Studies on .BETA.-lactam antibiotics. VI. Effect on antibacterial activity of .ALPHA.-substituents in the 2-(2-amino-4-thiazolyl)acetyl side chain of a cephalosporin nucleus.
- 1 January 1983
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 36 (1) , 36-41
- https://doi.org/10.7164/antibiotics.36.36
Abstract
Synthesis and in vitro antibacterial [gram negative bacteria, enterobacteria, Staphylococcus aureus] activity of semisynthetic cephalosporins having an .alpha.-substituted 2-(2-amino-4-thiazolyl)acetyl side chain at the 7-position were described.This publication has 4 references indexed in Scilit:
- Studies on .BETA.-lactam antibiotics. III Synthesis and enzymatic stability of 3-acyloxymethyl-7.BETA.-((z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetamido)-3-cephem-4-carboxylic acids.The Journal of Antibiotics, 1981
- Studies on .BETA.-lactam antibiotics. II Synthesis and structure-activity relationships of .ALPHA.-hydroxyiminoarylacetyl cephalosporins.The Journal of Antibiotics, 1981
- Synthesis and structure-activity relationships of 7.BETA.-[2-(2-aminothiazol-4-yl)acetamido]-cephalosporin derivatives. III. Synthesis and antibacterial activity of 7.BETA.-[2-amino-2-(2-aminothiazol-4-yl)acetamido]cephalosporins.The Journal of Antibiotics, 1980
- Nocardicin a, a new monocyclic .BETA.-lactam antibiotic. I. Discovery, isolation and characterization.The Journal of Antibiotics, 1976