Synthesis and Antiproliferative Activity of Steroidal Diaryl Ethers

Novel 13α-estrone derivatives have been synthesized via direct arylation of the phenolic hydroxy function. Chan–Lam couplings of arylboronic acids with 13α-estrone as a nucleophilic partner were carried out under copper catalysis. The antiproliferative activities of the newly synthesized diaryl ethe...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Kovács Édua
Ali Hazhmat
Minorics Renáta
Traj Péter
Resch Vivien Erzsébet
Paragi Gábor
Bruszel Bella
Zupkó István
Mernyák Erzsébet
Dokumentumtípus: Cikk
Megjelent: 2023
Sorozat:MOLECULES 28 No. 3
Tárgyszavak:
doi:10.3390/molecules28031196

mtmt:33594496
Online Access:http://publicatio.bibl.u-szeged.hu/28366
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520 3 |a Novel 13α-estrone derivatives have been synthesized via direct arylation of the phenolic hydroxy function. Chan–Lam couplings of arylboronic acids with 13α-estrone as a nucleophilic partner were carried out under copper catalysis. The antiproliferative activities of the newly synthesized diaryl ethers against a panel of human cancer cell lines (A2780, MCF-7, MDA-MB 231, HeLa, SiHa) were investigated by means of MTT assays. The quinoline derivative displayed substantial antiproliferative activity against MCF-7 and HeLa cell lines with low micromolar IC50 values. Disturbance of tubulin polymerization has been confirmed by microplate-based photometric assay. Computational calculations reveal significant interactions of the quinoline derivative with the taxoid binding site of tubulin. 
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700 0 1 |a Ali Hazhmat  |e aut 
700 0 1 |a Minorics Renáta  |e aut 
700 0 1 |a Traj Péter  |e aut 
700 0 1 |a Resch Vivien Erzsébet  |e aut 
700 0 1 |a Paragi Gábor  |e aut 
700 0 1 |a Bruszel Bella  |e aut 
700 0 1 |a Zupkó István  |e aut 
700 0 1 |a Mernyák Erzsébet  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/28366/1/molecules-28-01196-v3.pdf  |z Dokumentum-elérés