AU2022284249A1 - Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein - Google Patents

Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein Download PDF

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AU2022284249A1
AU2022284249A1 AU2022284249A AU2022284249A AU2022284249A1 AU 2022284249 A1 AU2022284249 A1 AU 2022284249A1 AU 2022284249 A AU2022284249 A AU 2022284249A AU 2022284249 A AU2022284249 A AU 2022284249A AU 2022284249 A1 AU2022284249 A1 AU 2022284249A1
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alkyl
compound
nhr
absent
mmol
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Sylvain Cottens
Magda DREWNIAK-SWITALSKA
Katarzyna Kaczanowska
Tomasz TOMCZYK
Andrzej TRACZ
Michal Walczak
Karolina WOJCIK
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Captor Therapeutics SA
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    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
    • A61K31/499Spiro-condensed pyrazines or piperazines
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    • 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
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    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D515/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D515/18Bridged systems
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  • Engineering & Computer Science (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)
  • Peptides Or Proteins (AREA)
  • Enzymes And Modification Thereof (AREA)
AU2022284249A 2021-06-01 2022-05-27 Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein Pending AU2022284249A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
PCT/PL2021/000030 WO2022255888A1 (en) 2021-06-01 2021-06-01 Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein
AUPCT/PL2021/000030 2021-06-01
PCT/EP2022/064481 WO2022253713A1 (en) 2021-06-01 2022-05-27 Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein

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AU2022284249A1 true AU2022284249A1 (en) 2023-12-07

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US (1) US20240294499A1 (https=)
EP (1) EP4347579A1 (https=)
JP (1) JP2024521895A (https=)
KR (1) KR20240029561A (https=)
CN (1) CN117957218A (https=)
AU (1) AU2022284249A1 (https=)
BR (1) BR112023025067A2 (https=)
CA (1) CA3218442A1 (https=)
IL (1) IL308676A (https=)
MX (1) MX2023014331A (https=)
WO (2) WO2022255888A1 (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022146151A1 (en) * 2020-12-30 2022-07-07 Captor Therapeutics S.A. Novel compounds which bind to cereblon, and methods of use thereof
IL311606A (en) * 2021-09-27 2024-05-01 Univ Pennsylvania Molluscum contagiosum infection inhibitors and methods of using them
WO2024015340A1 (en) * 2022-07-12 2024-01-18 Regents Of The University Of Michigan Cereblon ligands and uses thereof
WO2024123195A1 (en) * 2022-12-06 2024-06-13 Captor Therapeutics S.A. Targeted protein degradation using prodrugs of bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein
KR20250130610A (ko) * 2022-12-06 2025-09-02 캡터 테라퓨틱스 에스.에이. 유비퀴틴 리가제 및 표적 mcl-1 단백질에 결합하는 이작용성 화합물을 사용하는 표적화된 단백질 분해
WO2024167423A1 (en) 2023-02-07 2024-08-15 Captor Therapeutics S.A. Gspt1 degrader compounds
WO2025136129A1 (en) * 2023-12-22 2025-06-26 Captor Therapeutics S.A. Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target protein kinase c

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US6306663B1 (en) 1999-02-12 2001-10-23 Proteinex, Inc. Controlling protein levels in eucaryotic organisms
MY162157A (en) * 2007-04-16 2017-05-31 Abbott Lab Substituted indole mcl-1 inhibitors
CA2922341C (en) * 2013-08-28 2022-06-07 Vanderbilt University Substituted indole mcl-1 inhibitors
FR3015483B1 (fr) * 2013-12-23 2016-01-01 Servier Lab Nouveaux derives de thienopyrimidine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
WO2016105518A1 (en) * 2014-12-23 2016-06-30 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
BR112018068906A2 (pt) * 2016-03-16 2019-01-22 H. Lee Moffitt Cancer Center And Research Institute, Inc. composição, método, método de redução de risco, prevenção ou tratamento de um indivíduo que tem uma doença ou distúrbio autoimune, método de indução de degradação de uma proteína-alvo numa célula, método para reduzir o risco, prevenir ou tratar um estado da doença ou afecção num paciente em que a atividade proteica desregulada é responsável pelo referido estado da doença ou afecção, método para reduzir o risco, prevenir ou tratar câncer num indivíduo e método de tratamento de uma doença ou distúrbio genético num indivíduo
CN109152933B (zh) * 2016-04-21 2022-12-02 生物风险投资有限责任公司 诱导抗细胞凋亡bcl-2家族蛋白的降解的化合物及其用途
CN110506039A (zh) * 2016-10-11 2019-11-26 阿尔维纳斯股份有限公司 用于雄激素受体靶向降解的化合物和方法
KR20250117470A (ko) * 2016-12-23 2025-08-04 아비나스 오퍼레이션스, 인코포레이티드 급속 진행성 섬유육종 폴리펩티드의 표적화 분해를 위한 화합물 및 방법
IL312367A (en) * 2017-01-31 2024-06-01 Arvinas Operations Inc Cereblon ligands and bifunctional compounds comprising the same
CN107382862A (zh) * 2017-07-17 2017-11-24 大连理工大学 硫/氧代萘酰亚胺类化合物及其应用
CN118108706A (zh) * 2017-09-04 2024-05-31 C4医药公司 戊二酰亚胺
JP7852923B2 (ja) * 2019-11-27 2026-04-28 キャプター セラピューティクス エス.エー. セレブロンに結合するピペリジン-2,6-ジオン誘導体、及びその使用方法
WO2021105335A1 (en) * 2019-11-27 2021-06-03 Captor Therapeutics S.A. Piperidine-2, 6-dione derivatives which bind to cereblon, and methods of use thereof

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BR112023025067A2 (pt) 2024-03-12
CA3218442A1 (en) 2022-12-08
EP4347579A1 (en) 2024-04-10
US20240294499A1 (en) 2024-09-05
WO2022255888A1 (en) 2022-12-08
WO2022253713A1 (en) 2022-12-08
IL308676A (en) 2024-01-01
CN117957218A (zh) 2024-04-30
JP2024521895A (ja) 2024-06-04
KR20240029561A (ko) 2024-03-05
MX2023014331A (es) 2024-03-13

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