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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...

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Detalles Bibliográficos
Autores principales: Liang, Jing Lu, Cha, Hyo Chang, Jahng, Yurngdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
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.
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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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