SE7612960L - TIENAMYCIN DERIVATIVES - Google Patents
TIENAMYCIN DERIVATIVESInfo
- Publication number
- SE7612960L SE7612960L SE7612960A SE7612960A SE7612960L SE 7612960 L SE7612960 L SE 7612960L SE 7612960 A SE7612960 A SE 7612960A SE 7612960 A SE7612960 A SE 7612960A SE 7612960 L SE7612960 L SE 7612960L
- Authority
- SE
- Sweden
- Prior art keywords
- hydrogen
- pharmaceutically acceptable
- acceptable salts
- acyl
- 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
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
Abstract
N-Acyl derivatives and phosphorus-containing N-acyl derivatives of the antibiotic thienamycin of the general formula (II) <IMAGE> in which R<1> and R<2>, independently of each other, are selected from hydrogen, acyl and phosphorus-containing acyl, with the proviso that R<1> and R<2> are not both hydrogen and that, when R<1> or R<2> denotes acetyl, R<2> or R<1> is different from hydrogen and their non-toxic, pharmaceutically acceptable salts, are obtained by treating thienamycin with an appropriate acylating agent and converting the resulting compounds of the formula (II), where appropriate, into their non-toxic, pharmaceutically acceptable salts. The compounds which are obtained, and their pharmaceutically acceptable salts, are suitable for use as antibiotics.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US63429175A | 1975-11-21 | 1975-11-21 |
Publications (2)
Publication Number | Publication Date |
---|---|
SE7612960L true SE7612960L (en) | 1977-05-22 |
SE427840B SE427840B (en) | 1983-05-09 |
Family
ID=24543192
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7612960A SE427840B (en) | 1975-11-21 | 1976-11-19 | ANALOGY PROCEDURE FOR THE PREPARATION OF TIENAMYCIN DERIVATIVES |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS5277083A (en) |
CH (1) | CH632509A5 (en) |
DE (1) | DE2652675A1 (en) |
DK (1) | DK523276A (en) |
FR (1) | FR2332016A1 (en) |
GB (1) | GB1570986A (en) |
NL (1) | NL189298C (en) |
SE (1) | SE427840B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0008888B1 (en) * | 1978-08-23 | 1983-09-21 | Beecham Group Plc | Beta-lactam antibacterial compounds, their preparation and pharmaceutical compositions containing them |
DK456580A (en) * | 1979-10-29 | 1981-06-04 | Beecham Group Ltd | PROCEDURE FOR PREPARING BICYCLIC BETA-LACTAMRING COMPOUNDS |
EP0044142A1 (en) * | 1980-07-03 | 1982-01-20 | Beecham Group Plc | Process for the preparation of beta-lactam antibiotics |
WO2017132321A1 (en) * | 2016-01-29 | 2017-08-03 | The Johns Hopkins University | Novel inhibitors of bacterial growth |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1004670A (en) * | 1963-04-23 | 1965-09-15 | Beecham Res Lab | Penicillins |
GB1348985A (en) * | 1970-06-16 | 1974-03-27 | Merck & Co Inc | Esters of cephalosporin compounds |
-
1976
- 1976-11-19 GB GB48236/76A patent/GB1570986A/en not_active Expired
- 1976-11-19 DK DK523276A patent/DK523276A/en not_active Application Discontinuation
- 1976-11-19 SE SE7612960A patent/SE427840B/en not_active IP Right Cessation
- 1976-11-19 NL NLAANVRAGE7612940,A patent/NL189298C/en not_active IP Right Cessation
- 1976-11-19 DE DE19762652675 patent/DE2652675A1/en active Granted
- 1976-11-19 FR FR7634886A patent/FR2332016A1/en active Granted
- 1976-11-19 CH CH1462276A patent/CH632509A5/en not_active IP Right Cessation
- 1976-11-22 JP JP51139650A patent/JPS5277083A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
FR2332016B1 (en) | 1978-11-10 |
NL7612940A (en) | 1977-05-24 |
GB1570986A (en) | 1980-07-09 |
SE427840B (en) | 1983-05-09 |
JPS5277083A (en) | 1977-06-29 |
CH632509A5 (en) | 1982-10-15 |
DE2652675C2 (en) | 1990-02-01 |
FR2332016A1 (en) | 1977-06-17 |
DE2652675A1 (en) | 1977-06-02 |
JPS61346B2 (en) | 1986-01-08 |
NL189298B (en) | 1992-10-01 |
DK523276A (en) | 1977-05-22 |
NL189298C (en) | 1993-03-01 |
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