Diana G D, Carabateas P M, Johnson R E, Williams G L, Pancic F, Collins J C
J Med Chem. 1978 Sep;21(9):889-94. doi: 10.1021/jm00207a010.
The synthesis and in vitro antiviral evaluation of a series of substituted benzyl beta-diketones are described. The introduction of a styryl group onto the phenyl ring enhanced activity against herpesvirus type 2. The 4-methoxystyryl homologue 8 was evaluated extensively in vitro and was found to be effective against both RNA and DNA viruses. Compound 8 was evaluated in the mouse vagina against herpes simplex type 1 and produced a significant increase in survival rate as well as in survival time.