In this paper 11 compounds were isolated from the hydrolysates of the stems and leaves of Panax notoginseng(Burk) F.H.Chen by modern technologies of extraction,isolation,purification and identification,such as AB-8 macroporous absorption resin (MAR) , silica gel-column chromatography,R-phase high performance liquid ( RP-HPLC-UV-ELSD) and re-crystal.the structures of 11 compounds have beenestablished and 10 compounds have identified on the basis of physico-chemical and spectrographic evidence in the hydrolysate of the stems and leaves of Panax notoginseng(Burk) F.H.Chen. They were dammarane-20(22)en-3β,12β,25-panaxatriol(Ⅰ),20(R) -dammarane-3β,6α,12β,20,25-pentol(Ⅱ),20(R)-dammarane-3β,12β,20,25-triol(Ⅲ),20(S)-panaxadiol(Ⅳ),20(S)-protopanaxadiol (Ⅴ),20(R)-protopanaxadiol (Ⅵ),20(S)-panaxatriol(Ⅶ),20(S)-25-methoxyl-dammarane-3β,12β,20-triol (Ⅷ),20(S) -25- ethoxyl-dammarane-3β, 12β, 20-triol(Ⅸ),20(R) -25- ethoxyl–dammarane-3β, 12β, 20-triol(Ⅹ) .Among them compoundⅨandⅩwere found as the new product.using high performance liquid chromatography(HPLC) with evaporative light scattering detection(ELSD) determinate the quantitative of 20(S)-PD,20(R)-PPD,20(R)-25-OH-PPD in different parts hydrolysates of Panax Notoginseng。The results show that 20(S)-PD,20(R)-PPD,20(R)-25-OH-PPD are all highest in the hydrolysate of the stems and leaves of Panax notoginseng(Burk) F.H.Chen.Study systematically on the anticancer activity of 20(R)-PPD ,20(R)-25-OH-PPD,The result of vitro screening of pharmaco-activity study showed that, 20(R)-PPD,20(R)-25-OH-PPD showed obvious inhibition activity on tumor cells by used five cell system including breast cancer cells,liver cancer cells,prostatic carcinoma cells,colon cancer cells and lung cancer cells. |