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A new 5-alkylresorcinol glucoside derivative from Cybianthus magnus.

Authors :
Cabanillas, B.
Vásquez-Ocmín, P.
Zebiri, I.
Rengifo, E.
Sauvain, M.
Le, H.L.
Vaisberg, A.
Voutquenne-Nazabadioko, L.
Haddad, M.
Source :
Natural Product Research; Feb2016, Vol. 30 Issue 3, p293-298, 6p
Publication Year :
2016

Abstract

One new 5-alkylresorcinol glucoside (1) was isolated from leaves of Cybianthus magnus, along with 12 known compounds, isolated from four plants belonging to Myrsinaceae family (2, 3 isolated from C. magnus; 4–7, 10 and 11 isolated from Myrsine latifolia; 4, 8 and 9 isolated from Myrsine sessiflora; 6, 7, 10, 12 and 13 isolated from Myrsine congesta). Their structures were determined on the basis of spectroscopic analysis and by comparison of their spectral data with those reported in the literature. So far, only nine 5-alkylresorcinol glucosides were isolated from leaves of Grevillea robusta. Since resorcinols are known to exhibit strong cytotoxic activity, compounds 1 and 2 were tested against cell lines 3T3, H460, DU145 and MCF-7 for cytotoxicity in vitro and compounds 3–13 were tested for their antileishmanial activity. Compound 2 displayed a strong cytotoxic activity with IC<subscript>50</subscript> values ranging between 22 and 100 μM for all tested cell lines. Compounds 3–13 were not active against Leishmania amazonensis amastigotes. One new 5-alkylresorcinol glucoside (1) was isolated from leaves of Cybianthus magnus, along with 12 known compounds (2–13), isolated from four plants belonging to Myrsinaceae family. Their structures were determined on the basis of spectroscopic analysis and by comparison of their spectral data with those reported in the literature. Among the tested molecules, only compound 2 displayed a strong cytotoxic activity with IC<subscript>50</subscript> values ranging between 22 and 100 μM for all cell lines tested. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14786419
Volume :
30
Issue :
3
Database :
Complementary Index
Journal :
Natural Product Research
Publication Type :
Academic Journal
Accession number :
111556323
Full Text :
https://doi.org/10.1080/14786419.2015.1056188