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New potent steroid sulphatase inhibitors based on 6-(1-phenyl-1H-1,2,3-triazol-4-yl)naphthalen-2-yl sulphamate derivatives.
Ciupak, Olga; Dasko, Mateusz; Biernacki, Karol; Rachon, Janusz; Maslyk, Maciej; Kubinski, Konrad; Martyna, Aleksandra; Demkowicz, Sebastian.
Afiliação
  • Ciupak O; Department of Organic Chemistry, Faculty of Chemistry, Gdansk University of Technology, Gdansk, Poland.
  • Dasko M; Department of Inorganic Chemistry, Faculty of Chemistry, Gdansk University of Technology, Gdansk, Poland.
  • Biernacki K; Department of Organic Chemistry, Faculty of Chemistry, Gdansk University of Technology, Gdansk, Poland.
  • Rachon J; Department of Organic Chemistry, Faculty of Chemistry, Gdansk University of Technology, Gdansk, Poland.
  • Maslyk M; Department of Molecular Biology, The John Paul II Catholic University of Lublin, Lublin, Poland.
  • Kubinski K; Department of Molecular Biology, The John Paul II Catholic University of Lublin, Lublin, Poland.
  • Martyna A; Department of Molecular Biology, The John Paul II Catholic University of Lublin, Lublin, Poland.
  • Demkowicz S; Department of Organic Chemistry, Faculty of Chemistry, Gdansk University of Technology, Gdansk, Poland.
J Enzyme Inhib Med Chem ; 36(1): 238-247, 2021 Dec.
Article em En | MEDLINE | ID: mdl-33322953
ABSTRACT
In the present work, we report a new class of potent steroid sulphatase (STS) inhibitors based on 6-(1-phenyl-1H-1,2,3-triazol-4-yl)naphthalen-2-yl sulphamate derivatives. Within the set of new STS inhibitors, 6-(1-(1,2,3-trifluorophenyl)-1H-1,2,3-triazol-4-yl)naphthalen-2-yl sulphamate 3L demonstrated the highest activity in the enzymatic assay inhibiting the STS activity to 7.98% at 0.5 µM concentration. Furthermore, to verify whether the obtained STS inhibitors are able to pass through the cellular membrane effectively, cell line experiments have been carried out. We found that the lowest STS activities were measured in the presence of compound 3L (remaining STS activity of 5.22%, 27.48% and 99.0% at 100, 10 and 1 nM concentrations, respectively). The measured STS activities for Irosustat (used as a reference) were 5.72%, 12.93% and 16.83% in the same concentration range. Moreover, a determined IC50 value of 15.97 nM for 3L showed that this compound is a very promising candidate for further preclinical investigations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Sulfônicos / Esteril-Sulfatase / Inibidores Enzimáticos Limite: Humans Idioma: En Revista: J Enzyme Inhib Med Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Polônia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Sulfônicos / Esteril-Sulfatase / Inibidores Enzimáticos Limite: Humans Idioma: En Revista: J Enzyme Inhib Med Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Polônia