JP2025500917A - Metキナーゼの阻害剤 - Google Patents

Metキナーゼの阻害剤 Download PDF

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Publication number
JP2025500917A
JP2025500917A JP2024536124A JP2024536124A JP2025500917A JP 2025500917 A JP2025500917 A JP 2025500917A JP 2024536124 A JP2024536124 A JP 2024536124A JP 2024536124 A JP2024536124 A JP 2024536124A JP 2025500917 A JP2025500917 A JP 2025500917A
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Japan
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optionally substituted
pharma
solvate
acceptable salt
compound
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JP2024536124A
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Japanese (ja)
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JP2025500917A5 (https=
Inventor
エス. オウヤン,シャオフ
カノーニ,トウフィケ
ティホナス,ジョン,エス.
コックス,ジェイソン,エム.
カニア,ロバート
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キネート バイオファーマ インク.
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Publication of JP2025500917A publication Critical patent/JP2025500917A/ja
Publication of JP2025500917A5 publication Critical patent/JP2025500917A5/ja
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic 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
    • A61K31/535Heterocyclic 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
    • 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
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20Oxygen atoms
    • C07D215/22Oxygen atoms attached in position 2 or 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • 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
    • 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
    • C07D471/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
JP2024536124A 2021-12-16 2022-12-14 Metキナーゼの阻害剤 Pending JP2025500917A (ja)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
US202163290291P 2021-12-16 2021-12-16
US63/290,291 2021-12-16
US202263301267P 2022-01-20 2022-01-20
US63/301,267 2022-01-20
US202263380049P 2022-10-18 2022-10-18
US63/380,049 2022-10-18
US202263386647P 2022-12-08 2022-12-08
US63/386,647 2022-12-08
PCT/US2022/081504 WO2023114809A1 (en) 2021-12-16 2022-12-14 Inhibitors of met kinase

Publications (2)

Publication Number Publication Date
JP2025500917A true JP2025500917A (ja) 2025-01-15
JP2025500917A5 JP2025500917A5 (https=) 2025-12-23

Family

ID=85199244

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2024536124A Pending JP2025500917A (ja) 2021-12-16 2022-12-14 Metキナーゼの阻害剤

Country Status (12)

Country Link
US (2) US11753395B2 (https=)
EP (1) EP4448510A1 (https=)
JP (1) JP2025500917A (https=)
KR (1) KR20240121851A (https=)
AU (1) AU2022413540A1 (https=)
CA (1) CA3240907A1 (https=)
CL (1) CL2024001756A1 (https=)
CO (1) CO2024009144A2 (https=)
IL (1) IL313548A (https=)
MX (1) MX2024007444A (https=)
TW (1) TW202333709A (https=)
WO (1) WO2023114809A1 (https=)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023114809A1 (en) 2021-12-16 2023-06-22 Kinnate Biopharma Inc. Inhibitors of met kinase
CN121038792A (zh) * 2023-04-17 2025-11-28 赛琳治疗公司 用met激酶抑制剂治疗癌症
WO2024259060A1 (en) * 2023-06-16 2024-12-19 Kinnate Biopharma Inc. Inhibitors of met kinase
WO2025096463A1 (en) * 2023-10-30 2025-05-08 Vibliome Therapeutics, Llc Plk4 modulators

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US6334997B1 (en) 1994-03-25 2002-01-01 Isotechnika, Inc. Method of using deuterated calcium channel blockers
ES2293638T3 (es) 1994-03-25 2008-03-16 Isotechnika, Inc. Mejora de la eficacia de farmacos por deuteracion.
EP0860433B1 (en) 1995-11-07 2002-07-03 Kirin Beer Kabushiki Kaisha Quinoline derivatives and quinazoline derivatives inhibiting autophosphorylation of growth factor receptor originating in platelet and pharmaceutical compositions containing the same
JO2785B1 (en) 2003-05-27 2014-03-15 شركة جانسين فارماسوتيكا ان. في Quinazoline derivatives
US7459562B2 (en) 2004-04-23 2008-12-02 Bristol-Myers Squibb Company Monocyclic heterocycles as kinase inhibitors
US7439246B2 (en) 2004-06-28 2008-10-21 Bristol-Myers Squibb Company Fused heterocyclic kinase inhibitors
US20070155746A1 (en) 2005-12-23 2007-07-05 Kalypsys, Inc. Novel substituted pyridinyloxy and pyrimidinyloxy amides useful as inhibitors of protein kinases
JP2009539878A (ja) 2006-06-08 2009-11-19 アレイ バイオファーマ、インコーポレイテッド キノリン化合物および使用方法
US20090049035A1 (en) 2007-08-14 2009-02-19 International Business Machines Corporation System and method for indexing type-annotated web documents
JP2010126530A (ja) 2008-12-01 2010-06-10 Takeda Chem Ind Ltd 縮合複素環誘導体およびその用途
CN102573994B (zh) 2009-08-06 2015-06-24 默克专利有限公司 双环脲化合物
EP2423208A1 (en) 2010-08-28 2012-02-29 Lead Discovery Center GmbH Pharmaceutically active compounds as Axl inhibitors
CN102827186A (zh) 2011-06-16 2012-12-19 中国科学院上海药物研究所 一类吡啶并五元杂环衍生物及其制备方法和用途
JP2015507606A (ja) 2011-11-22 2015-03-12 デシフェラ ファーマシューティカルズ,エルエルシー 抗癌および抗増殖作用を示すピリドンアミドおよび類似体
WO2013180949A1 (en) * 2012-05-27 2013-12-05 Ning Xi Substituted quinoline compounds and methods of use
CN103508961B (zh) 2012-06-26 2015-07-22 中美冠科生物技术(太仓)有限公司 抗肿瘤药物
EP3003315B1 (en) 2013-06-06 2018-01-17 Lead Discovery Center GmbH A quinoline inhibitor of the macrophage stimulating 1 receptor mst1r
KR101505783B1 (ko) 2014-08-01 2015-03-25 씨제이헬스케어 주식회사 신규한 피롤로피리디닐옥시페닐아미드 유도체 및 이의 용도
SG11201707638UA (en) 2015-04-14 2017-10-30 Qurient Co Ltd Quinoline derivatives as tam rtk inhibitors
CN105153026B (zh) 2015-08-21 2018-02-02 江西科技师范大学 含联芳基酰胺结构的索拉非尼衍生物及其制备方法和应用
CN105732616B (zh) 2016-01-08 2018-07-27 江西科技师范大学 含联芳基酰胺结构的吡咯并吡啶类化合物及其制备方法和应用
CN109896997A (zh) 2017-12-08 2019-06-18 中国药科大学 N-酰基苯胺类c-Met激酶抑制剂的制备方法及其用途
UY38349A (es) 2018-08-30 2020-03-31 Array Biopharma Inc Compuestos de pirazolo[3,4-b]piridina como inhibidores de cinasas tam y met
CN111196814B (zh) 2018-11-19 2022-12-06 北京赛特明强医药科技有限公司 芳环连二噁烷并喹唑啉或喹啉类化合物、组合物及其应用
JP2022551422A (ja) * 2019-09-26 2022-12-09 エグゼリクシス, インコーポレイテッド ピリドン化合物およびタンパク質キナーゼの調節における使用の方法
WO2023114809A1 (en) 2021-12-16 2023-06-22 Kinnate Biopharma Inc. Inhibitors of met kinase

Also Published As

Publication number Publication date
AU2022413540A1 (en) 2024-07-18
US20230219929A1 (en) 2023-07-13
MX2024007444A (es) 2024-09-02
IL313548A (en) 2024-08-01
CL2024001756A1 (es) 2024-11-29
CA3240907A1 (en) 2023-06-22
CO2024009144A2 (es) 2024-08-08
US11753395B2 (en) 2023-09-12
WO2023114809A1 (en) 2023-06-22
TW202333709A (zh) 2023-09-01
EP4448510A1 (en) 2024-10-23
US20240067626A1 (en) 2024-02-29
US12595245B2 (en) 2026-04-07
KR20240121851A (ko) 2024-08-09

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