Abstract
Three new γ-butenolide derivatives 1–3, named spiculisporic acids B–D, were isolated from the culture of Aspergillus sp. HDf2, a marine-derived fungus that resides in the sea urchin, Anthocidaris crassispina. The structures of 1–3 were elucidated on the basis of spectroscopic methods, including MS and 2D NMR techniques. Their in vitro cytotoxic activities against two cell lines (SGC-7901, human gastric adenocarcinoma and SPC-A-1, human lung adenocarcinoma) and inhibitory activities against Staphylococcus aureus ATCC 51650 were investigated.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
4-Butyrolactone / analogs & derivatives*
-
4-Butyrolactone / chemistry
-
4-Butyrolactone / isolation & purification
-
4-Butyrolactone / pharmacology
-
Animals
-
Anti-Bacterial Agents / chemistry
-
Anti-Bacterial Agents / isolation & purification
-
Anti-Bacterial Agents / pharmacology
-
Aspergillus / chemistry*
-
Cell Line
-
Disk Diffusion Antimicrobial Tests
-
Humans
-
Inhibitory Concentration 50
-
Magnetic Resonance Spectroscopy
-
Molecular Conformation
-
Sea Urchins / microbiology*
-
Spectrometry, Mass, Electrospray Ionization
-
Staphylococcus aureus / drug effects
Substances
-
Anti-Bacterial Agents
-
spiculisporic acid B
-
spiculisporic acid C
-
spiculisporic acid D
-
4-Butyrolactone