Skip to main content
. 2010 Jul 5;88(1):25–30. doi: 10.1016/j.antiviral.2010.06.010

Table 1.

Activity of compounds against FCoV in fcwf-4 cells.

Compound Source Highest concentration tested CC50 Inhibition of CPE formation IC50
Nucleoside analogues
 Acyclovir GlaxoSmithKline (London, UK) 888 μM ≥888 μM NA
 Idoxuridine Pharmacy compound 141.2 μM ≥141.2 μM NA
 Ribavirin Roche (Basel, Switzerland) 12.8 μM ≥409.49 μM NA



Protease inhibitors
 Atazanavir Bristol-Myers Squibb (New York, USA) 17.75 μM 48.59 μM NA
 Indinavir Merck (Whitehouse station, USA) 70.237 μM ≥70.237 μM NA
 Lopinavir/ritonavir Abbott Laboratories (Abbott Park, USA) 3.125 μg/mL 47.04 μg/mL NA
 Nelfinavir Roche (Basel, Switzerland) 9.41 μM 11.45 μM + 8.19 μM
 Saquinavir Roche (Basel, Switzerland) 4.658 μM 95.83 μM NA



Reverse transcriptase inhibitors
 Efavirenz Merck (Whitehouse station, USA) 9.899 μM 52.14 μM NA
 Lamivudine GlaxoSmithKline (London, UK) 27.257 μM ≥27.257 μM NA
 Lamivudine/zidovudine GlaxoSmithKline (London, UK) 12.5 μg/mL ≥12.5 μg/mL NA
 Nelvirapine Boehringer Ingelheim (Ingelheim am Rhein, Germany) 46.94 μM ≥46.94 μM NA
 Stavudine Bristol-Myers Squibb (New York, USA) 55.754 μM ≥55.754 μM NA



Other
 Emodin Sigma, E7881 (St Louis, USA) 12.5 μM 67.41 μM NA
 Galanthus nivalis agglutinin Sigma, L8275 (St Louis, USA) 0.48 nM ≥1.92 nM + 0.0088 nM
 Promazine Sigma, P6656 (St Louis, USA) 100 nM ≥100 nM NA

NA: not available.