Two new protopanaxadiol type sapogenins, (3β,12β)-3,12,20-trihydroxydammar-24-en-26-al (1) and (3β,12β)-3,12,20-trihydroxydammar-24-en-26-oic acid (2), were isolated from the alkali hydrolysate of stems-leaves of Panax notoginseng, along with seven known analogues (3-9). Their structures were elucidated by spectroscopic analyses and single-crystal X-ray diffraction. Compound 2 and the known sapogenins 5-8 displayed weak to moderate inhibition of NO production in LPS-induced RAW264.7 macrophages with IC50 values from 44.5 to 143.6 μM, respectively.
Keywords: Panax notoginseng; Protopanaxadiol-type sapogenins; alkali hydrolysate; anti-inflammatory activity.