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New potent steroid sulphatase inhibitors based on 6-(1-phenyl-1 H -1,2,3-triazol-4-yl)naphthalen-2-yl sulphamate derivatives.
- Source :
-
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2021 Dec; Vol. 36 (1), pp. 238-247. - Publication Year :
- 2021
-
Abstract
- In the present work, we report a new class of potent steroid sulphatase (STS) inhibitors based on 6-(1-phenyl-1 H -1,2,3-triazol-4-yl)naphthalen-2-yl sulphamate derivatives. Within the set of new STS inhibitors, 6-(1-(1,2,3-trifluorophenyl)-1 H -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 IC <subscript>50</subscript> value of 15.97 nM for 3L showed that this compound is a very promising candidate for further preclinical investigations.
- Subjects :
- Dose-Response Relationship, Drug
Enzyme Inhibitors chemical synthesis
Enzyme Inhibitors chemistry
Humans
MCF-7 Cells
Molecular Structure
Steryl-Sulfatase isolation & purification
Steryl-Sulfatase metabolism
Structure-Activity Relationship
Sulfonic Acids chemical synthesis
Sulfonic Acids chemistry
Enzyme Inhibitors pharmacology
Steryl-Sulfatase antagonists & inhibitors
Sulfonic Acids pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1475-6374
- Volume :
- 36
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of enzyme inhibition and medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 33322953
- Full Text :
- https://doi.org/10.1080/14756366.2020.1858820