1.
Bioorg Med Chem Lett
; 11(10): 1281-4, 2001 May 21.
Artículo
en Inglés
| MEDLINE
| ID: mdl-11392537
RESUMEN
To prepare novel estrogen receptor (ER) ligands, we have developed a facile approach to substituted hexahydrochrysene and tetrahydrobenzo[a]fluorene systems. Substituents, including basic side chains, were added to these systems, and their binding affinity to ERalpha and ERbeta, and in some cases their transcriptional activity were evaluated.