Iloneoside: a cytotoxic ditigloylated pregnane glycoside from the leaves of <i>Gongronema latifolium</i> Benth

Gideon Ampoma Gyebi, Joseph O. Adebayo, Olufunke E. Olorundare, Antoni Pardede, Masayuki Ninomiya, Afolabi Olanrewaju Saheed, Abiola Babatunde, Mamoru Koketsu

Natural Product Research · 2017 · 16 citations · 6 references

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Abstract

Gongronema latifolium Benth (Asclepiadaceae) is an edible-green-leafy vegetable with known medicinal value. A chemical investigation of the 80% methanolic extract of the leaves led to the isolation of a new pregnane glycoside: iloneoside (3-O-[6-deoxy-3-O-methyl-β-D-allopyranosyl-(1→14)-β-D-oleandropyranosyl]-11,12-di-O-tigloyl-17β-marsdenin), together with four known constituents. Their chemical structures were determined by spectroscopic analysis. The isolates were tested for their in vitro growth inhibitory activity against human leukemia HL-60 cells. Iloneoside was the most active and gave apoptotic response. Molecular docking analysis demonstrated that iloneoside could be accommodated within hot spots of anti-apoptotic protein Bcl-2. These results suggest G. latifolium as a reliable source of potent anticancer compounds.

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