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Synthesis and Biological Activity of 23-Hydroxybetulinic Acid C-28 Ester Derivatives as Antitumor Agent Candidates
23-Hydroxybetulinic acid (1) served as the precursor for the synthesis of C-28 ester derivatives. The target compounds were evaluated in vitro for their antitumor activities against five cell lines (A549, BEL-7402, SF-763, B16 and HL-60). Among the obtained compounds, 6i had the most potent antitumo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268522/ https://www.ncbi.nlm.nih.gov/pubmed/22832884 http://dx.doi.org/10.3390/molecules17088832 |
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author | Bi, Yi Xu, Jinyi Sun, Fei Wu, Xiaoming Ye, Wencai Sun, Yijun Huang, Wenwen |
author_facet | Bi, Yi Xu, Jinyi Sun, Fei Wu, Xiaoming Ye, Wencai Sun, Yijun Huang, Wenwen |
author_sort | Bi, Yi |
collection | PubMed |
description | 23-Hydroxybetulinic acid (1) served as the precursor for the synthesis of C-28 ester derivatives. The target compounds were evaluated in vitro for their antitumor activities against five cell lines (A549, BEL-7402, SF-763, B16 and HL-60). Among the obtained compounds, 6i had the most potent antitumor activity, with the IC(50) values of 8.35 µM in HL-60 cells and showed similar antitumor activity as cyclophosphamide in H22 liver tumor and as 5-fluorouracil in B16 melanoma in vivo. |
format | Online Article Text |
id | pubmed-6268522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62685222018-12-12 Synthesis and Biological Activity of 23-Hydroxybetulinic Acid C-28 Ester Derivatives as Antitumor Agent Candidates Bi, Yi Xu, Jinyi Sun, Fei Wu, Xiaoming Ye, Wencai Sun, Yijun Huang, Wenwen Molecules Article 23-Hydroxybetulinic acid (1) served as the precursor for the synthesis of C-28 ester derivatives. The target compounds were evaluated in vitro for their antitumor activities against five cell lines (A549, BEL-7402, SF-763, B16 and HL-60). Among the obtained compounds, 6i had the most potent antitumor activity, with the IC(50) values of 8.35 µM in HL-60 cells and showed similar antitumor activity as cyclophosphamide in H22 liver tumor and as 5-fluorouracil in B16 melanoma in vivo. MDPI 2012-07-25 /pmc/articles/PMC6268522/ /pubmed/22832884 http://dx.doi.org/10.3390/molecules17088832 Text en © 2012 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 | Article Bi, Yi Xu, Jinyi Sun, Fei Wu, Xiaoming Ye, Wencai Sun, Yijun Huang, Wenwen Synthesis and Biological Activity of 23-Hydroxybetulinic Acid C-28 Ester Derivatives as Antitumor Agent Candidates |
title | Synthesis and Biological Activity of 23-Hydroxybetulinic Acid C-28 Ester Derivatives as Antitumor Agent Candidates |
title_full | Synthesis and Biological Activity of 23-Hydroxybetulinic Acid C-28 Ester Derivatives as Antitumor Agent Candidates |
title_fullStr | Synthesis and Biological Activity of 23-Hydroxybetulinic Acid C-28 Ester Derivatives as Antitumor Agent Candidates |
title_full_unstemmed | Synthesis and Biological Activity of 23-Hydroxybetulinic Acid C-28 Ester Derivatives as Antitumor Agent Candidates |
title_short | Synthesis and Biological Activity of 23-Hydroxybetulinic Acid C-28 Ester Derivatives as Antitumor Agent Candidates |
title_sort | synthesis and biological activity of 23-hydroxybetulinic acid c-28 ester derivatives as antitumor agent candidates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268522/ https://www.ncbi.nlm.nih.gov/pubmed/22832884 http://dx.doi.org/10.3390/molecules17088832 |
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