Natural‐Product‐Inspired Discovery of Trimethoxyphenyl‐1,2,4‐triazolosulfonamides as Potent Tubulin Polymerization Inhibitors

Abstract

AbstractAn approach of natural product‐inspired strategy and incorporation of an NP‐privileged motif has been investigated for the discovery of new tubulin polymerization inhibitors. Two series, N‐Arylsulfonyl‐3‐arylamino‐5‐amino‐1,2,4‐triazole derivatives, and their isomers were considered. The compounds were synthesized by construction of the N‐aryl‐1,2,4‐triazole‐3,5‐diamine motif and sulfonylation. Although the chemo‐ and regioselectivity in sulfonylation were challenging due to multiple ring‐tautomerizable‐NH and exocyclic NH2 functionalities present in the molecular motifs, the developed synthetic method enabled the preparation of designed molecular skeletons with biologically important motifs. The approach also led to explore interesting molecular regio‐ and stereochemical aspects valuable for activity. The X‐ray crystallography study indicated that the hydrogen bonding between the arylamine‐NH and the arylsulfonyl‐“O” unit and appropriate molecular‐functionality topology allowed the cis‐locking of two aryls, which is important for tubulin‐binding and antiproliferative properties. All synthesized compounds majorly showed characteristic antiproliferative effects in breast cancer cells (MCF‐7), and four compounds exhibited potent antiproliferative activity. One compound potently bound to tubulin at the colchicine site and inhibited tubulin polymerization in vitro. The compound significantly depolymerized microtubules in MCF‐7 cells, arrested the cells at the G2/M phase, and induced cell death. This study represents the importance of the design strategy in medicinal chemistry and the molecular structural features relevant to anticancer anti‐tubulin properties. The explored molecules have the potential for further development.