Cheng-Che Tsai

Aug 20, 2024 | sciencedirect.com | Mei-Chu Huang |Cheng-Che Tsai |Banruo Huang |F. Dean Toste

Schweinfurthins and their derivatives/analogues have been reported to be potent and selective inhibitors of cancer cell growth [1], [2], [3], [4], [5], [6]. Since the discovery of natural vedelianin, the first example of this family of compounds, several schweinfurthin derivatives have been isolated or synthesized and screened for their biological activities [5], [7], [8], [9], [10], [11], [12].