Table 1.
Drugs | Virus | Life cycle events |
---|---|---|
Compound SP-510-50 PI3K inhibitor: Idelalisib NVP-BEZ235 Dermaseptins Endocytosis inhibitor: Chlorpromazine anti-gHgL antibodies: CL40 and CL59 Amantadine analog: Tromantadine Saturated fatty alcohol: Docosanol |
HSV-1 HSV-2, HCMV KSHV, EBV HSV-1, HSV-2, EBV KSHV, EBV EBV EBV HSV-1 |
Virus binding or entry inhibitors |
Epigenetic therapy | ||
DNMT inhibitors: 5-azacytidine, RG108 HDAC inhibitors: MC1568, Sodium butyrate, Trichostatin A (TSA), Vorinostat (SAHA), Valproic Acid HMT inhibitors: DZNep (EZH2i) GSK126, GSK343 HDM inhibitors: ML342, DMOG, OG-L002, TCP |
HSV-1, HSV-2, HCMV, VZV, EBV, KSHV HSV-1, HCMV HSV-1 HSV-1 |
Repression of viral immediate early gene expression. Production of infectious progeny in quiescently infected cells. Latency reversal Significant activation of the lytic transcriptional program in HCMV Blockage of lytic HSV-1 replication in latently infected ganglion explant model Repression of viral IE gene expression |
Nucleoside analogs | ||
Trifluridine, Edoxudine, Brivudine, Cytarabine, Cidofovir, Acyclovir Ganciclovir, Penciclovir, Virdarabine, Indoxuridine Non-nucleoside inhibitors: Foscarnet PNU-183792 NSC 373989 Helicase-primase inhibitor: BAY 57-1293 T-0902611 BILS 179BS Protein-protein interaction inhibitor BILD1263 |
HSV-1, HSV-2, VZV, HCMV, EBV, HHV-6, HHV-7, KSHV HSV-1, HSV-2, VZV, HCMV HSV, VZV, HCMV KSHV HSV-1, HSV-2 HCMV HSV-1, HSV-2 HSV-1 |
DNA synthesis inhibitor. These drugs competitively stop the incorporation of dNTPs by the viral DNA polymerase and thereby end the elongation of viral DNA DNA synthesis inhibitors. Inhibit progression of the replication fork Inhibits viral replication |
Pyrazolo | ||
Quinoline, Benzothiophene Phosphorothioate oligonucleotides |
HSV-1 HCMV, EBV, KSHV |
Gene expression |
Acridones, Thiourea inhibitors
Phenylenediamine: Sulfonamides Ribosylbenzimidazoles |
HSV, EBV HCMV, KSHV HCMV |
Assembly or egress |