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Total synthesis and biological evaluation of fluorinated cryptophycins
Cryptophycins are cytotoxic natural products that exhibit considerable activities even against multi-drug-resistant tumor cell lines. As fluorinated pharmaceuticals have become more and more important during the past decades, fluorine-functionalized cryptophycins were synthesized and evaluated in ce...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511040/ https://www.ncbi.nlm.nih.gov/pubmed/23209540 http://dx.doi.org/10.3762/bjoc.8.231 |
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author | Weiß, Christine Bogner, Tobias Sammet, Benedikt Sewald, Norbert |
author_facet | Weiß, Christine Bogner, Tobias Sammet, Benedikt Sewald, Norbert |
author_sort | Weiß, Christine |
collection | PubMed |
description | Cryptophycins are cytotoxic natural products that exhibit considerable activities even against multi-drug-resistant tumor cell lines. As fluorinated pharmaceuticals have become more and more important during the past decades, fluorine-functionalized cryptophycins were synthesized and evaluated in cell-based cytotoxicity assays. The unit A trifluoromethyl-modified cryptophycin proved to be highly active against KB-3-1 cells and exhibited an IC(50) value in the low picomolar range. However, the replacement of the 3-chloro-4-methoxyphenyl-substituent in unit B by a pentafluorophenyl moiety resulted in a significant loss of activity. |
format | Online Article Text |
id | pubmed-3511040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-35110402012-12-03 Total synthesis and biological evaluation of fluorinated cryptophycins Weiß, Christine Bogner, Tobias Sammet, Benedikt Sewald, Norbert Beilstein J Org Chem Full Research Paper Cryptophycins are cytotoxic natural products that exhibit considerable activities even against multi-drug-resistant tumor cell lines. As fluorinated pharmaceuticals have become more and more important during the past decades, fluorine-functionalized cryptophycins were synthesized and evaluated in cell-based cytotoxicity assays. The unit A trifluoromethyl-modified cryptophycin proved to be highly active against KB-3-1 cells and exhibited an IC(50) value in the low picomolar range. However, the replacement of the 3-chloro-4-methoxyphenyl-substituent in unit B by a pentafluorophenyl moiety resulted in a significant loss of activity. Beilstein-Institut 2012-11-23 /pmc/articles/PMC3511040/ /pubmed/23209540 http://dx.doi.org/10.3762/bjoc.8.231 Text en Copyright © 2012, Weiß et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Weiß, Christine Bogner, Tobias Sammet, Benedikt Sewald, Norbert Total synthesis and biological evaluation of fluorinated cryptophycins |
title | Total synthesis and biological evaluation of fluorinated cryptophycins |
title_full | Total synthesis and biological evaluation of fluorinated cryptophycins |
title_fullStr | Total synthesis and biological evaluation of fluorinated cryptophycins |
title_full_unstemmed | Total synthesis and biological evaluation of fluorinated cryptophycins |
title_short | Total synthesis and biological evaluation of fluorinated cryptophycins |
title_sort | total synthesis and biological evaluation of fluorinated cryptophycins |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511040/ https://www.ncbi.nlm.nih.gov/pubmed/23209540 http://dx.doi.org/10.3762/bjoc.8.231 |
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