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Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity

Betulin derivatives are a widely studied group of compounds of natural origin due to their wide spectrum of biological activities. This paper describes new betulin derivatives, containing a phosphonate group. The allyl-vinyl isomerization and synthesis of acetylenic derivatives have been reported. S...

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Detalles Bibliográficos
Autores principales: Chrobak, Elwira, Bębenek, Ewa, Kadela-Tomanek, Monika, Latocha, Małgorzata, Jelsch, Christian, Wenger, Emmanuel, Boryczka, Stanisław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273377/
https://www.ncbi.nlm.nih.gov/pubmed/27571057
http://dx.doi.org/10.3390/molecules21091123
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author Chrobak, Elwira
Bębenek, Ewa
Kadela-Tomanek, Monika
Latocha, Małgorzata
Jelsch, Christian
Wenger, Emmanuel
Boryczka, Stanisław
author_facet Chrobak, Elwira
Bębenek, Ewa
Kadela-Tomanek, Monika
Latocha, Małgorzata
Jelsch, Christian
Wenger, Emmanuel
Boryczka, Stanisław
author_sort Chrobak, Elwira
collection PubMed
description Betulin derivatives are a widely studied group of compounds of natural origin due to their wide spectrum of biological activities. This paper describes new betulin derivatives, containing a phosphonate group. The allyl-vinyl isomerization and synthesis of acetylenic derivatives have been reported. Structural identification of products as E and Z isomers has been carried out using (1)H-, (13)C-, (31)P-NMR, and crystallographic analysis. The crystal structure in the orthorhombic space group and analysis of crystal packing contacts for 29-diethoxyphosphoryl-28-cyclopropylpropynoyloxy-lup-20E(29)-en-3β-ol 8a are reported. All new compounds were tested in vitro for their antiproliferative activity against human T47D (breast cancer), SNB-19 (glioblastoma), and C32 (melanoma) cell lines.
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spelling pubmed-62733772018-12-28 Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity Chrobak, Elwira Bębenek, Ewa Kadela-Tomanek, Monika Latocha, Małgorzata Jelsch, Christian Wenger, Emmanuel Boryczka, Stanisław Molecules Article Betulin derivatives are a widely studied group of compounds of natural origin due to their wide spectrum of biological activities. This paper describes new betulin derivatives, containing a phosphonate group. The allyl-vinyl isomerization and synthesis of acetylenic derivatives have been reported. Structural identification of products as E and Z isomers has been carried out using (1)H-, (13)C-, (31)P-NMR, and crystallographic analysis. The crystal structure in the orthorhombic space group and analysis of crystal packing contacts for 29-diethoxyphosphoryl-28-cyclopropylpropynoyloxy-lup-20E(29)-en-3β-ol 8a are reported. All new compounds were tested in vitro for their antiproliferative activity against human T47D (breast cancer), SNB-19 (glioblastoma), and C32 (melanoma) cell lines. MDPI 2016-08-26 /pmc/articles/PMC6273377/ /pubmed/27571057 http://dx.doi.org/10.3390/molecules21091123 Text en © 2016 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 (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chrobak, Elwira
Bębenek, Ewa
Kadela-Tomanek, Monika
Latocha, Małgorzata
Jelsch, Christian
Wenger, Emmanuel
Boryczka, Stanisław
Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity
title Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity
title_full Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity
title_fullStr Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity
title_full_unstemmed Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity
title_short Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity
title_sort betulin phosphonates; synthesis, structure, and cytotoxic activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273377/
https://www.ncbi.nlm.nih.gov/pubmed/27571057
http://dx.doi.org/10.3390/molecules21091123
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