JP2020502268A5 - - Google Patents

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Publication number
JP2020502268A5
JP2020502268A5 JP2019551913A JP2019551913A JP2020502268A5 JP 2020502268 A5 JP2020502268 A5 JP 2020502268A5 JP 2019551913 A JP2019551913 A JP 2019551913A JP 2019551913 A JP2019551913 A JP 2019551913A JP 2020502268 A5 JP2020502268 A5 JP 2020502268A5
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JP
Japan
Prior art keywords
alkyl
aryl
cycloalkyl
heterocyclyl
halogen
Prior art date
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Application number
JP2019551913A
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English (en)
Japanese (ja)
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JP2020502268A (ja
JP7046092B2 (ja
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Priority claimed from PCT/US2017/065665 external-priority patent/WO2018111787A1/en
Publication of JP2020502268A publication Critical patent/JP2020502268A/ja
Publication of JP2020502268A5 publication Critical patent/JP2020502268A5/ja
Application granted granted Critical
Publication of JP7046092B2 publication Critical patent/JP7046092B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2019551913A 2016-12-13 2017-12-12 Il-12、il-23および/またはifnアルファ応答の調節剤としてのホスフィンオキシドアルキルアミド置換ヘテロアリール化合物 Active JP7046092B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662433470P 2016-12-13 2016-12-13
US62/433,470 2016-12-13
PCT/US2017/065665 WO2018111787A1 (en) 2016-12-13 2017-12-12 Phosphine oxide alkyl amide substituted heteroaryl compounds as modulators of il-12, il-23, and/or ifn alpha responses

Publications (3)

Publication Number Publication Date
JP2020502268A JP2020502268A (ja) 2020-01-23
JP2020502268A5 true JP2020502268A5 (enExample) 2021-01-07
JP7046092B2 JP7046092B2 (ja) 2022-04-01

Family

ID=60888685

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2019551913A Active JP7046092B2 (ja) 2016-12-13 2017-12-12 Il-12、il-23および/またはifnアルファ応答の調節剤としてのホスフィンオキシドアルキルアミド置換ヘテロアリール化合物

Country Status (10)

Country Link
US (1) US10294256B2 (enExample)
EP (1) EP3555111B1 (enExample)
JP (1) JP7046092B2 (enExample)
KR (1) KR102602558B1 (enExample)
CN (1) CN110267964B (enExample)
AR (1) AR110351A1 (enExample)
ES (1) ES2907008T3 (enExample)
MA (1) MA48602A (enExample)
TW (1) TW201827423A (enExample)
WO (1) WO2018111787A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3083122A1 (en) 2017-11-21 2019-05-31 Bristol-Myers Squibb Company Sulfone pyridine alkyl amide-substituted heteroaryl compounds
AR117398A1 (es) 2018-03-12 2021-08-04 Abbvie Inc Inhibidores de la señalización mediada por tirosina cinasa 2
CN111936486B (zh) * 2018-03-22 2023-09-22 百时美施贵宝公司 用作IL-12、IL-23和/或IFNα响应的调节剂的包含吡啶的杂环化合物
RS66416B1 (sr) 2019-01-18 2025-02-28 Astrazeneca Ab 6'-[[(1s,3s)-3-[[5-(difluorometoksi)-2-pirimidinil]amino]ciklopentil]amino][1(2h),3'-bipiridin]-2-on kao inhibitor pcsk9 i metode njegove primene
US20230049130A1 (en) * 2020-01-19 2023-02-16 Crystal Pharmaceutical (Suzhou) Co., Ltd. Deucravacitinib crystal form, preparation method therefor and use thereof
CN114981262A (zh) 2020-12-22 2022-08-30 益方生物科技(上海)股份有限公司 杂芳基化合物及其制备方法和用途
US20240246944A1 (en) 2021-03-16 2024-07-25 Anrui Biomedical Technology (Guangzhou) Co., Ltd. Amino heteroaryl compounds and compositions
CN115724830A (zh) * 2021-08-31 2023-03-03 浙江文达医药科技有限公司 作为tyk2/jak1假激酶结构域(jh2)抑制剂的化合物及合成和使用方法
CA3236262A1 (en) 2021-10-25 2023-05-04 Isaac Marx Tyk2 degraders and uses thereof

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060270730A1 (en) 2003-08-07 2006-11-30 Andreas Katopodis Histone deacetylase inhibitors as immunosuppressants
MX2010012703A (es) * 2008-05-21 2010-12-21 Ariad Pharma Inc Derivados fosforosos como inhibidores de cinasa.
TW201100441A (en) * 2009-06-01 2011-01-01 Osi Pharm Inc Amino pyrimidine anticancer compounds
WO2013091011A1 (en) * 2011-12-21 2013-06-27 Biota Europe Ltd Heterocyclic urea compounds
AU2013204563B2 (en) * 2012-05-05 2016-05-19 Takeda Pharmaceutical Company Limited Compounds for inhibiting cell proliferation in EGFR-driven cancers
EP2922846B1 (en) 2012-11-08 2018-10-03 Bristol-Myers Squibb Company Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn-alpha
WO2014074660A1 (en) 2012-11-08 2014-05-15 Bristol-Myers Squibb Company ALKYL-AMIDE-SUBSTITUTED PYRIDYL COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFNα RESPONSES
WO2014181287A1 (en) * 2013-05-09 2014-11-13 Piramal Enterprises Limited Heterocyclyl compounds and uses thereof
TWI582077B (zh) * 2013-11-07 2017-05-11 必治妥美雅史谷比公司 作爲IL-12、IL-23及/或IFNα反應調節劑之經烷基-醯胺取代之吡啶化合物
EP2947460A1 (en) 2014-05-22 2015-11-25 Medizinische Universität Wien Personalized therapy of inflammation-associated cancer using methods of assessing the susceptibility of a subject to the treatment with EGFR inhibitors/antagonists

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