Synthetic Strategies Towards the Generation of Penicillin‐Containing Hybrids in the Search for Anticancer Activity

Abstract

An extended library of hybrids that combined a penicillin derivative with a peptoid moiety was designed and synthetized using either a solid‐phase or a mixed solid‐phase/solution‐phase strategy. The library was further evaluated for antiproliferative activity. While none of the different synthesized compounds showed significant cytotoxicity against a normal cell line, tumor cell results drew several conclusions, when comparing with our reference, the highly active triazolylpeptidyl penicillin derivative, TAF7f. Thus, when the 1,2,3‐triazole group was exchanged by its “retro‐inverse” analogue, no change was noted in the activity of the hybrids; however, better performance was generally obtained if the triazole is replaced by a glycine moiety. Additionally, the absence of hydrogen bond donor groups decreased the compounds activity, which could explain that, in general, this set of derivatives were less active than their peptide‐containing analogues. From this study, is indisputable that, regardless of the type of chain (peptide, peptoid or mixture) attached to penicillin, an isobutyl side chain placed in the position closest to penicillin and a benzyl in the next position are determinant for the activity.