JP2022141835A5 - - Google Patents

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Publication number
JP2022141835A5
JP2022141835A5 JP2022115300A JP2022115300A JP2022141835A5 JP 2022141835 A5 JP2022141835 A5 JP 2022141835A5 JP 2022115300 A JP2022115300 A JP 2022115300A JP 2022115300 A JP2022115300 A JP 2022115300A JP 2022141835 A5 JP2022141835 A5 JP 2022141835A5
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JP
Japan
Prior art keywords
pharmaceutically acceptable
group
acceptable salt
methyl
following formula
Prior art date
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JP2022115300A
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English (en)
Japanese (ja)
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JP2022141835A (ja
JP7331212B2 (ja
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Priority claimed from PCT/US2018/027005 external-priority patent/WO2018194885A1/en
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Publication of JP2022141835A publication Critical patent/JP2022141835A/ja
Publication of JP2022141835A5 publication Critical patent/JP2022141835A5/ja
Application granted granted Critical
Publication of JP7331212B2 publication Critical patent/JP7331212B2/ja
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JP2022115300A 2017-04-18 2022-07-20 フェニル-2-ヒドロキシ-アセチルアミノ-2-メチル-フェニル化合物 Active JP7331212B2 (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP17382207.3 2017-04-18
EP17382207 2017-04-18
PCT/US2018/027005 WO2018194885A1 (en) 2017-04-18 2018-04-11 Phenyl-2-hydroxy-acetylamino-2-methyl-phenyl compounds
JP2019556703A JP7110232B2 (ja) 2017-04-18 2018-04-11 フェニル-2-ヒドロキシ-アセチルアミノ-2-メチル-フェニル化合物

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2019556703A Division JP7110232B2 (ja) 2017-04-18 2018-04-11 フェニル-2-ヒドロキシ-アセチルアミノ-2-メチル-フェニル化合物

Publications (3)

Publication Number Publication Date
JP2022141835A JP2022141835A (ja) 2022-09-29
JP2022141835A5 true JP2022141835A5 (enExample) 2022-10-26
JP7331212B2 JP7331212B2 (ja) 2023-08-22

Family

ID=58606227

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2019556703A Active JP7110232B2 (ja) 2017-04-18 2018-04-11 フェニル-2-ヒドロキシ-アセチルアミノ-2-メチル-フェニル化合物
JP2022115300A Active JP7331212B2 (ja) 2017-04-18 2022-07-20 フェニル-2-ヒドロキシ-アセチルアミノ-2-メチル-フェニル化合物

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2019556703A Active JP7110232B2 (ja) 2017-04-18 2018-04-11 フェニル-2-ヒドロキシ-アセチルアミノ-2-メチル-フェニル化合物

Country Status (30)

Country Link
US (2) US11655214B2 (enExample)
EP (2) EP3612519B1 (enExample)
JP (2) JP7110232B2 (enExample)
KR (2) KR102575246B1 (enExample)
CN (2) CN110831927B (enExample)
AU (2) AU2018255191B2 (enExample)
BR (1) BR112019021867A2 (enExample)
CO (1) CO2019012767A2 (enExample)
CR (1) CR20190519A (enExample)
CY (1) CY1125150T1 (enExample)
DK (2) DK4039675T3 (enExample)
ES (2) ES2906847T3 (enExample)
FI (1) FI4039675T3 (enExample)
HR (2) HRP20220263T1 (enExample)
HU (2) HUE057745T2 (enExample)
IL (2) IL270005B (enExample)
LT (2) LT4039675T (enExample)
MX (2) MX389724B (enExample)
MY (1) MY199442A (enExample)
NZ (1) NZ758291A (enExample)
PH (1) PH12019502363B1 (enExample)
PL (2) PL3612519T3 (enExample)
PT (2) PT4039675T (enExample)
RS (2) RS62933B1 (enExample)
SA (1) SA519410320B1 (enExample)
SG (1) SG11201909680UA (enExample)
SI (2) SI3612519T1 (enExample)
SM (2) SMT202400357T1 (enExample)
WO (1) WO2018194885A1 (enExample)
ZA (1) ZA201906811B (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11201909680UA (en) * 2017-04-18 2019-11-28 Lilly Co Eli Phenyl-2-hydroxy-acetylamino-2-methyl-phenyl compounds
WO2019191115A1 (en) 2018-03-26 2019-10-03 Icahn School Of Medicine At Mount Sinai Methods of treating minimal residual cancer
KR20220068224A (ko) * 2019-08-29 2022-05-25 히버셀, 인크. Perk 억제 화합물
WO2021041976A1 (en) 2019-08-29 2021-03-04 Hibercell, Inc. Perk inhibiting indolinyl compounds
WO2021041970A1 (en) 2019-08-29 2021-03-04 Hibercell, Inc. Perk inhibiting imidazolopyrazine compounds
MX2022002446A (es) * 2019-08-29 2022-06-02 Hibercell Inc Compuestos de pirrolopirimidina inhibidores de perk.
WO2021231782A1 (en) * 2020-05-13 2021-11-18 Hibercell, Inc. Perk inhibitors for treating viral infections
WO2021231788A1 (en) * 2020-05-13 2021-11-18 Hibercell, Inc. Perk inhibiting pyrrolopyrimidine compounds to treat viral infections
CN113234029B (zh) * 2021-05-25 2022-03-22 白银康寓信生物科技有限公司 一种2-氨基-3,5-二卤代吡嗪的合成方法
AU2024242199A1 (en) * 2023-03-30 2025-10-30 Hibercell, Inc. Crystalline forms of (r)-2-amino-5-(4-(2-(3,5-difluorophenyl)-2-hydroxyacetamido)-2-methylphenyl)-n-isopropylnicotinamide and methods for using the same
GB202407386D0 (en) 2024-05-24 2024-07-10 Apollo Ap45 Ltd 1H-pyrazolo(4,3-D)pyrimidine derivatives

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US7863444B2 (en) 1997-03-19 2011-01-04 Abbott Laboratories 4-aminopyrrolopyrimidines as kinase inhibitors
TW200306819A (en) * 2002-01-25 2003-12-01 Vertex Pharma Indazole compounds useful as protein kinase inhibitors
CA2484209C (en) 2002-05-03 2013-06-11 Exelixis, Inc. Protein kinase modulators and methods of use
NZ544920A (en) 2003-07-23 2009-11-27 Bayer Healthcare Llc 4{4-[3-(4-chloro-3-trifluoromethylphenyl)-ureido]-3-fluorophenoxy}-pyridine-2-carboxylic acid methylamide and metabolites for the treatment and prevention of diseases and conditions
TW200804345A (en) 2005-08-30 2008-01-16 Novartis Ag Substituted benzimidazoles and methods of preparation
CA2620818A1 (en) * 2005-09-02 2007-03-08 Astellas Pharma Inc. Amide derivatives as rock inhibitors
EP2618146B1 (en) 2008-02-25 2015-06-17 Nestec S.A. Drug selection for breast cancer therapy using antibody-based arrays
US20120014911A1 (en) 2009-01-09 2012-01-19 Serge Fuchs Regulators of the Interferon-Alpha Receptor 1 (IFNAR1) Chain of the Interferon Receptor
CA2794153C (en) 2010-03-25 2018-01-02 Glaxosmithkline Llc Substituted indoline derivatives as perk inhibitors
EP2986286A1 (en) 2013-04-15 2016-02-24 Universita' Degli Studi di Bari Galloyl benzamide-based compounds as jnk modulators
WO2015056180A1 (en) 2013-10-15 2015-04-23 Glaxosmithkline Intellectual Property (No.2) Limited Indoline derivatives as inhibitors of perk
ES2685661T3 (es) 2013-11-08 2018-10-10 Ono Pharmaceutical Co., Ltd. Derivado de pirrolopirimidina
JP2017507967A (ja) 2014-03-11 2017-03-23 グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー2)、リミテッドGlaxosmithkline Intellectual Property (No.2) Limited Perk阻害剤として作用する化合物
WO2016004254A1 (en) 2014-07-01 2016-01-07 The Regents Of The University Of California Combined modulation of ire1
CA2967125C (en) 2014-11-14 2022-10-25 Nerviano Medical Sciences S.R.L. 6-amino-7-bicyclo-7-deaza-purine derivatives as protein kinase inhibitors
GB201508747D0 (en) 2015-05-21 2015-07-01 Univ Edinburgh Compounds
AU2016297754A1 (en) * 2015-07-24 2018-02-15 Blueprint Medicines Corporation Compounds useful for treating disorders related to KIT and PDGFR
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AU2017300123A1 (en) 2016-07-20 2019-01-31 Glaxosmithkline Intellectual Property Development Limited Isoquinoline derivatives as PERK inhibitors
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WO2018138358A1 (en) 2017-01-30 2018-08-02 Université de Liège Perk and ire-1a inhibitors against neurodevelopmental disorders
SG11201909680UA (en) 2017-04-18 2019-11-28 Lilly Co Eli Phenyl-2-hydroxy-acetylamino-2-methyl-phenyl compounds
JP7304855B2 (ja) 2017-11-14 2023-07-07 ザ チルドレンズ メディカル センター コーポレーション 新規イミダゾピリミジン化合物およびそれらの使用
EP3492454A1 (en) 2017-11-30 2019-06-05 Step Pharma S.A.S. Compounds
WO2019191115A1 (en) 2018-03-26 2019-10-03 Icahn School Of Medicine At Mount Sinai Methods of treating minimal residual cancer
CN112384283B (zh) 2018-07-06 2023-08-15 吉利德科学公司 治疗性的杂环化合物
US20220040183A1 (en) 2018-10-01 2022-02-10 INSERM (Institut National de la Santé et de la Recherche Médicale) Use of inhibitors of stress granule formation for targeting the regulation of immune responses

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