CY1119804T1 - Συντηγμενες τετρα- ή πεντα-κυκλικες διϋδροδιαζεπινοκαρβαζολονες ως αναστολεις parp - Google Patents

Συντηγμενες τετρα- ή πεντα-κυκλικες διϋδροδιαζεπινοκαρβαζολονες ως αναστολεις parp

Info

Publication number
CY1119804T1
CY1119804T1 CY20171101198T CY171101198T CY1119804T1 CY 1119804 T1 CY1119804 T1 CY 1119804T1 CY 20171101198 T CY20171101198 T CY 20171101198T CY 171101198 T CY171101198 T CY 171101198T CY 1119804 T1 CY1119804 T1 CY 1119804T1
Authority
CY
Cyprus
Prior art keywords
tetra
cyclic
pythrodiazepinocarbasolones
parp
suspensions
Prior art date
Application number
CY20171101198T
Other languages
Greek (el)
English (en)
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 CY1119804T1 publication Critical patent/CY1119804T1/el

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)
CY20171101198T 2011-12-31 2017-11-16 Συντηγμενες τετρα- ή πεντα-κυκλικες διϋδροδιαζεπινοκαρβαζολονες ως αναστολεις parp CY1119804T1 (el)

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
CY1119804T1 true CY1119804T1 (el) 2018-06-27

Family

ID=48696280

Family Applications (1)

Application Number Title Priority Date Filing Date
CY20171101198T CY1119804T1 (el) 2011-12-31 2017-11-16 Συντηγμενες τετρα- ή πεντα-κυκλικες διϋδροδιαζεπινοκαρβαζολονες ως αναστολεις parp

Country Status (29)

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

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IN2014DN06169A (Direct) 2011-12-31 2015-08-21 Beigene Ltd
US9193689B2 (en) 2012-03-07 2015-11-24 Institute Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
NO3044221T3 (Direct) 2013-09-11 2018-07-21
CN112521390A (zh) * 2015-08-25 2021-03-19 百济神州有限公司 制备parp抑制剂、结晶形式的方法及其用途
IL295050A (en) * 2016-04-01 2022-09-01 Recurium Ip Holdings Llc 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
CN115433187B (zh) * 2017-02-28 2023-10-27 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组合物及其用途
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
CN110891576A (zh) * 2017-07-17 2020-03-17 百济神州有限公司 使用包含parp抑制剂、替莫唑胺和/或放射疗法的组合治疗癌症
EP3801550A4 (en) * 2018-06-01 2022-02-16 BeiGene, Ltd. MAINTENANCE THERAPY OF A PARP INHIBITOR FOR THE TREATMENT OF STOMACH 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
CN113402502B (zh) * 2019-05-16 2022-10-14 百济神州(苏州)生物科技有限公司 一种parp抑制剂中间体制备的物料组合体系
KR20220016028A (ko) 2019-05-31 2022-02-08 베이진 엘티디 Parp 억제제 펠릿 제조 및 이의 제조방법
CA3148221A1 (en) 2019-08-06 2021-02-11 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
WO2025034702A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 for use in the treatment of 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
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
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder

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
KR100632079B1 (ko) 1999-01-11 2006-10-04 아구론 파마슈티컬스, 인크. 폴리(adp-리보오스) 중합 효소의 트리사이클릭 저해제
MXPA03004832A (es) * 2000-12-01 2004-05-04 Guilford Pharm Inc Compuestos y sus usos.
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
DK1585749T3 (da) * 2003-01-09 2008-09-22 Pfizer Diazepinoindol-derivater som kinaseinhibitorer
EP1633362B1 (en) 2003-05-28 2012-09-26 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
WO2007113671A1 (en) 2006-04-04 2007-10-11 Pfizer Products Inc. Combination therapy of (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4-yl)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide
MX2010005070A (es) 2007-11-15 2010-05-24 Angeletti P Ist Richerche Bio Derivados de piridazinona como inhibidores de parp.
US8012976B2 (en) * 2008-08-06 2011-09-06 Biomarin Pharmaceutical Inc. Dihydropyridophthalazinone inhibitors of poly(ADP-ribose)polymerase (PARP)
WO2011130661A1 (en) 2010-04-16 2011-10-20 Biomarin Pharmaceutical Inc. Methods of using dihydropyridophthalazinone inhibitors of poly (adp-ribose)polymerase (parp)
IN2014DN06169A (Direct) 2011-12-31 2015-08-21 Beigene Ltd
WO2015035606A1 (en) 2013-09-13 2015-03-19 Beigene, Ltd. Anti-pd1 antibodies and their use as therapeutics and diagnostics
CN106604742B (zh) 2014-07-03 2019-01-11 百济神州有限公司 抗pd-l1抗体及其作为治疗剂及诊断剂的用途
US9637488B2 (en) 2015-01-29 2017-05-02 Fuqiang Ruan Heterocyclic compounds as inhibitors of class I PI3KS
CN112521390A (zh) 2015-08-25 2021-03-19 百济神州有限公司 制备parp抑制剂、结晶形式的方法及其用途
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
CN115433187B (zh) 2017-02-28 2023-10-27 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组合物及其用途
CN110891576A (zh) 2017-07-17 2020-03-17 百济神州有限公司 使用包含parp抑制剂、替莫唑胺和/或放射疗法的组合治疗癌症

Also Published As

Publication number Publication date
PT2797921T (pt) 2017-11-14
EP3315500A1 (en) 2018-05-02
US9617273B2 (en) 2017-04-11
CN106220635A (zh) 2016-12-14
WO2013097225A1 (en) 2013-07-04
US20150175617A1 (en) 2015-06-25
CA2856309C (en) 2016-06-07
BR112014012628A2 (pt) 2017-06-13
EP2797921A4 (en) 2015-10-21
AU2011384858B2 (en) 2016-05-05
US20190016731A1 (en) 2019-01-17
ES2645814T3 (es) 2017-12-07
ME02855B (me) 2018-04-20
KR20140107353A (ko) 2014-09-04
IL233365A (en) 2016-08-31
IN2014DN06169A (Direct) 2015-08-21
BR112014012628B8 (pt) 2023-01-17
RS56616B1 (sr) 2018-02-28
CN103703004A (zh) 2014-04-02
CN103703004B (zh) 2016-06-29
HUE035153T2 (en) 2018-05-02
EA201491303A1 (ru) 2014-10-30
NZ624063A (en) 2016-09-30
DK2797921T3 (en) 2017-10-02
SI2797921T1 (en) 2018-01-31
SG11201401726VA (en) 2014-10-30
EP3315500B1 (en) 2020-03-18
KR101716012B1 (ko) 2017-03-13
US20160159811A1 (en) 2016-06-09
US20170305921A1 (en) 2017-10-26
JP2015503526A (ja) 2015-02-02
AU2011384858A1 (en) 2014-05-29
HK1192233A1 (zh) 2014-08-15
EA027533B1 (ru) 2017-08-31
US9260440B2 (en) 2016-02-16
IL233365A0 (en) 2014-08-31
SMT201700543T1 (it) 2018-01-11
MX2014007840A (es) 2014-08-21
CA2856309A1 (en) 2013-07-04
CN106220635B (zh) 2019-03-08
US10501467B2 (en) 2019-12-10
EP2797921B1 (en) 2017-09-06
LT2797921T (lt) 2017-11-27
EP2797921A1 (en) 2014-11-05
JP6034877B2 (ja) 2016-11-30
MX353578B (es) 2018-01-19
BR112014012628B1 (pt) 2021-02-09
HRP20171883T1 (hr) 2018-01-12
PL2797921T3 (pl) 2018-02-28
ZA201405560B (en) 2017-02-22
NO2797921T3 (Direct) 2018-02-03
US10112952B2 (en) 2018-10-30

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