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Cytotoxic and natural killer cell stimulatory constituents of Phyllanthus songboiensis.
- Source :
-
Phytochemistry [Phytochemistry] 2015 Mar; Vol. 111, pp. 132-40. Date of Electronic Publication: 2015 Jan 14. - Publication Year :
- 2015
-
Abstract
- A dichapetalin-type triterpenoid and a dibenzylbutyrolactone-type lignan, together with five known lignans, a known aromatic diterpenoid, and a known acylated phytosterol, were isolated from the aerial parts of Phyllanthus songboiensis, collected in Vietnam. Their structures were determined by interpretation of the spectroscopic data, and the inhibitory activity toward HT-29 human colon cancer cells of all isolates was evaluated by a cytotoxicity assay. The known arylnaphthalene lignan, (+)-acutissimalignan A, was highly cytotoxic toward HT-29 cells, with an IC50 value of 19 nM, but this compound was inactive as a DNA topoisomerase IIα (topo IIα) poison. The known phytosterol, (-)-β-sitosterol-3-O-β-D-(6-O-palmitoyl)glucopyranoside, was found to stimulate natural killer (NK) cells at a concentration of 10μM in the presence of interleukin 12 (IL-12).<br /> (Copyright © 2014 Elsevier Ltd. All rights reserved.)
- Subjects :
- Antineoplastic Agents, Phytogenic chemistry
Drug Screening Assays, Antitumor
HT29 Cells
Humans
Interleukin-12 metabolism
Killer Cells, Natural drug effects
Lignans chemistry
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Triterpenes chemistry
Vietnam
Antigens, Neoplasm metabolism
Antineoplastic Agents, Phytogenic isolation & purification
Antineoplastic Agents, Phytogenic pharmacology
DNA Topoisomerases, Type II metabolism
DNA-Binding Proteins metabolism
Lignans isolation & purification
Lignans pharmacology
Phyllanthus chemistry
Triterpenes isolation & purification
Triterpenes pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3700
- Volume :
- 111
- Database :
- MEDLINE
- Journal :
- Phytochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 25596805
- Full Text :
- https://doi.org/10.1016/j.phytochem.2014.12.014