JP2015517524A5 - - Google Patents

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Publication number
JP2015517524A5
JP2015517524A5 JP2015512752A JP2015512752A JP2015517524A5 JP 2015517524 A5 JP2015517524 A5 JP 2015517524A5 JP 2015512752 A JP2015512752 A JP 2015512752A JP 2015512752 A JP2015512752 A JP 2015512752A JP 2015517524 A5 JP2015517524 A5 JP 2015517524A5
Authority
JP
Japan
Prior art keywords
composition
salt
crystalline
methyl
monomesylate
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
JP2015512752A
Other languages
English (en)
Japanese (ja)
Other versions
JP2015517524A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2013/040933 external-priority patent/WO2013173326A1/en
Publication of JP2015517524A publication Critical patent/JP2015517524A/ja
Publication of JP2015517524A5 publication Critical patent/JP2015517524A5/ja
Pending legal-status Critical Current

Links

JP2015512752A 2012-05-14 2013-05-14 (4S,4aS,5aR,12aS)−4−ジメチルアミノ−3,10,12,12a−テトラヒドロキシ−7−[(メトキシ(メチル)アミノ)−メチル]−1,11−ジオキソ−1,4,4a,5,5a,6,11,12a−オクタヒドロ−ナフタセン−2−カルボン酸アミドの使用方法 Pending JP2015517524A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261646754P 2012-05-14 2012-05-14
US61/646,754 2012-05-14
PCT/US2013/040933 WO2013173326A1 (en) 2012-05-14 2013-05-14 Methods of using (4s,4as,5ar,12as)-4- dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide

Publications (2)

Publication Number Publication Date
JP2015517524A JP2015517524A (ja) 2015-06-22
JP2015517524A5 true JP2015517524A5 (enExample) 2016-06-30

Family

ID=49548796

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015512752A Pending JP2015517524A (ja) 2012-05-14 2013-05-14 (4S,4aS,5aR,12aS)−4−ジメチルアミノ−3,10,12,12a−テトラヒドロキシ−7−[(メトキシ(メチル)アミノ)−メチル]−1,11−ジオキソ−1,4,4a,5,5a,6,11,12a−オクタヒドロ−ナフタセン−2−カルボン酸アミドの使用方法

Country Status (6)

Country Link
US (1) US20130302442A1 (enExample)
EP (1) EP2849757A4 (enExample)
JP (1) JP2015517524A (enExample)
AU (1) AU2013262991A1 (enExample)
CA (1) CA2873412A1 (enExample)
WO (1) WO2013173326A1 (enExample)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012155146A1 (en) * 2011-05-12 2012-11-15 Paratek Pharmaceuticals, Inc. Crystalline salts of (4s,4as,5ar,12as)-4-dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide and methods of using the same
EP4268897A3 (en) * 2015-03-24 2024-01-03 Paratek Pharmaceuticals, Inc. Minocycline compounds for biodefense
US12297161B2 (en) * 2018-04-06 2025-05-13 Almirall, Llc Process for making sarecycline hydrochloride

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0375068A1 (en) * 1988-12-23 1990-06-27 Gist-Brocades N.V. Combining bismuth compounds and tetracyclines
US7871793B2 (en) * 2004-02-20 2011-01-18 Burnham Institute For Medical Research Antimicrobial carbohydrates and methods of using same
AU2007338681B2 (en) * 2006-12-21 2013-09-26 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds for treatment of inflammatory skin disorders
ES2548261T3 (es) * 2006-12-21 2015-10-15 Paratek Pharmaceuticals, Inc. Derivados de tetraciclina para el tratamiento de infecciones bacterianas, virales y parasitarias
JP5944825B2 (ja) * 2009-08-28 2016-07-05 テトラフェース ファーマシューティカルズ,インコーポレイテッド テトラサイクリン化合物
WO2012021829A1 (en) * 2010-08-12 2012-02-16 Tetraphase Pharmaceuticals, Inc. Methods of treating bacterial infections
WO2012155146A1 (en) * 2011-05-12 2012-11-15 Paratek Pharmaceuticals, Inc. Crystalline salts of (4s,4as,5ar,12as)-4-dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide and methods of using the same

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