RS56616B1 - Kondenzovani tetra ili penta-ciklični dihidrodiazepinokarbazoloni kao parp inhibitori - Google Patents

Kondenzovani tetra ili penta-ciklični dihidrodiazepinokarbazoloni kao parp inhibitori

Info

Publication number
RS56616B1
RS56616B1 RS20171228A RSP20171228A RS56616B1 RS 56616 B1 RS56616 B1 RS 56616B1 RS 20171228 A RS20171228 A RS 20171228A RS P20171228 A RSP20171228 A RS P20171228A RS 56616 B1 RS56616 B1 RS 56616B1
Authority
RS
Serbia
Prior art keywords
penta
parp inhibitors
dihydrodiazepinocarbazolones
cyclic
fused tetra
Prior art date
Application number
RS20171228A
Other languages
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 RS56616B1 publication Critical patent/RS56616B1/sr

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
RS20171228A 2011-12-31 2011-12-31 Kondenzovani tetra ili penta-ciklični dihidrodiazepinokarbazoloni kao parp inhibitori RS56616B1 (sr)

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
RS56616B1 true RS56616B1 (sr) 2018-02-28

Family

ID=48696280

Family Applications (1)

Application Number Title Priority Date Filing Date
RS20171228A RS56616B1 (sr) 2011-12-31 2011-12-31 Kondenzovani tetra ili penta-ciklični dihidrodiazepinokarbazoloni kao parp inhibitori

Country Status (29)

Country Link
US (4) US9260440B2 (sr)
EP (2) EP3315500B1 (sr)
JP (1) JP6034877B2 (sr)
KR (1) KR101716012B1 (sr)
CN (2) CN106220635B (sr)
AU (1) AU2011384858B2 (sr)
BR (1) BR112014012628B8 (sr)
CA (1) CA2856309C (sr)
CY (1) CY1119804T1 (sr)
DK (1) DK2797921T3 (sr)
EA (1) EA027533B1 (sr)
ES (1) ES2645814T3 (sr)
HK (1) HK1192233A1 (sr)
HR (1) HRP20171883T1 (sr)
HU (1) HUE035153T2 (sr)
IL (1) IL233365A (sr)
IN (1) IN2014DN06169A (sr)
LT (1) LT2797921T (sr)
ME (1) ME02855B (sr)
MX (1) MX353578B (sr)
NO (1) NO2797921T3 (sr)
NZ (1) NZ624063A (sr)
PL (1) PL2797921T3 (sr)
PT (1) PT2797921T (sr)
RS (1) RS56616B1 (sr)
SG (1) SG11201401726VA (sr)
SI (1) SI2797921T1 (sr)
WO (1) WO2013097225A1 (sr)
ZA (1) ZA201405560B (sr)

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WO2013097225A1 (en) 2011-12-31 2013-07-04 Beigene, Ltd. Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors
MX346147B (es) 2012-03-07 2017-03-09 Inst Of Cancer Research: Royal Cancer Hospital (The) Compuestos de 3-aril-5-substituido-isoquinolin-1-ona y su uso terapeutico.
CA2922469A1 (en) 2013-09-11 2015-03-19 Institute Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
MX2018002322A (es) * 2015-08-25 2018-04-11 Beigene Ltd Procedimiento para la preparacion de un inhibidor de poli(adp-ribosa)polimerasa, formas cristalinas, y usos del mismo.
CN112679495B (zh) 2016-04-01 2023-03-28 里科瑞尔姆Ip控股有限责任公司 雌激素受体调节剂
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
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
EA202192272A1 (ru) * 2019-05-31 2022-03-02 Бейджин, Лтд. Гранулированный препарат ингибитора parp и способ его получения
CN114269342A (zh) 2019-08-06 2022-04-01 里科瑞尔姆Ip控股有限责任公司 用于治疗突变的雌激素受体调节剂
WO2021046014A1 (en) 2019-09-03 2021-03-11 Teva Czech Industries S.R.O Solid state forms of pamiparib and process for preparation thereof

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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
AU781711B2 (en) 1999-01-11 2005-06-09 Agouron Pharmaceuticals, Inc. Tricyclic inhibitors of poly(ADP-ribose) polymerases
DE60142921D1 (de) 2000-12-01 2010-10-07 Eisai Inc Azaphenanthridone-derivate und deren verwendung als parp-inhibitoren
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
AU2004203977B2 (en) * 2003-01-09 2010-06-17 Pfizer Inc. Diazepinoindole derivatives as kinase inhibitors
US7268138B2 (en) 2003-05-28 2007-09-11 Mgi Gp, 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
JP5758630B2 (ja) 2007-11-15 2015-08-05 エンメエッセディ・イタリア・エッセ・エッレ・エッレ Parp阻害剤としてのピリダジノン誘導体
EP2326650B9 (en) * 2008-08-06 2014-09-10 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)
WO2013097225A1 (en) 2011-12-31 2013-07-04 Beigene, Ltd. Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors
HUE049281T2 (hu) 2013-09-13 2020-09-28 Beigene Switzerland Gmbh Anti-PD1 antitestek, valamint terapeutikumként és diagnosztikumként történõ alkalmazásuk
WO2016000619A1 (en) 2014-07-03 2016-01-07 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
MX2018002322A (es) 2015-08-25 2018-04-11 Beigene Ltd Procedimiento para la preparacion de un inhibidor de poli(adp-ribosa)polimerasa, formas cristalinas, y usos del mismo.
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
EP2797921A4 (en) 2015-10-21
NZ624063A (en) 2016-09-30
AU2011384858A1 (en) 2014-05-29
CN106220635A (zh) 2016-12-14
JP2015503526A (ja) 2015-02-02
US10112952B2 (en) 2018-10-30
PT2797921T (pt) 2017-11-14
MX2014007840A (es) 2014-08-21
CA2856309A1 (en) 2013-07-04
US20150175617A1 (en) 2015-06-25
CN103703004B (zh) 2016-06-29
SI2797921T1 (en) 2018-01-31
KR101716012B1 (ko) 2017-03-13
ZA201405560B (en) 2017-02-22
US9260440B2 (en) 2016-02-16
LT2797921T (lt) 2017-11-27
EP3315500B1 (en) 2020-03-18
HRP20171883T1 (hr) 2018-01-12
US9617273B2 (en) 2017-04-11
HUE035153T2 (en) 2018-05-02
EP2797921A1 (en) 2014-11-05
EP3315500A1 (en) 2018-05-02
CN106220635B (zh) 2019-03-08
MX353578B (es) 2018-01-19
WO2013097225A1 (en) 2013-07-04
ME02855B (me) 2018-04-20
BR112014012628A2 (pt) 2017-06-13
US20160159811A1 (en) 2016-06-09
AU2011384858B2 (en) 2016-05-05
US10501467B2 (en) 2019-12-10
US20170305921A1 (en) 2017-10-26
ES2645814T3 (es) 2017-12-07
EA027533B1 (ru) 2017-08-31
US20190016731A1 (en) 2019-01-17
CN103703004A (zh) 2014-04-02
IL233365A (en) 2016-08-31
SG11201401726VA (en) 2014-10-30
HK1192233A1 (zh) 2014-08-15
KR20140107353A (ko) 2014-09-04
BR112014012628B8 (pt) 2023-01-17
BR112014012628B1 (pt) 2021-02-09
IN2014DN06169A (sr) 2015-08-21
IL233365A0 (en) 2014-08-31
EA201491303A1 (ru) 2014-10-30
EP2797921B1 (en) 2017-09-06
NO2797921T3 (sr) 2018-02-03
PL2797921T3 (pl) 2018-02-28
CY1119804T1 (el) 2018-06-27
DK2797921T3 (en) 2017-10-02
CA2856309C (en) 2016-06-07
JP6034877B2 (ja) 2016-11-30

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