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Cephalotaxine is an alkaloid that has been found in Cephalotaxus and has anticancer and antiviral activities.1,2,3 It is cytotoxic to HL-60, NB4, MOLT-4, K562, Jurkat, and Raji cells (IC50s = 4.91, 16.88, 7.09, 22.59, 5.54, and 18.08 µM, respectively).1 Cephalotaxine (5-20 µM) induces mitochondrial apoptosis, as well as impairs lysosomal acidification and autophagic flux in HL-60 cells. It reduces infectivity and hepatitis B virus (HBV) surface antigen (HBsAg) secretion in HBV-infected HepG2 2.2.15 cells when used at concentrations ranging from 10 to 100 µM.2 Cephalotaxine (20, 40, and 80 µM) also reduces viral infectivity in Zika virus-infected Vero cells.3
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1. Cephalotaxine inhibits the survival of Leukemia cells by activating mitochondrial apoptosis pathway and inhibiting autophagy flow. Molecules 26(10), 2996 (2021).
2. Effect of cantharidin, cephalotaxine and homoharringtonine on "in vitro" models of hepatitis B virus (HBV) and bovine viral diarrhoea virus (BVDV) replication. Planta Med. 73(6), 552-558 (2007).
3. Cephalotaxine inhibits Zika infection by impeding viral replication and stability. Biochem. Biophys. Res. Commun. 22(4), 1052-1058 (2020).