Steroidal saponins from the rhizomes of Smilax sieboldii

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-(25 R)-5α-spirostan-6-one (laxogenin)3- O-β- d-glucopyranosyl-(1 → 4)- O-[α- l-arabinopyranosyl-(1 → 6)]-β- d-glucopyranoside, la...

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Published inPhytochemistry (Oxford) Vol. 31; no. 7; pp. 2445 - 2450
Main Authors Nikaido, Tamotsu, Ohmoto, Taichi, Kubo, Satoshi, Mimaki, Yoshihiro, Sashida, Yutaka
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Ltd 01.07.1992
Elsevier
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Abstract 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-(25 R)-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-(25 S)-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-(25 R)-5α-furostan-6-one 3- O-α- l-arabinopyranosyl-(1 ar 6)-β- d-glucopyranoside, 26- O-β- d-glucopyranosyl-3β,22ξ,26-trihydroxy-(25 R-5α-furostan-6-one 3- O-β- d-glucopyranosyl-(1 → 4)- O-[α- l-arabinopyranosyl-(1 ar 6)]-β- d-glucopyranoside and (25 R)-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.
AbstractList Six new steroidal saponins were isolated from the rhizomes of Smilax sieboldii. Their structures were determined by spectroscopic analysis and hydrolysis to be 3-beta-hydroxy-(25R)-5-alpha-spirostan-6-one (laxogenin) 3-O-beta-D-glucopyranosyl-(1 leads to 4)-O-[alpha-L-arabinopyranosyl-(1 leads to 6)]-beta-D-glucopyranoside, laxogenin 3-O-alpha-L-arabinopyranosyl-(1 leads to 6)-beta-D-glucopyranoside,3-beta,27-dihydroxy-(25S)-5-alpha-spirostan-6-one 3-O-beta-D-glucopyranosyl-(1 leads to 4)-O-[alpha-L-ara-binopyranosyl-(1 leads to 6)]-beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl-3-beta,22xi, 26-trihydroxy-(25R)-5-alpha-furostan-6-one 3-O-alpha-L-arabinopyranosyl-(1 leads to 6)-beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl-3-beta,22xi, 26-trihydroxy-(25R)-5-alpha-furostan-6-one 3-O-beta-D-glucopyranosyl-(1 leads to 4)-O-[alpha-L-arabinopyranosyl-(1 leads to 6)]-beta-D-glucopyranoside and (25R)-5-alpha-spirostan-3-beta-ol (tigogenin) 3-O-beta-D-glucopyranosyl-(1 leads to 4)-O-[alpha-L-arabinopyranosyl-(1 leads to 6)]-beta-D-glucopyranoside. The inhibition of cAMP phosphodiesterase by the saponins was evaluated.
Six new steroidal saponins were isolated from the rhizomes of Smilax sieboldii. Their structures were determined by spectroscopic analysis and hydrolysis to be 3 beta-hydroxy-(25R)-5 alpha-spirostan-6-one (laxogenin) 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]-beta-D-glucopyranoside, laxogenin 3-O-alpha-L-arabinopyranosyl-(1---6)-beta-D-glucopyranoside, 3 beta,27-dihydroxy-(25S)-5 alpha-spirostan-6-one 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]- beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl-3 beta,22 xi,26-trihydroxy-(25R)-5 alpha-furostan-6-one 3-O-alpha-L-arabinopyranosyl-(1---6)-beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl-3 beta,22 xi,26-trihydroxy-(25R)-5 alpha-furostan-6- one 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]- beta-D-glucopyranoside and (25R)-5 alpha-spirostan-3 beta-ol (tigogenin) 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl- (1---6)]-beta-D-glucopyranoside. The inhibition of cAMP phosphodiesterase by the saponins was evaluated.Six new steroidal saponins were isolated from the rhizomes of Smilax sieboldii. Their structures were determined by spectroscopic analysis and hydrolysis to be 3 beta-hydroxy-(25R)-5 alpha-spirostan-6-one (laxogenin) 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]-beta-D-glucopyranoside, laxogenin 3-O-alpha-L-arabinopyranosyl-(1---6)-beta-D-glucopyranoside, 3 beta,27-dihydroxy-(25S)-5 alpha-spirostan-6-one 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]- beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl-3 beta,22 xi,26-trihydroxy-(25R)-5 alpha-furostan-6-one 3-O-alpha-L-arabinopyranosyl-(1---6)-beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl-3 beta,22 xi,26-trihydroxy-(25R)-5 alpha-furostan-6- one 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]- beta-D-glucopyranoside and (25R)-5 alpha-spirostan-3 beta-ol (tigogenin) 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl- (1---6)]-beta-D-glucopyranoside. The inhibition of cAMP phosphodiesterase by the saponins was evaluated.
Six new steroidal saponins were isolated from the rhizomes of Smilax sieboldii. Their structures were determined by spectroscopic analysis and hydrolysis to be 3 beta-hydroxy-(25R)-5 alpha-spirostan-6-one (laxogenin) 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]-beta-D-glucopyranoside, laxogenin 3-O-alpha-L-arabinopyranosyl-(1---6)-beta-D-glucopyranoside, 3 beta,27-dihydroxy-(25S)-5 alpha-spirostan-6-one 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]- beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl-3 beta,22 xi,26-trihydroxy-(25R)-5 alpha-furostan-6-one 3-O-alpha-L-arabinopyranosyl-(1---6)-beta-D-glucopyranoside, 26-O-beta-D-glucopyranosyl-3 beta,22 xi,26-trihydroxy-(25R)-5 alpha-furostan-6- one 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl-(1- ---6)]- beta-D-glucopyranoside and (25R)-5 alpha-spirostan-3 beta-ol (tigogenin) 3-O-beta-D-glucopyranosyl-(1---4)-O-[alpha-L-arabinopyranosyl- (1---6)]-beta-D-glucopyranoside. The inhibition of cAMP phosphodiesterase by the saponins was evaluated.
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-(25 R)-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-(25 S)-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-(25 R)-5α-furostan-6-one 3- O-α- l-arabinopyranosyl-(1 ar 6)-β- d-glucopyranoside, 26- O-β- d-glucopyranosyl-3β,22ξ,26-trihydroxy-(25 R-5α-furostan-6-one 3- O-β- d-glucopyranosyl-(1 → 4)- O-[α- l-arabinopyranosyl-(1 ar 6)]-β- d-glucopyranoside and (25 R)-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.
Author Nikaido, Tamotsu
Kubo, Satoshi
Mimaki, Yoshihiro
Ohmoto, Taichi
Sashida, Yutaka
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Issue 7
Keywords cAMP phosphodiesterase
Liliaceae
laxogenin glycosides
steroidal saponins
Smilax sieboldii
spirostanol glycosides
inhibitory activity
tigogenin glycoside
furostanol glycosides
Steroid
Monocotyledones
Enzymatic activity
Molecular structure
Enzyme
Angiospermae
Rhizome
Isolation
Spermatophyta
Inhibition
Saponin
Language English
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PublicationTitle Phytochemistry (Oxford)
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Snippet Six new steroidal saponins were isolated from the rhizomes of Smilax sieboldii. Their structures were determined by spectroscopic analysis and hydrolysis to be...
Six new steroidal saponins were isolated from the rhizomes of Smilax sieboldii. Their structures were determined by spectroscopic analysis and hydrolysis to be...
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SubjectTerms 3',5'-Cyclic-AMP Phosphodiesterases
3',5'-Cyclic-AMP Phosphodiesterases - antagonists & inhibitors
antagonists & inhibitors
Biological and medical sciences
cAMP phosphodiesterase
Carbohydrate Sequence
chemical constituents of plants
Chemical constitution
chemical structure
chemistry
enzyme inhibitors
Fundamental and applied biological sciences. Psychology
furostanol glycosides
glycosides
Hydrolysis
inhibitory activity
isolation & purification
Japan
laxogenin glycosides
Liliaceae
Magnetic Resonance Spectroscopy
medicinal plants
molecular conformation
Molecular Sequence Data
Molecular Structure
pharmacology
phosphodiesterase I
Phytosterols
Phytosterols - chemistry
Phytosterols - isolation & purification
Phytosterols - pharmacology
Plant physiology and development
Plants
Plants - chemistry
rhizomes
Saponins
Saponins - chemistry
Saponins - isolation & purification
Saponins - pharmacology
Smilax
Smilax sieboldii
spectral analysis
spirostanol glycosides
steroid saponins
steroidal saponins
tigogenin glycoside
Title Steroidal saponins from the rhizomes of Smilax sieboldii
URI https://dx.doi.org/10.1016/0031-9422(92)83296-B
https://www.ncbi.nlm.nih.gov/pubmed/1369386
https://www.proquest.com/docview/48407803
https://www.proquest.com/docview/73096902
Volume 31
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