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Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity
Chemical decomposition of DMSO stock solutions is a common incident that can mislead biological screening campaigns. Here, we share our case study of 2‐aminothiazole 1, originating from an antimalarial class that undergoes chemical decomposition in DMSO at room temperature. As previously measured bi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360061/ https://www.ncbi.nlm.nih.gov/pubmed/33844432 http://dx.doi.org/10.1002/cmdc.202100067 |
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author | Ropponen, Henni‐Karoliina Bader, Chantal D. Diamanti, Eleonora Illarionov, Boris Rottmann, Matthias Fischer, Markus Witschel, Matthias Müller, Rolf Hirsch, Anna K. H. |
author_facet | Ropponen, Henni‐Karoliina Bader, Chantal D. Diamanti, Eleonora Illarionov, Boris Rottmann, Matthias Fischer, Markus Witschel, Matthias Müller, Rolf Hirsch, Anna K. H. |
author_sort | Ropponen, Henni‐Karoliina |
collection | PubMed |
description | Chemical decomposition of DMSO stock solutions is a common incident that can mislead biological screening campaigns. Here, we share our case study of 2‐aminothiazole 1, originating from an antimalarial class that undergoes chemical decomposition in DMSO at room temperature. As previously measured biological activities observed against Plasmodium falciparum NF54 and for the target enzyme PfIspE were not reproducible for a fresh batch, we tackled the challenge to understand where the activity originated from. Solvent‐ and temperature‐dependent studies using HRMS and NMR spectroscopy to monitor the decomposition led to the isolation and in vitro evaluation of several fractions against PfIspE. After four days of decomposition, we successfully isolated the oxygenated and dimerised compounds using SFC purification and correlated the observed activities to them. Due to the unstable nature of the two isolates, it is likely that they undergo further decomposition contributing to the overall instability of the compound. |
format | Online Article Text |
id | pubmed-8360061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83600612021-08-17 Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity Ropponen, Henni‐Karoliina Bader, Chantal D. Diamanti, Eleonora Illarionov, Boris Rottmann, Matthias Fischer, Markus Witschel, Matthias Müller, Rolf Hirsch, Anna K. H. ChemMedChem Communications Chemical decomposition of DMSO stock solutions is a common incident that can mislead biological screening campaigns. Here, we share our case study of 2‐aminothiazole 1, originating from an antimalarial class that undergoes chemical decomposition in DMSO at room temperature. As previously measured biological activities observed against Plasmodium falciparum NF54 and for the target enzyme PfIspE were not reproducible for a fresh batch, we tackled the challenge to understand where the activity originated from. Solvent‐ and temperature‐dependent studies using HRMS and NMR spectroscopy to monitor the decomposition led to the isolation and in vitro evaluation of several fractions against PfIspE. After four days of decomposition, we successfully isolated the oxygenated and dimerised compounds using SFC purification and correlated the observed activities to them. Due to the unstable nature of the two isolates, it is likely that they undergo further decomposition contributing to the overall instability of the compound. John Wiley and Sons Inc. 2021-05-07 2021-07-06 /pmc/articles/PMC8360061/ /pubmed/33844432 http://dx.doi.org/10.1002/cmdc.202100067 Text en © 2021 The Authors. ChemMedChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Ropponen, Henni‐Karoliina Bader, Chantal D. Diamanti, Eleonora Illarionov, Boris Rottmann, Matthias Fischer, Markus Witschel, Matthias Müller, Rolf Hirsch, Anna K. H. Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity |
title | Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity |
title_full | Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity |
title_fullStr | Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity |
title_full_unstemmed | Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity |
title_short | Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity |
title_sort | search for the active ingredients from a 2‐aminothiazole dmso stock solution with antimalarial activity |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360061/ https://www.ncbi.nlm.nih.gov/pubmed/33844432 http://dx.doi.org/10.1002/cmdc.202100067 |
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