PT2604610T - Derivado cetona de ftalazinona, processo para a sua preparação e seu uso farmacêutico - Google Patents

Derivado cetona de ftalazinona, processo para a sua preparação e seu uso farmacêutico

Info

Publication number
PT2604610T
PT2604610T PT118159862T PT11815986T PT2604610T PT 2604610 T PT2604610 T PT 2604610T PT 118159862 T PT118159862 T PT 118159862T PT 11815986 T PT11815986 T PT 11815986T PT 2604610 T PT2604610 T PT 2604610T
Authority
PT
Portugal
Prior art keywords
preparation
pharmaceutical use
ketone derivative
phthalazinone
phthalazinone ketone
Prior art date
Application number
PT118159862T
Other languages
English (en)
Portuguese (pt)
Inventor
Tang Pengcho
Li Xin
Li Xiangqin
Chen Yang
Wan Bin
Zhu Zhe
Original Assignee
Jiangsu Hansoh Pharmaceutical Co Ltd
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 Jiangsu Hansoh Pharmaceutical Co Ltd filed Critical Jiangsu Hansoh Pharmaceutical Co Ltd
Publication of PT2604610T publication Critical patent/PT2604610T/pt

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
    • A61K31/495Heterocyclic 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)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (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)
PT118159862T 2010-08-09 2011-07-26 Derivado cetona de ftalazinona, processo para a sua preparação e seu uso farmacêutico PT2604610T (pt)

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
PT2604610T true PT2604610T (pt) 2016-07-13

Family

ID=45567315

Family Applications (1)

Application Number Title Priority Date Filing Date
PT118159862T PT2604610T (pt) 2010-08-09 2011-07-26 Derivado cetona de ftalazinona, processo para a sua preparação e seu uso farmacêutico

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
AU2013368842B2 (en) 2012-12-31 2015-11-12 Cadila Healthcare Limited Substituted phthalazin-1 (2H)-one derivatives as selective inhibitors of poly (ADP-ribose) polymerase-1
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UY35834A (es) 2013-11-14 2015-05-29 Bristol Myers Squibb Company Una Corporación Del Estado De Delaware Piperazinas de pirazolo sustituido como inhibidores de caseína quinasa 1 delta y epsilon
PL3325623T6 (pl) 2015-07-23 2022-05-30 Institut Curie Zastosowanie skojarzenia cząsteczki dbait i inhibitorów parp do leczenia nowotworu
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WO2017101796A1 (zh) * 2015-12-16 2017-06-22 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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WO2018189214A1 (en) * 2017-04-12 2018-10-18 F. Hoffmann-La Roche Ag A method for labeling of aldehyde containing target molecules
MX2020002046A (es) * 2017-08-24 2020-09-17 Jiangsu Hengrui Medicine Co Forma cristalina del inhibidor de parp-1 y método de preparación de ésta.
CA3080644A1 (en) 2017-12-06 2019-06-13 Quanren WANG Use of parp inhibitor in treating chemotherapy-resistant ovarian cancer or breast cancer
US11345709B2 (en) 2018-01-09 2022-05-31 Jiangsu Hengrui Medicine Co., Ltd. Process for preparing 4-(4-fluoro-3-(2-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyrazine-7-carbonyl)benzyl)phthalazin-1(2h)-one
CA3088288A1 (en) * 2018-01-26 2019-08-01 Recordati Industria Chimica E Farmaceutica S.P.A Triazole, imidazole and pyrrole condensed piperazine derivatives and their use as modulators of mglu5 receptors
JP2021516229A (ja) * 2018-02-28 2021-07-01 ザ トラスティーズ オブ ザ ユニバーシティ オブ ペンシルバニア 低親和性ポリ(ad−リボース)ポリメラーゼ1依存性細胞毒性剤
CN111819282A (zh) 2018-03-13 2020-10-23 欧恩科斯欧公司 对抗癌症治疗中获得性耐药性的Dbait分子
CN112165944B (zh) * 2018-03-29 2024-04-09 德州大学系统董事会 转录激活蛋白的咪唑并哌嗪抑制剂
ES2989438T3 (es) 2018-09-19 2024-11-26 Novo Nordisk Healthcare Ag Activación de la piruvato cinasa R
WO2020061378A1 (en) 2018-09-19 2020-03-26 Forma Therapeutics, Inc. Treating sickle cell disease with a pyruvate kinase r activating compound
WO2020083187A1 (zh) * 2018-10-22 2020-04-30 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
CN115400087B (zh) * 2018-11-16 2023-10-20 江苏恒瑞医药股份有限公司 一种包含parp抑制剂的药物组合物
TW202110448A (zh) * 2019-05-28 2021-03-16 大陸商江蘇恆瑞醫藥股份有限公司 Parp抑制劑聯合vegfr抑制劑用於治療卵巢癌或乳腺癌的用途
AU2020350763A1 (en) 2019-09-19 2022-04-07 Novo Nordisk Health Care Ag Pyruvate kinase R (PKR) activating compositions
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
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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
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Also Published As

Publication number Publication date
JP2013535491A (ja) 2013-09-12
UA111161C2 (uk) 2016-04-11
US9566277B2 (en) 2017-02-14
EP2604610A4 (en) 2013-12-25
CN102686591A (zh) 2012-09-19
RU2564527C2 (ru) 2015-10-10
AU2011288876A1 (en) 2013-01-31
CA2806324A1 (en) 2012-02-16
CN102686591B (zh) 2014-03-19
AU2011288876A2 (en) 2013-02-21
PL2604610T3 (pl) 2016-11-30
BR112013002220B1 (pt) 2021-09-21
HUE029275T2 (en) 2017-02-28
US9273052B2 (en) 2016-03-01
KR20130110149A (ko) 2013-10-08
EP2604610B1 (en) 2016-05-11
AU2011288876B2 (en) 2014-08-21
JP5808408B2 (ja) 2015-11-10
US20130131068A1 (en) 2013-05-23
CN102372716A (zh) 2012-03-14
RU2013106754A (ru) 2014-09-20
ES2582315T3 (es) 2016-09-12
WO2012019427A1 (zh) 2012-02-16
CA2806324C (en) 2019-02-19
WO2012019427A8 (zh) 2012-05-10
KR101829940B1 (ko) 2018-02-19
BR112013002220A2 (pt) 2016-05-24
HK1174030A1 (en) 2013-05-31
US20160151367A1 (en) 2016-06-02
EP2604610A1 (en) 2013-06-19

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