PL3746446T3 - Inhibitory PRC2 - Google Patents

Inhibitory PRC2

Info

Publication number
PL3746446T3
PL3746446T3 PL19710816.0T PL19710816T PL3746446T3 PL 3746446 T3 PL3746446 T3 PL 3746446T3 PL 19710816 T PL19710816 T PL 19710816T PL 3746446 T3 PL3746446 T3 PL 3746446T3
Authority
PL
Poland
Prior art keywords
prc2
inhibitors
prc2 inhibitors
Prior art date
Application number
PL19710816.0T
Other languages
English (en)
Inventor
Matthew Arnold Marx
Matthew Randolph Lee
Thomas P. Bobinski
Aaron Craig BURNS
Nidhi Arora
James Gail Christensen
John Michael Ketcham
Original Assignee
Mirati Therapeutics, Inc.
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 Mirati Therapeutics, Inc. filed Critical Mirati Therapeutics, Inc.
Publication of PL3746446T3 publication Critical patent/PL3746446T3/pl

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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
PL19710816.0T 2018-01-31 2019-01-29 Inhibitory PRC2 PL3746446T3 (pl)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201862624176P 2018-01-31 2018-01-31
US201862672701P 2018-05-17 2018-05-17
US201862747736P 2018-10-19 2018-10-19
PCT/US2019/015677 WO2019152419A1 (en) 2018-01-31 2019-01-29 Prc2 inhibitors

Publications (1)

Publication Number Publication Date
PL3746446T3 true PL3746446T3 (pl) 2022-08-29

Family

ID=65763738

Family Applications (2)

Application Number Title Priority Date Filing Date
PL22165237.3T PL4043466T3 (pl) 2018-01-31 2019-01-29 Inhibitory PRC2
PL19710816.0T PL3746446T3 (pl) 2018-01-31 2019-01-29 Inhibitory PRC2

Family Applications Before (1)

Application Number Title Priority Date Filing Date
PL22165237.3T PL4043466T3 (pl) 2018-01-31 2019-01-29 Inhibitory PRC2

Country Status (19)

Country Link
US (5) US11485738B2 (pl)
EP (2) EP3746446B1 (pl)
JP (3) JP7025556B2 (pl)
KR (2) KR102776492B1 (pl)
CN (1) CN112004816B (pl)
AU (2) AU2019214861B2 (pl)
BR (1) BR112020015583B1 (pl)
CA (1) CA3089639C (pl)
DK (2) DK4043466T3 (pl)
ES (2) ES2991317T3 (pl)
FI (1) FI4043466T3 (pl)
HU (2) HUE059536T2 (pl)
IL (2) IL276156B (pl)
MX (2) MX2020007974A (pl)
NZ (1) NZ766447A (pl)
PL (2) PL4043466T3 (pl)
PT (2) PT4043466T (pl)
WO (1) WO2019152419A1 (pl)
ZA (2) ZA202004453B (pl)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ766447A (en) 2018-01-31 2021-12-24 Mirati Therapeutics Inc Prc2 inhibitors
CA3120791A1 (en) * 2018-11-30 2020-06-04 Tuojie Biotech (Shanghai) Co., Ltd. Pyrimidine and five-membered nitrogen heterocycle derivative, preparation method therefor, and medical uses thereof
WO2020219448A1 (en) 2019-04-22 2020-10-29 Mirati Therapeutics, Inc. Naphthyridine derivatives as prc2 inhibitors
JP7541538B2 (ja) * 2019-06-05 2024-08-28 ミラティ セラピューティクス,インク. 癌を処置するためのprc2阻害剤としてのイミダゾ[1,2-c]ピリミジン誘導体
CN112409385B (zh) * 2019-08-22 2024-08-13 上海青煜医药科技有限公司 氮杂芳基化合物及其应用
CN113004233B (zh) * 2019-12-18 2022-12-20 南京优氟医药科技有限公司 一种用于制备prc2抑制剂的化合物、其制备方法和用途
CN114907385A (zh) * 2021-02-10 2022-08-16 上海青煜医药科技有限公司 氮杂芳基化合物、其制备方法及应用
WO2023049724A1 (en) * 2021-09-24 2023-03-30 Oric Pharmaceuticals, Inc. Prc2 inhibitors for use in treating blood disorders
EP4587440A1 (en) * 2022-09-14 2025-07-23 Oric Pharmaceuticals, Inc. Physical forms of an inhibitor of prc2
GB202216323D0 (en) 2022-11-02 2022-12-14 Cerevance Ltd Novel compounds
EP4630004A1 (en) * 2022-12-05 2025-10-15 Oric Pharmaceuticals, Inc. Treatment of prostate cancer having androgen receptor variants
WO2024148008A1 (en) * 2023-01-03 2024-07-11 Oric Pharmaceuticals, Inc. Treatment of neuroendocrine prostate cancer
WO2024215699A1 (en) * 2023-04-11 2024-10-17 Oric Pharmaceuticals, Inc. Treatment of t-cell lymphoma
AU2024323161A1 (en) * 2023-08-04 2026-02-26 Oric Pharmaceuticals, Inc. Treatment of prostate cancer

Family Cites Families (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6921762B2 (en) 2001-11-16 2005-07-26 Amgen Inc. Substituted indolizine-like compounds and methods of use
WO2010021381A1 (ja) 2008-08-22 2010-02-25 武田薬品工業株式会社 縮合複素環誘導体およびその用途
JP5864546B2 (ja) 2010-05-07 2016-02-17 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC インダゾール
EA023788B1 (ru) 2010-05-07 2016-07-29 ГЛЭКСОСМИТКЛАЙН ЭлЭлСи Производные индола и фармацевтические композиции на их основе
US9175331B2 (en) 2010-09-10 2015-11-03 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
WO2012068589A2 (en) 2010-11-19 2012-05-24 Constellation Pharmaceuticals Modulators of methyl modifying enzymes, compositions and uses thereof
WO2012082436A2 (en) 2010-12-03 2012-06-21 Epizyme, Inc. Modulators of histone methyltransferase, and methods of use thereof
EP3323820B1 (en) 2011-02-28 2023-05-10 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
JO3438B1 (ar) 2011-04-13 2019-10-20 Epizyme Inc مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
TW201733984A (zh) 2011-04-13 2017-10-01 雅酶股份有限公司 經取代之苯化合物
ES2648820T3 (es) 2011-05-10 2018-01-08 Gilead Sciences, Inc. Compuestos heterocíclicos condensados como moduladores de los canales de sodio
CA2850570A1 (en) 2011-09-30 2013-04-04 Glaxosmithkline Llc Methods of treating cancer
WO2013063417A1 (en) 2011-10-27 2013-05-02 Memorial Sloan-Kettering Cancer Center Methyltransferase inhibitors for treating cancer
US9206128B2 (en) 2011-11-18 2015-12-08 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
WO2013075084A1 (en) 2011-11-18 2013-05-23 Constellation Pharmaceuticals Modulators of methyl modifying enzymes, compositions and uses thereof
EP2953941B1 (en) 2013-02-11 2017-04-05 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
WO2013120104A2 (en) 2012-02-10 2013-08-15 Constellation Pharmaceuticals Modulators of methyl modifying enzymes, compositions and uses thereof
JP6340361B2 (ja) 2012-04-13 2018-06-06 エピザイム,インコーポレイティド がんを処置するための組合せ治療
US9562041B2 (en) 2012-05-16 2017-02-07 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
US9105490B2 (en) 2012-09-27 2015-08-11 Taiwan Semiconductor Manufacturing Company, Ltd. Contact structure of semiconductor device
CA2884848C (en) 2012-09-28 2017-08-22 Pfizer Inc. Benzamide and heterobenzamide compounds
CA2887243C (en) 2012-10-15 2024-04-09 Epizyme, Inc. Methods of treating cancer
AU2013331380B2 (en) 2012-10-15 2018-03-22 Epizyme, Inc. Substituted benzene compounds
AU2013371541B2 (en) 2012-12-13 2016-10-13 Glaxosmithkline Llc Enhancer of Zeste Homolog 2 inhibitors
UA111305C2 (uk) 2012-12-21 2016-04-11 Пфайзер Інк. Конденсовані лактами арилу та гетероарилу
WO2014100665A1 (en) 2012-12-21 2014-06-26 Epizyme, Inc. 1,4-pyridone bicyclic heteroaryl compounds
WO2014100646A1 (en) 2012-12-21 2014-06-26 Epizyme, Inc. 1,4-pyridone compounds
WO2014144747A1 (en) 2013-03-15 2014-09-18 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
US9045477B2 (en) 2013-03-15 2015-06-02 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
EP2970281A4 (en) 2013-03-15 2016-08-03 Epizyme Inc SUBSTITUTED BENZOL COMPOUNDS
US9745305B2 (en) 2013-03-15 2017-08-29 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
US9243001B2 (en) 2013-03-15 2016-01-26 Epizyme, Inc. Substituted benzene compounds
US9505745B2 (en) 2013-04-30 2016-11-29 Glaxosmithkline Intellectual Property (No. 2) Limited Enhancer of zeste homolog 2 inhibitors
EP3004096A1 (en) 2013-06-06 2016-04-13 Glaxosmithkline Intellectual Property (No. 2) Limited Enhancer of zeste homolog 2 inhibitors
ES2640386T3 (es) 2013-07-10 2017-11-02 Glaxosmithkline Intellectual Property (No. 2) Limited Potenciador de inhibidores del homólogo Zeste 2
US9624205B2 (en) 2013-07-19 2017-04-18 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
WO2015010049A1 (en) 2013-07-19 2015-01-22 Epizyme, Inc. Substituted benzene compounds
EP3033334A1 (en) 2013-08-15 2016-06-22 Constellation Pharmaceuticals, Inc. Indole derivatives as modulators of methyl modifying enzymes, compositions and uses thereof
US9738630B2 (en) 2013-11-19 2017-08-22 Bristol-Myers Squibb Company Inhibitors of lysine methyl transferase
US9822103B2 (en) 2013-11-22 2017-11-21 Bristol-Myers Squibb Company Inhibitors of lysine methyl transferase
EP3111222A1 (en) 2014-02-26 2017-01-04 Glaxosmithkline Intellectual Property (No. 2) Limited Methods of treating cancer patients responding to ezh2 inhibitor gsk126
WO2015132765A1 (en) 2014-03-07 2015-09-11 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
HUE049417T2 (hu) 2014-03-17 2020-09-28 Daiichi Sankyo Co Ltd 1,3-benzodioxol származékok mint EZHl és/vagy EZH2 inhibitorok
WO2015193768A1 (en) 2014-06-17 2015-12-23 Pfizer Inc. Aryl fused lactams as ezh2 modulators
AP2016009605A0 (en) 2014-06-17 2016-12-31 Pfizer Substituted dihydroisoquinolinone compounds
CN107148419A (zh) 2014-10-28 2017-09-08 葛兰素史密斯克莱知识产权(第2 号)有限公司 Zeste增强子同源物2抑制剂
KR20170081213A (ko) 2014-11-06 2017-07-11 다나-파버 캔서 인스티튜트 인크. Ezh2 억제제 및 그의 용도
CA2966336A1 (en) 2014-11-06 2016-05-12 Dana-Farber Cancer Institute, Inc. Use of compositions modulating chromatin structure for graft versus host disease (gvhd)
AR102767A1 (es) 2014-12-05 2017-03-22 Lilly Co Eli Inhibidores de ezh2
WO2016102493A1 (en) 2014-12-22 2016-06-30 Bayer Pharma Aktiengesellschaft Imidazopyridine ezh2 inhibitors
IL236420A (en) * 2014-12-23 2016-06-30 Ron Schneider Methods and systems for producing an enlarged 3D image
EA032416B1 (ru) * 2014-12-23 2019-05-31 Новартис Аг Соединения триазолопиримидина и их применения
CN107438593B (zh) 2015-01-30 2020-10-30 基因泰克公司 治疗化合物及其用途
WO2016130396A1 (en) 2015-02-13 2016-08-18 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
TW201718598A (zh) 2015-08-27 2017-06-01 美國禮來大藥廠 Ezh2抑制劑
DK3378859T3 (da) 2015-11-19 2020-01-20 Jiangsu Hengrui Medicine Co Benzofuranderivater, fremgangsmåde til fremstilling deraf og anvendelse deraf i medicin
EP3386513A2 (en) 2015-12-07 2018-10-17 Epizyme Inc Inhibitors of ezh2 and methods of use thereof
WO2017174023A1 (zh) 2016-04-08 2017-10-12 南京明德新药研发股份有限公司 作为ezh2抑制剂的联苯化合物
EP3445365A4 (en) 2016-04-22 2019-10-16 Dana-Farber Cancer Institute, Inc. EZH2 INHIBITORS AND USES THEREOF
SG11201809560QA (en) 2016-05-05 2018-11-29 Glaxosmithkline Ip No 2 Ltd Enhancer of zeste homolog 2 inhibitors
US9957274B2 (en) 2016-05-06 2018-05-01 Abbvie Inc. Indane inhibitors of EED and methods of their use
JP7121660B2 (ja) 2016-06-01 2022-08-18 エピザイム,インコーポレイティド 癌を処置するためのezh2阻害剤の使用
US11147819B2 (en) 2016-06-17 2021-10-19 Epizyme, Inc. EZH2 inhibitors for treating cancer
WO2017221092A1 (en) * 2016-06-20 2017-12-28 Novartis Ag Triazolopyridine compounds and uses thereof
EP3472168B1 (en) * 2016-06-20 2024-01-10 Novartis AG Crystalline forms of triazolopyrimidine compound
US10676479B2 (en) * 2016-06-20 2020-06-09 Novartis Ag Imidazolepyridine compounds and uses thereof
US10266542B2 (en) 2017-03-15 2019-04-23 Mirati Therapeutics, Inc. EZH2 inhibitors
WO2019062435A1 (zh) 2017-09-28 2019-04-04 中国科学院上海药物研究所 三氮唑并嘧啶、三氮唑并吡啶化合物及其组合物用于治疗prc2介导的疾病
CN109942556A (zh) 2017-12-21 2019-06-28 上海青煜医药科技有限公司 嘧啶酮化合物及其应用
NZ766447A (en) * 2018-01-31 2021-12-24 Mirati Therapeutics Inc Prc2 inhibitors
CN110156787B (zh) 2018-02-13 2021-11-02 中国科学院上海药物研究所 一种三氮唑并嘧啶衍生化合物、包含其的药物组合物及其用途
CN110563722A (zh) 2018-06-06 2019-12-13 上海青煜医药科技有限公司 吡啶或哒嗪并环化合物及其应用
WO2020219448A1 (en) 2019-04-22 2020-10-29 Mirati Therapeutics, Inc. Naphthyridine derivatives as prc2 inhibitors
JP7541538B2 (ja) 2019-06-05 2024-08-28 ミラティ セラピューティクス,インク. 癌を処置するためのprc2阻害剤としてのイミダゾ[1,2-c]ピリミジン誘導体

Also Published As

Publication number Publication date
HUE059536T2 (hu) 2022-11-28
JP2021512092A (ja) 2021-05-13
PL4043466T3 (pl) 2025-04-07
JP2023109962A (ja) 2023-08-08
AU2019214861A1 (en) 2020-08-13
FI4043466T3 (fi) 2024-10-30
JP7495555B2 (ja) 2024-06-04
US12371435B2 (en) 2025-07-29
US20250282787A1 (en) 2025-09-11
PT4043466T (pt) 2024-10-14
KR20220139439A (ko) 2022-10-14
CA3089639C (en) 2024-06-18
EP4043466A1 (en) 2022-08-17
MX2020007974A (es) 2020-09-07
MX2021012501A (es) 2021-11-12
PT3746446T (pt) 2022-07-18
NZ766447A (en) 2021-12-24
ZA202107835B (en) 2022-07-27
NZ783240A (en) 2024-04-26
IL276156A (en) 2020-09-30
AU2021266351B2 (en) 2022-11-24
IL285354A (en) 2021-09-30
US20210032252A1 (en) 2021-02-04
KR102451529B1 (ko) 2022-10-06
US20210101904A1 (en) 2021-04-08
US11091495B2 (en) 2021-08-17
HUE069170T2 (hu) 2025-02-28
EP3746446A1 (en) 2020-12-09
BR112020015583A2 (pt) 2021-02-02
EP4043466B1 (en) 2024-08-21
CN112004816B (zh) 2024-01-05
JP2022068252A (ja) 2022-05-09
KR20200115570A (ko) 2020-10-07
ZA202004453B (en) 2022-11-30
US20230137025A1 (en) 2023-05-04
JP7025556B2 (ja) 2022-02-24
KR102776492B1 (ko) 2025-03-04
CN112004816A (zh) 2020-11-27
CA3089639A1 (en) 2019-08-08
WO2019152419A1 (en) 2019-08-08
DK4043466T3 (da) 2024-09-30
JP7288527B2 (ja) 2023-06-07
US11485738B2 (en) 2022-11-01
US20210230168A1 (en) 2021-07-29
ES2991317T3 (es) 2024-12-03
US11220509B2 (en) 2022-01-11
DK3746446T3 (da) 2022-06-27
EP3746446B1 (en) 2022-05-11
IL285354B (en) 2022-06-01
AU2019214861B2 (en) 2021-11-18
BR112020015583B1 (pt) 2022-12-06
WO2019152419A8 (en) 2019-11-07
IL276156B (en) 2021-08-31
AU2021266351A1 (en) 2021-12-09
ES2923290T3 (es) 2022-09-26

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