Cytotoxic cytochalasins from marine-derived fungus Arthrinium arundinis

Planta Med. 2015 Jan;81(2):160-6. doi: 10.1055/s-0034-1383403. Epub 2015 Jan 27.

Abstract

Four new cytochalasins, arthriniumnins A-D (1-4), a new natural product, ketocytochalasin (5), as well as five known cytochalasin analogues (6-10) were isolated and identified from the fungus Arthrinium arundinis ZSDS1-F3 from the sponge Phakellia fusca. Their structures were elucidated by NMR spectroscopic and mass spectrometric analyses, as well as single crystal X-ray diffraction. Compounds 6 and 9 showed cytotoxicity against K562, A549, Huh-7, H1975, MCF-7, U937, BGC823, HL60, Hela, and MOLT-4 cell lines, with IC50 values ranging from 1.13 to 47.4 µM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / isolation & purification
  • Antineoplastic Agents / pharmacology*
  • Ascomycota / chemistry*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Cytochalasins / chemistry
  • Cytochalasins / isolation & purification
  • Cytochalasins / pharmacology*
  • Drug Screening Assays, Antitumor
  • Humans
  • Molecular Structure
  • Porifera / microbiology*
  • X-Ray Diffraction

Substances

  • Antineoplastic Agents
  • Cytochalasins