Two new furostanol saponins 1–2 and a new spirostanol saponin 3 were isolated together with two known furostanol saponins 4–5 from the roots and rhizomes of Tupistra chinensis. Their structures were characterized as 1β,2β,3β,4β,5β,26-hexahydroxyfurost-20(22), 25(27)-dien-5,26-O-β-d-glucopyranoside (
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Two new furostanol saponins
1–
2 and a new spirostanol saponin
3 were isolated together with two known furostanol saponins
4–
5 from the roots and rhizomes of
Tupistra chinensis. Their structures were characterized as 1β,2β,3β,4β,5β,26-hexahydroxyfurost-20(22), 25(27)-dien-5,26-
O-β-d-glucopyranoside (
1), 1β,2β,3β,4β,5β,6β,7α,23ξ,26-nona-hydroxyfurost- 20(22),25(27)-dien-26-
O-β-d-glucopyranoside (
2), (20
S,22
R)-spirost-25 (27)-en-1β,3β,5β- trihydroxy-1-
O-β-d-xyloside (
3), tupisteroide B (
4) and 5β-furost-Δ
25(27)-en-1β,2β,3β,4β,5β,7α, 22ξ,26-octahydroxy-6-one-26-
O-β-d-glucopyranoside (
5), respectively, by extensive use of spectroscopic techniques and chemical evidence. Additionally, the
in vitro cytotoxic activity of
1–
4 was evaluated on human A549 and H1299 tumor cell lines, and compound
3 exhibited cytotoxicity against A549 cells (IC
50 86.63 ± 2.33 μmol·L
−1) and H1299 cells (IC
50 88.21 ± 1.34 μmol·L
−1).
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