Dammarane‐Type Saponins from the Leaves of Vietnamese Ginseng (Panax vietnamensis Ha & Grushv.) and Their Acetylcholinesterase Inhibition In Vitro and In Silico

Abstract Vietnamese ginseng ( Panax vietnamensis Ha & Grushv.) represents one of the famous Panax spp. for valuable applications in both traditional and modern medicine; in which, its rhizome part has mainly been used as the medicinal materials based on the bioactive ginsenosides such as ginsenoside Rb1, ginsenoside Rg1, ginsenoside Rd, and majonoside R2. In modern medicine, the development of medicinal materials and utilization of medicinal plants are crucially based on standard bioactive ingredients, so this study to evaluate the leaves of Vietnamese ginseng as source of bioactive ginsenoside led to the identification of seven ginsenosides ( 1 – 7 ). Of them, ginsenoside Rd ( 2 ) and pseudoginsenoside RS1 ( 5 ) showed inhibitory effects on acetylcholinesterase in vitro with the IC 50 values of 47.13 and 79.58 μM and supported by molecular docking analysis, in which ginsenoside Rd ( 2 ) and pseudoginsenoside RS1 ( 5 ) could play as allosteric inhibitors with high binding affinity (−8.5 and −9.4 kcal/mol) as evidenced by hydrogen bonding and hydrophobic interactions. The findings provided the scientific evidence for using the leaves of Vietnamese ginseng as an alternative source to the roots to enhance memory in traditional medicine as well as for further research on the anti‐dementia effects of 2 and 5 .