TW200621778A - 1β-methyl carbapenem derivatives - Google Patents
1β-methyl carbapenem derivativesInfo
- Publication number
- TW200621778A TW200621778A TW094138190A TW94138190A TW200621778A TW 200621778 A TW200621778 A TW 200621778A TW 094138190 A TW094138190 A TW 094138190A TW 94138190 A TW94138190 A TW 94138190A TW 200621778 A TW200621778 A TW 200621778A
- Authority
- TW
- Taiwan
- Prior art keywords
- group
- optionally substituted
- carbapenern
- infectious disease
- carbapenem derivatives
- 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
- A61P31/04—Antibacterial agents
-
- 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
Abstract
The present invention provides a carbapenern derivative having the prophylactic or therapeutic effect for the bacterial infectious disease, especially for infectious disease of the respiratory system. A carbapenern comound of the following formula (I), ?wherein, A represents an optionally substituted C1-6 alkyl group, an optionally substituted C2-4alkenyl group, a C3-6 cycloalkyl group, an optionally substituted 4-6 membered heterocylic group, a mono-substituted amino group or di-substituted amino group, n represents 1 or 2, X represents an oxygen atom or an sulfur atom?, the pharmaceutically acceptable salt or ester derivative thereof.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004319228 | 2004-11-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
TW200621778A true TW200621778A (en) | 2006-07-01 |
Family
ID=36319154
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW094138190A TW200621778A (en) | 2004-11-02 | 2005-11-01 | 1β-methyl carbapenem derivatives |
Country Status (2)
Country | Link |
---|---|
TW (1) | TW200621778A (en) |
WO (1) | WO2006049148A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112513043A (en) * | 2018-05-30 | 2021-03-16 | 维纳拓尔斯制药公司 | Broad spectrum carbapenems |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH023687A (en) * | 1988-06-22 | 1990-01-09 | Sankyo Co Ltd | 1-methylcarbapenem derivative |
JP3242677B2 (en) * | 1990-08-10 | 2001-12-25 | 住友製薬株式会社 | Novel β-lactam compound and method for producing the same |
JP2004043438A (en) * | 2002-05-15 | 2004-02-12 | Sankyo Co Ltd | Medicine containing 1-methylcarbapenem derivative |
-
2005
- 2005-11-01 TW TW094138190A patent/TW200621778A/en unknown
- 2005-11-01 WO PCT/JP2005/020069 patent/WO2006049148A1/en not_active Application Discontinuation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112513043A (en) * | 2018-05-30 | 2021-03-16 | 维纳拓尔斯制药公司 | Broad spectrum carbapenems |
Also Published As
Publication number | Publication date |
---|---|
WO2006049148A1 (en) | 2006-05-11 |
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