MXPA05012895A - Profarmaco inhibidor de beta-lactamasa. - Google Patents
Profarmaco inhibidor de beta-lactamasa.Info
- Publication number
- MXPA05012895A MXPA05012895A MXPA05012895A MXPA05012895A MXPA05012895A MX PA05012895 A MXPA05012895 A MX PA05012895A MX PA05012895 A MXPA05012895 A MX PA05012895A MX PA05012895 A MXPA05012895 A MX PA05012895A MX PA05012895 A MXPA05012895 A MX PA05012895A
- Authority
- MX
- Mexico
- Prior art keywords
- beta
- disclosed
- mammal
- present
- lactam antibiotic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic 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
- C07D499/86—Heterocyclic 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
- C07D499/861—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic 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
- C07D309/08—Heterocyclic 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
- C07D309/10—Oxygen atoms
- C07D309/12—Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/12—1,4-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-??-hidroximetilpenicilanico que tienen la estructura (ver 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.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47645603P | 2003-06-05 | 2003-06-05 | |
US49842203P | 2003-08-27 | 2003-08-27 | |
PCT/IB2004/001824 WO2004108733A1 (en) | 2003-06-05 | 2004-05-24 | Beta-lactamase inhibitor prodrug |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA05012895A true MXPA05012895A (es) | 2006-02-22 |
Family
ID=33514083
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MXPA05012895A MXPA05012895A (es) | 2003-06-05 | 2004-05-24 | 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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PA8579701A1 (es) * | 2002-08-23 | 2005-05-24 | Pfizer Prod Inc | Profarmaco inhibidor de beta-lactamasa |
EP1551558A1 (de) | 2002-10-14 | 2005-07-13 | H. Börger & Co. GmbH | Verfahren und vorrichtung zum fürdern von pulverfürmigem material |
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)
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 |
US4540689A (en) * | 1981-09-22 | 1985-09-10 | Kureha Kagaku Kogyo Kabushiki Kaisha | 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 |
US5703068A (en) * | 1990-08-20 | 1997-12-30 | Suntory Limited | Penem compounds |
GB9208492D0 (en) * | 1992-04-16 | 1992-06-03 | Glaxo Spa | Heterocyclic compounds |
JP3866298B2 (ja) * | 1997-12-29 | 2007-01-10 | リサーチ コーポレイション テクノロジーズ,インコーポレイティド | β−ラクタマーゼインヒビターとしての2β−置換化−6−アルキリデンペニシラン酸誘導体 |
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 |
-
2004
- 2004-05-24 BR BRPI0410936-8A patent/BRPI0410936A/pt not_active IP Right Cessation
- 2004-05-24 MX MXPA05012895A patent/MXPA05012895A/es not_active Application Discontinuation
- 2004-05-24 CA CA002528065A patent/CA2528065A1/en not_active Abandoned
- 2004-05-24 JP JP2006508430A patent/JP2006526612A/ja active Pending
- 2004-05-24 EP EP04734576A patent/EP1636240A1/en not_active Withdrawn
- 2004-05-24 WO PCT/IB2004/001824 patent/WO2004108733A1/en not_active Application Discontinuation
- 2004-06-01 CL CL200401343A patent/CL2004001343A1/es unknown
- 2004-06-02 UY UY28340A patent/UY28340A1/es not_active Application Discontinuation
- 2004-06-02 PE PE2004000557A patent/PE20050629A1/es not_active Application Discontinuation
- 2004-06-02 PA PA20048604001A patent/PA8604001A1/es unknown
- 2004-06-03 AR ARP040101928A patent/AR044482A1/es unknown
- 2004-06-04 TW TW093116149A patent/TW200504010A/zh unknown
- 2004-06-04 NL NL1026340A patent/NL1026340C2/nl not_active IP Right Cessation
- 2004-06-07 US US10/862,200 patent/US20050004093A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2004108733A1 (en) | 2004-12-16 |
UY28340A1 (es) | 2005-01-31 |
NL1026340C2 (nl) | 2005-09-14 |
PE20050629A1 (es) | 2005-08-25 |
PA8604001A1 (es) | 2004-12-16 |
AR044482A1 (es) | 2005-09-14 |
US20050004093A1 (en) | 2005-01-06 |
TW200504010A (en) | 2005-02-01 |
EP1636240A1 (en) | 2006-03-22 |
BRPI0410936A (pt) | 2006-06-27 |
JP2006526612A (ja) | 2006-11-24 |
CA2528065A1 (en) | 2004-12-16 |
CL2004001343A1 (es) | 2005-04-22 |
NL1026340A1 (nl) | 2004-12-07 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |