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. 2024 Feb 23;67(5):3205–3231. doi: 10.1021/acs.jmedchem.3c01543

Table 3. Peptide-Based Inhibitors of HCV Entry, Their Sequences, and the Available Inhibition Data.

target name sequence efficiency of inhibition
CD81 710–725178 ASWAIKWEYVVLLFLL ∼60% relative luciferase activity at 51 μMa
  CD81-binding nonapeptide182 SPQYWTGA motif NA
  CL58179 MANAGLQLLGFILAFLGW IC50 = 2.1 ± 0.5 μM
E2 hCD81-like nonapeptide184 ATWVCGPCT E2 inhibits binding of C9 clone to anti-hCD81 JS-81 with inhibition ratio of 67.5%
  SAHH-5181 PSGSNXSNIISNXFRED EC50 = 17–39 μMb
  C18183 WPWHNHR Relative level of HCV RNA ∼ 0.5 at 97 μMc
  E2–42180 QGSWFGCTWMNSTGF % of infectivity at C = 5 nM: 50–60%
a

Luciferase activity in Huh7.5 cells compared to the activity in PBS buffer.

b

Value depending on the HCV subtype.

c

In Huh7.5 cells infected with HCVcc.