Synthesis and Biological Evaluation of a Library of AGE‐Related Amino Acid Triazole Crosslinkers. Issue 33 (26th August 2020)

• Record Type: Journal Article
• Authors: Icik, Esra; Jolly, Anthony; Löffler, Paul; Agelidis, Nektarios; Bugdayci, Bakiye; Altevogt, Luca; Bilitewski, Ursula; Baro, Angelika; Laschat, Sabine
• Is Part Of: European journal of organic chemistry. Issue 33(2020)
• Page Start: 5368
• Page End: 5379
• Publication Date: 2020-08-26
• Subjects: Amino acids -- Biological activity -- Click chemistry -- Triazoles -- Triazolium; Chemistry, Organic -- Periodicals; Organic compounds -- Synthesis -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1002/ejoc.202000811
• Languages: English
• ISSNs: 1434-193X

Abstract

Abstract : Three N ‐Boc‐protected amino acids, l ‐serine, l ‐aspartic, and l ‐glutamic acid, were either converted into their methyl azidoalkanoates or various alkynes via Bestmann‐Ohira strategy or via reaction with propargylamine and propargyl bromide, respectively. The Cu‐catalyzed click reaction provided a library of amino acid based triazoles, which were further N ‐methylated to triazolium iodides or deprotected and precipitated as free amino acid triazole dihydrochlorides. The biological properties of all derivatives were investigated by cytotoxicity assay (against L929 mouse fibroblasts) and broth microdilution method ( E. coli ΔTolC and S. aureus ). First results reveal complete inactivity for triazolium iodides with cell viabilities and microbial growths nearly 100 %, indicating them as possible analogs of advanced glycation endproducts (AGEs). Abstract : Click reaction between l ‐amino acid derived azides and alkynes gave amino acid functionalized triazoles, which were further derivatized to charged triazolium iodides and free amino acid hydrochlorides. The products reveal high cell viabilities in a standard cytotoxicity assay making them attractive as AGE analogs.