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 in | Phytochemistry (Oxford) Vol. 31; no. 7; pp. 2445 - 2450 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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 |
Author_xml | – sequence: 1 givenname: Tamotsu surname: Nikaido fullname: Nikaido, Tamotsu organization: Faculty of Pharmaceutical Sciences, Toho University, 2-2-1, Miyama, Funabashi, Chiba 274, Japan – sequence: 2 givenname: Taichi surname: Ohmoto fullname: Ohmoto, Taichi organization: Faculty of Pharmaceutical Sciences, Toho University, 2-2-1, Miyama, Funabashi, Chiba 274, Japan – sequence: 3 givenname: Satoshi surname: Kubo fullname: Kubo, Satoshi – sequence: 4 givenname: Yoshihiro surname: Mimaki fullname: Mimaki, Yoshihiro – sequence: 5 givenname: Yutaka surname: Sashida fullname: Sashida, Yutaka |
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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 |
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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 |
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