JP2022507013A5 - - Google Patents

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Publication number
JP2022507013A5
JP2022507013A5 JP2021521390A JP2021521390A JP2022507013A5 JP 2022507013 A5 JP2022507013 A5 JP 2022507013A5 JP 2021521390 A JP2021521390 A JP 2021521390A JP 2021521390 A JP2021521390 A JP 2021521390A JP 2022507013 A5 JP2022507013 A5 JP 2022507013A5
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JP
Japan
Prior art keywords
salt
compound
ring
group
condensed
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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
JP2021521390A
Other languages
English (en)
Japanese (ja)
Other versions
JP2022507013A (ja
JP7532353B2 (ja
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Publication date
Priority claimed from GBGB1817047.2A external-priority patent/GB201817047D0/en
Application filed filed Critical
Publication of JP2022507013A publication Critical patent/JP2022507013A/ja
Publication of JP2022507013A5 publication Critical patent/JP2022507013A5/ja
Application granted granted Critical
Publication of JP7532353B2 publication Critical patent/JP7532353B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2021521390A 2018-10-19 2019-10-21 H4アンタゴニスト化合物としてのピラゾール誘導体 Active JP7532353B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1817047.2A GB201817047D0 (en) 2018-10-19 2018-10-19 H4 antagonist compounds
GB1817047.2 2018-10-19
PCT/GB2019/052997 WO2020079457A1 (en) 2018-10-19 2019-10-21 Pyrazole derivatives as h4 antagonist compounds

Publications (3)

Publication Number Publication Date
JP2022507013A JP2022507013A (ja) 2022-01-18
JP2022507013A5 true JP2022507013A5 (cg-RX-API-DMAC10.html) 2022-10-31
JP7532353B2 JP7532353B2 (ja) 2024-08-13

Family

ID=64453795

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2021521390A Active JP7532353B2 (ja) 2018-10-19 2019-10-21 H4アンタゴニスト化合物としてのピラゾール誘導体

Country Status (13)

Country Link
US (2) US12234227B2 (cg-RX-API-DMAC10.html)
EP (1) EP3867248B1 (cg-RX-API-DMAC10.html)
JP (1) JP7532353B2 (cg-RX-API-DMAC10.html)
KR (1) KR102873380B1 (cg-RX-API-DMAC10.html)
CN (1) CN113272297B (cg-RX-API-DMAC10.html)
AU (1) AU2019360428B2 (cg-RX-API-DMAC10.html)
BR (1) BR112021007372A2 (cg-RX-API-DMAC10.html)
CA (1) CA3116628A1 (cg-RX-API-DMAC10.html)
ES (1) ES3058587T3 (cg-RX-API-DMAC10.html)
GB (1) GB201817047D0 (cg-RX-API-DMAC10.html)
MX (1) MX2021004280A (cg-RX-API-DMAC10.html)
SG (1) SG11202103133QA (cg-RX-API-DMAC10.html)
WO (1) WO2020079457A1 (cg-RX-API-DMAC10.html)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB202005858D0 (en) * 2020-04-22 2020-06-03 Heptares Therapeutics Ltd H4 Antagonist compounds
GB202019667D0 (en) * 2020-12-14 2021-01-27 Heptares Therapeutics Ltd H4 antagonist comnpounds
KR102655210B1 (ko) * 2021-03-26 2024-04-08 주식회사 스탠다임 아데노신 a2a 수용체 길항제 및 이의 용도
WO2022232259A1 (en) * 2021-04-28 2022-11-03 Cornell University Soluble adenylyl cyclase (sac) inhibitors and uses thereof
EP4421067A4 (en) * 2021-10-19 2026-01-14 Unimatec Co Ltd PYRAZOLE COMPOUND CONTAINING FLUORIDE AND ITS PRODUCTION PROCESS
KR102621694B1 (ko) * 2022-09-15 2024-01-08 주식회사 스탠다임 아데노신 a2a 수용체 길항제 및 이의 용도

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000169475A (ja) 1998-07-24 2000-06-20 Dai Ichi Seiyaku Co Ltd ピラゾ―ル誘導体およびその塩
US6573377B1 (en) * 1998-07-24 2003-06-03 Daiichi Pharmaceuticals Co., Ltd. Pyrazole derivatives and salts thereof
WO2005054239A1 (en) 2003-12-05 2005-06-16 Bayer Healthcare Ag 2-aminopyrimidine derivatives
NL2000323C2 (nl) * 2005-12-20 2007-11-20 Pfizer Ltd Pyrimidine-derivaten.
EP2066645A2 (en) 2006-09-12 2009-06-10 UCB Pharma S.A. 2 amino-pyrimidine derivatives as h4 receptor antagonists, processes for preparing them and their use in pharmaceutical compositions
US7985745B2 (en) 2006-10-02 2011-07-26 Abbott Laboratories Method for pain treatment
CL2008000467A1 (es) 2007-02-14 2008-08-22 Janssen Pharmaceutica Nv Compuestos derivados de 2-aminopirimidina, moduladores del receptor histamina h4; su procedimiento de preparacion; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar un trastorno inflamatorio seleccionado de alegia, asma
WO2009068512A1 (en) 2007-11-30 2009-06-04 Palau Pharma, S. A. 2 -amino-pyrimidine derivatives as histamine h4 antagonists
PE20091524A1 (es) 2007-12-19 2009-09-25 Palau Pharma Sa Derivados de 2-aminopirimidina
RU2489430C2 (ru) 2007-12-21 2013-08-10 Палау Фарма, С.А. Производные 4-аминопиримидина
AR074199A1 (es) 2008-11-20 2010-12-29 Glaxosmithkline Llc Compuesto de 6-(4-pirimidinil)-1h-indazol, composiciones farmaceuticas que lo comprenden y su uso para preparar un medicamento util para el tratamiento o disminucion de la gravedad del cancer.
TW201035078A (en) 2009-03-20 2010-10-01 Incyte Corp Substituted heterocyclic compounds
WO2011059839A1 (en) 2009-10-29 2011-05-19 Sirtris Pharmaceuticals, Inc. Bicyclic pyridines and analogs as sirtuin modulators
JP5781537B2 (ja) 2009-12-23 2015-09-24 メディシス ファーマシューティカル コーポレイション ヒスタミンh4受容体アンタゴニストとしてのアミノアルキルピリミジン誘導体
AR093512A1 (es) 2012-11-16 2015-06-10 Merck Patent Gmbh Derivados heterociclicos como moduladores de la actividad de cinasas
JP2019525929A (ja) 2016-07-28 2019-09-12 メイヨ・ファウンデーション・フォー・メディカル・エデュケーション・アンド・リサーチ Parkin酵素機能の小分子活性化因子

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