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. 2017 Mar 3;8(5):960–963. doi: 10.1039/c6md00657d

Table 1. Antiviral activity of camphor-based compounds against the influenza virus A/Puerto Rico/8/34 (H1N1) in MDCK cells.

Compound CC50, μM IC50, μM SI log P a
1 >2142.9 155.8 ± 18.3 >14 2.71
4 301.9 ± 21.4 34.0 ± 4.2 9 4.29
5 137.6 ± 9.9 15.1 ± 1.0 9 4.85
6 93.9 ± 7.3 10.2 ± 1.4 9 5.34
7 580.1 ± 41.1 7.1 ± 0.8 82 3.53
8 102.9 ± 8.2 7.1 ± 0.5 14 3.68
9 100.0 ± 7.3 4.4 ± 0.5 23 3.26
10 51.6 ± 4.1 3.2 ± 0.4 16 3.79
11 >852.0 683.1 ± 62.8 1 4.11
12 69.3 ± 4.9 >34.1 >2 6.78
13 124.7 ± 10.1 14.3 ± 1.6 9 4.45
14 69.6 ± 5.2 7.8 ± 0.8 9 5.02
15 56.4 ± 3.8 15.3 ± 2.0 4 5.51
16 552.5 ± 31.1 12.2 ± 1.6 45 3.36
17 12.6 ± 1.0 6.8 ± 0.9 2 3.51
18 48.1 ± 3.3 1.9 ± 0.4 25 3.09
19 104.7 ± 8.7 8.4 ± 0.9 12 3.62
20 149.5 ± 11.7 >98.4 2 3.94
21 41.8 ± 2.2 7.1 ± 0.9 6 6.94
22 >974 >974 1 2.71
25 >533.8 73.7 ± 8.5 7 3.53
26 508.5 ± 36.1 7.8 ± 1.1 65 3.36
27 >1886.8 >1886.8 1 0.11
28 >1734.1 982.7 ± 75.3 >2 0.64
Rimantadine 335.2 ± 26.8 67.0 ± 4.9 5
Amantadine 284.1 ± 21.4 64.2 ± 4.7 4
Deitiforine 1266.2 ± 81.5 208.6 ± 15.4 6
Ribavirin >2000.0 24.6 ± 3.1 >81.0
Oseltamivir 160.3 ± 11.4 0.2 ± 0.03 781

alog P, the octanol–water partitioning coefficient, was calculated using ACDLabs/ChemSketch 12.01 (www.acdlabs.com).