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
EP11878508.8A EP2797921B1 (en) 2011-12-31 2011-12-31 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors
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
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 (22)

* 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
CA2865511A1 (en) 2012-03-07 2013-09-12 Institute Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
US9611223B2 (en) 2013-09-11 2017-04-04 Institute Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
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
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
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
WO2019228499A1 (en) * 2018-06-01 2019-12-05 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
SG11202112924RA (en) * 2019-05-31 2021-12-30 Beigene Ltd Parp inhibitor pellet preparation and preparation process therefor
WO2021026153A1 (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
US20250375445A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-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
PT1140936E (pt) 1999-01-11 2004-06-30 Agouron Pharma Inibidores triciclicos de poli(adp-ribose) polimerases
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
CA2527420C (en) 2003-05-28 2013-01-08 Guilford Pharmaceuticals, Inc. Compounds, methods and pharmaceutical compositions for inhibiting parp
BRPI0709731A2 (pt) 2006-04-04 2011-07-26 Pfizer Prod Inc terapia de combinaÇço de (2r,z)-2-amino-2-cicloexil-n-(5-(1-metil-1h-pirazol-4-il)-1- oxo-2,6-diidro-1h-[1,2]diazepino[4,5,6-cd]indol-8-il)acet amida
WO2007113647A1 (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-4υl)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide
KR101641596B1 (ko) 2007-11-15 2016-07-21 엠에스디 이탈리아 에스.알.엘. Parp 억제제로서의 피리다지논 유도체
SI2767537T1 (sl) * 2008-08-06 2017-08-31 Medivation Technologies, Inc. Dihidropiridoftalazinonski inhibitorji poli(adp-riboza) polimeraze (parp)
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
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
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
WO2018157794A1 (en) 2017-02-28 2018-09-07 Beigene, Ltd. Crystalline forms of salts of fused tera or penta-cyclic dihydrodiazepinocarazolones, and uses thereof
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
MX2014007840A (es) 2014-08-21
HRP20171883T1 (hr) 2018-01-12
CA2856309A1 (en) 2013-07-04
EP2797921B1 (en) 2017-09-06
US20160159811A1 (en) 2016-06-09
EP2797921A1 (en) 2014-11-05
NZ624063A (en) 2016-09-30
US20170305921A1 (en) 2017-10-26
SI2797921T1 (en) 2018-01-31
HK1192233A1 (zh) 2014-08-15
EA201491303A1 (ru) 2014-10-30
NO2797921T3 (enExample) 2018-02-03
EP2797921A4 (en) 2015-10-21
ES2645814T3 (es) 2017-12-07
JP2015503526A (ja) 2015-02-02
BR112014012628A2 (pt) 2017-06-13
US10501467B2 (en) 2019-12-10
CN103703004A (zh) 2014-04-02
AU2011384858B2 (en) 2016-05-05
IL233365A0 (en) 2014-08-31
MX353578B (es) 2018-01-19
IN2014DN06169A (enExample) 2015-08-21
EP3315500B1 (en) 2020-03-18
DK2797921T3 (en) 2017-10-02
PL2797921T3 (pl) 2018-02-28
BR112014012628B1 (pt) 2021-02-09
EP3315500A1 (en) 2018-05-02
CY1119804T1 (el) 2018-06-27
SG11201401726VA (en) 2014-10-30
US9260440B2 (en) 2016-02-16
CN103703004B (zh) 2016-06-29
WO2013097225A1 (en) 2013-07-04
CN106220635A (zh) 2016-12-14
KR101716012B1 (ko) 2017-03-13
US20150175617A1 (en) 2015-06-25
CA2856309C (en) 2016-06-07
CN106220635B (zh) 2019-03-08
US20190016731A1 (en) 2019-01-17
AU2011384858A1 (en) 2014-05-29
RS56616B1 (sr) 2018-02-28
SMT201700543T1 (it) 2018-01-11
BR112014012628B8 (pt) 2023-01-17
LT2797921T (lt) 2017-11-27
PT2797921T (pt) 2017-11-14
US9617273B2 (en) 2017-04-11
HUE035153T2 (en) 2018-05-02
EA027533B1 (ru) 2017-08-31
ZA201405560B (en) 2017-02-22
US10112952B2 (en) 2018-10-30
IL233365A (en) 2016-08-31
KR20140107353A (ko) 2014-09-04
JP6034877B2 (ja) 2016-11-30

Similar Documents

Publication Publication Date Title
ME02855B (me) KONDENZOVANI TETRA ILl PENTA-CIKLIČNI DIHIDRODIAZEPINOKARBAZOLONI KAO PARP INHIBITORI
HRP20200352T1 (hr) Novi kondenzirani pirimidinski spoj ili njegova sol
JP2013528600A5 (enExample)
HRP20160641T1 (hr) Fuzionirani triciklički spojevi kao inhibitori raf kinaze
HRP20241197T1 (hr) Makrociklični spojevi i primjene istih
IL277341B2 (en) Antifibrotic pyridinones
ME02181B (me) Ne-nukleozidni inhibitori reverzne transkriptaze
HRP20140195T1 (hr) Supstituirani derivati triazolopiridazina
HRP20160030T1 (hr) Derivati 6,7-dihidro-pirazolo[1,5-a]pirazin-4-ilamina koji su korisni kao inhibitori beta-sekretaze (bace)
AR078157A1 (es) Derivados de pirazol-[4,5-d]pirrolo[2,3-b]piridina inhibidores de tirosinquinasas jak 2, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento del cancer
SI20691B (sl) Triciklični inhibitorji poli(ADP-riboza) polimeraz
UY37925A (es) Formas cristalinas
WO2011113802A3 (en) Imidazopyridine and purine compounds, compositions and methods of use
RU2015148189A (ru) ПРОИЗВОДНЫЕ 2-АМИДОПИРИДО[4, 3-d]ПИРИМИДИН-5-ОНА И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ИНГИБИТОРОВ WEE-1
BR112012024017A2 (pt) compostos derivados de triazina dissubstituída farmaceuticamemnte ativios, composição farmacêutica, método para a síntese destes e uso dos mesmos
HRP20221495T1 (hr) Farmaceutske kompozicije koje sadrže derivate imidazotiadiazola i imidazopiridazina kao inhibitore proteazom aktiviranih receptora 4 (par4) za liječenje agregacije trombocita
HRP20160647T1 (hr) Novi heterociklički derivati i njihova uporaba u liječenju neuroloških poremećaja
JP2016506962A5 (enExample)
AR065531A1 (es) Derivados de pirimidina, procesos de obtencion y composiciones farmaceuticas.
HRP20170627T1 (hr) Derivati 2-metilmorfolin pirido-, pirazo- i pirimido-pirimidina kao inhibitori mtor
HRP20221018T1 (hr) Liječenje katapleksije
RU2016110096A (ru) Новое хинолин-замещенное соединение
ME02373B (me) Biciklična heterociklična jedinjenja kao inhibitori protein tirozin kinaze
RU2014141579A (ru) Гетероциклические соединения в качестве ингибиторов бета-лактамаз
JP2013523614A5 (enExample)