TW202333709A - Met激酶抑制劑 - Google Patents

Met激酶抑制劑 Download PDF

Info

Publication number
TW202333709A
TW202333709A TW111148006A TW111148006A TW202333709A TW 202333709 A TW202333709 A TW 202333709A TW 111148006 A TW111148006 A TW 111148006A TW 111148006 A TW111148006 A TW 111148006A TW 202333709 A TW202333709 A TW 202333709A
Authority
TW
Taiwan
Prior art keywords
optionally substituted
pharmaceutically acceptable
compound
solvate
acceptable salt
Prior art date
Application number
TW111148006A
Other languages
English (en)
Chinese (zh)
Inventor
小虎 歐陽
托菲克 卡諾尼
約翰 S 泰納斯
傑森 M 考克斯
羅伯特 S 肯尼亞
Original Assignee
美商奇奈特生物製藥公司
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 美商奇奈特生物製藥公司 filed Critical 美商奇奈特生物製藥公司
Publication of TW202333709A publication Critical patent/TW202333709A/zh

Links

Classifications

    • 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

Landscapes

  • 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)
TW111148006A 2021-12-16 2022-12-14 Met激酶抑制劑 TW202333709A (zh)

Applications Claiming Priority (8)

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

Publications (1)

Publication Number Publication Date
TW202333709A true TW202333709A (zh) 2023-09-01

Family

ID=85199244

Family Applications (1)

Application Number Title Priority Date Filing Date
TW111148006A TW202333709A (zh) 2021-12-16 2022-12-14 Met激酶抑制劑

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

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
JP2025500917A (ja) 2025-01-15
US11753395B2 (en) 2023-09-12
WO2023114809A1 (en) 2023-06-22
EP4448510A1 (en) 2024-10-23
US20240067626A1 (en) 2024-02-29
US12595245B2 (en) 2026-04-07
KR20240121851A (ko) 2024-08-09

Similar Documents

Publication Publication Date Title
TW202333709A (zh) Met激酶抑制劑
KR102644788B1 (ko) Erk1 및 erk2의 헤테로사이클릭 억제제 및 암 치료에서 이의 용도
KR102308488B1 (ko) 아릴- 또는 헤테로아릴-치환된 벤젠 화합물
EP3405192B1 (en) Bruton's tyrosine kinase inhibitors
JP6380862B2 (ja) 複数種類のキナーゼの阻害剤としての縮合三環式アミド系化合物
TWI618698B (zh) 新型嘧啶和吡啶類化合物及其用途
ES2813875T3 (es) Compuestos y procedimientos de uso
KR20170046180A (ko) 형질감염 중 재배열 (ret) 억제제로서의 신규 화합물
HK1202534A1 (en) Substituted benzene compounds
JP2013503194A (ja) Rafキナーゼを阻害するための1H−ピラゾロ[3,4−B]ピリジン化合物
CN113195471B (zh) 多取代吡啶酮类衍生物及其在医药上的应用
AU2019417418B2 (en) (pyridin-2-yl)amine derivatives as ΤGFβR1 (Alk5) inhibitors for the treatment of cancer
KR20190133199A (ko) 브루톤 타이로신 키나제 억제제
CA2990583A1 (en) 1,4-disubstituted imidazole derivative
TW202342018A (zh) Mek激酶抑制劑
KR101820541B1 (ko) 8-옥소디히드로퓨린 유도체
TW202031653A (zh) 新穎雜環芳香族醯胺衍生物及含有其之醫藥
TWI901073B (zh) 噻二唑酮衍生物及其組合物和應用
TW202325304A (zh) Raf激酶之抑制物
CN118742542A (zh) Met激酶的抑制剂
CN113735844B (zh) 2-甲酰基喹啉羧酰胺类化合物及其医药用途
EP4727943A1 (en) Inhibitors of met kinase
AU2013403333A1 (en) Phenyl linked quinolinyl modulators of ROR-gamma-t
RU2785567C2 (ru) Арил- или гетероарилзамещенные бензольные соединения