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MX2009006282A - Profarmacos solubles en agua de florfenicol y sus analogos. - Google Patents

Profarmacos solubles en agua de florfenicol y sus analogos.

Info

Publication number
MX2009006282A
MX2009006282A MX2009006282A MX2009006282A MX2009006282A MX 2009006282 A MX2009006282 A MX 2009006282A MX 2009006282 A MX2009006282 A MX 2009006282A MX 2009006282 A MX2009006282 A MX 2009006282A MX 2009006282 A MX2009006282 A MX 2009006282A
Authority
MX
Mexico
Prior art keywords
florfenicol
analogs
water
prodrug
prodrugs
Prior art date
Application number
MX2009006282A
Other languages
English (en)
Inventor
Tomasz W Glinka
Jason Zhang
Original Assignee
Schering Plough Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Schering Plough Ltd filed Critical Schering Plough Ltd
Publication of MX2009006282A publication Critical patent/MX2009006282A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C07D233/60Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by oxygen or sulfur atoms, attached to ring nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00Sulfones; Sulfoxides
    • C07C317/26Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C317/32Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06191Dipeptides containing heteroatoms different from O, S, or N

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Oncology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Communicable Diseases (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

La presente invención describe ciertos profármacos novedosos de florfenicol y/o de análogos de florfenicol, incluyendo profármacos de sales farmacéuticamente aceptables de florfenicol y sus análogos, incluyendo ésteres que contienen nitrógeno del grupo alcohol secundario de florfenicol y de sus análogos, y sales farmacéuticamente aceptables de los mismos, composiciones que los contienen, y métodos para administrarlos a sujetos; en modalidades particulares, los profármacos son suficientemente solubles en agua para servir las funciones necesarias de un profármaco soluble en agua de florfenicol o de un profármaco soluble en agua de un análogo de florfenicol; una cierta subclase de los compuestos también posee la estabilidad hidrolítica necesaria para mantener el profármaco en solución el sistema del sujeto hasta que existan las condiciones apropiadas cuando el profármaco puede hidrolizar, liberando florfenicol o el análogo de floríenicol en cuestión.
MX2009006282A 2006-12-13 2007-12-11 Profarmacos solubles en agua de florfenicol y sus analogos. MX2009006282A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US87486406P 2006-12-13 2006-12-13
PCT/US2007/025326 WO2008076259A1 (en) 2006-12-13 2007-12-11 Water-soluble prodrugs of florfenicol and its analogs

Publications (1)

Publication Number Publication Date
MX2009006282A true MX2009006282A (es) 2009-06-23

Family

ID=39304665

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009006282A MX2009006282A (es) 2006-12-13 2007-12-11 Profarmacos solubles en agua de florfenicol y sus analogos.

Country Status (6)

Country Link
US (1) US8084643B2 (es)
EP (1) EP2091909A1 (es)
CN (1) CN101605756A (es)
CA (1) CA2672586A1 (es)
MX (1) MX2009006282A (es)
WO (1) WO2008076259A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200505425A (en) * 2003-05-29 2005-02-16 Schering Plough Ltd Compositions and method for treating infection in cattle and swine
US8119667B2 (en) * 2005-12-29 2012-02-21 Schering-Plough Animal Health Corporation Carbonates of fenicol antibiotics
WO2008076256A1 (en) * 2006-12-13 2008-06-26 Schering-Plough Ltd. Water-soluble prodrugs of chloramphenicol, thiamphenicol, and analogs thereof
US8314252B2 (en) * 2008-07-30 2012-11-20 Intervet Inc. Process for preparing oxazoline-protected aminodiol compounds useful as intermediates to florfenicol
WO2010107446A1 (en) * 2009-03-19 2010-09-23 Green Earth Fuels, Llc Biodiesel cold soak filtering system
MX2013012820A (es) 2011-05-02 2014-02-10 Zoetis Llc Cefalosporinas novedosas utiles como agentes antibacteriales.
CN102417472B (zh) * 2011-12-12 2013-11-13 齐鲁动物保健品有限公司 一种氟苯尼考的制备方法
CN110078729A (zh) * 2019-06-11 2019-08-02 石家庄学院 一种水溶性氟苯尼考前药及其制备方法
CN111393341A (zh) * 2020-05-07 2020-07-10 中国农业大学 一种水溶性氟苯尼考氨基酸盐的制备方法
CN112194788B (zh) * 2020-09-15 2022-08-02 石家庄学院 一种水溶性氟苯尼考及其制备方法
CN115286544A (zh) * 2022-10-08 2022-11-04 世华合创生物技术开发(山东)有限公司 一种氟苯尼考衍生物、制备方法及其在抗细菌感染的应用
CN115304526B (zh) * 2022-10-11 2023-08-01 世华合创生物技术开发(山东)有限公司 一种水溶性氟苯尼考前药及其制备方法
CN116178309B (zh) * 2023-02-20 2024-11-29 华中农业大学 一种水溶性良好的氟苯尼考衍生物及其制备方法和应用

Family Cites Families (69)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR4604E (fr) 1904-08-18 1905-08-29 Societe Veuve Ch. Rossignol Et Cie Perfectionnements apportés aux jouets roulants
GB804986A (en) 1955-01-28 1958-11-26 Bayer Ag Acylaminopropanediols and the esters, acetals and ketals thereof
US2776992A (en) * 1956-03-14 1957-01-08 Du Pont Trifluoromethylsulfonylphenyldichloracetamidopropandiol
US3100781A (en) * 1957-11-20 1963-08-13 Zambon Spa Chloramphenicol glycinate and the production thereof
BE638755A (es) 1962-10-16
US3294818A (en) * 1964-04-06 1966-12-27 Warner Lambert Pharmaceutical Substituted dioxolanes and process for their production
GB1117616A (en) 1964-09-23 1968-06-19 Warner Lambert Pharmaceutical Process for preparing 1-(p-acetylphenyl)-2-(2,2-dichloroacetamido)-1,3-propanediol
US3405165A (en) * 1965-10-23 1968-10-08 Parke Davis & Co Sulfonic acid compound
US3475470A (en) * 1965-10-23 1969-10-28 Parke Davis & Co New amino acid ester complexes
GB1173562A (en) 1966-04-25 1969-12-10 Pierrel Spa Chloramphenicol Ester Salts, the Preparation therof and Compositions Containing them
NL6916355A (es) * 1968-11-02 1970-05-06
US3740411A (en) * 1970-06-23 1973-06-19 Sumitomo Chemical Co Water-soluble antibacterial compounds
US3770889A (en) * 1972-03-10 1973-11-06 Zenith Radio Corp Hinged chassis arrangement for receiver apparatus and the like
US3950360A (en) * 1972-06-08 1976-04-13 Sankyo Company Limited Antibiotic substances
US3984564A (en) * 1972-06-08 1976-10-05 Sankyo Company Limited Antibiotic substances B-41, their production and their use as insecticides and acaricides
SE434277B (sv) * 1976-04-19 1984-07-16 Merck & Co Inc Sett att framstella nya antihelmintiskt verkande foreningar genom odling av streptomyces avermitilis
US4199569A (en) * 1977-10-03 1980-04-22 Merck & Co., Inc. Selective hydrogenation products of C-076 compounds and derivatives thereof
US4235892A (en) * 1979-02-05 1980-11-25 Schering Corporation, Patent Dept. 1-Aryl-2-acylamido-3-fluoro-1-propanols, methods for their use as antibacterial agents and compositions useful therefor
ES488154A0 (es) * 1979-02-05 1981-04-16 Schering Corp Un procedimiento para la preparacion de un compuesto d-(treo-1-aril-2-acilamido-3-fluor-1-propanol
US4361557A (en) * 1980-01-28 1982-11-30 Schering Corporation 1-Aryl-2-acylamido-3-fluoro-1-propanol acylates, methods for their use as anti-bacterial agents and compositions useful therefor
US4820695A (en) * 1982-09-13 1989-04-11 Eli Lilly And Company C-20-dihydro-deoxy-(cyclic amino)-derivatives of macrolide antibiotics
JPS59112913A (ja) * 1982-12-20 1984-06-29 Takeda Chem Ind Ltd 水産用薬剤
US5105009A (en) * 1983-06-02 1992-04-14 Zambon S.P.A. Intermediates for the preparation of 1-(phenyl)-1-hydroxy-2-amino-3-fluoropropane derivatives
IT1173213B (it) * 1984-02-03 1987-06-18 Zambon Spa Procedimento per fluorurare alcuni derivati dall'1l-fenil-2-ammino-1,3-propandiolo e loro intermedi
US5243056A (en) * 1983-06-02 1993-09-07 Zambon S.P.A. Intermediates for the preparation of 1-(phenyl)-1-hydroxy-2-amino-3-fluoro propane derivatives
US5153328A (en) * 1984-02-03 1992-10-06 Zambon S.P.A. 2 Hydrocarbyl-4 substituted methyl 5 (4 substituted phenyl)-oxazolines
US5332835A (en) * 1984-02-03 1994-07-26 Zambon S.P.A. Process for fluorinating 1-phenyl-2-amino-1,3-propanediol compounds and new oxazoline compounds useful in this process
US4582918A (en) * 1984-09-19 1986-04-15 Schering Corporation Preparation of intermediates for (threo)-1-aryl-2-acylamido-3-fluoro-1-propanols
US4973750A (en) * 1984-09-19 1990-11-27 Schering Corporation Preparation of (threo)-1-aryl-2-acylamido-3-fluoro-1-propanols
ES8800986A1 (es) * 1985-07-27 1987-12-01 Pfizer Un procedimiento para la produccion de un nuevo derivado de avermectina
US4916154A (en) * 1986-09-12 1990-04-10 American Cyanamid Company 23-Imino derivatives of LL-F28249 compounds
IT1198238B (it) * 1986-12-23 1988-12-21 Zambon Spa Composti ad attivita' antibiotica
US4876352A (en) * 1988-09-14 1989-10-24 Schering Corporation Pressurized fluorination of hydroxy alkyl groups
US5227494A (en) * 1988-09-14 1993-07-13 Schering Corporation Process for preparing oxazoline compounds
IL98599A (en) * 1990-06-28 1995-06-29 Merck & Co Inc Stable salts of 4"-deoxy-4"-epi-methylamino avermectin b1a/b1b and insecticidal compositions containing them
US5082863A (en) * 1990-08-29 1992-01-21 Schering Corporation Pharmaceutical composition of florfenicol
WO1992007824A1 (en) * 1990-10-25 1992-05-14 Schering Corporation Process for preparing florfenicol, its analogs and oxazoline intermediates thereto
US5352832A (en) * 1992-12-18 1994-10-04 Schering Corporation Asymmetric process for preparing florfenicol, thiamphenicol chloramphenicol and oxazoline intermediates
US5399717A (en) * 1993-09-29 1995-03-21 Merck & Co., Inc. Glycosidation route to 4"-epi-methylamino-4"-deoxyavermectin B1
US5789599A (en) * 1994-05-06 1998-08-04 Drexel University Aziridine compounds, methods of preparation and reactions thereof
DE4437932A1 (de) * 1994-10-24 1996-04-25 Bayer Ag Verfahren zur Herstellung von in einer Seitenkette fluorierten Alkyloxazolen und neue, in einer Seitenkette fluorierte Alkyloxazole
US5958888A (en) * 1996-07-02 1999-09-28 Merial, Inc. Water miscible macrolide solutions
US6271255B1 (en) * 1996-07-05 2001-08-07 Biotica Technology Limited Erythromycins and process for their preparation
US5663361A (en) * 1996-08-19 1997-09-02 Schering Corporation Process for preparing intermediates to florfenicol
JP2003512290A (ja) * 1997-09-10 2003-04-02 メルク エンド カムパニー インコーポレーテッド 家畜抗菌剤としての8a−アザライド
US6339063B1 (en) * 1997-09-10 2002-01-15 Merck & Co., Inc. 9a-azalides as veterinary antimicrobial agents
AP9801420A0 (en) * 1998-01-02 1998-12-31 Pfizer Prod Inc Novel macrolides.
US6239112B1 (en) * 1998-07-09 2001-05-29 Merial, Inc. Water miscible macrolide solutions
CA2292359C (en) * 1999-01-28 2004-09-28 Pfizer Products Inc. Novel azalides and methods of making same
US6864240B1 (en) * 1999-06-15 2005-03-08 Elan Pharmaceuticals, Inc. Dipeptide inhibitors of β-secretase
US6514492B1 (en) 1999-07-14 2003-02-04 Schering-Plough Veterinary Corporation Taste masking of oral quinolone liquid preparations using ion exchange resins
CA2398485C (en) * 2000-01-27 2008-01-29 Pfizer Products Inc. Azalide antibiotic compositions
CN1297564C (zh) * 2001-04-27 2007-01-31 辉瑞产品公司 4″-取代-9-脱氧-9a-氮杂-9a-高红霉素A衍生物的制备方法
JP2003108949A (ja) * 2001-09-28 2003-04-11 Rohm Co Ltd 認証システム及び半導体装置
MXPA04008677A (es) * 2002-03-08 2004-12-06 Schering Plough Ltd Antibioticos novedosos del tipo florfenicol.
US6790867B2 (en) * 2002-05-20 2004-09-14 Schering-Plough Animal Health Corporation Compositions and method for treating infection in cattle and swine
US7439268B2 (en) * 2003-07-18 2008-10-21 Idexx Laboratories Compositions containing prodrugs of florfenicol and methods of use
NZ547592A (en) * 2003-12-23 2009-07-31 Schering Plough Ltd Florfenicol prodrug having improved water solubility
KR20060110344A (ko) * 2003-12-31 2006-10-24 쉐링-프라우 리미티드 이미다조[1,2-b]피리다진 유도체를 사용하여 동물에서기생충을 방제하는 방법
WO2005066119A2 (en) * 2003-12-31 2005-07-21 Schering-Plough Ltd. Antibacterial 1-(4-mono-and di-halomethylsulphonylphenyl)-2-acylamino-3-fluoropropanols and preparation thereof
PE20060693A1 (es) * 2004-09-23 2006-09-01 Schering Plough Ltd Nuevos derivados de trifluorometansulfonanilida oxamida eter
ATE446677T1 (de) * 2004-11-19 2009-11-15 Schering Plough Ltd Kontrolle von parasiten bei tieren mittels verwendung von parasitiziden 2-phenyl-3-(1h- pyrrol-2-yl) acrylonitril-derivaten
AR054380A1 (es) * 2005-06-09 2007-06-20 Schering Plough Ltd Control de parasitos en animales con derivados de n- ((feniloxi) fenil) -1,1,1-trifluorometansulfonamida y de n-(fenilsulfanil) fenil) -1,1,1-trifluorometansulfonamida
US8119667B2 (en) * 2005-12-29 2012-02-21 Schering-Plough Animal Health Corporation Carbonates of fenicol antibiotics
US20070238700A1 (en) 2006-04-10 2007-10-11 Winzenberg Kevin N N-phenyl-1,1,1-trifluoromethanesulfonamide hydrazone derivative compounds and their usage in controlling parasites
SE532251C2 (sv) 2006-11-28 2009-11-24 Theravac Pharmaceuticals Ab Nya formuleringar av TSLP för behandling av TH2-medierade inflammatoriska sjukdomar genom vaccinering
CA2672598A1 (en) 2006-12-13 2008-06-26 Schering-Plough Ltd. Water-soluble phenicol prodrugs in a lipophilic vehicle system
US20080153906A1 (en) * 2006-12-13 2008-06-26 Celly Chander S Water-Soluble Phenicol Prodrugs in a Lipophilic Vehicle System
WO2008076256A1 (en) 2006-12-13 2008-06-26 Schering-Plough Ltd. Water-soluble prodrugs of chloramphenicol, thiamphenicol, and analogs thereof

Also Published As

Publication number Publication date
US20080188556A1 (en) 2008-08-07
US8084643B2 (en) 2011-12-27
CA2672586A1 (en) 2008-06-26
EP2091909A1 (en) 2009-08-26
WO2008076259A1 (en) 2008-06-26
CN101605756A (zh) 2009-12-16

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