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. 2006 May 24;60(5):211–219. doi: 10.1016/j.biopha.2006.03.009

Table 8.

Antiviral activities of polyoxometalates against coronaviruses

EC50(μM) a
SI e
TGEV b FIPV c SARS-V d TGEV FIPV SARS-V
PM-504 1.4 ± 0.5 0.4 ± 0.3 3.5 ± 2.4 > 12.8 > 46.7 > 14.3
PM-518 2.1 ± 1.1 > 32.9 > 50 > 15.6 □1.0 < 1.0
PM-520 1.4 ± 1.3 0.76 ± 0.5 4.9 ± 1.4 > 20.4 >38.5 > 10.3
PM-523 2.5 ± 0.6 > 32.0 > 50 > 32.0 □1.0 < 1.0
PM-802 0.5 ± 0.5 0.03 ± 0.01 > 50 4.9 97.2 < 1.0
PM-803 0.34 ± 0.3 > 21.0 Nd 55.3 □1.0
PM-1001 0.14 ± 0.1 0.2 ± 0.1 0.7 ± 0.4 83.6 84.4 > 70.4
PM-1002 0.6 ± 0.4 Nd 0.25 ± 0.07 18.6 > 400
PM-1201 0.2 ± 0.14 > 9.0 Nd > 100 □1.0
PM-1207 1.9 ± 1.4 0.09 ± 0.04 0.9 ± 0.24 > 9.3 35.2 > 54.3
PM-1208 2.0 ± 1.8 > 3.6 2.7 ± 0.6 > 8.1 □1.0 > 18.4
PM-1210 1.6 ± 1.1 0.74 ± 0.4 0.76 ± 0.3 > 6.6 > 14.3 >65.8
PM-1213 1.7 ± 1.0 > 10.5 0.47 ± 0.14 > 18.2 □1.0 106.4
a

EC50 and CC50 were determined by the average of three independent experiments.

b

Transmissible gastroenteritis virus of swine.

c

Feline infectious peritonitis virus.

d

SARS coronavirus.

e

Selectivity index. SIs were calculated by CC50/EC50 in which the CC50s were determined by cytotoxicities for CPK cells (TGEV), for fcwf-4 cells (FIPV) and for Vero cells (SARS-V), respectively. The SIs greater than 30 are indicated in bold face.