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Synthesis, Characterization and HPLC Analysis of the (1S,2S,5R)-Diastereomer and the Enantiomer of the Clinical Candidate AR-15512

AR-15512 (formerly known as AVX-012 and WS-12) is a TRPM8 receptor agonist currently in phase 2b clinical trials for the treatment of dry eye. This bioactive compound with menthol-like cooling activity has three stereogenic centers, and its final structure and absolute configuration, (1R,2S,5R), hav...

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Autores principales: Rodríguez-Arévalo, Sergio, Pujol, Eugènia, Abás, Sònia, Galdeano, Carles, Escolano, Carmen, Vázquez, Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914790/
https://www.ncbi.nlm.nih.gov/pubmed/33572112
http://dx.doi.org/10.3390/molecules26040906
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author Rodríguez-Arévalo, Sergio
Pujol, Eugènia
Abás, Sònia
Galdeano, Carles
Escolano, Carmen
Vázquez, Santiago
author_facet Rodríguez-Arévalo, Sergio
Pujol, Eugènia
Abás, Sònia
Galdeano, Carles
Escolano, Carmen
Vázquez, Santiago
author_sort Rodríguez-Arévalo, Sergio
collection PubMed
description AR-15512 (formerly known as AVX-012 and WS-12) is a TRPM8 receptor agonist currently in phase 2b clinical trials for the treatment of dry eye. This bioactive compound with menthol-like cooling activity has three stereogenic centers, and its final structure and absolute configuration, (1R,2S,5R), have been previously solved by cryo-electron microscopy. The route of synthesis of AR-15512 has also been reported, revealing that epimerization processes at the C-1 can occur at specific stages of the synthesis. In order to confirm that the desired configuration of AR-15512 does not change throughout the process and to discard the presence of the enantiomer in the final product due to possible contamination of the initial starting material, both the enantiomer of AR-15512 and the diastereomer at the C-1 were synthesized and fully characterized. In addition, the absolute configuration of the (1S,2S,5R)-diastereomer was determined by X-ray crystallographic analysis, and new HPLC methods were designed and developed for the identification of the two stereoisomers and their comparison with the clinical candidate AR-15512.
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spelling pubmed-79147902021-03-01 Synthesis, Characterization and HPLC Analysis of the (1S,2S,5R)-Diastereomer and the Enantiomer of the Clinical Candidate AR-15512 Rodríguez-Arévalo, Sergio Pujol, Eugènia Abás, Sònia Galdeano, Carles Escolano, Carmen Vázquez, Santiago Molecules Article AR-15512 (formerly known as AVX-012 and WS-12) is a TRPM8 receptor agonist currently in phase 2b clinical trials for the treatment of dry eye. This bioactive compound with menthol-like cooling activity has three stereogenic centers, and its final structure and absolute configuration, (1R,2S,5R), have been previously solved by cryo-electron microscopy. The route of synthesis of AR-15512 has also been reported, revealing that epimerization processes at the C-1 can occur at specific stages of the synthesis. In order to confirm that the desired configuration of AR-15512 does not change throughout the process and to discard the presence of the enantiomer in the final product due to possible contamination of the initial starting material, both the enantiomer of AR-15512 and the diastereomer at the C-1 were synthesized and fully characterized. In addition, the absolute configuration of the (1S,2S,5R)-diastereomer was determined by X-ray crystallographic analysis, and new HPLC methods were designed and developed for the identification of the two stereoisomers and their comparison with the clinical candidate AR-15512. MDPI 2021-02-09 /pmc/articles/PMC7914790/ /pubmed/33572112 http://dx.doi.org/10.3390/molecules26040906 Text en © 2021 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
Rodríguez-Arévalo, Sergio
Pujol, Eugènia
Abás, Sònia
Galdeano, Carles
Escolano, Carmen
Vázquez, Santiago
Synthesis, Characterization and HPLC Analysis of the (1S,2S,5R)-Diastereomer and the Enantiomer of the Clinical Candidate AR-15512
title Synthesis, Characterization and HPLC Analysis of the (1S,2S,5R)-Diastereomer and the Enantiomer of the Clinical Candidate AR-15512
title_full Synthesis, Characterization and HPLC Analysis of the (1S,2S,5R)-Diastereomer and the Enantiomer of the Clinical Candidate AR-15512
title_fullStr Synthesis, Characterization and HPLC Analysis of the (1S,2S,5R)-Diastereomer and the Enantiomer of the Clinical Candidate AR-15512
title_full_unstemmed Synthesis, Characterization and HPLC Analysis of the (1S,2S,5R)-Diastereomer and the Enantiomer of the Clinical Candidate AR-15512
title_short Synthesis, Characterization and HPLC Analysis of the (1S,2S,5R)-Diastereomer and the Enantiomer of the Clinical Candidate AR-15512
title_sort synthesis, characterization and hplc analysis of the (1s,2s,5r)-diastereomer and the enantiomer of the clinical candidate ar-15512
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914790/
https://www.ncbi.nlm.nih.gov/pubmed/33572112
http://dx.doi.org/10.3390/molecules26040906
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