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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...

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Autores principales: Weiß, Christine, Bogner, Tobias, Sammet, Benedikt, Sewald, Norbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
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.
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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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