A new pregnenolone analogues as privileged scaffolds in inhibition of CYP17 hydroxylase enzyme. Synthesis and in silico molecular docking study

作者：Al Masoudi Najim A^*; Mahdi Kuthiar M; Abdul Rida Nabeel A; Saeed Bahjat A; Engel Mathias

来源：Steroids, 2015, 100: 52-59.

DOI：10.1016/j.steroids.2015.05.002

• CYP17 hydroxylase
• Imine analogues
• Molecular docking
• Pregnenolone
• Prostate cancer

A new series of 17-(N-(arylimino)-5-pregnen-3 beta-ol derivatives 19-32 as well as carboxylate and acrylate analogues of pregnenolone 37-40 were synthesized and evaluated for their inhibitory activity against human CYP17 hydroxylase expressed in Escherichia coli. Compounds 32 and 37 were the Most potent analogues in this series, showing inhibition activity with IC50 = 2.11 and 1.29 mu M, respectively. However, the analogue 37 revealed a better selectivity profile (83.21% inhibition of hydroxylase), which is a leading candidate for further development. Molecular docking study of 37 showed binding with the amino acid residues of CYP17 through hydrogen bonds and hydrophobic interaction.

• 出版日期2015-8