A new biologically active acylated triterpene saponin from Silene fortunei.J Nat Prod. 1999 Jan; 62(1):133-6.JN
Abstract
A new acylated triterpene-saponin (1), together with a mixture of the known jenisseensosides C and D, has been isolated from the roots of Silene fortunei. The structure of the new compound was established by chemical means and spectroscopic methods as 3-O-[beta-D-galactopyranosyl-(1-->2)-beta-D-glucuronopyranosyl]-28 -O- [[alpha-L-arabinopyranosyl-(1-->2)-alpha-L-arabinopyranosyl- (1-->3)-b eta-D-xylopyranosyl-(1-->4)-alpha-L-rhamnopyranosyl-(1-->2)]-[beta-D- glucopyranosyl-(1-->3)]-4-O-acetyl-beta-D-fucopyranosyl]quillaic acid. This saponin showed a significant enhancement of granulocyte phagocytosis in vitro.
MeSH
Pub Type(s)
Journal Article
Language
eng
PubMed ID
9917300
Citation
Lacaille-Dubois, M A., et al. "A New Biologically Active Acylated Triterpene Saponin From Silene Fortunei." Journal of Natural Products, vol. 62, no. 1, 1999, pp. 133-6.
Lacaille-Dubois MA, Hanquet B, Cui ZH, et al. A new biologically active acylated triterpene saponin from Silene fortunei. J Nat Prod. 1999;62(1):133-6.
Lacaille-Dubois, M. A., Hanquet, B., Cui, Z. H., Lou, Z. C., & Wagner, H. (1999). A new biologically active acylated triterpene saponin from Silene fortunei. Journal of Natural Products, 62(1), 133-6.
Lacaille-Dubois MA, et al. A New Biologically Active Acylated Triterpene Saponin From Silene Fortunei. J Nat Prod. 1999;62(1):133-6. PubMed PMID: 9917300.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - A new biologically active acylated triterpene saponin from Silene fortunei.
AU - Lacaille-Dubois,M A,
AU - Hanquet,B,
AU - Cui,Z H,
AU - Lou,Z C,
AU - Wagner,H,
PY - 1999/1/23/pubmed
PY - 1999/1/23/medline
PY - 1999/1/23/entrez
SP - 133
EP - 6
JF - Journal of natural products
JO - J Nat Prod
VL - 62
IS - 1
N2 - A new acylated triterpene-saponin (1), together with a mixture of the known jenisseensosides C and D, has been isolated from the roots of Silene fortunei. The structure of the new compound was established by chemical means and spectroscopic methods as 3-O-[beta-D-galactopyranosyl-(1-->2)-beta-D-glucuronopyranosyl]-28 -O- [[alpha-L-arabinopyranosyl-(1-->2)-alpha-L-arabinopyranosyl- (1-->3)-b eta-D-xylopyranosyl-(1-->4)-alpha-L-rhamnopyranosyl-(1-->2)]-[beta-D- glucopyranosyl-(1-->3)]-4-O-acetyl-beta-D-fucopyranosyl]quillaic acid. This saponin showed a significant enhancement of granulocyte phagocytosis in vitro.
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/9917300/A_new_biologically_active_acylated_triterpene_saponin_from_Silene_fortunei_
L2 - https://doi.org/10.1021/np980172y
DB - PRIME
DP - Unbound Medicine
ER -