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Lichen secondary metabolites as DNA-interacting agents
J. Plsíkova, J. Stepankova, J. Kasparkova, V. Brabec, M. Backor, M. Kozurkova,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Benzoates pharmacology MeSH
- Benzofurans pharmacology MeSH
- Circular Dichroism MeSH
- DNA drug effects metabolism MeSH
- Emodin analogs & derivatives pharmacology MeSH
- Hydroxybenzoates pharmacology MeSH
- Topoisomerase I Inhibitors pharmacology MeSH
- Topoisomerase II Inhibitors pharmacology MeSH
- Intercalating Agents pharmacology MeSH
- Kinetics MeSH
- Nucleic Acid Conformation MeSH
- Humans MeSH
- Lichens chemistry metabolism MeSH
- Cattle MeSH
- Spectrophotometry, Ultraviolet MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Cattle MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
A series of lichen secondary metabolites (parietin, atranorin, usnic and gyrophoric acid) and their interactions with calf thymus DNA were investigated using molecular biophysics and biochemical methods. The binding constants K were estimated to range from 4.3×10(5) to 2.4×10(7)M(-1) and the percentage of hypochromism was found to be 16-34% (from spectral titration). The results of spectral measurement indicate that the compounds act as effective DNA-interacting agents. Electrophoretic separation studies prove that from all the metabolites tested in this study, only gyrophoric acid exhibited an inhibitory effect on Topo I (25μM).
References provided by Crossref.org
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- $a A series of lichen secondary metabolites (parietin, atranorin, usnic and gyrophoric acid) and their interactions with calf thymus DNA were investigated using molecular biophysics and biochemical methods. The binding constants K were estimated to range from 4.3×10(5) to 2.4×10(7)M(-1) and the percentage of hypochromism was found to be 16-34% (from spectral titration). The results of spectral measurement indicate that the compounds act as effective DNA-interacting agents. Electrophoretic separation studies prove that from all the metabolites tested in this study, only gyrophoric acid exhibited an inhibitory effect on Topo I (25μM).
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