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Table 2 Inhibitory activity of N30 against eight influenza strains

From: A novel benzo-heterocyclic amine derivative N30 inhibits influenza virus replication by depression of Inosine-5’-Monophospate Dehydrogenase activity

Strain

N30

RBV

OC

AH

IC50(μM)

SI

IC50(μM)

SI

IC50(μM)

SI

IC50(μM)

SI

A/FortMonmouth/1/1947

1.93 ± 0.16

34.54

1.64 ± 0.72

>121.95

0.25 ± 0.01

>200

0.65 ± 0.59

>307.69

A/tianjinjinnan/15/2009

1.67 ± 0.49

39.92

2.54 ± 1.25

>78.74

2.57 ± 0.10

>19.45

18.24 ± 0.24

>10.96

A/liaoningzhenxing/1109/2010

3.43 ± 3.36

19.44

4.92 ± 3.02

>40.65

3.20 ± 0.21

>15.58

10.13 ± 0.04

>19.74

A/wuhan/359/1995

1.31 ± 0.87

50.89

8.23 ± 6.31

>24.30

0.12 ± 0.01

>416.67

15.64 ± 0.31

>12.78

A/fujiantongan/196/2009

1.13 ± 0.43

59.00

4.42 ± 0.74

>45.25

0.28 ± 0.01

>178.57

78.84 ± 3.04

>2.54

A/hunanzhuhui/1222/2010

1.76 ± 0.24

37.89

2.34 ± 0.98

>85.47

0.78 ± 0.02

>64.10

57.24 ± 2.23

>3.49

BV/shenzhen/155/2005

1.16 ± 0.69

57.47

1.70 ± 0.57

>117.65

1.02 ± 0.08

>49.02

>200

-

BY/fujianxinluo/54/2006

0.70 ± 0.18

95.24

2.48 ± 0.53

>80.65

0.56 ± 0.02

>89.28

>200

-

  1. Note: The TC50 of N30, OC, RBV and Amantadine were 66.67 μM, >50 μM, >200 μM, >200 μM, respectively
  2. “−”: no antiviral activity at the maximal nontoxic concentration