CO5261620A1 - CARBAPENEM COMPOUNDS, USE OF THE SAME AND INTERMEDIATE COMPOUNDS FOR THE SAME - Google Patents
CARBAPENEM COMPOUNDS, USE OF THE SAME AND INTERMEDIATE COMPOUNDS FOR THE SAMEInfo
- Publication number
- CO5261620A1 CO5261620A1 CO00091283A CO00091283A CO5261620A1 CO 5261620 A1 CO5261620 A1 CO 5261620A1 CO 00091283 A CO00091283 A CO 00091283A CO 00091283 A CO00091283 A CO 00091283A CO 5261620 A1 CO5261620 A1 CO 5261620A1
- Authority
- CO
- Colombia
- Prior art keywords
- same
- compounds
- formula
- optionally substituted
- lower alkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
- C07D477/10—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and with 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
- C07D477/12—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and with 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 hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6
- C07D477/16—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and with 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 hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6 with hetero atoms or carbon atoms 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 3
- C07D477/20—Sulfur atoms
-
- 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
-
- 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
Abstract
Un compuesto de carbapenem de la fórmula (I)<EMI FILE="00091283_1" ID="1" IMF=JPEG >en donde R1 es un grupo acilo de un a-aminoácido en donde el amino está opcionalmente sustituido por alquilo inferior, R2 es un átomo de hidrógeno o un alquilo inferior, R3 es un fenilo opcionalmente sustituido, o una sal del mismo farmacéuticamente aceptable. Un agente antibacteriano que comprende el compuesto de carbapenem de la reivindicación 1, el cual es representado por la fórmula (I), o una sal farmacéuticamente aceptable del mismo como ingrediente activo. Un compuesto de carbapenem de la fórmula (ll)<EMI FILE="00091283_2" ID="2" IMF=JPEG >en donde R2 es un átomo de hidrógeno u un alquilo inferior, yR3 es un fenilo opcionalmente sustituido, o una sal del mismo.A carbapenem compound of the formula (I) <EMI FILE = "00091283_1" ID = "1" IMF = JPEG> wherein R1 is an acyl group of an amino acid wherein the amino is optionally substituted by lower alkyl, R2 it is a hydrogen atom or a lower alkyl, R3 is an optionally substituted phenyl, or a pharmaceutically acceptable salt thereof. An antibacterial agent comprising the carbapenem compound of claim 1, which is represented by formula (I), or a pharmaceutically acceptable salt thereof as an active ingredient. A carbapenem compound of the formula (ll) <EMI FILE = "00091283_2" ID = "2" IMF = JPEG> wherein R2 is a hydrogen atom or a lower alkyl, and R3 is an optionally substituted phenyl, or a salt of the same.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34553599 | 1999-12-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO5261620A1 true CO5261620A1 (en) | 2003-03-31 |
Family
ID=18377257
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO00091283A CO5261620A1 (en) | 1999-12-03 | 2000-11-29 | CARBAPENEM COMPOUNDS, USE OF THE SAME AND INTERMEDIATE COMPOUNDS FOR THE SAME |
Country Status (4)
Country | Link |
---|---|
AR (1) | AR026682A1 (en) |
AU (1) | AU1419501A (en) |
CO (1) | CO5261620A1 (en) |
WO (1) | WO2001040228A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114716487B (en) * | 2022-02-24 | 2024-03-08 | 四川农业大学 | Furanodiester compound and preparation method and application thereof |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3965099A (en) * | 1974-06-26 | 1976-06-22 | Smithkline Corporation | Cephalosporin esters with antibacterial activity |
US4503040A (en) * | 1984-02-27 | 1985-03-05 | Pfizer Inc. | 6-(Aminoacyloxymethyl)penicillanic acid 1,1-dioxides as beta-lactamase inhibitors |
JP2847693B2 (en) * | 1992-06-18 | 1999-01-20 | 田辺製薬株式会社 | Removal method of carboxyl group protecting group |
JPH06298769A (en) * | 1993-04-13 | 1994-10-25 | Fujisawa Pharmaceut Co Ltd | Ampicillin phenyl ester and its salt |
JP2000239275A (en) * | 1998-12-25 | 2000-09-05 | Sankyo Co Ltd | Carbapenem ester derivative |
-
2000
- 2000-11-21 AU AU14195/01A patent/AU1419501A/en not_active Abandoned
- 2000-11-21 WO PCT/JP2000/008223 patent/WO2001040228A1/en active Application Filing
- 2000-11-29 CO CO00091283A patent/CO5261620A1/en not_active Application Discontinuation
- 2000-12-01 AR ARP000106344A patent/AR026682A1/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
AU1419501A (en) | 2001-06-12 |
AR026682A1 (en) | 2003-02-19 |
WO2001040228A1 (en) | 2001-06-07 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Application refused |