PA8604001A1 - Profarmaco inhibidor de beta-lactamasa - Google Patents

Profarmaco inhibidor de beta-lactamasa

Info

Publication number
PA8604001A1
PA8604001A1 PA20048604001A PA8604001A PA8604001A1 PA 8604001 A1 PA8604001 A1 PA 8604001A1 PA 20048604001 A PA20048604001 A PA 20048604001A PA 8604001 A PA8604001 A PA 8604001A PA 8604001 A1 PA8604001 A1 PA 8604001A1
Authority
PA
Panama
Prior art keywords
beta
lactama
antibiotic
same
mammer
Prior art date
Application number
PA20048604001A
Other languages
English (en)
Inventor
Dale Gordon Mcleod
Donnell John Paul O
Anthony Marfat
Original Assignee
Pfizer Prod Inc
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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of PA8604001A1 publication Critical patent/PA8604001A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D499/00Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D499/86Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with only atoms other than nitrogen atoms directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
    • C07D499/861Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with only atoms other than nitrogen atoms directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2 with a hydrocarbon radical or a substituted hydrocarbon radical, directly attached in position 6
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/10Oxygen atoms
    • C07D309/12Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/101,4-Dioxanes; Hydrogenated 1,4-dioxanes
    • C07D319/121,4-Dioxanes; Hydrogenated 1,4-dioxanes not condensed with other rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

SE DAN A CONOCER PROFARMACOS DE SULFONA DEL ACIDO 6-ß-HIDROXIMETILPENICILANICO QUE TIENE LA ESTRUCTURA EN LA QUE R ES H O METILO, CADA X ES METILENO, E Y ES O, O EN LA QUE R ES H, CADA X ES O E Y ES METILENO, Y SOLVATOS DE LOS MISMOS. SE DAN A CONOCER TAMBIEN COMPOSICIONES FARMACEUTICAS QUE COMPRENDEN UN PROFARMACO DE LA PRESENTE INVENCION, O UN SOLVATO DEL MISMO, UN ANTIBIOTICO BETA-LACTAMA OPCIONAL Y AL MENOS UN VEHICULO FARMACEUTICAMENTE ACEPTABLE. SE DA A CONOCER ADEMAS UN PROCEDIMIENTO PARA AUMENTAR LA EFICACIA TERAPEUTICA DE UN ANTIBIOTICO BETA-LACTAMA EN UN MAMIFERO MEDIANTE LA ADMINISTRACION DE UNA CANTIDAD EFICAZ DE UN ANTIBIOTICO BETA-LACTAMA Y UNA CANTIDAD QUE AUMENTA LA EFICACIA DE UN PROFARMACO DE LA PRESENTE INVENCION, O UN SOLVATO DEL MISMO. SE DA A CONOCER ADICIONALMENTE UN PROCEDIMIENTO PARA TRATAR UNA INFECCION BACTERIANA EN UN MAMIFERO MEDIANTE LA ADMINISTRACION DE UNA CANTIDAD TERAPEUTICAMENTE EFICAZ DE UNA COMPOSICION FARMACEUTICA DE LA PRESENTE INVENCION A UN MAMIFERO NECESITADO DE ELLO.
PA20048604001A 2003-06-05 2004-06-02 Profarmaco inhibidor de beta-lactamasa PA8604001A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US47645603P 2003-06-05 2003-06-05
US49842203P 2003-08-27 2003-08-27

Publications (1)

Publication Number Publication Date
PA8604001A1 true PA8604001A1 (es) 2004-12-16

Family

ID=33514083

Family Applications (1)

Application Number Title Priority Date Filing Date
PA20048604001A PA8604001A1 (es) 2003-06-05 2004-06-02 Profarmaco inhibidor de beta-lactamasa

Country Status (14)

Country Link
US (1) US20050004093A1 (es)
EP (1) EP1636240A1 (es)
JP (1) JP2006526612A (es)
AR (1) AR044482A1 (es)
BR (1) BRPI0410936A (es)
CA (1) CA2528065A1 (es)
CL (1) CL2004001343A1 (es)
MX (1) MXPA05012895A (es)
NL (1) NL1026340C2 (es)
PA (1) PA8604001A1 (es)
PE (1) PE20050629A1 (es)
TW (1) TW200504010A (es)
UY (1) UY28340A1 (es)
WO (1) WO2004108733A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE20321762U1 (de) 1988-05-11 2009-08-27 H. Börger & Co. GmbH Vorrichtung zum Fördern von pulverförmigem Material
PA8579701A1 (es) * 2002-08-23 2005-05-24 Pfizer Prod Inc Profarmaco inhibidor de beta-lactamasa
GB201407506D0 (en) 2014-04-29 2014-06-11 Glaxosmithkline Ip Dev Ltd Novel compound
US9737505B2 (en) 2014-04-29 2017-08-22 Glaxosmithkline Intellectual Property Development Limited Prodrug of 1,1′-(1,6-dioxo-1,6-hexanediyl)bis-D-proline

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE34011B1 (en) * 1969-03-13 1975-01-08 Leo Pharm Prod Ltd New penicillin esters
IE34019B1 (en) * 1969-03-18 1975-01-08 Leo Pharm Prod Ltd New semi-synthetic penicillin esters
US3957764A (en) * 1969-11-11 1976-05-18 Lovens Kemiske Fabrik Produktionsaktieselskab 6-aminopenicillanic acid derivatives
US3862181A (en) * 1970-10-28 1975-01-21 Squibb & Sons Inc Process for preparing cephalosporins
US4397783A (en) * 1979-03-05 1983-08-09 Pfizer Inc. Process for converting 6,6-disubstituted penicillanic acid derivatives to the 6-β-congeners
US4287181A (en) * 1979-10-22 1981-09-01 Pfizer Inc. Derivatives of 6β-hydroxyalkylpenicillanic acids as β-lactamase inhibitors
US4432970A (en) * 1979-11-23 1984-02-21 Pfizer Inc. 6-beta-Halopenicillanic acid 1,1-dioxides as beta-lactamase inhibitors
GB2076812A (en) * 1980-05-22 1981-12-09 Ciba Geigy Ag Penam-dioxide compounds, processes for their manufacture, and their use
AU559689B2 (en) * 1981-09-22 1987-03-19 Kureha Kagaku Kogyo K.K. Penicillin derivative
US4406887A (en) * 1981-10-13 1983-09-27 Bristol-Myers Company Method for treating resistant bacteria including anaerobes
US4377590A (en) * 1982-05-10 1983-03-22 Pfizer Inc. Derivatives of ampicillin and amoxicillin with beta-lactamase inhibitors
US4428935A (en) * 1982-05-24 1984-01-31 Pfizer Inc. Penicillanic acid dioxide prodrug
US4826833A (en) * 1984-01-30 1989-05-02 Pfizer Inc. 6-(Substituted)methylene-penicillanic and 6-(substituted)hydroxymethylpenicillanic acids and derivatives thereof
US4521533A (en) * 1984-07-12 1985-06-04 Pfizer Inc. Salts of 6-alpha-(aminomethyl)penicillanic acid 1,1-dioxide esters and beta-lactam antibiotics
US4762921A (en) * 1985-04-18 1988-08-09 Pfizer Inc. 6-(1-acyl-1-hydroxymethyl)penicillanic acid derivatives
US5200403A (en) * 1987-07-10 1993-04-06 Farmitalia Carlo Erba S.R.L. Inhibition of βlactamase with 6 β-(substituted methyl)-penicillanic acid derivatives
JPH03206038A (ja) * 1990-01-08 1991-09-09 Yoshitomi Pharmaceut Ind Ltd 抗菌剤
GB9001405D0 (en) * 1990-01-22 1990-03-21 Leo Pharm Prod Ltd New intermediates,their production and use
EP0544906B1 (en) * 1990-08-20 1999-11-10 Suntory Limited Antibacterial penem esters derivatives
GB9208492D0 (en) * 1992-04-16 1992-06-03 Glaxo Spa Heterocyclic compounds
WO1999033838A1 (en) * 1997-12-29 1999-07-08 Research Corporation Technologies, Inc. 2-β-SUBSTITUTED-6-ALKYLIDENE PENICILLANIC ACID DERIVATIVES AS β-LACTAMASE INHIBITORS
ATE288438T1 (de) * 1999-03-03 2005-02-15 Astur Pharma Sa Verfahren zur herstellung von dioxopenicillansäurederivaten
PA8579701A1 (es) * 2002-08-23 2005-05-24 Pfizer Prod Inc Profarmaco inhibidor de beta-lactamasa

Also Published As

Publication number Publication date
AR044482A1 (es) 2005-09-14
TW200504010A (en) 2005-02-01
EP1636240A1 (en) 2006-03-22
MXPA05012895A (es) 2006-02-22
PE20050629A1 (es) 2005-08-25
WO2004108733A1 (en) 2004-12-16
UY28340A1 (es) 2005-01-31
BRPI0410936A (pt) 2006-06-27
US20050004093A1 (en) 2005-01-06
NL1026340C2 (nl) 2005-09-14
CL2004001343A1 (es) 2005-04-22
CA2528065A1 (en) 2004-12-16
NL1026340A1 (nl) 2004-12-07
JP2006526612A (ja) 2006-11-24

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