Structure-activity relationship of pamamycins: effects of alkyl substituents

J Antibiot (Tokyo). 1995 Oct;48(10):1159-64. doi: 10.7164/antibiotics.48.1159.

Abstract

Nine new pamamycin homologues were isolated from the culture broth of Streptomyces alboniger IFO 12738 using a combination of ODS and NH2 HPLCs, and their structures determined by GC-MS. The structural differences in these homologues are in the numbers and positions of methyl and ethyl groups. The aerial mycelium-inducing and growth-inhibitory activities in S. alboniger of these homologues and their antibiotic activity against Bacillus subtilis were examined. The effects of the alkyl substituents on these activities are discussed.

Publication types

  • Comparative Study

MeSH terms

  • Antifungal Agents / chemistry*
  • Antifungal Agents / isolation & purification
  • Antifungal Agents / pharmacology
  • Fermentation
  • Gas Chromatography-Mass Spectrometry
  • Macrolides
  • Microbial Sensitivity Tests
  • Organic Chemicals
  • Streptomyces
  • Structure-Activity Relationship

Substances

  • Antifungal Agents
  • Macrolides
  • Organic Chemicals
  • pamamycin