Steroidal saponins from the rhizomes of Smilax sieboldii
1992; Elsevier BV; Volume: 31; Issue: 7 Linguagem: Inglês
10.1016/0031-9422(92)83296-b
ISSN1873-3700
AutoresTamotsu Nikaido, Taichi Ohmoto, Satoshi Kubo, Yoshihiro Mimaki, Yutaka Sashida,
Tópico(s)Polysaccharides and Plant Cell Walls
ResumoSix 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) )-α-d-glucopyranoside, 26-O-β-d-glucopyranosyl-3β,22ξ,26-trihydroxy-(25R)-5α-furostan-6-one 3-O-α-l-arabinopyranosyl-(1 ar 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 ar 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.
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