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Recent Advances in the Studies on Luotonins
Luotonins are alkaloids from the aerial parts of Peganum nigellastrum Bunge. that display three major skeleton types. Luotonins A, B, and E are pyrroloquinazolino-quinoline alkaloids, luotonins C and D are canthin-6-one alkaloids, and luotonin F is a 4(3H)-quinazolinone alkaloid. All six luotonins h...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264391/ https://www.ncbi.nlm.nih.gov/pubmed/21677601 http://dx.doi.org/10.3390/molecules16064861 |
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author | Liang, Jing Lu Cha, Hyo Chang Jahng, Yurngdong |
author_facet | Liang, Jing Lu Cha, Hyo Chang Jahng, Yurngdong |
author_sort | Liang, Jing Lu |
collection | PubMed |
description | Luotonins are alkaloids from the aerial parts of Peganum nigellastrum Bunge. that display three major skeleton types. Luotonins A, B, and E are pyrroloquinazolino-quinoline alkaloids, luotonins C and D are canthin-6-one alkaloids, and luotonin F is a 4(3H)-quinazolinone alkaloid. All six luotonins have shown promising cytotoxicities towards selected human cancer cell lines, especially against leukemia P-388 cells. Luotonin A is the most active one, with its activity stemming from topoisomerase I-dependent DNA-cleavage. Such intriguing biological activities and unique structures have led not only to the development of synthetic methods for the efficient synthesis of these compounds, but also to interest in structural modifications for improving the biological properties. Recent progress in the study of luotonins is covered. |
format | Online Article Text |
id | pubmed-6264391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62643912018-12-10 Recent Advances in the Studies on Luotonins Liang, Jing Lu Cha, Hyo Chang Jahng, Yurngdong Molecules Review Luotonins are alkaloids from the aerial parts of Peganum nigellastrum Bunge. that display three major skeleton types. Luotonins A, B, and E are pyrroloquinazolino-quinoline alkaloids, luotonins C and D are canthin-6-one alkaloids, and luotonin F is a 4(3H)-quinazolinone alkaloid. All six luotonins have shown promising cytotoxicities towards selected human cancer cell lines, especially against leukemia P-388 cells. Luotonin A is the most active one, with its activity stemming from topoisomerase I-dependent DNA-cleavage. Such intriguing biological activities and unique structures have led not only to the development of synthetic methods for the efficient synthesis of these compounds, but also to interest in structural modifications for improving the biological properties. Recent progress in the study of luotonins is covered. MDPI 2011-06-14 /pmc/articles/PMC6264391/ /pubmed/21677601 http://dx.doi.org/10.3390/molecules16064861 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Liang, Jing Lu Cha, Hyo Chang Jahng, Yurngdong Recent Advances in the Studies on Luotonins |
title | Recent Advances in the Studies on Luotonins |
title_full | Recent Advances in the Studies on Luotonins |
title_fullStr | Recent Advances in the Studies on Luotonins |
title_full_unstemmed | Recent Advances in the Studies on Luotonins |
title_short | Recent Advances in the Studies on Luotonins |
title_sort | recent advances in the studies on luotonins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264391/ https://www.ncbi.nlm.nih.gov/pubmed/21677601 http://dx.doi.org/10.3390/molecules16064861 |
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