JP2022554169A5 - - Google Patents

Info

Publication number
JP2022554169A5
JP2022554169A5 JP2022523904A JP2022523904A JP2022554169A5 JP 2022554169 A5 JP2022554169 A5 JP 2022554169A5 JP 2022523904 A JP2022523904 A JP 2022523904A JP 2022523904 A JP2022523904 A JP 2022523904A JP 2022554169 A5 JP2022554169 A5 JP 2022554169A5
Authority
JP
Japan
Prior art keywords
carboxamide
trifluoroethyl
pyrrolidine
methylphenyl
amino
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.)
Granted
Application number
JP2022523904A
Other languages
English (en)
Japanese (ja)
Other versions
JP7626910B2 (ja
JP2022554169A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2020/057132 external-priority patent/WO2021081375A1/en
Publication of JP2022554169A publication Critical patent/JP2022554169A/ja
Publication of JP2022554169A5 publication Critical patent/JP2022554169A5/ja
Application granted granted Critical
Publication of JP7626910B2 publication Critical patent/JP7626910B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2022523904A 2019-10-24 2020-10-23 Rafキナーゼの阻害剤 Active JP7626910B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201962925596P 2019-10-24 2019-10-24
US62/925,596 2019-10-24
US202063044898P 2020-06-26 2020-06-26
US63/044,898 2020-06-26
PCT/US2020/057132 WO2021081375A1 (en) 2019-10-24 2020-10-23 Inhibitors of raf kinases

Publications (3)

Publication Number Publication Date
JP2022554169A JP2022554169A (ja) 2022-12-28
JP2022554169A5 true JP2022554169A5 (https=) 2023-10-30
JP7626910B2 JP7626910B2 (ja) 2025-02-05

Family

ID=75619376

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022523904A Active JP7626910B2 (ja) 2019-10-24 2020-10-23 Rafキナーゼの阻害剤

Country Status (16)

Country Link
US (3) US11098031B1 (https=)
EP (1) EP4048259A4 (https=)
JP (1) JP7626910B2 (https=)
KR (1) KR20220104702A (https=)
CN (1) CN114845711B (https=)
AU (1) AU2020371727B2 (https=)
BR (1) BR112022007612A2 (https=)
CA (1) CA3158530A1 (https=)
CL (1) CL2022000998A1 (https=)
CO (1) CO2022006712A2 (https=)
IL (1) IL292424B1 (https=)
MX (1) MX2022004937A (https=)
PH (1) PH12022550976A1 (https=)
TW (1) TWI899110B (https=)
WO (1) WO2021081375A1 (https=)
ZA (1) ZA202204284B (https=)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW202106684A (zh) 2019-05-03 2021-02-16 美商奇奈特生物製藥公司 Raf激酶抑制劑
JP7626910B2 (ja) 2019-10-24 2025-02-05 ピエール ファーブル メディカモン Rafキナーゼの阻害剤
JP7214925B2 (ja) * 2019-12-06 2023-01-30 メッドシャイン ディスカバリー インコーポレイテッド Pan-RAFキナーゼ阻害剤としてのビアリール化合物
PH12022551513A1 (en) 2019-12-20 2023-04-24 Mirati Therapeutics Inc Sos1 inhibitors
WO2022060996A1 (en) * 2020-09-18 2022-03-24 Kinnate Biopharma Inc. Inhibitors of raf kinases
WO2022081469A1 (en) 2020-10-12 2022-04-21 Kinnate Biopharma Inc. Inhibitors of raf kinases
BR112023021913A2 (pt) * 2021-04-23 2024-01-16 Kinnate Biopharma Inc Tratamento de câncer com inibidor de raf
EP4326255A4 (en) * 2021-04-23 2025-03-12 Pierre Fabre Medicament Solid state forms of (s)-n-(3-(2-(((r)-1-hydroxypropan-2-yl)amino)-6-morpholinopyridin-4-yl)-4-methylphenyl)-3-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and salts thereof
EP4373806A4 (en) * 2021-07-19 2025-06-18 Pierre Fabre Medicament Preparation method of 3- (2, 2, 2-trifluoroethyl) pyrrolidine hydrochloride
WO2023061492A1 (zh) * 2021-10-14 2023-04-20 华领医药技术(上海)有限公司 2-氧代-3-氮杂双环[3.1.0]己烷衍生物
WO2023070053A1 (en) * 2021-10-21 2023-04-27 Kinnate Biopharma Inc. Inhibitors of raf kinases
CA3240192A1 (en) * 2021-12-09 2023-06-15 Daniel L. Flynn Raf kinase inhibitors and methods of use thereof
CA3240263A1 (en) 2021-12-09 2023-06-15 Daniel L. Flynn Raf kinase inhibitors and methods of use thereof
EP4472968A1 (en) * 2022-02-03 2024-12-11 Pierre Fabre Medicament Inhibitors of raf kinases
EP4486722A4 (en) * 2022-03-02 2026-03-25 Nico Therapeutics Inc COMPOUNDS, COMPOSITIONS AND PROCESSES

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2293638T3 (es) 1994-03-25 2008-03-16 Isotechnika, Inc. Mejora de la eficacia de farmacos por deuteracion.
US6334997B1 (en) 1994-03-25 2002-01-01 Isotechnika, Inc. Method of using deuterated calcium channel blockers
US6187799B1 (en) 1997-05-23 2001-02-13 Onyx Pharmaceuticals Inhibition of raf kinase activity using aryl ureas
US20070244120A1 (en) 2000-08-18 2007-10-18 Jacques Dumas Inhibition of raf kinase using substituted heterocyclic ureas
GB9823873D0 (en) 1998-10-30 1998-12-30 Pharmacia & Upjohn Spa 2-ureido-thiazole derivatives,process for their preparation,and their use as antitumour agents
WO2003068229A1 (en) 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors
US7459562B2 (en) 2004-04-23 2008-12-02 Bristol-Myers Squibb Company Monocyclic heterocycles as kinase inhibitors
US20070054916A1 (en) 2004-10-01 2007-03-08 Amgen Inc. Aryl nitrogen-containing bicyclic compounds and methods of use
CA2592118C (en) 2004-12-23 2015-11-17 Deciphera Pharmaceuticals, Llc Urea derivatives as enzyme modulators
US8188113B2 (en) 2006-09-14 2012-05-29 Deciphera Pharmaceuticals, Inc. Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
CL2008001933A1 (es) 2007-06-29 2009-09-25 Millennium Pharm Inc Compuestos derivados de pirimidina, inhibidores de la raf quinasa; compuestos intermediarios; procedimiento de preparacion; composicion farmaceutica; y su uso para tratar trastornos proliferativos, cardiacos, neurodegenerativos, inflamatorios, oseos, inmunologicos enfermedad viral, entre otros.
EA018551B1 (ru) 2008-02-22 2013-08-30 Айрм Ллк ГЕТЕРОЦИКЛИЧЕСКИЕ СОЕДИНЕНИЯ И СОДЕРЖАЩИЕ ИХ КОМПОЗИЦИИ В КАЧЕСТВЕ ИНГИБИТОРОВ КИНАЗ c-KIT И PDGFR
EP2112150B1 (en) 2008-04-22 2013-10-16 Forma Therapeutics, Inc. Improved raf inhibitors
JP2012514044A (ja) 2008-12-30 2012-06-21 ミレニアム ファーマシューティカルズ, インコーポレイテッド Rafキナーゼ阻害剤として有用なヘテロアリール化合物
AR090151A1 (es) 2012-03-07 2014-10-22 Lilly Co Eli Compuestos inhibidores de raf
SI3366293T1 (sl) 2012-06-07 2020-08-31 Deciphera Pharmaceuticals, Llc Dihidronafthiridini in sorodne spojine uporabne kot kinazni inhibitorji za zdravljenje proliferativnih bolezni
US9242969B2 (en) 2013-03-14 2016-01-26 Novartis Ag Biaryl amide compounds as kinase inhibitors
UY36294A (es) 2014-09-12 2016-04-29 Novartis Ag Compuestos y composiciones como inhibidores de quinasa
EP3191467B1 (en) 2014-09-12 2020-10-21 Novartis AG Compounds and compositions as kinase inhibitors
CN107074828B (zh) * 2014-09-12 2020-05-19 诺华股份有限公司 用作raf激酶抑制剂的化合物和组合物
CA3026876A1 (en) 2016-06-10 2017-12-14 Novartis Ag Therapeutic uses of a c-raf inhibitor
AU2017329090B9 (en) 2016-09-19 2019-09-05 Novartis Ag Therapeutic combinations comprising a RAF inhibitor and a ERK inhibitor
WO2020168172A1 (en) 2019-02-15 2020-08-20 Zamboni Chem Solutions Inc. Conjugate compounds for the degradation of raf
WO2020198058A1 (en) * 2019-03-22 2020-10-01 Kinnate Biopharma Inc. Inhibitors of raf kinases
TW202106684A (zh) 2019-05-03 2021-02-16 美商奇奈特生物製藥公司 Raf激酶抑制劑
JP7626910B2 (ja) 2019-10-24 2025-02-05 ピエール ファーブル メディカモン Rafキナーゼの阻害剤
WO2022060996A1 (en) 2020-09-18 2022-03-24 Kinnate Biopharma Inc. Inhibitors of raf kinases
WO2022081469A1 (en) 2020-10-12 2022-04-21 Kinnate Biopharma Inc. Inhibitors of raf kinases
BR112023021913A2 (pt) 2021-04-23 2024-01-16 Kinnate Biopharma Inc Tratamento de câncer com inibidor de raf
EP4326255A4 (en) 2021-04-23 2025-03-12 Pierre Fabre Medicament Solid state forms of (s)-n-(3-(2-(((r)-1-hydroxypropan-2-yl)amino)-6-morpholinopyridin-4-yl)-4-methylphenyl)-3-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and salts thereof

Similar Documents

Publication Publication Date Title
JP2022554169A5 (https=)
RU2014108140A (ru) Соединение на основе хинозолина в качестве ингибиторов серен-треониновых киназ
JP2014521696A5 (https=)
RU2481336C2 (ru) Циклопента(d)пиримидины в качестве ингибиторов протеинкиназ акт
RU2455288C2 (ru) Соединения и композиции 5-(4-(галогеналкокси)фенил)пиримидин-2-амина в качестве ингибиторов киназ
JP2020506946A5 (https=)
JP2010508338A5 (https=)
JP2022534261A5 (https=)
RU2013133800A (ru) Селективные к bcl-2 агенты, вызывающие апоптоз, для лечения рака и иммунных заболеваний
JP2022553351A5 (https=)
RU2009115830A (ru) Пиридинкарбоксамиды в качестве ингибиторов 11-бета-hsd1
JP2013503903A5 (https=)
JP2018531981A5 (https=)
JP2018516932A5 (https=)
JP2018527336A5 (https=)
JP2018511587A5 (https=)
JP2010508307A5 (https=)
JP2022502362A5 (https=)
RU2010145463A (ru) Производные замещенного 2-фенилпиридина
JP2017081918A5 (https=)
JP2019536764A5 (https=)
RU2018131766A (ru) 6-гетероциклил-4-морфолин-4-илпиридин-2-оны, пригодные для лечения рака и диабета
JP2019505595A5 (https=)
RU2006101541A (ru) Производные пиперазина и способ их применения
HRP20250833T1 (hr) Derivati alfa-d-galaktopiranozida supstituirani triazolil metilom