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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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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. |
format | Online Article Text |
id | pubmed-6273377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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