1.Two new cyclic bisbibenzyl derivatives from Hebertus dicranus.
Chang-Long XU ; Jin-Xin WANG ; Hui-Liang LI
Chinese Journal of Natural Medicines (English Ed.) 2016;14(6):457-461
In the present study, two new cyclic bisbibenzyls (1, 2) co-occuring with a known compound, isoplagiochins C (3) were isolated from Hebertus dicranus. The structures were determined mainly by extensive 1D and 2D NMR experiments, and the absolute configurations of 1 and 2 were established by the circular dichroism spectrum. Furthermore, all these three rare compounds were tested in vitro for inhibitory activity against the growth of human cancer cell lines (A549, HCT116, MDA-MB-231, and BEL7404) by the MTT assay, and compound 2 exhibited moderately inhibitory activity with IC50 values ranging from 13.89 to 31.62 μmol·L(-1). In conclusion, our results provided a basis for future development and modification of these compounds for cancer therapy.
Antineoplastic Agents, Phytogenic
;
chemistry
;
isolation & purification
;
Cell Line, Tumor
;
Drugs, Chinese Herbal
;
chemistry
;
isolation & purification
;
Hepatophyta
;
chemistry
;
Humans
;
Molecular Structure
2.Scapaundulin C, a novel labdane diterpenoid isolated from Chinese liverwort Scapania undulate, inhibits acetylcholinesterase activity.
Ya-Qi KANG ; Jin-Chuan ZHOU ; Pei-Hong FAN ; Shu-Qi WANG ; Hong-Xiang LOU
Chinese Journal of Natural Medicines (English Ed.) 2015;13(12):933-936
In the present study, scapaundulin C (1), a new labdane diterpenoid, and four related known compounds scapaundulin A (2), 5α, 8α, 9α-trihydroxy-13E-labden-12-one (3), 5α, 8α-dihydroxy-13E-labden-12-one (4), and (13S)-15-hydroxylabd-8 (17)-en-19-oic acid (5), were isolated from the Chinese liverwort Scapania undulate (L.) Dum., using column chromatography. The structures of these compounds were determined on the basis of 1D- and 2D-NMR analyses. The acetylcholinesterase (AchE) inhibitory activity was evaluated using a bioautographic TLC assay and the cytotoxic activity was evaluated by the MTT method. All the compounds were reported for the first time to exhibit moderate AchE inhibitory activity with minimal inhibitory quantities ranging from 250 to 500 ng. All the compounds were tested for their cytotoxicity against five human tumor cell lines, A549, K562, A2780, Hela, and HT29, and compounds 3 and 4 exhibited moderate inhibitory effects on the growth of A2780 cells.
Acetylcholinesterase
;
analysis
;
Cholinesterase Inhibitors
;
chemistry
;
isolation & purification
;
Diterpenes
;
chemistry
;
isolation & purification
;
Hepatophyta
;
chemistry
;
Humans
;
Magnetic Resonance Spectroscopy
;
Molecular Structure
;
Plant Extracts
;
chemistry
;
isolation & purification