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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
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.
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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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