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. 2014 Apr 7;20(13):3457–3467. doi: 10.3748/wjg.v20.i13.3457

Table 2.

Antiviral agents targeting viral entry

Stages of HCV entry process Target Antiviral agents Ref.
HCV particle/attachment HCV E1 and E2 Neutralizing antibodies [102,103]
Heparin [41,55]
Lectins [106,107]
EGCG [109,110]
Oleanane-type triterpenes [111]
Virion-associated lipoprotein Anti-apoE mAb [108]
Receptor-mediated endocytosis SRBI Anti-SR-BI mAb [113]
ITX 5061 [117]
CD81 Anti-CD81 mAb [114]
CLDN1 Anti-CLDN1mAb [115]
CLDN1-derived peptide [116]
EGFR Erlotinib [50]
NPC1L1 Ezetimibe [52]
TfR1 Anti-TfR1 mAb [51]
Internalization Amphipathic DNA polymers [118]
Arbidol [122]
Tamoxifen [123]
Endosomal fusion Fusion E2-derived peptide [121]
CD81-derived peptide [124]
Curcumin [125]
Phenothiazines [126]
Ferroquine [127]
aUY11 [128]
HCV II-1/GS-563253 [129]
Regulation Ras Tipifarnib [78]
PKA H89 [96]
MKNK1 RO4475417 [93]
PI3K Wortmanin [99]

Targets within the different stages of Hepatitis C virus (HCV) entry process are depicted, followed by examples of compounds targeting the respective entry step. Stages of development and references are indicated. GAGs: Glycosaminoglycans; CLDN1: Claudin-1; OCLN: Occludin; LDLR: Low-density lipoprotein receptor; EGFR: Epidermal growth factor receptor.