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Unravelling the Antiproliferative Activity of 1,2,5-oxadiazole Derivatives.
Ehrsam, Daniel; Porta, Fabiola; Mori, Matteo; Schwabedissen, Henriette E Meyer Zu; Dalla Via, Lisa; Garcia-Argaez, Aìda Nelly; Basile, Livia; Meneghetti, Fiorella; Villa, Stefania; Gelain, Arianna.
Afiliação
  • Ehrsam D; Biopharmacy, Department of Pharmaceutical Sciences, University of Basel, Basel, Switzerland.
  • Porta F; Biopharmacy, Department of Pharmaceutical Sciences, University of Basel, Basel, Switzerland.
  • Mori M; Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.
  • Schwabedissen HEMZ; Biopharmacy, Department of Pharmaceutical Sciences, University of Basel, Basel, Switzerland.
  • Dalla Via L; Department of Pharmaceutical and Pharmacological Sciences, University of Padua, Padua, Italy.
  • Garcia-Argaez AN; Department of Pharmaceutical and Pharmacological Sciences, University of Padua, Padua, Italy.
  • Basile L; Department of Drug Sciences, Section of Medicinal Chemistry, University of Catania, Catania, Italy.
  • Meneghetti F; Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.
  • Villa S; Department of Pharmaceutical Sciences, University of Milan, Milan, Italy stefania.villa@unimi.it.
  • Gelain A; Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.
Anticancer Res ; 39(7): 3453-3461, 2019 Jul.
Article em En | MEDLINE | ID: mdl-31262869
ABSTRACT

AIM:

To develop several new derivatives aimed to complete the studies concerning the antiproliferative profile of the oxadiazole derivative MD77. MATERIALS AND

METHODS:

The substitution pattern around the phenyl rings of this compound was analyzed through the synthesis of positional isomers and of analogues bearing different substituents at the para positions (2-12).

RESULTS:

The results of the antiproliferative activity of these derivatives versus HCT-116 and HeLa cancer cell lines shed light on the effects of the presence, nature and position of such substituents. Notably, derivative 4, a regioisomer of 1 in which the substituents at the para positions of the phenyl rings were inverted, showed the best antiproliferative profile, exhibiting a significant activity also against MCF7 and MDA-MB 468 cancer cell lines.

CONCLUSION:

Preliminary results showed the ability of compound 4 to reduce the viability of cancer cells by counteracting human recombinant topoisomerase II α relaxation activity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxidiazóis / Antineoplásicos Limite: Humans Idioma: En Revista: Anticancer Res Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxidiazóis / Antineoplásicos Limite: Humans Idioma: En Revista: Anticancer Res Ano de publicação: 2019 Tipo de documento: Article