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Targeting HIV entry through interaction with envelope glycoprotein 120 (gp120): Synthesis and antiviral evaluation of 1,3,5-triazines with aromatic amino acids

AutorLozano, V. ; Aguado, Leire ; Hoorelbeke, B.; Renders, M.; Camarasa Rius, María José ; Schols, D.; Balzarini, Jan; San-Félix, Ana ; Peréz-Pérez, María-Jesús
Fecha de publicación2011
EditorAmerican Chemical Society
CitaciónJournal of Medicinal Chemistry 54: 5335-5348 (2011)
ResumenOn the basis of the interesting inhibitory properties that lectins show against HIV-replication through their interaction with glycoprotein 120 (gp120), we here describe the design, synthesis, and anti-HIV evaluation of three series of 1,3,5-triazine derivatives (monomers, dimers, and trimers) functionalized with aromatic amino acids meant to mimic interactions that lectins establish with gp120. While monomers were inactive against HIV replication, dimers showed limited anti-HIV activity that is, however, considerably more significant in the trimers series, with EC50 values in the lower μM range. These findings most likely reflect the requirement of multivalency of the 1,3,5-triazine derivatives to display anti-HIV activity, as lectins do. The pronounced anti-HIV activity (EC50 ∼ 20 μM) is accompanied by the absence of toxicity in CEM T-cell line (CC50 > 250 μM). Moreover, SPR experiments revealed that the prototype trimers with a central core of 2,4,6-triethylbenzene and six l-Trp or six l-Tyr residues at the periphery were efficient binders of CXCR4- and CCR5-tropic HIV-1 gp120 (estimated KD: lower micromolar range). The collected data support the interest of this novel family of anti-HIV agents and qualify them as potential novel microbicide lead compounds.
Versión del editorhttp://dx.doi.org/10.1021/jm200560r
Identificadoresdoi: 10.1021/jm200560r
issn: 0022-2623
e-issn: 1520-4804
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