JP2016504376A5 - - Google Patents

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Publication number
JP2016504376A5
JP2016504376A5 JP2015551201A JP2015551201A JP2016504376A5 JP 2016504376 A5 JP2016504376 A5 JP 2016504376A5 JP 2015551201 A JP2015551201 A JP 2015551201A JP 2015551201 A JP2015551201 A JP 2015551201A JP 2016504376 A5 JP2016504376 A5 JP 2016504376A5
Authority
JP
Japan
Prior art keywords
alkyl
optionally substituted
compound
inhibitor
ligand
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.)
Pending
Application number
JP2015551201A
Other languages
English (en)
Japanese (ja)
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JP2016504376A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2014/050168 external-priority patent/WO2014108408A1/en
Publication of JP2016504376A publication Critical patent/JP2016504376A/ja
Publication of JP2016504376A5 publication Critical patent/JP2016504376A5/ja
Pending legal-status Critical Current

Links

JP2015551201A 2013-01-08 2014-01-07 ナフチリジノン誘導体及びウイルス性疾患の治療、改善又は予防におけるそれらの使用 Pending JP2016504376A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361750032P 2013-01-08 2013-01-08
US61/750,032 2013-01-08
PCT/EP2014/050168 WO2014108408A1 (en) 2013-01-08 2014-01-07 Naphthyridinone derivatives and their use in the treatment, amelioration or prevention of a viral disease

Publications (2)

Publication Number Publication Date
JP2016504376A JP2016504376A (ja) 2016-02-12
JP2016504376A5 true JP2016504376A5 (en:Method) 2017-02-16

Family

ID=50073147

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015551201A Pending JP2016504376A (ja) 2013-01-08 2014-01-07 ナフチリジノン誘導体及びウイルス性疾患の治療、改善又は予防におけるそれらの使用

Country Status (12)

Country Link
US (3) US9199987B2 (en:Method)
EP (1) EP2945945B1 (en:Method)
JP (1) JP2016504376A (en:Method)
KR (1) KR20150103672A (en:Method)
CN (1) CN104903319B (en:Method)
BR (1) BR112015013414A2 (en:Method)
CA (1) CA2894821A1 (en:Method)
ES (1) ES2597803T3 (en:Method)
HK (1) HK1211288A1 (en:Method)
MX (1) MX2015008292A (en:Method)
RU (1) RU2015132977A (en:Method)
WO (1) WO2014108408A1 (en:Method)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ736259A (en) 2015-04-28 2019-09-27 Shionogi & Co Substituted polycyclic pyridone derivative and prodrugs thereof
LT3290424T (lt) 2015-04-28 2023-03-10 Shionogi & Co., Ltd Pakeisto policiklinio piridono dariniai ir jo provaistas
KR102084109B1 (ko) * 2015-12-15 2020-03-03 시오노기세야쿠 가부시키가이샤 캡 의존적 엔도뉴클레아제 저해제 및 항인플루엔자 약을 조합하는 것을 특징으로 하는 인플루엔자 치료용 의약
CR20190123A (es) 2016-08-10 2019-04-30 Shionogi & Co Composiciones farmacéuticas que contienen derivados de piridona policíclicos sustituídos y profármacos de los mismos
JP2020176263A (ja) * 2019-04-19 2020-10-29 住友化学株式会社 フィルム及び農園芸用施設

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5475109A (en) 1994-10-17 1995-12-12 Merck & Co., Inc. Dioxobutanoic acid derivatives as inhibitors of influenza endonuclease
US6559145B2 (en) * 2000-07-12 2003-05-06 Pharmacia & Upjohn Company Heterocycle carboxamides as antiviral agents
EP1790638B1 (en) 2004-09-15 2013-04-03 Shionogi Co., Ltd. Carbamoylpyridone derivative having hiv integrase inhibitory activity
US20070072831A1 (en) 2005-05-16 2007-03-29 Gilead Sciences, Inc. Integrase inhibitor compounds
US20110166123A1 (en) * 2008-01-07 2011-07-07 Aardea Biosciences, Inc. Novel compositions and methods of use
TWI518084B (zh) 2009-03-26 2016-01-21 鹽野義製藥股份有限公司 哌喃酮與吡啶酮衍生物之製造方法
JP5697163B2 (ja) 2009-03-26 2015-04-08 塩野義製薬株式会社 置換された3−ヒドロキシ−4−ピリドン誘導体
WO2011000566A2 (en) 2009-06-30 2011-01-06 Savira Pharmaceuticals Gmbh Compounds and pharmaceutical compositions for the treatment of negative-sense ssrna virus infections
WO2011041143A1 (en) 2009-10-01 2011-04-07 Merck Sharp & Dohme Corp. HETEROCYCLIC-FUSED PYRAZOLO[4,3-c]PYRIDIN-3-ONE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS

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