Synthesis of new derivatives of 21-imidazolyl-16-dehydropregnenolone as inhibitors of 5α-reductase 2 and with cytotoxic activity in cancer cells
Keywords: 16-Dehydropregnenolone acetate derivatives; Alicyclic ester moiety at C-3 of the steroidal skeleton; 5-α-reductase; Cytotoxic activity; Cell lines: PC-3; MCF7; SK-LU-1;