ZA201405560B - Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors - Google Patents

Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors

Info

Publication number
ZA201405560B
ZA201405560B ZA2014/05560A ZA201405560A ZA201405560B ZA 201405560 B ZA201405560 B ZA 201405560B ZA 2014/05560 A ZA2014/05560 A ZA 2014/05560A ZA 201405560 A ZA201405560 A ZA 201405560A ZA 201405560 B ZA201405560 B ZA 201405560B
Authority
ZA
South Africa
Prior art keywords
penta
parp inhibitors
dihydrodiazepinocarbazolones
cyclic
fused tetra
Prior art date
Application number
ZA2014/05560A
Other languages
English (en)
Inventor
Bo Ren
Hexiang Wang
Changyou Zhou
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 ZA201405560B publication Critical patent/ZA201405560B/en

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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)
  • 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)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Engineering & Computer Science (AREA)
  • Rheumatology (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)
ZA2014/05560A 2011-12-31 2014-07-28 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors ZA201405560B (en)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number Publication Date
ZA201405560B true ZA201405560B (en) 2017-02-22

Family

ID=48696280

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA2014/05560A ZA201405560B (en) 2011-12-31 2014-07-28 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors

Country Status (29)

Country Link
US (4) US9260440B2 (enEXAMPLES)
EP (2) EP3315500B1 (enEXAMPLES)
JP (1) JP6034877B2 (enEXAMPLES)
KR (1) KR101716012B1 (enEXAMPLES)
CN (2) CN103703004B (enEXAMPLES)
AU (1) AU2011384858B2 (enEXAMPLES)
BR (1) BR112014012628B8 (enEXAMPLES)
CA (1) CA2856309C (enEXAMPLES)
CY (1) CY1119804T1 (enEXAMPLES)
DK (1) DK2797921T3 (enEXAMPLES)
EA (1) EA027533B1 (enEXAMPLES)
ES (1) ES2645814T3 (enEXAMPLES)
HR (1) HRP20171883T1 (enEXAMPLES)
HU (1) HUE035153T2 (enEXAMPLES)
IL (1) IL233365A (enEXAMPLES)
IN (1) IN2014DN06169A (enEXAMPLES)
LT (1) LT2797921T (enEXAMPLES)
ME (1) ME02855B (enEXAMPLES)
MX (1) MX353578B (enEXAMPLES)
NO (1) NO2797921T3 (enEXAMPLES)
NZ (1) NZ624063A (enEXAMPLES)
PL (1) PL2797921T3 (enEXAMPLES)
PT (1) PT2797921T (enEXAMPLES)
RS (1) RS56616B1 (enEXAMPLES)
SG (1) SG11201401726VA (enEXAMPLES)
SI (1) SI2797921T1 (enEXAMPLES)
SM (1) SMT201700543T1 (enEXAMPLES)
WO (1) WO2013097225A1 (enEXAMPLES)
ZA (1) ZA201405560B (enEXAMPLES)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112014012628B8 (pt) 2011-12-31 2023-01-17 Beigene Ltd Dihidrodiazepinocarbazolonas tetra ou pentacíclicas fundidas como inibidoras de parp
CN104302358B (zh) 2012-03-07 2017-12-05 癌症研究协会:皇家癌症医院 3‑芳基‑5‑取代的异喹啉‑1‑酮化合物和它们的治疗用途
NO3044221T3 (enEXAMPLES) 2013-09-11 2018-07-21
EA037366B1 (ru) * 2015-08-25 2021-03-18 Бейджин, Лтд. Способ получения ингибитора parp, кристаллические формы и их применения
AU2017242027B2 (en) 2016-04-01 2020-10-08 Recurium Ip Holdings, Llc Estrogen receptor modulators
EP3519051B1 (en) 2016-09-27 2021-09-22 Beigene, Ltd. Treatment of cancers using combination comprising parp inhibitors
CN110392687B (zh) * 2017-02-28 2022-08-02 百济神州(苏州)生物科技有限公司 稠合的四环或五环二氢二氮杂䓬并咔唑酮的盐的结晶形式及其用途
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
WO2019015561A1 (en) * 2017-07-17 2019-01-24 Beigene, Ltd. TREATMENT OF CANCERS USING A COMBINATION COMPRISING INHIBITORS OF PARP, TEMOZOLOMIDE AND / OR RADIOTHERAPY
US20210205323A1 (en) * 2018-06-01 2021-07-08 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
MX2021014339A (es) * 2019-05-31 2022-01-06 Beigene Ltd Preparacion de granulo inhibidor de parp y proceso de preparacion del mismo.
US11278532B2 (en) 2019-08-06 2022-03-22 Recurium Ip Holdings, Llc Estrogen receptor modulators for treating mutants
WO2021046014A1 (en) 2019-09-03 2021-03-11 Teva Czech Industries S.R.O Solid state forms of pamiparib and process for preparation thereof
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 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
OA11749A (en) 1999-01-11 2005-07-19 Agouron Pharma Tricyclic inhibitors of poly(adp-ribose)polymerases.
ES2354249T3 (es) 2000-12-01 2011-03-11 Eisai Inc. Derivados de azafenantridona y su uso como inhibidores de parp.
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
AP2048A (en) 2003-01-09 2009-09-24 Pfizer Diazepinoindole derivatives as kinase inhibitors
EP1633362B1 (en) 2003-05-28 2012-09-26 Eisai Inc. Compounds, methods and pharmaceutical compositions for inhibiting parp
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
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
RU2490265C2 (ru) 2007-11-15 2013-08-20 Институто Ди Ричерке Ди Биолоджиа Молеколаре П. Анджелетти С.П.А. Пиридазиноновые производные в качестве ингибиторов parp
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)
BR112014012628B8 (pt) 2011-12-31 2023-01-17 Beigene Ltd Dihidrodiazepinocarbazolonas tetra ou pentacíclicas fundidas como inibidoras de parp
CN107011441B (zh) 2013-09-13 2020-12-01 百济神州(广州)生物科技有限公司 抗pd1抗体及其作为治疗剂与诊断剂的用途
US10544225B2 (en) 2014-07-03 2020-01-28 Beigene, Ltd. Anti-PD-L1 antibodies and their use as therapeutics and diagnostics
US9637488B2 (en) 2015-01-29 2017-05-02 Fuqiang Ruan Heterocyclic compounds as inhibitors of class I PI3KS
EA037366B1 (ru) 2015-08-25 2021-03-18 Бейджин, Лтд. Способ получения ингибитора parp, кристаллические формы и их применения
EP3519051B1 (en) 2016-09-27 2021-09-22 Beigene, Ltd. Treatment of cancers using combination comprising parp inhibitors
CN110392687B (zh) 2017-02-28 2022-08-02 百济神州(苏州)生物科技有限公司 稠合的四环或五环二氢二氮杂䓬并咔唑酮的盐的结晶形式及其用途
WO2019015561A1 (en) 2017-07-17 2019-01-24 Beigene, Ltd. TREATMENT OF CANCERS USING A COMBINATION COMPRISING INHIBITORS OF PARP, TEMOZOLOMIDE AND / OR RADIOTHERAPY

Also Published As

Publication number Publication date
CN103703004B (zh) 2016-06-29
CN106220635A (zh) 2016-12-14
BR112014012628B1 (pt) 2021-02-09
KR20140107353A (ko) 2014-09-04
NZ624063A (en) 2016-09-30
EP2797921A1 (en) 2014-11-05
HRP20171883T1 (hr) 2018-01-12
CN103703004A (zh) 2014-04-02
ES2645814T3 (es) 2017-12-07
BR112014012628B8 (pt) 2023-01-17
NO2797921T3 (enEXAMPLES) 2018-02-03
BR112014012628A2 (pt) 2017-06-13
LT2797921T (lt) 2017-11-27
AU2011384858B2 (en) 2016-05-05
MX353578B (es) 2018-01-19
WO2013097225A1 (en) 2013-07-04
PL2797921T3 (pl) 2018-02-28
ME02855B (me) 2018-04-20
US20170305921A1 (en) 2017-10-26
RS56616B1 (sr) 2018-02-28
CN106220635B (zh) 2019-03-08
SMT201700543T1 (it) 2018-01-11
IL233365A0 (en) 2014-08-31
CA2856309A1 (en) 2013-07-04
DK2797921T3 (en) 2017-10-02
EP2797921B1 (en) 2017-09-06
SG11201401726VA (en) 2014-10-30
EA027533B1 (ru) 2017-08-31
MX2014007840A (es) 2014-08-21
SI2797921T1 (en) 2018-01-31
PT2797921T (pt) 2017-11-14
US10501467B2 (en) 2019-12-10
US20160159811A1 (en) 2016-06-09
KR101716012B1 (ko) 2017-03-13
US9260440B2 (en) 2016-02-16
IL233365A (en) 2016-08-31
CY1119804T1 (el) 2018-06-27
US10112952B2 (en) 2018-10-30
CA2856309C (en) 2016-06-07
HUE035153T2 (en) 2018-05-02
EP3315500B1 (en) 2020-03-18
US20190016731A1 (en) 2019-01-17
HK1192233A1 (zh) 2014-08-15
EA201491303A1 (ru) 2014-10-30
EP3315500A1 (en) 2018-05-02
AU2011384858A1 (en) 2014-05-29
US20150175617A1 (en) 2015-06-25
JP2015503526A (ja) 2015-02-02
JP6034877B2 (ja) 2016-11-30
US9617273B2 (en) 2017-04-11
IN2014DN06169A (enEXAMPLES) 2015-08-21
EP2797921A4 (en) 2015-10-21

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