
Phytochemistry p. 2445 - 2450 (1992)
Update date:2022-08-03
Topics:
Kubo, Satoshi
Mimaki, Yoshihiro
Sashida, Yutaka
Nikaido, Tamotsu
Ohmoto, Taichi
Six new steroidal saponins were isolated from the rhizomes of Smilax sieboldii.Their structures were determined by spectroscopic analysis and hydrolysis to be 3β-hydroxy-(25R)-5α-spirostan-6-one (laxogenin) 3-O-β-D-glucopyranosyl-(1<*>4-O-<α-L-arabinopyranosyl-(1<*>6)>-β-D-glucopyranoside, laxogenin 3-O-α-L-arabinopyranosyl-(1<*>6)-β-D-glucopyranoside, 3β,27-dihydroxy-(25S)-5α-spirostan-6-one 3-O-β-D-glucopyranosyl-(1<*>4)-O-<α-L-arabinopyranosyl-(1<*>6)>-β-D-glucopyranoside, 26-O-β-D-glucopyranosyl-3β,22ξ,26-trihydroxy-(25R)-5α-furostan-6-one 3-O-α-L-arabinopyranosyl-(1<*>6)-β-D-glucopyranoside, 26-O-β-D-glucopyranosyl-3β,22ξ,26-trihydroxy-(25R)-5α-furostan-6-one 3-O-β-D-glucopyranosyl-(1<*>4)-O-<α-L-arabinopyranosyl-(1<*>6)>-β-D-glucopyranoside and (25R)-5α-spirostan-3β-ol (tigogenin) 3-O-β-D-glucopyranosyl-(1<*>4)-O-<α-L-arabinopyranosyl-(1<*>6)>-β-D-glucopyranoside.The inhibition of cAMP phosphodiesterase by the saponins was evaluated. Key Word Index - Smilax sieboldii; Liliaceae; steroidal saponins; spirostanol glycosides; furostanol glycosides; laxogenin glycosides; tigogenin glycoside; cAMP phosphdiesterase; inhibitory activity.
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(2017)Doi:10.1021/jm400718n
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(1992)