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. 2013 Nov 22;54:65–116. doi: 10.1007/978-3-642-41004-8_4

Table 4.4.

PM-19 dose response for the mice infected with HSV-2

Compound Dose (mg/kg−1/kg−1) Number of survivors/total Survival days
Experiment 1
No treatment 0/24 (0)a 6.83 ± 0.46 (0)a
PM-19 0.03 (on days 0–2) 0/12 (0) 6.83 ± 0.42 (0)
0.1 (on days 0–2) 2/12 (17) 8.00 ± 1.03 (17)
0.3 (on days 0–2) 7/12 (58)**b 11.50 ± 0.94 (68)**b
1.0 (on days 0–2) 9/12 (75)** 12.08 ± 1.02 (77)**
ACV 25.0 (on days 0–5) 2/12 (17) 7.64 ± 1.22 (12)
50.0 (on days 0–5) 2/12 (17) 9.08 ± 0.84 (33)*
Experiment 2
No treatment 2/24 (8) 7.13 ± 0.47 (0)
PM-19 1.0 (on days 0–2) 9/12 (75)** 13.08 ± 0.48 (84)**
2.5 (on days 0–2) 8/12 (67)** 11.50 ± 1.07 (61)**
5.0 (on days 0–2) 7/12 (58)** 11.40 ± 1.02 (60)**
10.0 (on days 0–2) 9/12 (75)** 12.50 ± 0.87 (75)**
25.0 (on days 0–2) 11/12 (92)** 14.00 ± 0.00 (97)**
50.0 (on days 0–2) 9/12 (75)** 12.33 ± 0.92 (73)**
ACV 25.0 (on days 0–2) 0/12 (0) 7.92 ± 0.78 (11)
50.0 (on days 0–2) 0/12 (0) 7.33 ± 0.38 (3)
100.0 (on days 0–2) 1/12 (8) 3.85 ± 1.54 (−50)

Mice were treated i.p. with indicated doses of the test compounds once daily from day 0 (immediately after infection) until day 2 or 5 after i.p. infection with HSV-2 (2.8 × 102 pfu)

aNumber in parenthesis indicates the percentage of mice that were still alive on day 14 after infection

bSignificantly different from corresponding tumor control group (*p < 0.05; **p < 0.01)