Claims
- 1. Compounds represented by the formula ##STR39## and pharmaceutically acceptable salts and esters thereof in racemic or optically active forms wherein
- n is 1, 2 or 3; m is 1, 2 or 3;
- Z represents --COOH, --SO.sub.3 H, ##STR40## or alkali metal salts thereof; R, R.sub.1, R.sub.2 and R.sub.3 independently represent hydrogen, lower alkyl, hydroxy lower alkyl, amino lower alkyl, carboxy lower alkyl, thio lower alkyl, lower alkoxy lower alkyl, carbonylamino lower alkyl, aminocarbonyl lower alkyl, cyano lower alkyl, fluoro lower alkyl, carbamoyloxy lower alkyl, or sulfamoyloxy with the proviso that when m is 2 or 3, R, R.sub.1, R.sub.2 and R.sub.3 independently additionally represent hydroxy, amino, cyano, fluoro, carbamoyloxy, carbonylamino or --SO.sub.3 H;
- each X independently represents --CH--, --N--, --S-- or --O-- with the proviso that at least one X is --N--.
- 2. Compounds of claim 1 wherein n is 1 or 2, m is 1, R, R.sub.1, R.sub.2 and R.sub.3 are independently hydrogen or lower alkyl; Z is --SO.sub.3 H or --COOH and two non-adjacent X's are --N--.
- 3. Compounds of claim 1 wherein n is 1, m is 1, R.sub.1 and R.sub.3 ore each hydrogen, R and R.sub.2 are independently hydrogen or lower alkyl, Z is --SO.sub.3 H and the heterocyclic ring is 2-imidazole.
- 4. A compound of claim 1 which is 5R,6S,8R-2-(1-carboxymethyl-4-imidazolylmethylthio)-6-(1-hydroxyethyl)penem-3-carboxylic acid.
- 5. A compound of claim 1 which is 5R,6S,8R-2-(carboxymethyl-5-imidazolylmethylthio)-6-(1-hydroxyethyl)penem carboxylic acid.
- 6. A compound of claim 1 which is 5R,6S,8R-2-(4-sulfonic acid methyl-5-imidazolylmethylthio)-6-(1-hydroxymethyl)penem-3-carboxylic acid.
- 7. A pharmaceutical composition comprising an antibacterial effective amount of a compound of claim 1 in admixture with a pharmaceutically acceptable carrier therefor.
- 8. A composition according to claim 7 wherein said antibacterial compound is 5R,6S,8R-2-(1-carboxymethyl-4-imidazoyl-methylthio)-6-(1-hydroxyethyl)penem-3-carboxylic acid.
- 9. A composition according to claim 7 wherein said antibacterial compound is 5R,6S,8R-2-(carboxymethyl-5-imidazolylmethylthio)-6-(1-hydroxyethyl)penem carboxylic acid.
- 10. A composition according to claim 7 wherein said antibacterial compound is 5R,6S,8R-2-(4-sulfonic acid methyl-5-imidazolylmethylthio)-6-(1-hydroxymethyl)-penem-3-carboxylic acid.
- 11. A method of preventing bacterial infections in warm blooded animals in need of such treatment which comprises administering an antibacterial effective amount of a compound of claim 1.
- 12. The method of claim 11 wherein the compound administered is 5R,6S,8R-2-(1-carboxymethyl-4-imidazolylmethylthio)-6-(1-hydroxymethyl)penem-3-carboxylic acid.
- 13. The method of claim 11 wherein the compound administered is bacterial compound is 5R,6S,8R-2-(carboxymethyl-5-imidazolylmethylthio)-6-(1-hydroxyethyl)penem carboxylic acid.
- 14. The method of claim 11 wherein the compound administered is 5R,6S,8R-2-(4-sulfonic acid methyl-5-imidazolylmethylthio)-6-hydroxymethyl)penem-3-carboxylic acid.
RELATED APPLICATIONS
This application is a continuation-in-part of U.S. patent application Ser. No. 555,738, filed Nov. 28, 1983, now abandoned.
US Referenced Citations (2)
Number |
Name |
Date |
Kind |
4260618 |
Christensen et al. |
Apr 1981 |
|
4431654 |
Girijavallabhan |
Feb 1984 |
|
Foreign Referenced Citations (1)
Number |
Date |
Country |
2013674A |
Aug 1979 |
GBX |
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
555738 |
Nov 1983 |
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