Repozytorium publikacji - Politechnika Gdańska

Steroid sulfatase (STS) is responsible for the hydrolysis of biologically inactive sulfated steroids into their active un-sulfated forms and promotes the growth of various hormone-dependent cancers (e.g., breast cancer). Therefore, the STS enzyme is a promising therapeutic target for the treatment of steroid-sensitive cancers. Herein, we report the synthesis and biological evaluation of sulfamate analogs as potential STS inhibitors based on N-acylated tyramines that contain C–F bonds. The inhibitory effects of the analogs were tested using STS isolated from human placenta. Of the analogs tested, 4-(2-perfluoroundecanoylaminoethyl)-phenyl sulfamate, 5r, demonstrated the greatest inhibitory effect, with an IC50 value of 2.18 μm (IC50 value of 2.13 μm for coumarin-7-O-sulfamate was used as a reference). These findings were supported by the results our computational analyses performed using molecular docking techniques.

Autorzy

• dr inż. Mateusz Daśko link otwiera się w nowej karcie ,
• prof. dr hab. inż. Janusz Rachoń link otwiera się w nowej karcie ,
• Maciej Masłyk,
• Konrad Kubiński,
• dr hab. inż. Sebastian Demkowicz link otwiera się w nowej karcie