KR20220154094A - Ulk1/2 억제제를 이용한 단일 및 병용 요법 - Google Patents

Ulk1/2 억제제를 이용한 단일 및 병용 요법 Download PDF

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KR20220154094A
KR20220154094A KR1020227028939A KR20227028939A KR20220154094A KR 20220154094 A KR20220154094 A KR 20220154094A KR 1020227028939 A KR1020227028939 A KR 1020227028939A KR 20227028939 A KR20227028939 A KR 20227028939A KR 20220154094 A KR20220154094 A KR 20220154094A
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optionally substituted
cancer
inhibitor
alkyl
ulk
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니콜라스 디 피 코스포드
루벤 제이 쇼
니콜 에이 바카스
앨리슨 에스 림퍼트
소냐 엔 브런
미첼 바모스
Original Assignee
솔크 인스티튜트 포 바이올로지칼 스터디즈
샌포드 번햄 프레비즈 메디컬 디스커버리 인스티튜트
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/502Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
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    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
KR1020227028939A 2020-02-14 2021-02-12 Ulk1/2 억제제를 이용한 단일 및 병용 요법 Pending KR20220154094A (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202062977041P 2020-02-14 2020-02-14
US62/977,041 2020-02-14
PCT/US2021/018044 WO2021163633A1 (en) 2020-02-14 2021-02-12 Mono and combination therapies with ulk1/2 inhibitors

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KR20220154094A true KR20220154094A (ko) 2022-11-21

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KR1020227028939A Pending KR20220154094A (ko) 2020-02-14 2021-02-12 Ulk1/2 억제제를 이용한 단일 및 병용 요법

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US (1) US20230130766A1 (https=)
EP (1) EP4103186A4 (https=)
JP (1) JP2023513797A (https=)
KR (1) KR20220154094A (https=)
CN (1) CN115484956A (https=)
AU (1) AU2021218740A1 (https=)
WO (1) WO2021163633A1 (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20220153582A (ko) 2020-02-14 2022-11-18 솔크 인스티튜트 포 바이올로지칼 스터디즈 마크로시클릭 ulk1/2 억제제
WO2022072668A1 (en) * 2020-09-30 2022-04-07 Salk Institute For Biological Studies Patient selection biomarkers for treatment with ulk inhibitors
WO2024140401A1 (zh) * 2022-12-30 2024-07-04 捷思英达控股有限公司 作为激酶抑制剂的杂环化合物以及包括其的组合物
WO2025045182A1 (zh) * 2023-09-01 2025-03-06 深圳众格生物科技有限公司 Ulk1抑制剂及其制备方法和用途
WO2025166124A1 (en) * 2024-02-02 2025-08-07 Deciphera Pharmaceuticals, Llc Ulk inhibitors and methods of use thereof
WO2025166180A1 (en) * 2024-02-02 2025-08-07 Deciphera Pharmaceuticals, Llc Ulk inhibitors and methods of use thereof
WO2025166161A1 (en) * 2024-02-02 2025-08-07 Deciphera Pharmaceuticals, Llc Ulk inhibitors and methods of use thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MXPA06013165A (es) * 2004-05-14 2007-02-13 Pfizer Prod Inc Derivados de pirimidina para el tratamiento de crecimiento de celulas anormal.
WO2006037117A1 (en) * 2004-09-27 2006-04-06 Amgen Inc. Substituted heterocyclic compounds and methods of use
DK3185868T3 (da) * 2014-08-25 2022-05-23 Salk Inst For Biological Studi Hidtil ukendte ULK1-inhibitorer og fremgangsmåder til anvendelse af samme
RS62017B1 (sr) * 2014-09-17 2021-07-30 Celgene Car Llc Mk2 inhibitori i njihova upotreba

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AU2021218740A1 (en) 2022-09-22
US20230130766A1 (en) 2023-04-27
JP2023513797A (ja) 2023-04-03
WO2021163633A1 (en) 2021-08-19
EP4103186A1 (en) 2022-12-21
CN115484956A (zh) 2022-12-16
CA3171335A1 (en) 2021-08-19
EP4103186A4 (en) 2024-03-06

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