KR102604803B1 - 신규 plk1 분해 유도 화합물 - Google Patents

신규 plk1 분해 유도 화합물 Download PDF

Info

Publication number
KR102604803B1
KR102604803B1 KR1020227042318A KR20227042318A KR102604803B1 KR 102604803 B1 KR102604803 B1 KR 102604803B1 KR 1020227042318 A KR1020227042318 A KR 1020227042318A KR 20227042318 A KR20227042318 A KR 20227042318A KR 102604803 B1 KR102604803 B1 KR 102604803B1
Authority
KR
South Korea
Prior art keywords
amino
methyl
μmol
mmol
cancer
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
KR1020227042318A
Other languages
English (en)
Korean (ko)
Other versions
KR20230024267A (ko
Inventor
류수희
민임숙
이한규
김성훈
류혜국
강금영
김상윤
정소현
이준규
이기쁨
Original Assignee
(주) 업테라
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 (주) 업테라 filed Critical (주) 업테라
Publication of KR20230024267A publication Critical patent/KR20230024267A/ko
Application granted granted Critical
Publication of KR102604803B1 publication Critical patent/KR102604803B1/ko
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • 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
    • A61K31/55Heterocyclic 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
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/545Heterocyclic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/55Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • 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
    • 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
    • C07D487/10Spiro-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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
KR1020227042318A 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물 Active KR102604803B1 (ko)

Applications Claiming Priority (17)

Application Number Priority Date Filing Date Title
KR1020210105358 2021-08-10
KR20210105358 2021-08-10
KR1020210106488 2021-08-12
KR20210106488 2021-08-12
KR1020210117389 2021-09-03
KR20210117389 2021-09-03
KR20210126757 2021-09-24
KR1020210126757 2021-09-24
KR20220008456 2022-01-20
KR1020220008456 2022-01-20
KR20220020996 2022-02-17
KR1020220020996 2022-02-17
KR20220054880 2022-05-03
KR1020220054880 2022-05-03
KR1020220075838 2022-06-21
KR20220075838 2022-06-21
PCT/KR2022/011962 WO2023018237A1 (en) 2021-08-10 2022-08-10 Novel plk1 degradation inducing compound

Publications (2)

Publication Number Publication Date
KR20230024267A KR20230024267A (ko) 2023-02-20
KR102604803B1 true KR102604803B1 (ko) 2023-11-22

Family

ID=85200656

Family Applications (5)

Application Number Title Priority Date Filing Date
KR1020227042318A Active KR102604803B1 (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물
KR1020227036596A Active KR102604802B1 (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물
KR1020247013823A Pending KR20240060721A (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물
KR1020227036557A Active KR102604801B1 (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물
KR1020227046443A Active KR102662205B1 (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물

Family Applications After (4)

Application Number Title Priority Date Filing Date
KR1020227036596A Active KR102604802B1 (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물
KR1020247013823A Pending KR20240060721A (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물
KR1020227036557A Active KR102604801B1 (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물
KR1020227046443A Active KR102662205B1 (ko) 2021-08-10 2022-08-10 신규 plk1 분해 유도 화합물

Country Status (15)

Country Link
US (4) US11939334B2 (https=)
EP (4) EP4157849A4 (https=)
JP (4) JP7555156B2 (https=)
KR (5) KR102604803B1 (https=)
CN (2) CN116322700B (https=)
AU (1) AU2022327025A1 (https=)
CA (1) CA3228601A1 (https=)
CL (1) CL2024000373A1 (https=)
CO (1) CO2024001256A2 (https=)
CR (1) CR20240120A (https=)
EC (1) ECSP24010109A (https=)
IL (1) IL310678A (https=)
MX (1) MX2024001774A (https=)
PE (1) PE20240894A1 (https=)
WO (5) WO2023018236A1 (https=)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20230158158A1 (en) * 2020-03-27 2023-05-25 Uppthera Pyrazolo quinazoline derivative compounds inducing selective degradation of plk1
UY39892A (es) 2021-08-10 2023-03-31 Novartis Pharma Ag Compuestos y composiciones para tratar afecciones asociadas con la actividad de STING
CN120603831A (zh) * 2022-11-29 2025-09-05 厄普特拉株式会社 具有增加的刚性的plk1降解诱导化合物
KR20250037591A (ko) * 2023-02-02 2025-03-17 (주) 업테라 신규 plk1 분해 유도 화합물
WO2024188209A1 (zh) * 2023-03-10 2024-09-19 标新生物医药科技(上海)有限公司 新颖的e3泛素连接酶配体、蛋白降解剂及其应用
KR20260022390A (ko) 2023-06-08 2026-02-19 누릭스 테라퓨틱스 인코포레이티드 Smarca2의 선택적 분해제로서의 이작용성 아진 접합체 및 이의 치료적 용도
CN121816348A (zh) 2023-08-11 2026-04-07 深圳众格生物科技有限公司 一种降解irak4的蛋白降解靶向嵌合体化合物及其应用
CN117126133A (zh) * 2023-08-14 2023-11-28 中国海洋大学 一种化合物及其用途
WO2025062330A1 (en) 2023-09-20 2025-03-27 Aurigene Oncology Limited Heterocyclic compounds as cbp selective degraders
WO2025125575A1 (en) 2023-12-14 2025-06-19 Astrazeneca Ab Irak4 protacs
WO2025239662A1 (ko) * 2024-05-13 2025-11-20 (주) 업테라 분해 약물-항체 접합체용 plk1 분해 유도 화합물
CN118724841A (zh) * 2024-06-14 2024-10-01 南通华祥医药科技有限公司 一种n-氨基哌啶二盐酸盐的制备方法
WO2026013577A1 (en) * 2024-07-10 2026-01-15 Monte Rosa Therapeutics Ag Piperidine-2, 6-dione derivatives useful for the targeted degradation of vav1
WO2026013576A1 (en) * 2024-07-10 2026-01-15 Monte Rosa Therapeutics Ag Dihydrouracil derivatives useful for the targeted degradation of vav1
WO2026026773A1 (zh) * 2024-07-29 2026-02-05 杭州胶联生物医药科技有限公司 作为vav1蛋白靶点降解剂的新型取代杂环类化合物
WO2026041138A1 (zh) * 2024-08-22 2026-02-26 武汉人福创新药物研发中心有限公司 作为vav1降解剂的苯并杂环类化合物及其用途

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009153197A1 (en) 2008-06-18 2009-12-23 F. Hoffmann-La Roche Ag Halo-substituted pyrimidodiazepines as plkl inhibitors
CN106977584A (zh) 2017-04-19 2017-07-25 吉林大学 靶向泛素化降解plk1和brd4蛋白的化合物及其应用
CN109879877A (zh) 2019-03-04 2019-06-14 吉林大学 一种可降解plk1和brd4蛋白的化合物及其应用
US20200038513A1 (en) 2018-07-26 2020-02-06 Arvinas Operations, Inc. Modulators of fak proteolysis and associated methods of use

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2649324A1 (en) * 2006-04-12 2007-10-25 Jean-Damien Charrier Tetrahydropteridines useful as inhibitors of protein kinases
TW200808325A (en) * 2006-07-06 2008-02-16 Astrazeneca Ab Novel compounds
WO2008113711A1 (en) * 2007-03-22 2008-09-25 F. Hoffmann-La Roche Ag Substituted pyrimidodiazepines useful as plk1 inhibitors
US9694084B2 (en) * 2014-12-23 2017-07-04 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
AU2016349781A1 (en) * 2015-11-02 2018-05-10 Yale University Proteolysis targeting chimera compounds and methods of preparing and using same
CN106543185B (zh) * 2016-11-10 2017-12-15 吉林大学 一种靶向泛素化降解plk1和brd4蛋白的化合物及其应用
BR112019015484A2 (pt) * 2017-01-31 2020-04-28 Arvinas Operations Inc ligantes de cereblon e compostos bifuncionais compreendendo os mesmos
CN111018857B (zh) * 2018-10-09 2023-06-02 嘉兴优博生物技术有限公司 靶向蛋白酶降解平台(ted)
JP7785663B2 (ja) 2019-09-16 2025-12-15 ノバルティス アーゲー 二機能性分解誘導薬及びそれらの使用方法
AU2020356484A1 (en) * 2019-09-27 2022-03-17 Dana-Farber Cancer Institute, Inc. ERK5 degraders as therapeutics in cancer and inflammatory diseases
US20230158158A1 (en) * 2020-03-27 2023-05-25 Uppthera Pyrazolo quinazoline derivative compounds inducing selective degradation of plk1

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009153197A1 (en) 2008-06-18 2009-12-23 F. Hoffmann-La Roche Ag Halo-substituted pyrimidodiazepines as plkl inhibitors
CN106977584A (zh) 2017-04-19 2017-07-25 吉林大学 靶向泛素化降解plk1和brd4蛋白的化合物及其应用
US20200038513A1 (en) 2018-07-26 2020-02-06 Arvinas Operations, Inc. Modulators of fak proteolysis and associated methods of use
CN109879877A (zh) 2019-03-04 2019-06-14 吉林大学 一种可降解plk1和brd4蛋白的化合物及其应用

Also Published As

Publication number Publication date
KR20230024302A (ko) 2023-02-20
CR20240120A (es) 2024-05-22
CN116261458B (zh) 2024-05-24
CO2024001256A2 (es) 2024-03-18
KR102604802B1 (ko) 2023-11-22
WO2023018238A1 (en) 2023-02-16
EP4384520A4 (en) 2025-09-03
MX2024001774A (es) 2024-04-24
US20230219966A1 (en) 2023-07-13
EP4157849A4 (en) 2024-12-11
JP7555156B2 (ja) 2024-09-24
EP4157850A1 (en) 2023-04-05
KR20230024267A (ko) 2023-02-20
KR20230024250A (ko) 2023-02-20
KR102604801B1 (ko) 2023-11-22
EP4384520A1 (en) 2024-06-19
ECSP24010109A (es) 2024-05-31
PE20240894A1 (es) 2024-04-24
KR102662205B1 (ko) 2024-04-30
EP4384521A1 (en) 2024-06-19
CN116322700B (zh) 2024-08-20
CA3228601A1 (en) 2023-02-16
US20250101025A1 (en) 2025-03-27
CN116322700A (zh) 2023-06-23
WO2023017442A1 (en) 2023-02-16
KR20240060721A (ko) 2024-05-08
JP2024530495A (ja) 2024-08-21
US11912710B2 (en) 2024-02-27
WO2023018237A1 (en) 2023-02-16
JP7555155B2 (ja) 2024-09-24
JP2023540728A (ja) 2023-09-26
US20250114460A1 (en) 2025-04-10
EP4384521A4 (en) 2025-09-03
JP2023540729A (ja) 2023-09-26
CL2024000373A1 (es) 2024-07-19
EP4157850A4 (en) 2024-11-20
KR20230024251A (ko) 2023-02-20
CN116261458A (zh) 2023-06-13
US20230242541A1 (en) 2023-08-03
WO2023018236A1 (en) 2023-02-16
EP4157849A1 (en) 2023-04-05
AU2022327025A1 (en) 2024-03-21
US11939334B2 (en) 2024-03-26
IL310678A (en) 2024-04-01
JP2024530195A (ja) 2024-08-16
WO2023017446A1 (en) 2023-02-16

Similar Documents

Publication Publication Date Title
KR102604803B1 (ko) 신규 plk1 분해 유도 화합물
KR102529222B1 (ko) Plk1 선택적 분해 유도 화합물
JP6789962B2 (ja) CDK阻害剤としてのピラゾロ[1,5−a][1,3,5]トリアジンとピラゾロ[1,5−a]ピリミジン誘導体
KR20220125306A (ko) RORγt 억제제, 이의 제조 방법 및 이의 용도
KR102920418B1 (ko) 키나아제 억제 활성을 갖는 화합물
CN120265288A (zh) Bcl-xl降解化合物
CA3232178A1 (en) Pyridazinyl amino derivatives as alk5 inhibitors
CA2942598A1 (en) N-[2-(3-amino-2,5-dimethyl-1,1-dioxido-5,6-dihydro-2h-1,2,4-thiadiazin-5-yl)-1,3-thiazol-4-yl] amides
CN117794936A (zh) 新型plk1降解诱导化合物
KR20250037591A (ko) 신규 plk1 분해 유도 화합물
KR20250133441A (ko) 2,4-디아닐리노피리미딘 기반의 오로라-a 키나아제 선택적 분해 유도 화합물
KR20250105638A (ko) 경직성이 증가된 plk1 분해 유도 화합물

Legal Events

Date Code Title Description
PA0105 International application

St.27 status event code: A-0-1-A10-A15-nap-PA0105

PA0201 Request for examination

St.27 status event code: A-1-2-D10-D11-exm-PA0201

PA0302 Request for accelerated examination

St.27 status event code: A-1-2-D10-D17-exm-PA0302

St.27 status event code: A-1-2-D10-D16-exm-PA0302

D13-X000 Search requested

St.27 status event code: A-1-2-D10-D13-srh-X000

D14-X000 Search report completed

St.27 status event code: A-1-2-D10-D14-srh-X000

PG1501 Laying open of application

St.27 status event code: A-1-1-Q10-Q12-nap-PG1501

E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

St.27 status event code: A-1-2-D10-D21-exm-PE0902

T11-X000 Administrative time limit extension requested

St.27 status event code: U-3-3-T10-T11-oth-X000

E13-X000 Pre-grant limitation requested

St.27 status event code: A-2-3-E10-E13-lim-X000

P11-X000 Amendment of application requested

St.27 status event code: A-2-2-P10-P11-nap-X000

P13-X000 Application amended

St.27 status event code: A-2-2-P10-P13-nap-X000

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

St.27 status event code: A-1-2-D10-D22-exm-PE0701

PR0701 Registration of establishment

St.27 status event code: A-2-4-F10-F11-exm-PR0701

PR1002 Payment of registration fee

St.27 status event code: A-2-2-U10-U12-oth-PR1002

Fee payment year number: 1

PG1601 Publication of registration

St.27 status event code: A-4-4-Q10-Q13-nap-PG1601