ME02855B - KONDENZOVANI TETRA ILl PENTA-CIKLIČNI DIHIDRODIAZEPINOKARBAZOLONI KAO PARP INHIBITORI - Google Patents

KONDENZOVANI TETRA ILl PENTA-CIKLIČNI DIHIDRODIAZEPINOKARBAZOLONI KAO PARP INHIBITORI

Info

Publication number
ME02855B
ME02855B MEP-2017-278A MEP28617A ME02855B ME 02855 B ME02855 B ME 02855B ME P28617 A MEP28617 A ME P28617A ME 02855 B ME02855 B ME 02855B
Authority
ME
Montenegro
Prior art keywords
alkyl
heterocyclyl
heteroaryl
cycloalkyl
aryl
Prior art date
Application number
MEP-2017-278A
Other languages
German (de)
English (en)
French (fr)
Unknown language (me)
Inventor
Changyou Zhou
Bo Ren
Hexiang Wang
Original Assignee
Beigene 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 Beigene Ltd filed Critical Beigene Ltd
Publication of ME02855B publication Critical patent/ME02855B/me

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
    • C07D487/06Peri-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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • 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
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/55171,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • 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
    • C07D471/12Heterocyclic 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 three hetero rings
    • C07D471/16Peri-condensed systems
    • 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
    • C07D471/22Heterocyclic 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 systems contains four or more hetero rings
    • 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
    • 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
    • C07D487/12Heterocyclic 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 three hetero rings
    • C07D487/14Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
MEP-2017-278A 2011-12-31 2011-12-31 KONDENZOVANI TETRA ILl PENTA-CIKLIČNI DIHIDRODIAZEPINOKARBAZOLONI KAO PARP INHIBITORI ME02855B (me)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/CN2011/085148 WO2013097225A1 (en) 2011-12-31 2011-12-31 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors
EP11878508.8A EP2797921B1 (en) 2011-12-31 2011-12-31 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors

Publications (1)

Publication Number Publication Date
ME02855B true ME02855B (me) 2018-04-20

Family

ID=48696280

Family Applications (1)

Application Number Title Priority Date Filing Date
MEP-2017-278A ME02855B (me) 2011-12-31 2011-12-31 KONDENZOVANI TETRA ILl PENTA-CIKLIČNI DIHIDRODIAZEPINOKARBAZOLONI KAO PARP INHIBITORI

Country Status (29)

Country Link
US (4) US9260440B2 (enExample)
EP (2) EP2797921B1 (enExample)
JP (1) JP6034877B2 (enExample)
KR (1) KR101716012B1 (enExample)
CN (2) CN103703004B (enExample)
AU (1) AU2011384858B2 (enExample)
BR (1) BR112014012628B8 (enExample)
CA (1) CA2856309C (enExample)
CY (1) CY1119804T1 (enExample)
DK (1) DK2797921T3 (enExample)
EA (1) EA027533B1 (enExample)
ES (1) ES2645814T3 (enExample)
HR (1) HRP20171883T1 (enExample)
HU (1) HUE035153T2 (enExample)
IL (1) IL233365A (enExample)
IN (1) IN2014DN06169A (enExample)
LT (1) LT2797921T (enExample)
ME (1) ME02855B (enExample)
MX (1) MX353578B (enExample)
NO (1) NO2797921T3 (enExample)
NZ (1) NZ624063A (enExample)
PL (1) PL2797921T3 (enExample)
PT (1) PT2797921T (enExample)
RS (1) RS56616B1 (enExample)
SG (1) SG11201401726VA (enExample)
SI (1) SI2797921T1 (enExample)
SM (1) SMT201700543T1 (enExample)
WO (1) WO2013097225A1 (enExample)
ZA (1) ZA201405560B (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ME02855B (me) 2011-12-31 2018-04-20 Beigene Ltd KONDENZOVANI TETRA ILl PENTA-CIKLIČNI DIHIDRODIAZEPINOKARBAZOLONI KAO PARP INHIBITORI
RU2696572C2 (ru) 2012-03-07 2019-08-05 Инститьют Оф Кансер Ресёрч: Ройял Кансер Хоспитал (Зе) 3-арил-5-замещенные соединения изохинолин-1-она и их терапевтическое применение
CN105722835B (zh) 2013-09-11 2018-07-31 癌症研究协会:皇家癌症医院 3-芳基-5-取代的-异喹啉-1-酮化合物及它们的疗法应用
IL257442B2 (en) * 2015-08-25 2023-03-01 Beigene Ltd Process for preparing parp inhibitor, crystalline forms and their uses
IL285318B (en) * 2016-04-01 2022-09-01 Kalyra Pharmaceuticals Inc Estrogen receptor modulators
CN110087730B (zh) * 2016-09-27 2023-03-28 百济神州(苏州)生物科技有限公司 使用包含parp抑制剂的组合产品治疗癌症
WO2018157794A1 (en) * 2017-02-28 2018-09-07 Beigene, Ltd. Crystalline forms of salts of fused tera or penta-cyclic dihydrodiazepinocarazolones, and uses thereof
CN106883232B (zh) 2017-03-31 2019-01-22 苏州康润医药有限公司 一种氮杂非那烯-3-酮的衍生物及其制备方法与应用
TW201908317A (zh) * 2017-07-17 2019-03-01 開曼群島商百濟神州有限公司 使用parp抑制劑、替莫唑胺及/或放射療法的組合治療癌症
AU2019275722A1 (en) * 2018-06-01 2020-11-12 Beigene, Ltd. Maintenance therapy of a PARP inhibitor in treating gastric cancer
CN111171031B (zh) * 2019-05-10 2021-04-09 百济神州(苏州)生物科技有限公司 一种含parp抑制剂倍半水合物产物的制备方法
CN111171002B (zh) * 2019-05-16 2021-04-06 百济神州(苏州)生物科技有限公司 一种parp抑制剂中间体的制备方法
JP2022534093A (ja) 2019-05-31 2022-07-27 ベイジーン リミテッド Parp阻害剤ペレット製剤及びその調製方法
JP2022543832A (ja) 2019-08-06 2022-10-14 リキュリウム アイピー ホールディングス リミテッド ライアビリティー カンパニー 変異体を治療するためのエストロゲン受容体調節剤
WO2021046014A1 (en) 2019-09-03 2021-03-11 Teva Czech Industries S.R.O Solid state forms of pamiparib and process for preparation thereof
TW202508595A (zh) 2023-05-04 2025-03-01 美商銳新醫藥公司 用於ras相關疾病或病症之組合療法
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025080946A2 (en) 2023-10-12 2025-04-17 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025217307A1 (en) 2024-04-09 2025-10-16 Revolution Medicines, Inc. Methods for predicting response to a ras(on) inhibitor and combination therapies
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE445326B (sv) 1983-04-05 1986-06-16 Malmstroem Anders E H Sett och anordning for forhindrande av veggturbulens
US6799298B2 (en) 1998-03-11 2004-09-28 Overture Services, Inc. Technique for locating an item of interest within a stored representation of data
PL210415B1 (pl) 1999-01-11 2012-01-31 Agouron Pharma Pochodne indolu, środek farmaceutyczny i zastosowanie pochodnych indolu
US6887996B2 (en) 2000-12-01 2005-05-03 Guilford Pharmaceuticals Inc. Compounds and their use
US6423705B1 (en) 2001-01-25 2002-07-23 Pfizer Inc. Combination therapy
US6906096B2 (en) 2002-06-28 2005-06-14 Irm Llc 4,7-Disubstituted indoles and methods of making
SI1585749T1 (sl) 2003-01-09 2008-10-31 Pfizer Derivati diazepinoindola kot inhibitorji kinaze
AU2004242947B2 (en) 2003-05-28 2010-04-29 Eisai Inc. Compounds, methods and pharmaceutical compositions for inhibiting PARP
CA2648369A1 (en) 2006-04-04 2007-10-11 Pfizer Products Inc. Polymorphic forms of (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4?l)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide
AU2007232279B2 (en) 2006-04-04 2010-05-06 Pfizer Products Inc. Combination therapy of (2R)-2-amino-2-cyclohexyl-N-(2-(1-methyl-1H-pyrazol-4-yl)-6- oxo-5,6-dihydro-1H-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide
EP2220073B1 (en) 2007-11-15 2014-09-03 MSD Italia S.r.l. Pyridazinone derivatives as parp inhibitors
CN104478875B (zh) 2008-08-06 2017-04-12 麦迪韦逊科技有限公司 聚(adp‑核糖)聚合酶(parp)的二氢吡啶并酞嗪酮抑制剂
WO2011130661A1 (en) 2010-04-16 2011-10-20 Biomarin Pharmaceutical Inc. Methods of using dihydropyridophthalazinone inhibitors of poly (adp-ribose)polymerase (parp)
ME02855B (me) 2011-12-31 2018-04-20 Beigene Ltd KONDENZOVANI TETRA ILl PENTA-CIKLIČNI DIHIDRODIAZEPINOKARBAZOLONI KAO PARP INHIBITORI
EP3044234B9 (en) 2013-09-13 2020-08-26 BeiGene Switzerland GmbH Anti-pd1 antibodies and their use as therapeutics and diagnostics
TWI726608B (zh) 2014-07-03 2021-05-01 英屬開曼群島商百濟神州有限公司 抗pd-l1抗體及其作為治療及診斷之用途
US9637488B2 (en) 2015-01-29 2017-05-02 Fuqiang Ruan Heterocyclic compounds as inhibitors of class I PI3KS
IL257442B2 (en) 2015-08-25 2023-03-01 Beigene Ltd Process for preparing parp inhibitor, crystalline forms and their uses
CN110087730B (zh) 2016-09-27 2023-03-28 百济神州(苏州)生物科技有限公司 使用包含parp抑制剂的组合产品治疗癌症
WO2018157794A1 (en) 2017-02-28 2018-09-07 Beigene, Ltd. Crystalline forms of salts of fused tera or penta-cyclic dihydrodiazepinocarazolones, and uses thereof
TW201908317A (zh) 2017-07-17 2019-03-01 開曼群島商百濟神州有限公司 使用parp抑制劑、替莫唑胺及/或放射療法的組合治療癌症

Also Published As

Publication number Publication date
EP3315500B1 (en) 2020-03-18
HRP20171883T1 (hr) 2018-01-12
SI2797921T1 (en) 2018-01-31
US9617273B2 (en) 2017-04-11
KR20140107353A (ko) 2014-09-04
ZA201405560B (en) 2017-02-22
BR112014012628B8 (pt) 2023-01-17
AU2011384858A1 (en) 2014-05-29
KR101716012B1 (ko) 2017-03-13
CN103703004B (zh) 2016-06-29
JP2015503526A (ja) 2015-02-02
ES2645814T3 (es) 2017-12-07
NO2797921T3 (enExample) 2018-02-03
SMT201700543T1 (it) 2018-01-11
US20170305921A1 (en) 2017-10-26
US9260440B2 (en) 2016-02-16
EP2797921A4 (en) 2015-10-21
EP3315500A1 (en) 2018-05-02
JP6034877B2 (ja) 2016-11-30
DK2797921T3 (en) 2017-10-02
CN103703004A (zh) 2014-04-02
US20160159811A1 (en) 2016-06-09
CA2856309A1 (en) 2013-07-04
US10501467B2 (en) 2019-12-10
HUE035153T2 (en) 2018-05-02
PL2797921T3 (pl) 2018-02-28
CY1119804T1 (el) 2018-06-27
RS56616B1 (sr) 2018-02-28
EA027533B1 (ru) 2017-08-31
MX353578B (es) 2018-01-19
WO2013097225A1 (en) 2013-07-04
SG11201401726VA (en) 2014-10-30
US20190016731A1 (en) 2019-01-17
MX2014007840A (es) 2014-08-21
EP2797921B1 (en) 2017-09-06
NZ624063A (en) 2016-09-30
BR112014012628B1 (pt) 2021-02-09
HK1192233A1 (zh) 2014-08-15
EP2797921A1 (en) 2014-11-05
BR112014012628A2 (pt) 2017-06-13
CA2856309C (en) 2016-06-07
IN2014DN06169A (enExample) 2015-08-21
LT2797921T (lt) 2017-11-27
PT2797921T (pt) 2017-11-14
AU2011384858B2 (en) 2016-05-05
CN106220635A (zh) 2016-12-14
CN106220635B (zh) 2019-03-08
US10112952B2 (en) 2018-10-30
IL233365A (en) 2016-08-31
IL233365A0 (en) 2014-08-31
EA201491303A1 (ru) 2014-10-30
US20150175617A1 (en) 2015-06-25

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