1.
Bioorg Med Chem Lett
; 28(23-24): 3708-3711, 2018 12 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30389287
RESUMO
We synthesized six novel BBR derivatives that were designed to avoid metabolic activation via ipso-substitution and evaluated for their degree of toxicity and hURAT1 inhibition. It was found that all of the derivatives demonstrate lower cytotoxicity in mouse hepatocytes and lower levels of metabolic activation than BBR, while maintaining their inhibitory activity toward the uric acid transporter. We propose that these derivatives could serve as effective uricosuric agents that have much better safety profiles than BBR.