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Objective To study the chemical constituents in the dried roots of Panax notoginseng.Methods The constituents were isolated and purified with chromatographic methods.Their structures were elucidated by spectroscopic methods(1D,2D NMR,UV,IR,[α]D,and HRESI-TOF-MS)and chemical analyses.Results Twenty saponins including 20(S)-ginsenoside Rh1(1),6-O-β-D-(6′-acetyl)-glucopyranosyl-24-ene-dammar-3β,6α,12β,20S-tetraol(2),ginseno-side Rf(3),notoginsenoside R2(4),ginsenoside Rg2(5),ginsenoside Rg1(6),notoginsenoside Rt(7),koryoginsenoside R1(8),6-O-(β-D-glucopyranosyl)-20-O-(β-D-xylopyranosyl)-3β,6α,12β,20(S)-tetrahydroxy-dammar-24-ene(9),pseudoginsenoside Rt3(10),notoginsenoside R1(11),ginsenoside Re(12),notoginsenoside N(13),ginsenoside F1(14),ginsenoside U(15),ginsenoside Rk3(16),3β,12β-dihydroxydammar-(E)-20(22),24-diene-6-O-β-D-xylopyranosyl-(1→2)-β-D-glucopyranoside(17),ginsenoside Rh4(18),pseudoginsenoside Rt5(19),and vinaginsenoside R22(20)were obtained.Conclusion Compounds 2,19,and 20 are isolated from this species for the first time.The 1H-NMR data of compound 19 and1H-NMR and 13C-NMR data of compound 20 are first reported.Meanwhile,the NMR data ofβ-D-xylopyranosyl group in compound 9 is corrected.
Objective To study the chemical constituents in the dried roots of Panax notoginseng. Methods The constituents were isolated and purified with chromatographic methods. Their structures were elucidated by spectroscopic methods (1D, 2D NMR, UV, IR, [α] D, and HRESI- TOF-MS) and chemical analyzes. Results Twenty saponins including 20 (S) -ginsenoside Rh1 (1), 6-O-β- D- (6’-acetyl) -glucopyranosyl-24-ene-dammar- (3), notoginsenoside R2 (4), ginsenoside Rg2 (5), ginsenoside Rg1 (6), notoginsenoside Rt (7), koryoginsenoside R1 - (β-D-glucopyranosyl) -20-O- (β-D-xylopyranosyl) -3β, 6α, 12β, 20 (S) -tetrahydroxy-dammar-24- ene (9), pseudoginsenoside Rt3 (10), notoginsenoside Ginsenoside R1 (11), ginsenoside Re (12), notoginsenoside N (13), ginsenoside F1 (14), ginsenoside U (15), ginsenoside Rk3 (16), 3β, 12β-dihydroxydammar- (E) -20 24-diene-6-O-β-D-xylopyranosyl- (1 → 2) -β-D-glucopyranoside (17), ginsenoside Rh4 (18), pseudoginsenoside Rt5 (19), and vinaginsenoside R22 (20) Conclusion Compo 1H-NMR data of compound 19 and 1H-NMR and 13C-NMR data of compound 20 are first reported. Meanwhile, the NMR data of β-D-xylopyranosyl group in compound 9 is corrected.