| Literature DB >> 29945796 |
Adriano Aloisi1, Adrien Franchet2, Dominique Ferrandon2, Alberto Bianco1, Cécilia Ménard-Moyon3.
Abstract
Fipronil is a phenyl pyrazole molecule widely used across the world as both insecticide and veterinary drug. The main goal of this work was to synthesize a fluorescently labeled fipronil derivative for cellular imaging without affecting its intrinsic properties. We selected fluorescein as fluorescent probe and we investigated different strategies for stable chemical ligation between both entities, such as thiourea and direct peptide bond. While thiourea bond displayed low stability, direct peptide bond was difficult to achieve due to problems of steric hindrance. The best result was obtained by conjugation using click chemistry, which allowed to obtain fipronil stably labeled with the fluorescent probe.Entities:
Keywords: Azide-alkyne cycloaddition; Fipronil; Fluorescein; Stability
Mesh:
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Year: 2018 PMID: 29945796 DOI: 10.1016/j.bmcl.2018.06.036
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823