1.
Chem Pharm Bull (Tokyo)
; 54(5): 682-6, 2006 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16651766
RESUMO
Nineteen biscoumarins bearing free and modified hydroxyl substituents at benzoyloxyphenyl linker have been synthesized by multiple step synthesis. Among these biscoumarins, thirteen were found to be active molecules against HIV-1 integrase (HIV-1 IN). The structure-activity relationship of the nineteen compounds on HIV IN may be useful for the design of potent therapeutic agents.