
doi: 10.1248/cpb.58.587
pmid: 20410650
A new neolignan, (7R,8R)-5-O-demethylbilagrewin (1), together with four known lignans (2-5), were isolated from the heartwood of Santalum album (Santalaceae). The structure of 1 was determined by analysis of extensive spectroscopic data. The isolated compounds and derivatives were evaluated for their cytotoxic activities against HL-60 human promyelocytic leukemia cells and A549 human lung adenocarcinoma cells. Compounds 1 and 2 exhibited cytotoxicity against HL-60 cells with IC(50) values of 1.5+/-0.02 and 4.3+/-0.13 microM, and against A549 cells with IC(50) values of 13.6+/-0.32 and 19.9+/-1.27 microM, respectively. The aldehyde group of 1 and 2 was revealed to be a structural requirement for the appearance of cytotoxicity in this type of lignans. These tumor cell deaths were shown to be mediated through induction of apoptosis.
Leukemia, Lung Neoplasms, Molecular Structure, Cytotoxins, apoptosis, neolignan, Apoptosis, DNA Fragmentation, A549 cell, Adenocarcinoma, Antineoplastic Agents, Phytogenic, Lignans, Santalaceae, Santalum, Cell Line, Tumor, Neoplasms, Humans, HL-60 cell, <i>Santalum album</i>
Leukemia, Lung Neoplasms, Molecular Structure, Cytotoxins, apoptosis, neolignan, Apoptosis, DNA Fragmentation, A549 cell, Adenocarcinoma, Antineoplastic Agents, Phytogenic, Lignans, Santalaceae, Santalum, Cell Line, Tumor, Neoplasms, Humans, HL-60 cell, <i>Santalum album</i>
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