MX353578B - Dihidrodiazpinocarbazolonas tetra o penta-ciclicas fusionadas como inhibidores de poli (adp-ribosa) polimerasa (parp). - Google Patents

Dihidrodiazpinocarbazolonas tetra o penta-ciclicas fusionadas como inhibidores de poli (adp-ribosa) polimerasa (parp).

Info

Publication number
MX353578B
MX353578B MX2014007840A MX2014007840A MX353578B MX 353578 B MX353578 B MX 353578B MX 2014007840 A MX2014007840 A MX 2014007840A MX 2014007840 A MX2014007840 A MX 2014007840A MX 353578 B MX353578 B MX 353578B
Authority
MX
Mexico
Prior art keywords
penta
parp inhibitors
fused tetra
cyclic
dihydrodiazepinocarbazolones
Prior art date
Application number
MX2014007840A
Other languages
English (en)
Other versions
MX2014007840A (es
Inventor
Zhou Changyou
Ren Bo
Wang Hexiang
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 MX2014007840A publication Critical patent/MX2014007840A/es
Publication of MX353578B publication Critical patent/MX353578B/es

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

Abstract

La presente invención se refiere a ciertos compuestos tetra o penta-cíclicos fusionados, y sales de los mismos, composiciones de los mismos, y métodos de uso de los mismos.
MX2014007840A 2011-12-31 2011-12-31 Dihidrodiazpinocarbazolonas tetra o penta-ciclicas fusionadas como inhibidores de poli (adp-ribosa) polimerasa (parp). MX353578B (es)

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 (2)

Publication Number Publication Date
MX2014007840A MX2014007840A (es) 2014-08-21
MX353578B true MX353578B (es) 2018-01-19

Family

ID=48696280

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2014007840A MX353578B (es) 2011-12-31 2011-12-31 Dihidrodiazpinocarbazolonas tetra o penta-ciclicas fusionadas como inhibidores de poli (adp-ribosa) polimerasa (parp).

Country Status (29)

Country Link
US (4) US9260440B2 (es)
EP (2) EP2797921B1 (es)
JP (1) JP6034877B2 (es)
KR (1) KR101716012B1 (es)
CN (2) CN103703004B (es)
AU (1) AU2011384858B2 (es)
BR (1) BR112014012628B8 (es)
CA (1) CA2856309C (es)
CY (1) CY1119804T1 (es)
DK (1) DK2797921T3 (es)
EA (1) EA027533B1 (es)
ES (1) ES2645814T3 (es)
HK (1) HK1192233A1 (es)
HR (1) HRP20171883T1 (es)
HU (1) HUE035153T2 (es)
IL (1) IL233365A (es)
IN (1) IN2014DN06169A (es)
LT (1) LT2797921T (es)
ME (1) ME02855B (es)
MX (1) MX353578B (es)
NO (1) NO2797921T3 (es)
NZ (1) NZ624063A (es)
PL (1) PL2797921T3 (es)
PT (1) PT2797921T (es)
RS (1) RS56616B1 (es)
SG (1) SG11201401726VA (es)
SI (1) SI2797921T1 (es)
WO (1) WO2013097225A1 (es)
ZA (1) ZA201405560B (es)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2797921B1 (en) 2011-12-31 2017-09-06 BeiGene, Ltd. Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors
ES2611504T3 (es) 2012-03-07 2017-05-09 Institute Of Cancer Research: Royal Cancer Hospital (The) Compuestos de isoquinolin-1-ona 3-aril-5-sustituida y sus usos terapéuticos
NO3044221T3 (es) 2013-09-11 2018-07-21
NZ739876A (en) * 2015-08-25 2022-09-30 Beigene Ltd Process for preparing parp inhibitor, crystalline forms, and uses thereof
BR112018070161A2 (pt) 2016-04-01 2019-02-12 Zeno Royalties & Milestones, LLC moduladores de receptores de estrogênio
TWI806840B (zh) * 2016-09-27 2023-07-01 英屬開曼群島商百濟神州有限公司 使用包含parp抑制劑的組合產品治療癌症
TW201840564A (zh) * 2017-02-28 2018-11-16 英屬開曼群島商百濟神州有限公司 稠合的四環或五環二氫二氮呯幷哢唑酮的鹽的結晶形式及其用途
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
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
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
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
EP3977984A4 (en) 2019-05-31 2023-01-11 BeiGene, Ltd. PREPARATION OF PARP INHIBITOR TABLET AND METHOD OF PREPARATION THEREOF
BR112022002138A2 (pt) 2019-08-06 2022-04-19 Recurium Ip Holdings Llc Moduladores do receptor de estrogênio para tratamento de mutantes
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
KR100632079B1 (ko) 1999-01-11 2006-10-04 아구론 파마슈티컬스, 인크. 폴리(adp-리보오스) 중합 효소의 트리사이클릭 저해제
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
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SI1585749T1 (sl) * 2003-01-09 2008-10-31 Pfizer Derivati diazepinoindola kot inhibitorji kinaze
MXPA05012812A (es) 2003-05-28 2006-02-28 Guilford Pharm Inc Compuestos, metodos y composiciones farmaceuticas para inhibir poli(adenosina-5'-difosfo-ribosa)polimerasa(parp).
MX2008012791A (es) 2006-04-04 2008-10-15 Pfizer Prod Inc Terapia de combinacion de (2r,z)-2-amino-2-ciclohexil-n-(5-(1-meti l-1h-pirazol-4-il)-1-oxo-2,6-dihidro-1h-[1,2]diazepinos[4,5,6-cd[ indol-8-il)acetamida.
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
EP2220073B1 (en) 2007-11-15 2014-09-03 MSD Italia S.r.l. Pyridazinone derivatives as parp inhibitors
PT2326650E (pt) 2008-08-06 2014-05-06 Biomarin Pharm Inc Inibidores de di-hidropiridoftalazinona de poli(adpribose) polimerase (parp)
WO2011130661A1 (en) 2010-04-16 2011-10-20 Biomarin Pharmaceutical Inc. Methods of using dihydropyridophthalazinone inhibitors of poly (adp-ribose)polymerase (parp)
EP2797921B1 (en) 2011-12-31 2017-09-06 BeiGene, Ltd. Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors
CN112552401B (zh) 2013-09-13 2023-08-25 广州百济神州生物制药有限公司 抗pd1抗体及其作为治疗剂与诊断剂的用途
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US9637488B2 (en) 2015-01-29 2017-05-02 Fuqiang Ruan Heterocyclic compounds as inhibitors of class I PI3KS
NZ739876A (en) 2015-08-25 2022-09-30 Beigene Ltd Process for preparing parp inhibitor, crystalline forms, and uses thereof
TWI806840B (zh) 2016-09-27 2023-07-01 英屬開曼群島商百濟神州有限公司 使用包含parp抑制劑的組合產品治療癌症
TW201840564A (zh) 2017-02-28 2018-11-16 英屬開曼群島商百濟神州有限公司 稠合的四環或五環二氫二氮呯幷哢唑酮的鹽的結晶形式及其用途
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
EP3315500A1 (en) 2018-05-02
EA201491303A1 (ru) 2014-10-30
CN106220635B (zh) 2019-03-08
NZ624063A (en) 2016-09-30
HRP20171883T1 (hr) 2018-01-12
BR112014012628B1 (pt) 2021-02-09
WO2013097225A1 (en) 2013-07-04
SI2797921T1 (en) 2018-01-31
JP6034877B2 (ja) 2016-11-30
EP3315500B1 (en) 2020-03-18
LT2797921T (lt) 2017-11-27
IL233365A0 (en) 2014-08-31
US20160159811A1 (en) 2016-06-09
KR101716012B1 (ko) 2017-03-13
CN103703004A (zh) 2014-04-02
PL2797921T3 (pl) 2018-02-28
US20170305921A1 (en) 2017-10-26
AU2011384858A1 (en) 2014-05-29
BR112014012628B8 (pt) 2023-01-17
US20190016731A1 (en) 2019-01-17
CY1119804T1 (el) 2018-06-27
HK1192233A1 (zh) 2014-08-15
CA2856309C (en) 2016-06-07
EP2797921A1 (en) 2014-11-05
MX2014007840A (es) 2014-08-21
IN2014DN06169A (es) 2015-08-21
PT2797921T (pt) 2017-11-14
ME02855B (me) 2018-04-20
JP2015503526A (ja) 2015-02-02
HUE035153T2 (en) 2018-05-02
AU2011384858B2 (en) 2016-05-05
IL233365A (en) 2016-08-31
EA027533B1 (ru) 2017-08-31
EP2797921B1 (en) 2017-09-06
SG11201401726VA (en) 2014-10-30
ZA201405560B (en) 2017-02-22
NO2797921T3 (es) 2018-02-03
DK2797921T3 (en) 2017-10-02
KR20140107353A (ko) 2014-09-04
CN103703004B (zh) 2016-06-29
RS56616B1 (sr) 2018-02-28
US9260440B2 (en) 2016-02-16
CN106220635A (zh) 2016-12-14
US9617273B2 (en) 2017-04-11
US20150175617A1 (en) 2015-06-25
US10112952B2 (en) 2018-10-30
BR112014012628A2 (pt) 2017-06-13
EP2797921A4 (en) 2015-10-21
US10501467B2 (en) 2019-12-10
CA2856309A1 (en) 2013-07-04
ES2645814T3 (es) 2017-12-07

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