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  2. 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

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

  • Front Chem. 2020 Jun 30:8:495. doi: 10.3389/fchem.2020.00495.
Roberta Listro 1 Silvia Stotani 1 2 Giacomo Rossino 1 Marta Rui 1 Alessio Malacrida 3 Guido Cavaletti 3 Michela Cortesi 4 Chiara Arienti 4 Anna Tesei 4 Daniela Rossi 1 Marcello Di Giacomo 1 Mariarosaria Miloso 3 Simona Collina 1
Affiliations

Affiliations

  • 1 Medicinal Chemistry and Pharmaceutical Technology Section, Department of Drug Sciences, University of Pavia, Pavia, Italy.
  • 2 Medicinal Chemistry, Taros Chemicals GmbH and Co. KG, Dortmund, Germany.
  • 3 Experimental Neurology Unit, School of Medicine and Surgery & Milan Center for Neuroscience, University of Milan Bicocca, Monza, Italy.
  • 4 Biosciences Laboratory, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRCCS), Meldola, Italy.
Abstract

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.

Keywords

cancer; compound library; drug discovery; glioblastoma; multiple myeloma.

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