Marineosins A and B, cytotoxic spiroaminals from a marine-derived actinomycete

Org Lett. 2008 Dec 18;10(24):5505-8. doi: 10.1021/ol8020644.

Abstract

Two novel spiroaminals, marineosins A and B (1, 2), containing two pyrrole functionalities, were isolated from cultures of a marine sediment-derived actinomycete related to the genus Streptomyces. The marineosins, which appear to be derived from unknown modifications of prodigiosin-like pigment pathways, showed significant inhibition of human colon carcinoma (HCT-116) in an in vitro assay (IC50 = 0.5 microM for marineosin A) and selective activities in diverse cancer cell types.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Anticarcinogenic Agents / chemistry*
  • Anticarcinogenic Agents / isolation & purification
  • Anticarcinogenic Agents / pharmacology
  • Antifungal Agents / chemistry*
  • Antifungal Agents / isolation & purification
  • Antifungal Agents / pharmacology
  • Candida albicans / drug effects
  • Cell Line, Tumor
  • Drug Screening Assays, Antitumor
  • Humans
  • Marine Biology
  • Molecular Conformation
  • Pyrroles / chemistry*
  • Pyrroles / isolation & purification
  • Pyrroles / pharmacology
  • Spiro Compounds / chemistry*
  • Spiro Compounds / isolation & purification
  • Spiro Compounds / pharmacology
  • Streptomyces / chemistry*

Substances

  • Anticarcinogenic Agents
  • Antifungal Agents
  • Pyrroles
  • Spiro Compounds
  • marineosin A
  • marineosin B