JP2013514345A5 - - Google Patents

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Publication number
JP2013514345A5
JP2013514345A5 JP2012543942A JP2012543942A JP2013514345A5 JP 2013514345 A5 JP2013514345 A5 JP 2013514345A5 JP 2012543942 A JP2012543942 A JP 2012543942A JP 2012543942 A JP2012543942 A JP 2012543942A JP 2013514345 A5 JP2013514345 A5 JP 2013514345A5
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JP
Japan
Prior art keywords
pharmaceutically acceptable
acceptable salt
optionally substituted
represented
methyl
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JP2012543942A
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English (en)
Japanese (ja)
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JP2013514345A (ja
JP5793766B2 (ja
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Priority claimed from PCT/IB2010/055596 external-priority patent/WO2011073845A1/en
Publication of JP2013514345A publication Critical patent/JP2013514345A/ja
Publication of JP2013514345A5 publication Critical patent/JP2013514345A5/ja
Application granted granted Critical
Publication of JP5793766B2 publication Critical patent/JP5793766B2/ja
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JP2012543942A 2009-12-16 2010-12-06 抗菌剤として有用なｎ−結合型ヒドロキサム酸誘導体 Active JP5793766B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US28703509P 2009-12-16 2009-12-16
US61/287,035 2009-12-16
PCT/IB2010/055596 WO2011073845A1 (en) 2009-12-16 2010-12-06 N-linked hydroxamic acid derivatives useful as antibacterial agents

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2015142292A Division JP2016006064A (ja) 2009-12-16 2015-07-16 抗菌剤として有用なｎ−結合型ヒドロキサム酸誘導体

Publications (3)

Publication Number Publication Date
JP2013514345A JP2013514345A (ja) 2013-04-25
JP2013514345A5 true JP2013514345A5 (enExample) 2014-02-06
JP5793766B2 JP5793766B2 (ja) 2015-10-14

Family

ID=43571291

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2012543942A Active JP5793766B2 (ja) 2009-12-16 2010-12-06 抗菌剤として有用なｎ−結合型ヒドロキサム酸誘導体
JP2015142292A Pending JP2016006064A (ja) 2009-12-16 2015-07-16 抗菌剤として有用なｎ−結合型ヒドロキサム酸誘導体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2015142292A Pending JP2016006064A (ja) 2009-12-16 2015-07-16 抗菌剤として有用なｎ−結合型ヒドロキサム酸誘導体

Country Status (10)

Country Link
US (4) US8664401B2 (enExample)
EP (1) EP2512474B1 (enExample)
JP (2) JP5793766B2 (enExample)
CA (2) CA2899583A1 (enExample)
DK (1) DK2512474T3 (enExample)
ES (1) ES2525820T3 (enExample)
PL (1) PL2512474T3 (enExample)
PT (1) PT2512474E (enExample)
SI (1) SI2512474T1 (enExample)
WO (1) WO2011073845A1 (enExample)

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BR112018073580A2 (pt) * 2016-05-17 2019-03-19 Idorsia Pharmaceuticals Ltd derivados de 6-(buta-1,3-diyn-1-il) benzo [d] tiazol
SG11201810656WA (en) 2016-06-14 2018-12-28 Novartis Ag Crystalline form of (r)-4-(5-(cyclopropylethynyl)isoxazol-3-yl)-n-hydroxy-2-methyl-2-(methylsulfonyl)butanamide as an antibacterial agent
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MX2019010302A (es) 2017-03-30 2019-11-21 Hoffmann La Roche Isoquinolinas como inhibidores de hpk1.
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BR112020017453A2 (pt) * 2018-03-15 2020-12-22 Pfizer Inc Fosfatos e boronatos de piridinona e pirimidinona úteis como agentes antibacterianos
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TW202024053A (zh) 2018-10-02 2020-07-01 美商建南德克公司 異喹啉化合物及其用途
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CA2830866A1 (en) 2011-04-08 2012-10-11 Pfizer Inc. Imidazole, pyrazole, and triazole derivatives useful as antibacterial agents
MX2013011526A (es) 2011-04-08 2013-12-06 Pfizer Derivados de isoxazol utiles como agentes antibacteriales .

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