Novel steroid sulfatase inhibitors based on N ‐thiophosphorylated 3‐(4‐aminophenyl)‐coumarin‐7‐O‐sulfamates - Publication - Bridge of Knowledge

Your account

login

Search

Novel steroid sulfatase inhibitors based on N ‐thiophosphorylated 3‐(4‐aminophenyl)‐coumarin‐7‐O‐sulfamates

Abstract

In the present work, we described convenient methods for the synthesis ofN-thiophosphorylated 3-(4-aminophenyl)-coumarin-7-O-sulfamates as steroid sulfatase(STS) inhibitors. To design the structures of the potential STS inhibitors, molecularmodeling techniques were used. A computational docking method was used to deter-mine the binding modes of the synthesized inhibitors as well as to identify potentialinteractions between specified functional groups on the inhibitors and the amino acidresidues present in the active site of the enzyme. The inhibitory activities of the syn-thesized compounds were tested in an enzymatic assay with STS isolated from ahuman placenta. Within the set of newly synthesized compounds,9edemonstratedthe highest inhibitory activity in the enzymatic assay with an IC50value of 0.201μM(the IC50value of667-COUMATEin the same test was 0.062μM). Furthermore, wetried to verify if the obtained STS inhibitors are able to pass through the cellular mem-brane effectively in cell line experiments. In the course of our study, we determinedthe STS activity in the MCF-7 cell line after incubation in the presence of the inhibitors(at 100 nM concentration). For this evaluation, we included newly synthesized com-pounds9a-gand theirN-phosphorylated analogs6a-h, whose synthesis has been pre-viously described. We found that the lowest STS activities were measured in thepresence ofN-phosphorylated derivatives6e(0.1% of STS activity) and6f(0.2% ofSTS activity). The measured STS activity in the presence of667-COUMATE(used as areference) was 0.1%. Moreover, at concentrations up to 1μM, the most active com-pounds (6e,6f,9b,and9e) did not exert any toxic effects on zebrafish embryos.

Citations

  • 6

    CrossRef

  • 0

    Web of Science

  • 7

    Scopus

Authors (10)

Cite as

Full text

download paper
downloaded 61 times
Publication version
Accepted or Published Version
License
Copyright (2019 Wiley Periodicals, Inc.)

Keywords

Details

Category:
Articles
Type:
artykuły w czasopismach
Published in:
DRUG DEVELOPMENT RESEARCH no. 80, pages 857 - 866,
ISSN: 0272-4391
Language:
English
Publication year:
2019
Bibliographic description:
Daśko M., Demkowicz S., Biernacki K., Harrous A., Rachoń J., Kozak W., Martyna A., Masłyk M., Kubiński K., Boguszewska‐czubara A.: Novel steroid sulfatase inhibitors based on N ‐thiophosphorylated 3‐(4‐aminophenyl)‐coumarin‐7‐O‐sulfamates// DRUG DEVELOPMENT RESEARCH -Vol. 80,iss. 6 (2019), s.857-866
DOI:
Digital Object Identifier (open in new tab) 10.1002/ddr.21569
Verified by:
Gdańsk University of Technology

seen 164 times

Recommended for you

Synthesis and steroid sulfatase inhibitory activities of N-phosphorylated 3-(4-aminophenyl)-coumarin-7-O-sulfamates

  • M. Daśko,
  • M. Masłyk,
  • K. Kubiński
  • + 3 authors
2016

Synthesis and biological evaluation of fluorinated N-benzoyl and N-phenylacetoyl derivatives of 3-(4-aminophenyl)-coumarin-7-O-sulfamate as steroid sulfatase inhibitors

2017

Synthesis and biological evaluation of fluorinated 3-phenylcoumarin-7-O-sulfamate derivatives as steroid sulfatase inhibitors

2016

Synthesis and biological evaluation of N-acylated tyramine sulfamates containing C-F bonds as steroid sulfatase inhibitors

2017
Meta Tags