Published As

Publication number Publication date
EA035039B1 (ru) 2020-04-21
TW201922746A (zh) 2019-06-16
WO2016020320A1 (fr) 2016-02-11
DK3395818T3 (en) 2021-12-13
CA2956992A1 (fr) 2016-02-11
CU20170009A7 (es) 2017-07-04
US20180256591A1 (en) 2018-09-13
US20160287604A1 (en) 2016-10-06
IL250220A0 (en) 2017-03-30
US9993484B2 (en) 2018-06-12
AU2019204125B2 (en) 2020-06-25
UY36254A (es) 2016-02-29
MX2017001637A (es) 2017-04-27
WO2016020320A8 (fr) 2017-04-06
IL250220B (en) 2019-09-26
SI3395818T1 (sl) 2022-01-31
CO2017001035A2 (es) 2017-05-31
CA2956992C (fr) 2024-10-29
MX2020010333A (es) 2022-08-03
NZ765780A (en) 2023-11-24
ECSP17007538A (es) 2017-03-31
DK3177619T3 (en) 2018-08-06
LT3177619T (lt) 2018-08-10
PH12021550792A1 (en) 2021-12-13
TW201613920A (en) 2016-04-16
TN2017000027A1 (en) 2018-07-04
US9549932B2 (en) 2017-01-24
MA40523B1 (fr) 2018-09-28
RS62609B1 (sr) 2021-12-31
US10772893B2 (en) 2020-09-15
MX394442B (es) 2025-03-24
US11529356B2 (en) 2022-12-20
CN110204544A (zh) 2019-09-06
PT3177619T (pt) 2018-07-24
SA517380830B1 (ar) 2021-01-18
CN110256427B (zh) 2022-02-22
NZ728416A (en) 2021-11-26
PH12017500204A1 (en) 2017-07-10
SI3177619T1 (en) 2018-08-31
KR20200130755A (ko) 2020-11-19
US20170216304A1 (en) 2017-08-03
NI201700011A (es) 2017-04-20
TWI656121B (zh) 2019-04-11
PH12017500204B1 (en) 2022-07-29
KR20170040300A (ko) 2017-04-12
UA123928C2 (uk) 2021-06-23
EA201891861A1 (ru) 2019-01-31
EP3395818A1 (fr) 2018-10-31
CN106795156A (zh) 2017-05-31
CY1120673T1 (el) 2019-12-11
JP6266839B2 (ja) 2018-01-24
EP3177619A1 (fr) 2017-06-14
DOP2017000038A (es) 2018-04-15
US20200383991A1 (en) 2020-12-10
UA121036C2 (uk) 2020-03-25
AP2017009702A0 (en) 2017-01-31
IL268969B (en) 2020-03-31
CN106795156B (zh) 2019-07-30
JP6507216B2 (ja) 2019-04-24
EA201790306A1 (ru) 2017-08-31
ES2900599T3 (es) 2022-03-17
EP3177619B1 (fr) 2018-04-25
CR20170034A (es) 2017-04-06
CY1124855T1 (el) 2022-11-25
JP2018062517A (ja) 2018-04-19
BR112017002221B1 (pt) 2023-02-28
HRP20211770T1 (hr) 2022-02-18
CL2017000287A1 (es) 2017-11-10
MX376270B (es) 2025-03-07
CN110204544B (zh) 2022-04-12
EA031678B1 (ru) 2019-02-28
IL268969A (en) 2019-10-31
TWI700283B (zh) 2020-08-01
CU24419B1 (es) 2019-05-03
ES2679625T3 (es) 2018-08-29
HUE038533T2 (hu) 2018-10-29
ZA202101003B (en) 2022-09-28
SG11201700750UA (en) 2017-02-27
JO3447B1 (ar) 2020-07-05
RS57445B1 (sr) 2018-09-28
MY192883A (en) 2022-09-13
LT3395818T (lt) 2021-11-25
HRP20181143T1 (hr) 2018-09-21
PE20170666A1 (es) 2017-06-15
PL3177619T3 (pl) 2018-09-28
JP2017523987A (ja) 2017-08-24
EP3395818B1 (fr) 2021-09-22
PL3395818T3 (pl) 2022-01-31
KR102317169B1 (ko) 2021-10-27
CN110256427A (zh) 2019-09-20
AU2015299173B2 (en) 2019-03-14
HUE056676T2 (hu) 2022-02-28
AU2019204125A1 (en) 2019-07-04
KR102180006B1 (ko) 2020-11-18
BR112017002221A2 (pt) 2018-05-22

Similar Documents

Publication Publication Date Title
MA40523B1 (fr) 2-(morpholin-4-yl)-1,7-naphthyridines
MA41135B1 (fr) Benzamides substitués 1,3-thiazol-2-yl
MA35422B1 (fr) Imidazopyridazines amino-substituees
MA45020A (fr) Dérivés sulfonamides aromatiques
MA59379B1 (fr) Aminothiazoles substitués en tant qu'inhibiteurs de dgkzeta pour l'activation immunitaire
MA33768B1 (fr) Triazolopyridines
MA35826B1 (fr) Triazolopyridines substituées et leur utilisation à titre d'inhibiteurs de ttk
MA47447B1 (fr) 2-hétéroaryl-3-oxo-2,3-dihydropyridazine-4-carboxamides pour le traitement du cancer
WO2019035863A8 (fr) Activateurs de la pyruvate kinase destinés à être utilisés dans le traitement de troubles hématologiques
MA41562A1 (fr) Agonistes d'apj 4-hydroxy-3-(heteroaryl)pyridine-2-one a utiliser dans le traitement de troubles cardio-vasculaires
EA202090448A1 (ru) Дигидрооксадиазиноны
MA39317A1 (fr) Dérivés de nucléosides à substitution 4'-difluorométhyle utilisés en tant qu'inhibiteurs de la réplication de l'arn du virus de la grippe
WO2019007696A1 (fr) Nouveaux composés et compositions pharmaceutiques de ceux-ci destinés au traitement de la fibrose
MA38358A1 (fr) Formulations de composés organiques
JOP20200100A1 (ar) مشتقات بيرازولو-بيرولو-بيريميدين-ديون جديدة كمثبِّطات لـ p2x3
MA43913A (fr) Modulateurs allostériques positifs du récepteur m1 muscarinique
MA47082B1 (fr) Amides aromatiques d'acide carboxylique en tant qu'antagonistes des recepteurs bradykinin b1
MA38679A1 (fr) Modulateurs du récepteur de cxcr7
MA42769B1 (fr) Dérivés de fluoroindole en tant que modulateurs allostériques positifs du récepteur muscarinique m1
MA43553B1 (fr) 2-(morpholin-4-yl)-1,7-naphthyridines
MA37849A1 (fr) Dérivés de diazépinone à utiliser pour le traitement du syndrome de l'x fragile, de la maladie de parkinson ou de la maladie du reflux
MA38642A1 (fr) Compositions pharmaceutiques de composes triazolopyridines substitues pour une utilsation en tant qu'agents anticancereux
MA38774A1 (fr) Pyrazolo-pyridinamines substituees inhibiteurs de mknk1 kinase pour une utilisation dans les troubles hyperproliferatifs et/ou relatifs a l'angiogenese.
MA39041A1 (fr) Thiénopyrimidines en tant qu'inhibiteurs de mknk1 et de mknk2
MA39256A1 (fr) Benzimidazol-2-amines en tant qu'inhibiteurs midh1