PL2604610T3 - Pochodna ketonu ftalazynonowego, sposób jej wytwarzania oraz jej farmaceutyczne zastosowanie - Google Patents

Pochodna ketonu ftalazynonowego, sposób jej wytwarzania oraz jej farmaceutyczne zastosowanie

Info

Publication number
PL2604610T3
PL2604610T3 PL11815986.2T PL11815986T PL2604610T3 PL 2604610 T3 PL2604610 T3 PL 2604610T3 PL 11815986 T PL11815986 T PL 11815986T PL 2604610 T3 PL2604610 T3 PL 2604610T3
Authority
PL
Poland
Prior art keywords
preparation
pharmaceutical use
ketone derivative
phthalazinone
phthalazinone ketone
Prior art date
Application number
PL11815986.2T
Other languages
English (en)
Polish (pl)
Inventor
Pengcho Tang
Xin Li
Xiangqin Li
Yang Chen
Bin Wang
Zhe Zhu
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 filed Critical
Publication of PL2604610T3 publication Critical patent/PL2604610T3/pl

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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
    • A61K31/495Heterocyclic 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/502Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41881,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
    • 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
    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic 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
    • A61K31/535Heterocyclic 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
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • 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
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
PL11815986.2T 2010-08-09 2011-07-26 Pochodna ketonu ftalazynonowego, sposób jej wytwarzania oraz jej farmaceutyczne zastosowanie PL2604610T3 (pl)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010102483075A CN102372716A (zh) 2010-08-09 2010-08-09 酞嗪酮类衍生物、其制备方法及其在医药上的应用

Publications (1)

Publication Number Publication Date
PL2604610T3 true PL2604610T3 (pl) 2016-11-30

Family

ID=45567315

Family Applications (1)

Application Number Title Priority Date Filing Date
PL11815986.2T PL2604610T3 (pl) 2010-08-09 2011-07-26 Pochodna ketonu ftalazynonowego, sposób jej wytwarzania oraz jej farmaceutyczne zastosowanie

Country Status (15)

Country Link
US (2) US9273052B2 (enExample)
EP (1) EP2604610B1 (enExample)
JP (1) JP5808408B2 (enExample)
KR (1) KR101829940B1 (enExample)
CN (2) CN102372716A (enExample)
AU (1) AU2011288876B2 (enExample)
BR (1) BR112013002220B1 (enExample)
CA (1) CA2806324C (enExample)
ES (1) ES2582315T3 (enExample)
HU (1) HUE029275T2 (enExample)
PL (1) PL2604610T3 (enExample)
PT (1) PT2604610T (enExample)
RU (1) RU2564527C2 (enExample)
UA (1) UA111161C2 (enExample)
WO (1) WO2012019427A1 (enExample)

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CN102702108A (zh) * 2012-06-27 2012-10-03 上海大学 1,2-二氢酞嗪类化合物及其合成方法
CN103570725B (zh) * 2012-08-01 2017-03-22 中国科学院上海药物研究所 哌嗪并三唑类化合物及其制备方法和用途
CN102863393A (zh) * 2012-09-26 2013-01-09 上海大学 1,2-二氢酞嗪类化合物及其合成方法
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AR098414A1 (es) 2013-11-14 2016-05-26 Bristol Myers Squibb Co PIPERAZINAS DE PIRAZOLO SUSTITUIDO COMO INHIBIDORES DE CASEÍNA QUINASA 1 d/e
ES2879434T3 (es) 2015-07-23 2021-11-22 Inst Curie Uso de una combinación de molécula Dbait e inhibidores de PARP para tratamiento del cáncer
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CN106749261A (zh) 2015-11-23 2017-05-31 中国科学院上海药物研究所 一类取代三唑并哌嗪类parp抑制剂及其制备方法和用途
CN107207504B (zh) * 2015-12-16 2020-03-10 四川科伦博泰生物医药股份有限公司 酞嗪酮衍生物、其制备方法及用途
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WO2018162439A1 (en) 2017-03-08 2018-09-13 Onxeo New predictive biomarker for the sensitivity to a treatment of cancer with a dbait molecule
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WO2018191389A1 (en) * 2017-04-12 2018-10-18 Roche Sequencing Solutions, Inc. A method for sequencing reaction with tagged nucleoside obtained via pictet spengler reaction
US11180505B2 (en) 2017-08-24 2021-11-23 Jiangsu Hengrui Medicine Co., Ltd. Crystal form of PARP-1 inhibitor and preparation method therefor
CN111093706B (zh) * 2017-12-06 2022-06-21 江苏恒瑞医药股份有限公司 Parp抑制剂用于治疗化疗耐药的卵巢癌或乳腺癌的用途
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CA3129516A1 (en) 2018-02-28 2019-09-06 The Trustees Of The University Of Pennsylvania Low affinity poly(ad-ribose) polymerase 1 dependent cytotoxic agents
KR20200130856A (ko) 2018-03-13 2020-11-20 옹쎄오 암 치료에서 획득한 내성에 대한 디베이트 분자
AU2019245403B2 (en) * 2018-03-29 2025-02-06 Board Of Regents, The University Of Texas System Imidazopiperazine inhibitors of transcription activating proteins
WO2020061255A1 (en) 2018-09-19 2020-03-26 Forma Therapeutics, Inc. Activating pyruvate kinase r
US10675274B2 (en) 2018-09-19 2020-06-09 Forma Therapeutics, Inc. Activating pyruvate kinase R
CN112584836A (zh) * 2018-10-22 2021-03-30 江苏恒瑞医药股份有限公司 一种ar拮抗剂联合parp抑制剂在制备治疗前列腺癌的药物中的用途
US12318385B2 (en) 2018-11-16 2025-06-03 Jiangsu Hengrui Medicine Co., Ltd. Pharmaceutical composition comprising PARP inhibitors
WO2020238932A1 (zh) * 2019-05-28 2020-12-03 江苏恒瑞医药股份有限公司 Parp抑制剂联合vegfr抑制剂用于治疗卵巢癌或乳腺癌的用途
HUE072832T2 (hu) 2019-09-19 2025-12-28 Novo Nordisk Healthcare Ag Piruvát kináz R-t (PKR) aktiváló készítmények
CN112870365A (zh) * 2019-11-29 2021-06-01 江苏恒瑞医药股份有限公司 Ezh2抑制剂和/或parp抑制剂与化疗药物联合在制备治疗肿瘤药物中的用途
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
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CN111732594B (zh) * 2020-08-18 2022-03-04 苏州富士莱医药股份有限公司 一种氟唑帕利的制备方法
CN116348112A (zh) 2020-10-02 2023-06-27 德州大学系统董事会 转录激活蛋白的咪唑并哌嗪抑制剂
JP2023544173A (ja) 2020-10-02 2023-10-20 ボード オブ レジェンツ,ザ ユニバーシティ オブ テキサス システム 転写活性化タンパク質のイミダゾピペラジン阻害剤
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Also Published As

Publication number Publication date
US20130131068A1 (en) 2013-05-23
CN102372716A (zh) 2012-03-14
RU2013106754A (ru) 2014-09-20
CN102686591B (zh) 2014-03-19
US20160151367A1 (en) 2016-06-02
AU2011288876A2 (en) 2013-02-21
RU2564527C2 (ru) 2015-10-10
JP5808408B2 (ja) 2015-11-10
WO2012019427A8 (zh) 2012-05-10
CA2806324C (en) 2019-02-19
AU2011288876A1 (en) 2013-01-31
EP2604610A1 (en) 2013-06-19
KR101829940B1 (ko) 2018-02-19
UA111161C2 (uk) 2016-04-11
HK1174030A1 (en) 2013-05-31
JP2013535491A (ja) 2013-09-12
CA2806324A1 (en) 2012-02-16
BR112013002220A2 (pt) 2016-05-24
ES2582315T3 (es) 2016-09-12
EP2604610B1 (en) 2016-05-11
AU2011288876B2 (en) 2014-08-21
CN102686591A (zh) 2012-09-19
WO2012019427A1 (zh) 2012-02-16
KR20130110149A (ko) 2013-10-08
EP2604610A4 (en) 2013-12-25
US9273052B2 (en) 2016-03-01
BR112013002220B1 (pt) 2021-09-21
US9566277B2 (en) 2017-02-14
HUE029275T2 (en) 2017-02-28
PT2604610T (pt) 2016-07-13

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