1.
Bioorg Med Chem Lett
; 24(16): 3739-43, 2014 Aug 15.
Artículo
en Inglés
| MEDLINE
| ID: mdl-25086680
RESUMEN
We have developed a series of substituted 4-(thiophen-2-ylmethyl)-2H-phthalazin-1-ones as potent PARP-1 inhibitors. Preliminary biological evaluation indicated that most compounds possessed inhibitory potencies comparable to, or higher than AZD-2281. Among these compounds, 18q appeared to be the most notable one, which displayed an 8-fold improvement in enzymatic activity compared to AZD-2281. These efforts lay the foundation for our further investigation.