Antibacterial activity and chemical modifications of PS-5 at the C-3 side chain

J Antibiot (Tokyo). 1990 Oct;43(10):1254-70. doi: 10.7164/antibiotics.43.1254.

Abstract

Using PS-5 as starting material, the effects of chemical modification at the C-3 side chain were studied on the antibacterial activity against Gram-positive and Gram-negative bacteria including beta-lactamase-producers. Among 35 side chains tested, 4-pyridylthio showed the highest antibacterial activity against the Gram-positive bacteria, and D-cysteinyl against the Gram-negative microbes. In general, compared with acetamidoethylthio in PS-5, basic side chains showed improved antibacterial activity against the staphylococci and pseudomonads, whereas the antibiotic activity against the Gram-negative bacteria decreased with bulky side chains. The introduction of 6-aminopenicillanate and 7-aminocephalosporanate to the C-3 side chain of carbapenem significantly reduced the antibacterial activity against the beta-lactamase-producing microbes.

MeSH terms

  • Gram-Negative Bacteria / drug effects*
  • Gram-Positive Bacteria / drug effects*
  • Structure-Activity Relationship
  • Thienamycins / chemistry
  • Thienamycins / metabolism
  • Thienamycins / pharmacology*
  • beta-Lactamase Inhibitors

Substances

  • Thienamycins
  • beta-Lactamase Inhibitors
  • PS 5