“…This contrasting activity trend for IV-AE between to the two receptors is notable, as LasR and AbaR share very similar native ligands (OdDHL and OH-dDHL, respectively), and have high sequence homology in their ligand-binding sites (note, this site is only putative in the case of AbaR). 61, 65 Additional biochemical studies are warranted to probe this disparity further. Lastly, the type V triazoles containing multiple HL groups displayed modest LasR agonistic and antagonistic activities at best, suggesting that while additional study of such multivalent structures could be fruitful, ligand redesign ( e.g.…”