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. 2020 Jan 29;12(2):154. doi: 10.3390/v12020154

Table 4.

The overview of miscellaneous small molecules with anti-HSV activity.

Compound Antiherpetic and Cytotoxicity Assays, Strains, Cells, and Reference Agents Results Additional Information Source
Trichobotrysin A (108) Vero cells, HSV-1
PRA
ACV IC50 3.50 μM
IC50 3.08 μM Deep-sea-derived fungus Trichobotrys effuse
Tetramic acid derivatives
[81]
Trichobotrysin B (109) IC50 9.37 μM
Trichobotrysin D (110) IC50 3.12 μM
(E)-2-(2,4-hexa-diynyliden)-1,6-dioxaspiro[4.5]
dec-3-ene (111)
Vero cells, HSV-1 (clinical isolate with >99% homology to isolate SK087 US4–6 genes), HSV-2 (clinical isolate >99% homology to isolate 99-62039 US4 gene)
CPE, YRA
Time-of-addition, adsorption inhibition, virucidal, penetration inhibition assays
Macromolecular synthesis inhibition analysis
ACV HSV-1 EC50 0.9 μg/mL; SI > 1000 / HSV-2 EC50 0.7 μg/mL; SI > 1000
EC50, SI: HSV-1/HSV-2
0.146 μg/mL; > 205 / 0.127 μg/mL; > 236
Tanacetum vulgare
Spiroketal-enol ether derivative.
Mechanism of antiviral activity elucidated on petroleum ether extract and 111
(inhibition of viral gene expression).
[82]
Monogalactosyl diglyceride (112) and digalactosyl diglyceride (DGDG) Vero cells, HSV-1, HSV-2
PRA
ACV HSV-1 IC50 0.64 μg/mL and HSV-2 IC50 0.80 μg/mL
HSV-1 IC50 36.00 μg/mL for 112 and 40.00 μg/mL for DGDG, respectively. HSV-2 IC50 41.00 μg/mL for 112 and 43.20 μg/mL for DGDG, respectively. Clinacanthus nutans [83]
Methyl (N-benzoyl-(2′R,3′S)-3′-phenylisoserinate) (113) Vero cells, HSV-1 (MacIntyre strain)
CPE
ACV IC50 1 µg/mL, SI ˃ 250
HSV-1 IC50 10.7 µg/mL, SI ˃ 46.7 Taxol derivatives. The activity may be associated with their influence on mitotic division. [68]
N-benzoyl-(2′R,3′S)-3′-phenylisoserine (114) HSV-1 IC50 21.7 µg/mL, SI ˃ 23