Acylated triterpene saponins from Silene jenisseensis.Phytochemistry. 1995 Sep; 40(2):509-14.P
Abstract
From the roots of Silene jenisseensis a new trans-p-methoxycinnamoyl triterpene saponin has been isolated along with its cis-p-methoxycinnamoyl isomer as an inseparable mixture. Their structures were established by chemical means and spectroscopic methods including 1D- and 2D-homonuclear and heteronuclear correlation NMR spectroscopy as 3-O-[beta-D-galactopyranosyl-(1 --> 2)-beta-D-glucuronopyranosyl]-28-O-[beta-D-glucopyranosyl-(1 --> 2)-alpha-L-rhamnopyranosyl- (1 --> 2)-beta-D-4-O-trans-p-methoxycinnamoyl-fucopyranosyl] quillaic acid and its cis-isomer, respectively. They did not show any activity in the in vitro chemoluminescence granulocytes assay, but exhibited only a weak inhibitory effect in the cyclooxygenase inhibition assay.
Links
MeSH
Pub Type(s)
Journal Article
Language
eng
PubMed ID
7546560
Citation
Lacaille-Dubois, M A., et al. "Acylated Triterpene Saponins From Silene Jenisseensis." Phytochemistry, vol. 40, no. 2, 1995, pp. 509-14.
Lacaille-Dubois MA, Hanquet B, Cui ZH, et al. Acylated triterpene saponins from Silene jenisseensis. Phytochemistry. 1995;40(2):509-14.
Lacaille-Dubois, M. A., Hanquet, B., Cui, Z. H., Lou, Z. C., & Wagner, H. (1995). Acylated triterpene saponins from Silene jenisseensis. Phytochemistry, 40(2), 509-14.
Lacaille-Dubois MA, et al. Acylated Triterpene Saponins From Silene Jenisseensis. Phytochemistry. 1995;40(2):509-14. PubMed PMID: 7546560.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Acylated triterpene saponins from Silene jenisseensis.
AU - Lacaille-Dubois,M A,
AU - Hanquet,B,
AU - Cui,Z H,
AU - Lou,Z C,
AU - Wagner,H,
PY - 1995/9/1/pubmed
PY - 1995/9/1/medline
PY - 1995/9/1/entrez
SP - 509
EP - 14
JF - Phytochemistry
JO - Phytochemistry
VL - 40
IS - 2
N2 - From the roots of Silene jenisseensis a new trans-p-methoxycinnamoyl triterpene saponin has been isolated along with its cis-p-methoxycinnamoyl isomer as an inseparable mixture. Their structures were established by chemical means and spectroscopic methods including 1D- and 2D-homonuclear and heteronuclear correlation NMR spectroscopy as 3-O-[beta-D-galactopyranosyl-(1 --> 2)-beta-D-glucuronopyranosyl]-28-O-[beta-D-glucopyranosyl-(1 --> 2)-alpha-L-rhamnopyranosyl- (1 --> 2)-beta-D-4-O-trans-p-methoxycinnamoyl-fucopyranosyl] quillaic acid and its cis-isomer, respectively. They did not show any activity in the in vitro chemoluminescence granulocytes assay, but exhibited only a weak inhibitory effect in the cyclooxygenase inhibition assay.
SN - 0031-9422
UR - https://www.unboundmedicine.com/medline/citation/7546560/Acylated_triterpene_saponins_from_Silene_jenisseensis_
L2 - https://linkinghub.elsevier.com/retrieve/pii/003194229500222S
DB - PRIME
DP - Unbound Medicine
ER -