JP2014520077A5 - - Google Patents

Download PDF

Info

Publication number
JP2014520077A5
JP2014520077A5 JP2014510546A JP2014510546A JP2014520077A5 JP 2014520077 A5 JP2014520077 A5 JP 2014520077A5 JP 2014510546 A JP2014510546 A JP 2014510546A JP 2014510546 A JP2014510546 A JP 2014510546A JP 2014520077 A5 JP2014520077 A5 JP 2014520077A5
Authority
JP
Japan
Prior art keywords
crystalline salt
salt
crystalline
synthesis
pharmaceutical composition
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.)
Granted
Application number
JP2014510546A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014520077A (ja
JP6574572B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2012/037838 external-priority patent/WO2012155146A1/en
Publication of JP2014520077A publication Critical patent/JP2014520077A/ja
Publication of JP2014520077A5 publication Critical patent/JP2014520077A5/ja
Application granted granted Critical
Publication of JP6574572B2 publication Critical patent/JP6574572B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2014510546A 2011-05-12 2012-05-14 (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結晶塩及びそれを使用する方法 Active JP6574572B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161485179P 2011-05-12 2011-05-12
US61/485,179 2011-05-12
PCT/US2012/037838 WO2012155146A1 (en) 2011-05-12 2012-05-14 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

Related Child Applications (2)

Application Number Title Priority Date Filing Date
JP2017032823A Division JP2017132775A (ja) 2011-05-12 2017-02-24 (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結晶塩及びそれを使用する方法
JP2019043868A Division JP6876082B2 (ja) 2011-05-12 2019-03-11 (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結晶塩及びそれを使用する方法

Publications (3)

Publication Number Publication Date
JP2014520077A JP2014520077A (ja) 2014-08-21
JP2014520077A5 true JP2014520077A5 (enExample) 2015-06-25
JP6574572B2 JP6574572B2 (ja) 2019-09-11

Family

ID=47139728

Family Applications (5)

Application Number Title Priority Date Filing Date
JP2014510546A Active JP6574572B2 (ja) 2011-05-12 2012-05-14 (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結晶塩及びそれを使用する方法
JP2017032823A Withdrawn JP2017132775A (ja) 2011-05-12 2017-02-24 (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結晶塩及びそれを使用する方法
JP2019043868A Active JP6876082B2 (ja) 2011-05-12 2019-03-11 (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結晶塩及びそれを使用する方法
JP2021017922A Pending JP2021098695A (ja) 2011-05-12 2021-02-08 (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結晶塩及びそれを使用する方法
JP2023060582A Pending JP2023093519A (ja) 2011-05-12 2023-04-04 (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結晶塩及びそれを使用する方法

Family Applications After (4)

Application Number Title Priority Date Filing Date
JP2017032823A Withdrawn JP2017132775A (ja) 2011-05-12 2017-02-24 (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結晶塩及びそれを使用する方法
JP2019043868A Active JP6876082B2 (ja) 2011-05-12 2019-03-11 (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結晶塩及びそれを使用する方法
JP2021017922A Pending JP2021098695A (ja) 2011-05-12 2021-02-08 (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結晶塩及びそれを使用する方法
JP2023060582A Pending JP2023093519A (ja) 2011-05-12 2023-04-04 (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結晶塩及びそれを使用する方法

Country Status (14)

Country Link
US (4) US9255068B2 (enExample)
EP (2) EP2707003B1 (enExample)
JP (5) JP6574572B2 (enExample)
CA (1) CA2835876C (enExample)
DK (1) DK2707003T3 (enExample)
ES (2) ES2739626T3 (enExample)
HR (1) HRP20191295T8 (enExample)
HU (1) HUE044536T2 (enExample)
LT (1) LT2707003T (enExample)
PL (1) PL2707003T3 (enExample)
PT (1) PT2707003T (enExample)
SI (1) SI2707003T1 (enExample)
TR (1) TR201911086T4 (enExample)
WO (1) WO2012155146A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8856782B2 (en) 2007-03-01 2014-10-07 George Mason Research Foundation, Inc. On-demand disposable virtual work system
US9098698B2 (en) 2008-09-12 2015-08-04 George Mason Research Foundation, Inc. Methods and apparatus for application isolation
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
WO2013082437A1 (en) 2011-12-02 2013-06-06 Invincia, Inc. Methods and apparatus for control and detection of malicious content using a sandbox environment
JP2015517524A (ja) * 2012-05-14 2015-06-22 パラテック ファーマシューティカルズ インコーポレイテッド (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
ES2978198T3 (es) * 2016-10-19 2024-09-06 Tetraphase Pharmaceuticals Inc Formas cristalinas de eravaciclina
EP3654988B1 (en) * 2017-07-21 2023-09-06 Almirall, LLC Sarecycline for the treatment of non-inflammatory acne lesions
US12297161B2 (en) 2018-04-06 2025-05-13 Almirall, Llc Process for making sarecycline hydrochloride
EP4357798A4 (en) 2021-06-14 2025-05-21 Hioki E.E. Corporation SHORT-CIRCUIT DETECTION DEVICE AND SHORT-CIRCUIT DETECTION METHOD

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2990331A (en) 1956-11-23 1961-06-27 Pfizer & Co C Stable solutions of salts of tetracyclines for parenteral administration
US2980584A (en) 1957-10-29 1961-04-18 Pfizer & Co C Parenteral magnesium oxytetracycline acetic or lactic acid carboxamide vehicle preparation
US3062717A (en) 1958-12-11 1962-11-06 Pfizer & Co C Intramuscular calcium tetracycline acetic or lactic acid carboxamide vehicle preparation
US3165531A (en) 1962-03-08 1965-01-12 Pfizer & Co C 13-substituted-6-deoxytetracyclines and process utilizing the same
US3454697A (en) 1965-06-08 1969-07-08 American Cyanamid Co Tetracycline antibiotic compositions for oral use
NL6607516A (enExample) 1966-05-31 1967-12-01
DE1767891C3 (de) 1968-06-28 1980-10-30 Pfizer Verfahren zur Herstellung von wäßrigen arzneilichen Lösungen für die parenterale, perorale und lokale Anwendung mit einem Gehalt an einem Tetracyclinderivat
US3957980A (en) 1972-10-26 1976-05-18 Pfizer Inc. Doxycycline parenteral compositions
DE2442829A1 (de) 1974-09-06 1976-03-18 Merck Patent Gmbh Tetracyclische verbindungen und verfahren zu ihrer herstellung
US4018889A (en) 1976-01-02 1977-04-19 Pfizer Inc. Oxytetracycline compositions
US4126680A (en) 1977-04-27 1978-11-21 Pfizer Inc. Tetracycline antibiotic compositions
CA2103189C (en) 1992-11-17 2005-05-03 Lorne M. Golub Tetracyclines including non-antimicrobial chemically-modified tetracyclines inhibit excessive collagen crosslinking during diabetes
US5834450A (en) 1994-02-17 1998-11-10 Pfizer Inc. 9- (substituted amino) -alpha-6-deoxy-5-oxy tetracycline derivatives, their preparation and their use as antibiotics
US5789395A (en) 1996-08-30 1998-08-04 The Research Foundation Of State University Of New York Method of using tetracycline compounds for inhibition of endogenous nitric oxide production
US6277061B1 (en) 1998-03-31 2001-08-21 The Research Foundation Of State University Of New York Method of inhibiting membrane-type matrix metalloproteinase
ES2548261T3 (es) * 2006-12-21 2015-10-15 Paratek Pharmaceuticals, Inc. Derivados de tetraciclina para el tratamiento de infecciones bacterianas, virales y parasitarias
AU2007338681B2 (en) 2006-12-21 2013-09-26 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds for treatment of inflammatory skin disorders
WO2009111064A2 (en) * 2008-03-05 2009-09-11 Paratek Pharmaceuticals, Inc. Minocycline compounds and methods of use thereof
TW202021946A (zh) * 2008-05-19 2020-06-16 美商派洛泰克藥物股份有限公司 四環素化合物之甲苯磺酸鹽及同素異形體
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
JP2015517524A (ja) * 2012-05-14 2015-06-22 パラテック ファーマシューティカルズ インコーポレイテッド (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

Similar Documents

Publication Publication Date Title
JP2014520077A5 (enExample)
MY184756A (en) Novel compounds for selective histone deacetylase inhibitors, and pharmaceutical composition comprising the same
UY32174A (es) Nuevos heterociclos sustituidos, composiciones farmaceuticas conteniendolos, procedimientos de preparacion y aplicaciones
WO2015002994A3 (en) Heteroaryl inhibitors of sumo activating enzyme
HRP20191295T1 (hr) Kristalne soli amida (4s,4as,5ar,12as)-4-dimetilamino-3,10,12,12a-tetrahidroksi-7-[(metoksi(metil)amino)-metil]-1,11-diokso-1,4,4a,5,5a,6,11,12a-oktahidro-naftacen-2-karboksilne kiseline i postupci uporabe istih
NZ631027A (en) Imidazothiadiazole and imidazopyrazine derivatives as protease activated receptor 4 (par4) inhibitors for treating platelet aggregation
ME02558B (me) Inhibitori replikacije virusa gripa
AR084824A1 (es) Procesos para preparar isoquinolinonas y formas solidas de isoquinolinonas
HRP20250119T1 (hr) Kdm1a inhibitor i njegova primjena u terapiji
MX2014012741A (es) Derivados de imidazotiadiazol e imidazopirazina como inhibidores del receptor 4 activado de proteasa (par4) para tratamiento de agregacion plaquetaria.
HK1221418A1 (zh) 释放修饰药物的水凝胶-连接的前药
JP2017061566A5 (enExample)
CA2914620C (en) Heterocyclic derivatives and use thereof
RU2018114480A (ru) Соли и твердые формы монобактамного антибиотика
MX2017005422A (es) Inhibidores de histona desacetilasa y sus usos en terapia.
WO2014022382A3 (en) Antibacterial protein kinase inhibitors
Szermerski et al. Synthesis, biological evaluation and molecular docking studies of benzyloxyacetohydroxamic acids as LpxC inhibitors
HRP20161135T1 (hr) Oblici u krutom stanju n-((s)-2,3-dihidroksi-propil)-3-(2-fluoro-4-jodo-fenilamino)-izonikotinamida
JP2015517524A5 (enExample)
WO2012122450A3 (en) Peptide deformylase inhibitors
WO2014195977A3 (en) Novel polymorphs of vismodegib
IL273751B2 (en) Salts of (R)-9-(5,2-difluorophenethyl)-4-ethyl-2-methyl-1-oxa-9,4-diazaspiro[5.5]undecan-3-one
BR112023024037A2 (pt) Sal farmaceuticamente aceitável de derivado de pirazoloheteroarila, formas cristalinas, composição farmacêutica, usos dos mesmos e métodos para preparar as referidas formas cristalinas e composição farmacêutica
WO2013015657A3 (ko) 혈관생성억제 작용을 갖는 신규한 화합물, 이의 제조방법 및 이를 포함하는 약학적 조성물
CN104961666B (zh) 2‑巯基乙酰胺类截短侧耳素衍生物及制备方法与医药用途