JP7007302B2 - メニン-mll相互作用の阻害剤 - Google Patents

メニン-mll相互作用の阻害剤 Download PDF

Info

Publication number
JP7007302B2
JP7007302B2 JP2018564288A JP2018564288A JP7007302B2 JP 7007302 B2 JP7007302 B2 JP 7007302B2 JP 2018564288 A JP2018564288 A JP 2018564288A JP 2018564288 A JP2018564288 A JP 2018564288A JP 7007302 B2 JP7007302 B2 JP 7007302B2
Authority
JP
Japan
Prior art keywords
methyl
diazaspiro
fluoro
pyrimidine
nonane
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
JP2018564288A
Other languages
English (en)
Japanese (ja)
Other versions
JP2019517548A5 (enExample
JP2019517548A (ja
Inventor
カケーシャン サルバチオン
エー.クレアモン デイビッド
ウェイン ディラード ローレンス
トン チョンクオ
ファン イー
チア ランチー
ディー.ロテスタ スティーブン
マーカス アンドリュー
モラールズ-ラモス エンジェル
ビー.シン スレッシュ
ベンカトラマン シャンカー
ユアン チン
チョン ヤーチュン
チョアン リンハン
ディー.ペアレント スティーブン
エル.ヒューストン トラビス
Original Assignee
ヴァイティー ファーマシューティカルズ,エルエルシー
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 ヴァイティー ファーマシューティカルズ,エルエルシー filed Critical ヴァイティー ファーマシューティカルズ,エルエルシー
Publication of JP2019517548A publication Critical patent/JP2019517548A/ja
Publication of JP2019517548A5 publication Critical patent/JP2019517548A5/ja
Priority to JP2022000946A priority Critical patent/JP7461390B2/ja
Application granted granted Critical
Publication of JP7007302B2 publication Critical patent/JP7007302B2/ja
Priority to JP2024000278A priority patent/JP2024045176A/ja
Priority to JP2025083421A priority patent/JP2025113339A/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

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
    • C07D487/10Spiro-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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Diabetes (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Obesity (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
JP2018564288A 2016-06-10 2017-06-08 メニン-mll相互作用の阻害剤 Active JP7007302B2 (ja)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2022000946A JP7461390B2 (ja) 2016-06-10 2022-01-06 メニン-mll相互作用の阻害剤
JP2024000278A JP2024045176A (ja) 2016-06-10 2024-01-04 メニン-mll相互作用の阻害剤
JP2025083421A JP2025113339A (ja) 2016-06-10 2025-05-19 メニン-mll相互作用の阻害剤

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662348496P 2016-06-10 2016-06-10
US62/348,496 2016-06-10
PCT/US2017/036506 WO2017214367A1 (en) 2016-06-10 2017-06-08 Inhibitors of the menin-mll interaction

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2022000946A Division JP7461390B2 (ja) 2016-06-10 2022-01-06 メニン-mll相互作用の阻害剤

Publications (3)

Publication Number Publication Date
JP2019517548A JP2019517548A (ja) 2019-06-24
JP2019517548A5 JP2019517548A5 (enExample) 2020-07-27
JP7007302B2 true JP7007302B2 (ja) 2022-01-24

Family

ID=59325631

Family Applications (4)

Application Number Title Priority Date Filing Date
JP2018564288A Active JP7007302B2 (ja) 2016-06-10 2017-06-08 メニン-mll相互作用の阻害剤
JP2022000946A Active JP7461390B2 (ja) 2016-06-10 2022-01-06 メニン-mll相互作用の阻害剤
JP2024000278A Pending JP2024045176A (ja) 2016-06-10 2024-01-04 メニン-mll相互作用の阻害剤
JP2025083421A Pending JP2025113339A (ja) 2016-06-10 2025-05-19 メニン-mll相互作用の阻害剤

Family Applications After (3)

Application Number Title Priority Date Filing Date
JP2022000946A Active JP7461390B2 (ja) 2016-06-10 2022-01-06 メニン-mll相互作用の阻害剤
JP2024000278A Pending JP2024045176A (ja) 2016-06-10 2024-01-04 メニン-mll相互作用の阻害剤
JP2025083421A Pending JP2025113339A (ja) 2016-06-10 2025-05-19 メニン-mll相互作用の阻害剤

Country Status (21)

Country Link
US (4) US10683302B2 (enExample)
EP (2) EP3805215A1 (enExample)
JP (4) JP7007302B2 (enExample)
KR (3) KR20220123727A (enExample)
CN (1) CN109743875B (enExample)
AU (3) AU2017278950B2 (enExample)
BR (1) BR122024002146A2 (enExample)
CA (1) CA3024180A1 (enExample)
CY (1) CY1124834T1 (enExample)
DK (1) DK3468966T3 (enExample)
ES (1) ES2831084T3 (enExample)
HR (1) HRP20201771T1 (enExample)
HU (1) HUE051451T2 (enExample)
IL (4) IL263586B (enExample)
LT (1) LT3468966T (enExample)
MX (3) MX381228B (enExample)
PL (1) PL3468966T3 (enExample)
PT (1) PT3468966T (enExample)
SI (1) SI3468966T1 (enExample)
WO (1) WO2017214367A1 (enExample)
ZA (1) ZA201900150B (enExample)

Families Citing this family (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016040330A1 (en) 2014-09-09 2016-03-17 The Regents Of The University Of Michigan Thienopyrimidine and thienopyridine compounds and methods of use thereof
WO2016197027A1 (en) 2015-06-04 2016-12-08 Kura Oncology, Inc. Methods and compositions for inhibiting the interaction of menin with mll proteins
AR104020A1 (es) 2015-06-04 2017-06-21 Kura Oncology Inc Métodos y composiciones para inhibir la interacción de menina con proteínas mill
BR112018068702A2 (pt) 2016-03-16 2019-01-15 Kura Oncology Inc inibidores bicíclicos em ponte de menin-mll e métodos de uso
CN114539284A (zh) 2016-03-16 2022-05-27 库拉肿瘤学公司 经取代的menin-mll抑制剂及使用方法
US10899738B2 (en) 2016-05-02 2021-01-26 The Regents Of The University Of Michigan Piperidines as menin inhibitors
HRP20201771T1 (hr) 2016-06-10 2021-02-19 Vitae Pharmaceuticals, Llc Inhibitori interakcije menin-mll
US10611778B2 (en) 2016-09-14 2020-04-07 Janssen Pharmaceutica Nv Fused bicyclic inhibitors of menin-MLL interaction
AU2017326487B2 (en) 2016-09-14 2021-08-05 Janssen Pharmaceutica Nv Spiro bicyclic inhibitors of menin-MLL interaction
US12084462B2 (en) 2016-09-14 2024-09-10 Janssen Pharmaceutica Nv Spiro bicyclic inhibitors of menin-MLL interaction
MX391405B (es) 2016-12-15 2025-03-21 Janssen Pharmaceutica Nv Inhibidores de azepano de la interacción menina-mll.
US11944627B2 (en) 2017-03-24 2024-04-02 Kura Oncology, Inc. Methods for treating hematological malignancies and Ewing's sarcoma
BR112019020130A2 (pt) 2017-03-31 2020-04-22 Univ Michigan Regents piperidinas como inibidores covalentes de menin
US11147272B2 (en) 2017-04-10 2021-10-19 Mitsui Chemicals Argro, Inc. Pyridone compounds and agricultural and horticultural fungicides comprising the same as active ingredients
US11542248B2 (en) 2017-06-08 2023-01-03 Kura Oncology, Inc. Methods and compositions for inhibiting the interaction of menin with MLL proteins
WO2019060365A1 (en) 2017-09-20 2019-03-28 Kura Oncology, Inc. SUBSTITUTED MÉNINE-MLL INHIBITORS AND METHODS OF USE
BR112020012461A2 (pt) * 2017-12-20 2020-11-24 Janssen Pharmaceutica Nv inibidores exo-aza espiro da interação menin-mll
US11396517B1 (en) 2017-12-20 2022-07-26 Janssen Pharmaceutica Nv Exo-aza spiro inhibitors of menin-MLL interaction
JP7239562B2 (ja) 2018-03-30 2023-03-14 住友ファーマ株式会社 光学活性な架橋型環状2級アミン誘導体
EP3845533A4 (en) 2018-08-27 2022-04-27 Sumitomo Dainippon Pharma Co., Ltd. OPTICALLY ACTIVE AZABICYCLIC DERIVATIVE
US10815241B2 (en) 2018-08-27 2020-10-27 Sumitomo Dainippon Pharma Co., Ltd. Optically active azabicyclo ring derivative
WO2020114474A1 (zh) * 2018-12-06 2020-06-11 苏州信诺维医药科技有限公司 一种杂环化合物、其应用及含其的药物组合物
TW202039512A (zh) 2018-12-06 2020-11-01 日商第一三共股份有限公司 環烷-1,3-二胺化合物
WO2020142559A1 (en) 2018-12-31 2020-07-09 Biomea Fusion, Llc Inhibitors of menin-mll interaction
CN114040760B (zh) 2018-12-31 2025-05-09 拜欧米富士恩公司 Menin-mll相互作用的不可逆抑制剂
PE20221454A1 (es) 2019-10-09 2022-09-21 Novartis Ag Derivados de 2-azaespiro[3.4]octano como agonistas de m4
CN114555592B (zh) 2019-10-09 2024-09-06 诺华股份有限公司 作为m4激动剂的2-氮杂螺[3.4]辛烷衍生物
AU2020404305A1 (en) 2019-12-19 2022-08-04 Janssen Pharmaceutica Nv Substituted straight chain spiro derivatives
JP7454520B2 (ja) * 2020-02-26 2024-03-22 住友ファーマ株式会社 光学活性なアザビシクロ環誘導体からなる医薬
CN111297863B (zh) * 2020-03-30 2021-06-25 四川大学华西医院 menin-MLL抑制剂在制备治疗子宫内膜癌的药物中的应用
CN120393025A (zh) * 2020-04-07 2025-08-01 赛达克斯制药股份有限公司 Menin抑制剂和cyp3a4抑制剂的组合及其使用方法
WO2022086986A1 (en) * 2020-10-21 2022-04-28 Kura Oncology, Inc. Treatment of hematological malignancies with inhibitors of menin
CN114516873A (zh) * 2020-11-18 2022-05-20 苏州优理生物医药科技有限公司 一种螺环类化合物、包含其药物组合物及其应用
RU2752079C1 (ru) * 2020-12-01 2021-07-22 Федеральное государственное автономное образовательное учреждение высшего образования "Пермский государственный национальный исследовательский университет" (Е)-(6-(2-гидроксифенил)-2-иминио-4,7,8-триоксо-1,3-дифенил-1,3,6-триазаспиро[4.4]нонан-9-илиден)(4-метоксифенил)метаноат, обладающий противомикробной активностью, и способ его получения
MX2023013176A (es) 2021-05-08 2023-12-01 Janssen Pharmaceutica Nv Derivados espiro sustituidos.
CN117321049A (zh) 2021-05-08 2023-12-29 詹森药业有限公司 取代的螺环衍生物
KR20240006638A (ko) * 2021-05-11 2024-01-15 얀센 파마슈티카 엔브이 조합 요법
JP2024518497A (ja) * 2021-05-11 2024-05-01 ヤンセン ファーマシューティカ エヌ.ベー. 併用療法
AU2022274325A1 (en) 2021-05-14 2023-10-05 Syndax Pharmaceuticals, Inc. Inhibitors of the menin-mll interaction
PE20242359A1 (es) 2021-06-01 2024-12-16 Janssen Pharmaceutica Nv Derivados de fenil-1h-pirrolo[2,3-c]piridina sustituidos
WO2022253309A1 (zh) * 2021-06-03 2022-12-08 首药控股(北京)股份有限公司 取代的杂环化合物及其应用
CA3218340A1 (en) 2021-06-03 2022-12-08 Janssen Pharmaceutica Nv Pyridazines or 1,2,4-triazines substituted by spirocyclic amines
WO2022257047A1 (en) * 2021-06-09 2022-12-15 Acerand Therapeutics (Hong Kong) Limited Diazaspirobicylic compounds as protein-protein interaction inhibitors and applications thereof
IL309359A (en) * 2021-06-17 2024-02-01 Janssen Pharmaceutica Nv (r)-n-ethyl-5-fluoro-n-isopropyl-2-((5-(2-(6-((2-methoxyethyl)(methyl)amino)-2-methylhexan-3-yl)-2,6-diazaspiro[3.4]octan-6-yl)-1,2,4-triazin-6-yl)oxy)benzamide besylate salt for the treatment of diseases such as cancer
CN115515958B (zh) * 2021-08-04 2023-09-29 成都苑东生物制药股份有限公司 一种新型磺酰胺类menin-MLL相互作用抑制剂、其制备方法及医药用途
WO2023011446A1 (zh) * 2021-08-04 2023-02-09 成都苑东生物制药股份有限公司 一种新型磺酰胺类menin-MLL相互作用抑制剂、其制备方法及医药用途
US12251385B2 (en) 2021-08-11 2025-03-18 Biomea Fusion, Inc. Covalent inhibitors of menin-MLL interaction for diabetes mellitus
WO2023022912A1 (en) 2021-08-20 2023-02-23 Biomea Fusion, Inc. Crystalline form of n-[4-[4-(4-morpholinyl)-7h-pyrrolo[2,3-d]pyrimidin-6-yl]phenyl]-4-[[3(r)-[(1-oxo -2-propen-1-yl)amino]-1-piperidinyl]methyl]-2-pyridinecarboxamide, an irreversible menin-mll inhibitor for the treatment of cancer
CN113769098B (zh) * 2021-09-22 2022-09-30 中国医学科学院肿瘤医院深圳医院 MLL-menin抑制剂组合物在制备抗肝癌药物中的应用
IL313033A (en) * 2021-12-03 2024-07-01 Bionova Pharmaceuticals Shanghai Ltd Carbonyl substituted diazaspiro compounds and its use
US20250074910A1 (en) * 2021-12-31 2025-03-06 Hitgen Inc. Menin inhibitor and use thereof
KR20240161147A (ko) 2022-03-14 2024-11-12 슬랩 파마슈티컬스 엘엘씨 다중 사이클릭 화합물
CN117069719A (zh) * 2022-08-17 2023-11-17 烨辉医药科技(上海)有限公司 二氮杂螺环-哒嗪化合物及其用途
WO2024046457A1 (en) * 2022-09-02 2024-03-07 Hutchmed Limited Triazine compounds and uses thereof
CN120529900A (zh) 2022-11-24 2025-08-22 奥莱松基因组股份有限公司 用于治疗癌症的LSD1抑制剂和Menin抑制剂的组合
CN118271341A (zh) * 2022-12-30 2024-07-02 成都先导药物开发股份有限公司 Menin抑制剂及其用途
WO2024155719A1 (en) 2023-01-18 2024-07-25 Biomea Fusion, Inc. Crystalline forms of n-[4-[4-(4-morpholinyl)-7h-pyrrolo[2,3-d]pyrimidin-6-yl]phenyl]-4-[[3(r)-[(l-oxo-2-propen-l-yl)amino]-l-piperidinyl]methyl]-2- pyridinecarboxamide as a covalentinhibitor of menin-mll interaction
WO2024213101A1 (zh) * 2023-04-13 2024-10-17 首药控股(北京)股份有限公司 取代的杂环化合物
CN118994033B (zh) * 2023-05-17 2025-09-16 成都先导药物开发股份有限公司 一种sdnx-5613的合成方法及其中间体化合物
CN116969891A (zh) * 2023-07-28 2023-10-31 杭州国瑞生物科技有限公司 一种7-甲基-5-醛基-1h-吲唑的合成方法
TW202525797A (zh) * 2023-08-28 2025-07-01 美商錫達斯醫藥股份有限公司 作為menin-mll交互作用之抑制劑的芳基醚類似物
WO2025059366A1 (en) * 2023-09-13 2025-03-20 Kumquat Biosciences Inc. Ras inhibitors
WO2025097148A2 (en) 2023-11-04 2025-05-08 Syndax Pharmaceuticals, Inc. Salts and polymorphic forms of menin inhibitors and pharmaceutical compositions thereof
WO2025188611A1 (en) * 2024-03-04 2025-09-12 Dana-Farber Cancer Institute, Inc. Chemical matters for targeting leukemic complex proteins

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014517016A (ja) 2011-06-10 2014-07-17 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング Btk阻害活性を有するピリミジンおよびピリミジン化合物の組成物と製造方法
WO2015191701A1 (en) 2014-06-10 2015-12-17 The Trustees Of The University Of Pennsylvania Scaffolds for inhibitors of menin-mll interactions
JP2016512514A (ja) 2013-03-13 2016-04-28 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン チエノピリミジン及びチエノピリジン化合物を含有する組成物並びにそれらの使用方法
CN105732636A (zh) 2014-12-30 2016-07-06 广东东阳光药业有限公司 杂芳化合物及其在药物中的应用
JP2018538330A (ja) 2015-12-22 2018-12-27 ヴァイティー ファーマシューティカルズ,インコーポレイテッド menin−MLL相互作用の阻害剤

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2086544C1 (ru) 1991-06-13 1997-08-10 Хоффманн-Ля Рош АГ Бензолсульфонамидные производные пиримидина или их соли, фармацевтическая композиция для лечения заболеваний, связанных с активностью эндотелина
US6124477A (en) 1996-06-27 2000-09-26 Bioavailability Systems, Llc Anti-first-pass effect compounds
US5820915A (en) 1996-06-27 1998-10-13 Bioavailability Systems, L.L.C. Method for the preparation of a first-pass effective citrus-derived substance and product thereof
US5990154A (en) 1997-05-30 1999-11-23 Bioavailability Systems, L.L.C. Anti-first-pass effect compounds and citrus extract
US6063809A (en) 1997-08-26 2000-05-16 Bioavailability Systems, Llc Anti-first-pass effect compounds
US20040058982A1 (en) 1999-02-17 2004-03-25 Bioavailability System, Llc Pharmaceutical compositions
US6248776B1 (en) 1997-08-26 2001-06-19 Bioavailability Systems, L.L.C. Anti-first-pass effect compounds
US5993887A (en) 1998-06-29 1999-11-30 Bioavailability Systems, L.L.C. Safe citrus juice and process for preparation
WO2004037827A1 (en) 2000-10-20 2004-05-06 Bioavailability Systems, Llc Synthesis of spiro ortho esters, spiro ortho carbonates, and intermediates
US7968569B2 (en) 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
US7807845B2 (en) 2004-03-11 2010-10-05 Sequoia Pharmaceuticals, Inc. Resistance-repellent retroviral protease inhibitors
AU2005244121B2 (en) 2004-05-07 2012-01-19 Sequoia Pharmaceuticals, Inc. Resistance-repellent retroviral protease inhibitors
US20090281114A1 (en) 2008-05-08 2009-11-12 Fabre-Kramer Pharmaceuticals, Inc. Indolylalkyl derivatives of pyrimidinylpiperazine and metabolites thereof for treatment of anxiety, depression, and sexual dysfunction
CL2009001152A1 (es) 2008-05-13 2009-10-16 Array Biopharma Inc Compuestos derivados de n-(4-(cicloalquilo nitrogenado-1-il)-1h-pirrolo[2,3-b]piridin-3-il)amida, inhibidores de cinasa; proceso de preparacion; composicion farmaceutica; y su uso para el tratamiento de una enfermedad proliferativa.
US8466159B2 (en) 2011-10-21 2013-06-18 Abbvie Inc. Methods for treating HCV
KR20140040594A (ko) 2012-09-26 2014-04-03 아로그 파마슈티칼스, 엘엘씨 돌연변이체 c-kit의 억제 방법
US11596636B2 (en) 2014-01-14 2023-03-07 The Trustees Of The University Of Pennsylvania Tailored combinatorial epigenetic therapies for P53 gain-of-function tumors
US20170232030A1 (en) 2014-08-13 2017-08-17 Epizyme, Inc. Combination therapy for treating cancer
WO2016197027A1 (en) 2015-06-04 2016-12-08 Kura Oncology, Inc. Methods and compositions for inhibiting the interaction of menin with mll proteins
EP4643952A2 (en) 2016-01-26 2025-11-05 Memorial Sloan Kettering Cancer Center Targeting chromatin regulators for inhibiting leukemogenic gene expression in npm1
BR112018068702A2 (pt) 2016-03-16 2019-01-15 Kura Oncology Inc inibidores bicíclicos em ponte de menin-mll e métodos de uso
US10899738B2 (en) 2016-05-02 2021-01-26 The Regents Of The University Of Michigan Piperidines as menin inhibitors
WO2017197036A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Spirocyclic degronimers for target protein degradation
HRP20201771T1 (hr) 2016-06-10 2021-02-19 Vitae Pharmaceuticals, Llc Inhibitori interakcije menin-mll
CA3036987A1 (en) 2016-09-16 2018-03-22 Vitae Pharmaceuticals, Inc. Inhibitors of the menin-mll interaction
US11944627B2 (en) 2017-03-24 2024-04-02 Kura Oncology, Inc. Methods for treating hematological malignancies and Ewing's sarcoma
BR112020012461A2 (pt) 2017-12-20 2020-11-24 Janssen Pharmaceutica Nv inibidores exo-aza espiro da interação menin-mll
EP3740491A1 (en) 2018-01-18 2020-11-25 Array Biopharma, Inc. Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors
CN111936465A (zh) 2018-03-30 2020-11-13 密歇根大学董事会 作为共价menin抑制剂的哌啶化合物
JP7470105B2 (ja) 2018-09-13 2024-04-17 メルク・シャープ・アンド・ドーム・エルエルシー 非マイクロサテライト高不安定性/ミスマッチ修復の良好な結腸直腸がんを処置するためのpd-1アンタゴニストおよびlag3アンタゴニストの組み合わせ
EP3856173A4 (en) 2018-09-26 2022-07-06 Kura Oncology, Inc. TREATMENT OF HEMOPATHY MALIGNANCE WITH MENIN INHIBITORS
CN114040760B (zh) 2018-12-31 2025-05-09 拜欧米富士恩公司 Menin-mll相互作用的不可逆抑制剂
CN120393025A (zh) 2020-04-07 2025-08-01 赛达克斯制药股份有限公司 Menin抑制剂和cyp3a4抑制剂的组合及其使用方法
WO2022241122A1 (en) 2021-05-12 2022-11-17 Syndax Pharmaceuticals, Inc. Combinations for treatment of cancer
AU2022274325A1 (en) 2021-05-14 2023-10-05 Syndax Pharmaceuticals, Inc. Inhibitors of the menin-mll interaction
US12251385B2 (en) 2021-08-11 2025-03-18 Biomea Fusion, Inc. Covalent inhibitors of menin-MLL interaction for diabetes mellitus
JP2025503385A (ja) 2021-12-15 2025-02-04 ダナ-ファーバー キャンサー インスティテュート,インコーポレイテッド メニン-mllエピジェネティック複合体を破壊することによる消化管間質腫瘍(gist)の治療的標的化

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014517016A (ja) 2011-06-10 2014-07-17 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング Btk阻害活性を有するピリミジンおよびピリミジン化合物の組成物と製造方法
JP2016512514A (ja) 2013-03-13 2016-04-28 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン チエノピリミジン及びチエノピリジン化合物を含有する組成物並びにそれらの使用方法
WO2015191701A1 (en) 2014-06-10 2015-12-17 The Trustees Of The University Of Pennsylvania Scaffolds for inhibitors of menin-mll interactions
CN105732636A (zh) 2014-12-30 2016-07-06 广东东阳光药业有限公司 杂芳化合物及其在药物中的应用
JP2018538330A (ja) 2015-12-22 2018-12-27 ヴァイティー ファーマシューティカルズ,インコーポレイテッド menin−MLL相互作用の阻害剤

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
SHI, Aibin et al.,Structual insights into inhibition of the bivalent menin-MLL interaction by small molecules in leukemia,Blood,2012年11月29日,vol.120, no.23,pp.4461-4469

Also Published As

Publication number Publication date
RU2019100040A (ru) 2020-07-13
AU2021258089A1 (en) 2021-11-25
KR20220123727A (ko) 2022-09-08
HUE051451T2 (hu) 2021-03-01
DK3468966T3 (da) 2020-11-09
IL283267B (en) 2022-12-01
CN109743875B (zh) 2022-04-29
WO2017214367A1 (en) 2017-12-14
AU2024202700A1 (en) 2024-05-16
MX2023002982A (es) 2023-04-10
LT3468966T (lt) 2021-02-25
AU2017278950A1 (en) 2019-01-03
IL298381B1 (en) 2025-08-01
US12312359B2 (en) 2025-05-27
KR20190017012A (ko) 2019-02-19
IL283267A (en) 2021-07-29
US20230174541A1 (en) 2023-06-08
CN109743875A (zh) 2019-05-10
JP7461390B2 (ja) 2024-04-03
PT3468966T (pt) 2020-11-10
US20210053974A1 (en) 2021-02-25
IL321844A (en) 2025-08-01
IL283267B2 (en) 2023-04-01
BR122024002146A2 (pt) 2024-03-05
ZA201900150B (en) 2023-04-26
AU2017278950B2 (en) 2021-07-29
KR20250079083A (ko) 2025-06-04
JP2022058514A (ja) 2022-04-12
IL263586A (en) 2019-01-31
RU2019100040A3 (enExample) 2020-07-15
US10683302B2 (en) 2020-06-16
MX381228B (es) 2025-03-12
KR102436430B1 (ko) 2022-08-24
JP2025113339A (ja) 2025-08-01
PL3468966T3 (pl) 2021-04-06
SI3468966T1 (sl) 2021-03-31
NZ748203A (en) 2025-06-27
EP3468966B1 (en) 2020-08-05
IL263586B (en) 2021-06-30
EP3805215A1 (en) 2021-04-14
IL298381A (en) 2023-01-01
EP3468966A1 (en) 2019-04-17
CA3024180A1 (en) 2017-12-14
US11479557B2 (en) 2022-10-25
IL298381B2 (en) 2025-12-01
ES2831084T3 (es) 2021-06-07
HRP20201771T1 (hr) 2021-02-19
AU2021258089B2 (en) 2024-01-25
US20190144459A1 (en) 2019-05-16
JP2024045176A (ja) 2024-04-02
MX2018015252A (es) 2019-04-25
BR112018075260A2 (pt) 2019-03-12
US20250326764A1 (en) 2025-10-23
MX2021003939A (es) 2021-05-27
CY1124834T1 (el) 2022-07-22
JP2019517548A (ja) 2019-06-24

Similar Documents

Publication Publication Date Title
JP7461390B2 (ja) メニン-mll相互作用の阻害剤
US11739085B2 (en) Inhibitors of the menin-MLL interaction
TW202311262A (zh) Menin-mll交互作用之抑制劑
RU2799820C2 (ru) Ингибиторы взаимодействия менин-mll
RU2829484C2 (ru) Ингибиторы взаимодействия менин-mll
BR112018075260B1 (pt) Compostos inibidores da interação de menina-llm, composição farmacêutica, sal, forma cristalina e uso dos mesmos
HK40007344B (en) Inhibitors of the menin-mll interaction
HK40007344A (en) Inhibitors of the menin-mll interaction

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20200608

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20200608

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20210422

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20210511

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20210806

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20210831

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20211124

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20211207

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20220106

R150 Certificate of patent or registration of utility model

Ref document number: 7007302

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250