Avtor/Urednik | Bacsa, Ildikó; Herman, Bianka Edina; Jójárt, Rebeka; Herman, Kevin Stefán; Wólfling, János; Schneider, Gyula; Tömböly, Csaba; Lanišnik-Rižner, Tea; Szécsi, Mihály; Mernyák, Erzsébet | |
Naslov | Synthesis and structure-activity relationships of 2- and/or 4-halogenated 13[beta]- and 13[alpha]-estrone derivatives as enzyme inhibitors of estrogen biosynthesis | |
Tip | članek | |
Vol. in št. | Letnik 33, št. 1 | |
Leto izdaje | 2018 | |
Obseg | str. 1271-1282 | |
ISSN | 1475-6366 - Journal of enzyme inhibition and medicinal chemistry | |
Jezik | eng | |
Abstrakt | Ring A halogenated 13[alpha], 13[beta], and 17-deoxy-13[alpha]-estrone derivatives were synthesised with N-halosuccinimides as electrophile triggers. Substitutions occurred at positions C-2 and/or C-4. The potential inhibitory action of the halogenated estrones on human aromatase, steroid sulfatase, or 17[beta]-hydroxysteroid dehydrogenase 1 activity was investigated via in vitro radiosubstrate incubation. Potent submicromolar or low micromolar inhibitors were identified with occasional dual or multiple inhibitory properties. Valuable structure-activity relationships were established from the comparison of the inhibitory data obtained. Kinetic experiments performed with selected compounds revealed competitive reversible inhibition mechanisms against 17[beta]-hydroxysteroid dehydrogenase 1 and competitive irreversible manner in the inhibition of the steroid sulfatase enzyme. | |
Proste vsebinske oznake | estrogen biosynthesis enzyme inhibitors estrogen biosinteza encimski inhibitorji |