A Dimeric Sesquiterpenoid from a Malaysian Meiogyne as a New Inhibitor of Bcl-xL/BakBH3 Domain Peptide Interaction

A Dimeric Sesquiterpenoid from a Malaysian <i>Meiogyne</i> as a New Inhibitor of Bcl-xL/BakBH3 Domain Peptide Interaction Endiandric Acid Analogues from <i>Beilschmiedia ferruginea</i> as Dual Inhibitors of Bcl-xL/Bak and Mcl-1/Bid Interactions Dual inhibitors of the pro-survival proteins Bcl-2 and Mcl-1 derived from natural compound meiogynin A Anacardic Acids from <i>Knema hookeriana</i> as Modulators of Bcl-xL/Bak and Mcl-1/Bid Interactions Natural Inhibitors of the RhoA–p115 Complex from the Bark of <i>Meiogyne baillonii</i> (+)- and (−)-Ecarlottones, Uncommon Chalconoids from <i>Fissistigma latifolium</i> with Pro-Apoptotic Activity Antiplasmodial Sesquiterpene Alkaloids from the Roots of <i>Maytenus mekongensis</i> Antiplasmodial Sesquiterpene Alkaloids from the Roots of Maytenus mekongensis Sesquiterpenoids and Plasmin-Inhibitory Flavonoids from <i>Blumea </i><i>b</i><i>alsamifera</i> Synthesis and biological activities of new di- and trimeric quinoline derivatives