Search Results - "Frattaruolo, L."

An ancient remedial repurposing: synthesis of new pinocembrin fatty acid acyl derivatives as potential antimicrobial/anti-inflammatory agents by Tundis, R., Frattaruolo, L., Carullo, G., Armentano, B., Badolato, M., Loizzo, M. R., Aiello, F., Cappello, A. R.

“…Five new pinocembrin derivatives (MC1-MC5) were synthesized by Steglich reaction, and investigated for their antimicrobial, antioxidant, and anti-inflammatory…”
Get full text

Thioalbamide inhibits FoF1-ATPase in breast cancer cells and reduces tumor proliferation and invasiveness in breast cancer in vivo models by Frattaruolo, L., Malivindi, R., Brindisi, M., Rago, V., Curcio, R., Lauria, G., Fiorillo, M., Dolce, V., Truman, A.W., Cappello, A.R.

“…Thioalbamide is a ribosomally synthesized and post-translationally modified peptide (RiPP) belonging to the family of thioamitides, a rare class of microbial…”
Get full text

Thioalbamide inhibits F o F 1 -ATPase in breast cancer cells and reduces tumor proliferation and invasiveness in breast cancer in vivo models by Frattaruolo, L, Malivindi, R, Brindisi, M, Rago, V, Curcio, R, Lauria, G, Fiorillo, M, Dolce, V, Truman, A W, Cappello, A R

“…Thioalbamide is a ribosomally synthesized and post-translationally modified peptide (RiPP) belonging to the family of thioamitides, a rare class of microbial…”
Get full text