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Synthesis and evaluation of AKR1C inhibitory properties of A-ring halogenated oestrone derivatives
Published in Journal of Enzyme Inhibition and Medicinal Chemistry, 2021
Maša Sinreih, Rebeka Jójárt, Zoltán Kele, Tomaž Büdefeld, Gábor Paragi, Erzsébet Mernyák, Tea Lanišnik Rižner
In summary here, we can say that there was no formation of new hydrogen or halogen bonds with the flexible loops that might have been responsible for the selectivity, although hydrophobic interactions might have particularly important roles in the selectivities of these compounds. Hence, the variations of atoms at positions 2 and 4 in the sterane skeletons might fine-tune these effects.