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AR107828A1 - 2-amino-n-[7-metoxi-2,3-dihidroimidazo-[1,2-c]quinazolin-5-il]pirimidin-5-carboxamidas como inhibidor de pi3k - Google Patents

2-amino-n-[7-metoxi-2,3-dihidroimidazo-[1,2-c]quinazolin-5-il]pirimidin-5-carboxamidas como inhibidor de pi3k

Info

Publication number
AR107828A1
AR107828A1 ARP170100571A ARP170100571A AR107828A1 AR 107828 A1 AR107828 A1 AR 107828A1 AR P170100571 A ARP170100571 A AR P170100571A AR P170100571 A ARP170100571 A AR P170100571A AR 107828 A1 AR107828 A1 AR 107828A1
Authority
AR
Argentina
Prior art keywords
dihydroimidazo
compounds
carboxamids
metoxi
quinazolin
Prior art date
Application number
ARP170100571A
Other languages
English (en)
Inventor
Andreas Lender
Dieter Lang
Michael Gerisch
Oliver Politz
Ningshu Liu
Schwarz Thomas Dr
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 AR107828A1 publication Critical patent/AR107828A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-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
    • A61K31/5355Non-condensed oxazines and containing further heterocyclic rings
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Compuestos de 2,3-dihidroimidazo[1,2-c]quinazolina, composiciones farmacéuticas que contienen dichos compuestos y al uso de dichos compuestos o composiciones para la inhibición de fosfatidilinositol-3-quinasa (PI3K) y para el tratamiento de enfermedades asociadas con la actividad de fosfatidilinositol-3-quinasa (PI3K), en particular para el tratamiento de trastorno hiperproliferativos y/o angiogénicos, como único agente o en combinación con otros ingredientes activos. Reivindicación 1: Un compuesto de fórmula general (1), caracterizado porque: R¹ representa un átomo de hidrógeno o un grupo -C(=O)H; y R¹’ representa un grupo -(CH₂)₂OH; o: R¹ y R¹’, junto con el átomo de N al cual están unidos, forman un grupo morfolinilo el cual es sustituido con 1 ó 2 sustituyentes seleccionados independientemente entre -OH y =O; o una sal, solvato, hidrato o estereoisómero fisiológicamente aceptable del mismo.
ARP170100571A 2016-03-08 2017-03-08 2-amino-n-[7-metoxi-2,3-dihidroimidazo-[1,2-c]quinazolin-5-il]pirimidin-5-carboxamidas como inhibidor de pi3k AR107828A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP16159156 2016-03-08

Publications (1)

Publication Number Publication Date
AR107828A1 true AR107828A1 (es) 2018-06-13

Family

ID=55521577

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP170100571A AR107828A1 (es) 2016-03-08 2017-03-08 2-amino-n-[7-metoxi-2,3-dihidroimidazo-[1,2-c]quinazolin-5-il]pirimidin-5-carboxamidas como inhibidor de pi3k

Country Status (9)

Country Link
US (1) US10844066B2 (es)
EP (1) EP3426657B1 (es)
JP (1) JP6935415B2 (es)
CN (1) CN108884098B (es)
AR (1) AR107828A1 (es)
CA (1) CA3016584A1 (es)
TW (1) TW201736375A (es)
UY (1) UY37149A (es)
WO (1) WO2017153220A1 (es)

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EP3018127A1 (en) 2014-11-07 2016-05-11 Bayer Pharma Aktiengesellschaft Synthesis of copanlisib and its dihydrochloride salt
CN107864625B (zh) 2015-03-09 2021-05-28 拜耳制药股份公司 含有取代的2,3-二氢咪唑并[1,2-c]喹唑啉的组合产品
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
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
CN109729716B (zh) 2016-09-23 2022-03-15 拜耳制药股份公司 Pi3k-抑制剂的组合产品
ES2928773T3 (es) 2017-01-17 2022-11-22 Heparegenix Gmbh Inhibidores de proteína cinasas para fomentar la regeneración hepática o reducir o prevenir la muerte de hepatocitos
EP3585437B1 (en) 2017-02-24 2022-12-21 Bayer Pharma Aktiengesellschaft Combinations of copanlisib with anti-pd-1 antibody
EP3645005A1 (en) 2017-06-28 2020-05-06 Bayer Consumer Care AG Combination of a pi3k-inhibitor with an androgen receptor antagonist
FR3072024A1 (fr) * 2017-10-11 2019-04-12 Olivier Petitjean Prevention et traitement de l’hyperplasie benigne de la prostate a l‘aide d’un inhibiteur selectif de la production d’especes reactives de l’oxygene d’origine mitochondriale
KR102618168B1 (ko) * 2018-07-06 2023-12-27 일양약품주식회사 프리온 질환의 예방 또는 치료를 위한 약제학적 조성물
CN109674817B (zh) * 2019-01-31 2021-06-29 哈尔滨医科大学 三氧化二砷在制备治疗晚期动脉粥样硬化药物中的用途
CN110656152A (zh) * 2019-10-11 2020-01-07 郑州大学 一种艾曲波帕介导巨噬细胞抗血管生成作用验证方法
CN114223613B (zh) * 2021-11-30 2023-03-21 西安医学院 一种基于aav8-pcsk9诱导的高胆固醇血症和动脉粥样硬化小鼠模型及构建方法
AU2024306046A1 (en) * 2023-06-26 2026-01-22 Athos Therapeutics, Inc. Small molecules for the treatment of autoimmune disorders

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HRP20131159B1 (hr) 2002-09-30 2019-11-01 Bayer Ip Gmbh Taljeni azol-pirimidin derivati
AR064106A1 (es) 2006-12-05 2009-03-11 Bayer Schering Pharma Ag Derivados de 2,3-dihidroimidazo [1,2-c] quinazolina sustituida utiles para el tratamiento de enfermedades y trastornos hiper-proliferativos asociados con la angiogenesis
WO2009091550A2 (en) 2008-01-14 2009-07-23 Bayer Healthcare Llc Sulfone substituted 2,3-dihydroimidazo [1,2-c] quinazoline derivatives useful for treating hyper-proliferative disorders and diseases with angiogenesis
EP2168583A1 (en) 2008-09-24 2010-03-31 Bayer Schering Pharma Aktiengesellschaft Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines for the treatment of myeloma
CA2796253A1 (en) 2010-04-16 2011-10-20 Bayer Intellectual Property Gmbh Substituted 2,3-dihydroimidazo[1,2-c]quinazoline-containing combinations
JO3733B1 (ar) 2011-04-05 2021-01-31 Bayer Ip Gmbh استخدام 3,2-دايهيدروايميدازو[1, 2 -c]كوينازولينات مستبدلة
EP2508525A1 (en) 2011-04-05 2012-10-10 Bayer Pharma Aktiengesellschaft Substituted 2,3-dihydroimidazo[1,2-c]quinazoline salts
UA119537C2 (uk) 2013-04-08 2019-07-10 Байєр Фарма Акцієнгезелльшафт ЗАСТОСУВАННЯ ЗАМІЩЕНИХ 2,3-ДИГІДРОІМІДАЗО[1,2-c]ХІНАЗОЛІНІВ ДЛЯ ЛІКУВАННЯ ЛІМФОМ
EP3077002B1 (en) 2013-12-03 2020-04-22 Bayer Pharma Aktiengesellschaft Combination of pi3k-inhibitors
EP3018131A1 (en) 2014-11-07 2016-05-11 Bayer Pharma Aktiengesellschaft Synthesis of copanlisib and its dihydrochloride salt
EP3018127A1 (en) 2014-11-07 2016-05-11 Bayer Pharma Aktiengesellschaft Synthesis of copanlisib and its dihydrochloride salt
KR20180013850A (ko) 2015-03-09 2018-02-07 바이엘 파마 악티엔게젤샤프트 치환된 2,3-디히드로이미다조[1,2-c]퀴나졸린의 용도
CN107864625B (zh) 2015-03-09 2021-05-28 拜耳制药股份公司 含有取代的2,3-二氢咪唑并[1,2-c]喹唑啉的组合产品
BR112018015782A2 (pt) 2016-02-01 2019-01-02 Bayer Pharma AG biomarcadores de copanlisibe
JP2019512003A (ja) 2016-02-01 2019-05-09 バイエル ファーマ アクチエンゲゼルシャフト コパンリシブバイオマーカー
CN109729716B (zh) 2016-09-23 2022-03-15 拜耳制药股份公司 Pi3k-抑制剂的组合产品

Also Published As

Publication number Publication date
JP2019507770A (ja) 2019-03-22
US20190092775A1 (en) 2019-03-28
CN108884098A (zh) 2018-11-23
CA3016584A1 (en) 2017-09-14
JP6935415B2 (ja) 2021-09-15
UY37149A (es) 2017-10-31
TW201736375A (zh) 2017-10-16
WO2017153220A1 (en) 2017-09-14
EP3426657B1 (en) 2022-07-13
EP3426657A1 (en) 2019-01-16
US10844066B2 (en) 2020-11-24
CN108884098B (zh) 2021-09-14

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