TY - JOUR
T1 - Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L.
AU - Li, Yongxin
AU - Yu, Shanjiang
AU - Liu, Dong
AU - Proksch, Peter
AU - Lin, Wenhan
PY - 2012/1/15
Y1 - 2012/1/15
N2 - Four new polyphenols namely excoecariphenols A-D (1-4) were isolated from the Chinese mangrove plant Excoecaria agallocha L. together with 23 known phenolic compounds. The structures of new compounds were elucidated on the basis of extensive spectroscopic analyses including IR, MS, NMR, and CD data. Excoecariphenols A and B presented as the unusual flavane-based 1-thioglycosides. Part of the isolated polyphenols were tested against hepatitis C NS3-4A protease and HCV RNA in huh 7.5 cells. Excoecariphenol D, corilagin, geraniin, and chebulagic acid showed potential inhibition toward HCV NS3-4A protease with IC 50 values in a range of 3.45-9.03 μM, while excoecariphenol D and corilagin inhibited HCV RNA in huh 7.5 cells significantly. A primary structure-activity relationship (SAR) is discussed.
AB - Four new polyphenols namely excoecariphenols A-D (1-4) were isolated from the Chinese mangrove plant Excoecaria agallocha L. together with 23 known phenolic compounds. The structures of new compounds were elucidated on the basis of extensive spectroscopic analyses including IR, MS, NMR, and CD data. Excoecariphenols A and B presented as the unusual flavane-based 1-thioglycosides. Part of the isolated polyphenols were tested against hepatitis C NS3-4A protease and HCV RNA in huh 7.5 cells. Excoecariphenol D, corilagin, geraniin, and chebulagic acid showed potential inhibition toward HCV NS3-4A protease with IC 50 values in a range of 3.45-9.03 μM, while excoecariphenol D and corilagin inhibited HCV RNA in huh 7.5 cells significantly. A primary structure-activity relationship (SAR) is discussed.
KW - Excoecaria agallocha L.
KW - Excoecariphenols A-D
KW - HCV RNA inhibition
KW - Huh 7.5 cells
KW - Mangrove plant
KW - NS3-4A protein kinase inhibition
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000299653500067
UR - https://openalex.org/W2137085874
UR - https://www.scopus.com/pages/publications/84855675976
U2 - 10.1016/j.bmcl.2011.11.109
DO - 10.1016/j.bmcl.2011.11.109
M3 - Journal Article
SN - 0960-894X
VL - 22
SP - 1099
EP - 1102
JO - Bioorganic and Medicinal Chemistry Letters
JF - Bioorganic and Medicinal Chemistry Letters
IS - 2
ER -