MX371108B - Pirimidopirimidinonas utiles como iniciadores de wee-1 cinasa. - Google Patents

Pirimidopirimidinonas utiles como iniciadores de wee-1 cinasa.

Info

Publication number
MX371108B
MX371108B MX2016007801A MX2016007801A MX371108B MX 371108 B MX371108 B MX 371108B MX 2016007801 A MX2016007801 A MX 2016007801A MX 2016007801 A MX2016007801 A MX 2016007801A MX 371108 B MX371108 B MX 371108B
Authority
MX
Mexico
Prior art keywords
wee
useful
pyrimidopyrimidinones
kinase inhibitors
compounds
Prior art date
Application number
MX2016007801A
Other languages
English (en)
Other versions
MX2016007801A (es
Inventor
Harrison Timothy
Trevitt Graham
Roderick O´Dowd Colin
John Wilkinson Andrew
robin hewitt Peter
Burkamp Frank
d shepherd Steven
Miel Hugues
Original Assignee
Almac Discovery 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 Almac Discovery Ltd filed Critical Almac Discovery Ltd
Publication of MX2016007801A publication Critical patent/MX2016007801A/es
Publication of MX371108B publication Critical patent/MX371108B/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
    • C07D487/04Ortho-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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D475/00Heterocyclic compounds containing pteridine ring 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Abstract

La presente invención se relaciona con compuestos que son útiles como inhibidores de la actividad de Wee-1 cinasa. La presente invención también se relaciona con composiciones farmacéuticas que comprenden estos compuestos y con métodos para utilizar estos compuestos en el tratamiento de cáncer y métodos para tratar cáncer.
MX2016007801A 2013-12-19 2014-12-19 Pirimidopirimidinonas utiles como iniciadores de wee-1 cinasa. MX371108B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1322602.2A GB201322602D0 (en) 2013-12-19 2013-12-19 Pharmaceutical compounds
PCT/GB2014/053793 WO2015092431A1 (en) 2013-12-19 2014-12-19 Pyrimidopyrimidinones useful as wee-1 kinase inhibitors

Publications (2)

Publication Number Publication Date
MX2016007801A MX2016007801A (es) 2016-09-07
MX371108B true MX371108B (es) 2020-01-17

Family

ID=50071157

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2016007801A MX371108B (es) 2013-12-19 2014-12-19 Pirimidopirimidinonas utiles como iniciadores de wee-1 cinasa.

Country Status (27)

Country Link
US (1) US9850247B2 (es)
EP (1) EP3083625B1 (es)
JP (1) JP6437559B2 (es)
KR (1) KR102405462B1 (es)
CN (1) CN105829315B (es)
AU (1) AU2014369457B2 (es)
BR (1) BR112016014151B1 (es)
CA (1) CA2933755C (es)
CY (1) CY1120035T1 (es)
DK (1) DK3083625T3 (es)
ES (1) ES2650013T3 (es)
GB (1) GB201322602D0 (es)
HR (1) HRP20180080T1 (es)
HU (1) HUE037908T2 (es)
IL (1) IL245672B (es)
LT (1) LT3083625T (es)
MX (1) MX371108B (es)
NO (1) NO3083625T3 (es)
NZ (1) NZ720178A (es)
PL (1) PL3083625T3 (es)
PT (1) PT3083625T (es)
RS (1) RS56731B1 (es)
RU (1) RU2691105C1 (es)
SG (1) SG11201603814TA (es)
SI (1) SI3083625T1 (es)
WO (1) WO2015092431A1 (es)
ZA (1) ZA201603337B (es)

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CN109906227B (zh) * 2016-11-16 2022-03-11 上海瑛派药业有限公司 8,9-二氢咪唑[1,2-a]嘧啶并[5,4-e]嘧啶-5(6H)-酮类化合物
CA3048376A1 (en) 2016-12-27 2018-07-05 Riken Bmp-signal-inhibiting compound
WO2018133829A1 (zh) * 2017-01-23 2018-07-26 南京明德新药研发股份有限公司 作为Wee1抑制剂的1,2-二氢-3H-吡唑[3,4-d]嘧啶-3-酮衍生物
GB201703881D0 (en) * 2017-03-10 2017-04-26 Almac Discovery Ltd Pharmaceutical compounds
AU2018243667A1 (en) 2017-03-31 2019-10-17 Seagen Inc. Combinations of Chk1- and Wee1 - inhibitors
CN110914277B (zh) * 2017-07-10 2022-08-09 上海瑛派药业有限公司 咪唑并[1,2-b]嘧啶并[4,5-d]哒嗪-5(6H)-酮类化合物及其应用
CN109422754A (zh) * 2017-08-24 2019-03-05 上海迪诺医药科技有限公司 吡唑并[3,4-d]嘧啶-3-酮衍生物、其药物组合物及应用
US11299493B2 (en) 2017-10-09 2022-04-12 Nuvation Bio Inc. Heterocyclic compounds and uses thereof
AU2018347307A1 (en) 2017-10-09 2020-04-23 Nuvation Bio Inc. Heterocyclic compounds and uses thereof
BR112020008664A8 (pt) 2017-11-01 2023-01-17 Shijiazhuang Sagacity New Drug Dev Co Ltd Composto macrocíclico que atua como inibidor de weel e aplicações do mesmo
US20200405723A1 (en) * 2018-02-28 2020-12-31 The Regents Of The University Of Colorado, A Body Corporate Wee1 kinase inhibitors and methods of treating cancer using the same
MX2021003531A (es) 2018-09-27 2021-07-21 Betta Pharmaceuticals Co Ltd Inhibidor de fgfr4 y su uso.
CN112955454A (zh) 2018-10-26 2021-06-11 石家庄智康弘仁新药开发有限公司 作为Wee1抑制剂的嘧啶并吡唑酮类衍生物及其应用
CN113614087B (zh) 2019-03-22 2023-06-02 首药控股(北京)股份有限公司 Wee1抑制剂及其制备和用途
EP3952878A4 (en) * 2019-04-09 2023-01-04 Nuvation Bio Inc. HETEROCYCLIC COMPOUNDS AND USES THEREOF
EP3952879A4 (en) * 2019-04-09 2023-01-04 Nuvation Bio Inc. HETEROCYCLIC COMPOUNDS AND USES THEREOF
JP2022526831A (ja) 2019-04-09 2022-05-26 ニューベイション・バイオ・インコーポレイテッド ヘテロ環式化合物およびその使用
EP3964510A4 (en) 2019-04-30 2023-04-26 Wuxi Biocity Biopharmaceutics Co., Ltd. WEE1 INHIBITOR COMPOUND CRYSTAL FORM AND USE
CN112142763B (zh) * 2019-06-28 2024-01-26 上海医药集团股份有限公司 一种吡唑酮并嘧啶类化合物、其制备方法及应用
EP4169919A1 (en) 2020-06-17 2023-04-26 Wigen Biomedicine Technology (Shanghai) Co., Ltd. Pyrazolo[3,4-d]pyrimidine-3-ketone derivative as wee-1 inhibitor
US20230416247A1 (en) * 2020-10-01 2023-12-28 University Of Washington Drug-like molecules and methods for the therapeutic targeting of microrna-21
CA3201152A1 (en) * 2020-12-18 2022-06-23 Xiaoyang Dong Nitrogen containing 2,3-dihydroquinazolinone compounds as nav1.8 inhibitors
JP2024515318A (ja) 2021-04-30 2024-04-08 ウィゲン・バイオメディシン・テクノロジー・(シャンハイ)・カンパニー・リミテッド Wee-1阻害剤としての縮合環状化合物、その調製方法およびその使用
CN116836184A (zh) * 2022-03-25 2023-10-03 药雅科技(上海)有限公司 Wee1激酶抑制剂的制备及其应用
WO2023217201A2 (zh) * 2022-05-10 2023-11-16 杭州德睿智药科技有限公司 作为Wee1抑制剂的新型嘧啶并杂环类新化合物及其应用

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WO2013013031A1 (en) * 2011-07-19 2013-01-24 Abbvie Inc. Pyridazino [4, 5 -d] pyrimidin- (6h) -one inhibitors of wee - 1 kinase
JP2014530867A (ja) * 2011-10-20 2014-11-20 アッヴィ・インコーポレイテッド キナーゼのピリドピリミジノン阻害剤
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CN102816164A (zh) * 2012-08-31 2012-12-12 北京理工大学 一种合成7-氨基-2,3-二氢嘧啶[4,5-d]嘧啶-4(1H)-酮的方法

Also Published As

Publication number Publication date
BR112016014151B1 (pt) 2023-01-17
SI3083625T1 (en) 2018-03-30
KR20160098499A (ko) 2016-08-18
NO3083625T3 (es) 2018-03-31
MX2016007801A (es) 2016-09-07
AU2014369457B2 (en) 2018-08-09
BR112016014151A2 (es) 2017-08-08
EP3083625A1 (en) 2016-10-26
RU2691105C1 (ru) 2019-06-11
GB201322602D0 (en) 2014-02-05
KR102405462B1 (ko) 2022-06-03
ES2650013T3 (es) 2018-01-16
HUE037908T2 (hu) 2018-09-28
SG11201603814TA (en) 2016-07-28
PL3083625T3 (pl) 2018-03-30
IL245672A0 (en) 2016-06-30
RU2016123363A (ru) 2018-01-25
US20160318936A1 (en) 2016-11-03
NZ720178A (en) 2022-05-27
CA2933755C (en) 2023-01-31
CA2933755A1 (en) 2015-06-25
JP6437559B2 (ja) 2018-12-12
WO2015092431A1 (en) 2015-06-25
HRP20180080T1 (hr) 2018-03-09
PT3083625T (pt) 2018-02-06
JP2017500335A (ja) 2017-01-05
IL245672B (en) 2021-10-31
US9850247B2 (en) 2017-12-26
ZA201603337B (en) 2018-07-25
EP3083625B1 (en) 2017-11-01
CY1120035T1 (el) 2018-12-12
AU2014369457A1 (en) 2016-06-09
RS56731B1 (sr) 2018-03-30
DK3083625T3 (en) 2017-12-18
CN105829315B (zh) 2019-03-08
LT3083625T (lt) 2017-12-27
CN105829315A (zh) 2016-08-03

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