A new secalonic acid derivative,
F-7 (
1
), was isolated from the endophytic
Aspergillus aculeatus
MBT 102, associated with
Rosa damascena
. The planar structure of
1
was established on the basis of 1D and 2D NMR and ESI-TOF-MS spectra.
The relative configuration of
1
was determined applying
a combined quantum mechanical/NMR approach and, afterward, the comparison
of calculated and experimental electronic circular dichroism spectra
determined the assignment of its absolute configuration. The compound
possesses strong cytotoxic activity against triple negative breast
cancer (TNBC) cells. It was found to induce apoptosis, as evidenced
by scanning electron microscopy and phase contrast microscopy. Furthermore,
flow cytometry analyses demonstrated that
1
induced mitochondrial
damage and reactive oxygen species mediated apoptosis, arresting the
G1 phase of the cells in a dose-dependent manner. Also, the compound
causes significant microtubule disruption in TNBC cells. Subsequently,
1
restricted the cell migration leading to the concomitant
increase in expression of cleaved caspase and PARP.