An efficient and facile microwave-assisted solution phase parallel synthesis for a 26-member library of N,N'-disubstituted thiourea analogs were accomplished successfully. The reaction time for synthesis of analogs was drastically reduced from a reported 8-12 h to only 10 min. Compounds were more than 95% pure, as characterized by modern analytical techniques, i.e. (1)H &(13)C NMR and FT-IR. The solid phase structural analysis has also been performed by single crystal XRD analysis. Synthesized compounds were preliminary screened for their in vitro urease inhibition and antifungal activity. Most of the compounds were found to be potent inhibitors of urease. However, the most significant activity was found for 11 with IC₅₀ of 1.67 μM. The docking scores correlate with the IC₅₀ values of inhibitors.
Keywords: Antifungal; DPPH radical scavenging; Microwave synthesis; N,N′-Disubstituted thioureas; Single crystal XRD; Urease inhibition.
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