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Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents
Despite the fact that significant advances in treatment of common cancers have been achieved over the years, orphan tumors still represent an important unmet medical need. Due to their complex multifactorial origin and limited number of cases, such pathologies often have very limited treatment optio...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338850/ https://www.ncbi.nlm.nih.gov/pubmed/32695745 http://dx.doi.org/10.3389/fchem.2020.00495 |
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author | Listro, Roberta Stotani, Silvia Rossino, Giacomo Rui, Marta Malacrida, Alessio Cavaletti, Guido Cortesi, Michela Arienti, Chiara Tesei, Anna Rossi, Daniela Giacomo, Marcello Di Miloso, Mariarosaria Collina, Simona |
author_facet | Listro, Roberta Stotani, Silvia Rossino, Giacomo Rui, Marta Malacrida, Alessio Cavaletti, Guido Cortesi, Michela Arienti, Chiara Tesei, Anna Rossi, Daniela Giacomo, Marcello Di Miloso, Mariarosaria Collina, Simona |
author_sort | Listro, Roberta |
collection | PubMed |
description | Despite the fact that significant advances in treatment of common cancers have been achieved over the years, orphan tumors still represent an important unmet medical need. Due to their complex multifactorial origin and limited number of cases, such pathologies often have very limited treatment options and poor prognosis. In the search for new anticancer agents, our group recently identified RC-106, a Sigma receptor modulator endowed with proteasome inhibition activity. This compound showed antiproliferative activity toward different cancer cell lines, among them glioblastoma (GB) and multiple myeloma (MM), two currently unmet medical conditions. In this work, we directed our efforts toward the exploration of chemical space around RC-106 to identify new active compounds potentially useful in cancer treatment. Thanks to a combinatorial approach, we prepared 41 derivatives of the compound and evaluated their cytotoxic potential against MM and GB. Three novel potential anticancer agents have been identified. |
format | Online Article Text |
id | pubmed-7338850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73388502020-07-20 Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents Listro, Roberta Stotani, Silvia Rossino, Giacomo Rui, Marta Malacrida, Alessio Cavaletti, Guido Cortesi, Michela Arienti, Chiara Tesei, Anna Rossi, Daniela Giacomo, Marcello Di Miloso, Mariarosaria Collina, Simona Front Chem Chemistry Despite the fact that significant advances in treatment of common cancers have been achieved over the years, orphan tumors still represent an important unmet medical need. Due to their complex multifactorial origin and limited number of cases, such pathologies often have very limited treatment options and poor prognosis. In the search for new anticancer agents, our group recently identified RC-106, a Sigma receptor modulator endowed with proteasome inhibition activity. This compound showed antiproliferative activity toward different cancer cell lines, among them glioblastoma (GB) and multiple myeloma (MM), two currently unmet medical conditions. In this work, we directed our efforts toward the exploration of chemical space around RC-106 to identify new active compounds potentially useful in cancer treatment. Thanks to a combinatorial approach, we prepared 41 derivatives of the compound and evaluated their cytotoxic potential against MM and GB. Three novel potential anticancer agents have been identified. Frontiers Media S.A. 2020-06-30 /pmc/articles/PMC7338850/ /pubmed/32695745 http://dx.doi.org/10.3389/fchem.2020.00495 Text en Copyright © 2020 Listro, Stotani, Rossino, Rui, Malacrida, Cavaletti, Cortesi, Arienti, Tesei, Rossi, Giacomo, Miloso and Collina. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Listro, Roberta Stotani, Silvia Rossino, Giacomo Rui, Marta Malacrida, Alessio Cavaletti, Guido Cortesi, Michela Arienti, Chiara Tesei, Anna Rossi, Daniela Giacomo, Marcello Di Miloso, Mariarosaria Collina, Simona Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents |
title | Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents |
title_full | Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents |
title_fullStr | Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents |
title_full_unstemmed | Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents |
title_short | Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents |
title_sort | exploring the rc-106 chemical space: design and synthesis of novel (e)-1-(3-arylbut-2-en-1-yl)-4-(substituted) piperazine derivatives as potential anticancer agents |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338850/ https://www.ncbi.nlm.nih.gov/pubmed/32695745 http://dx.doi.org/10.3389/fchem.2020.00495 |
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