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Table 1 Summary of chemical drugs targeting Rho protein as antiviral targets

From: Rho-GTPases subfamily: cellular defectors orchestrating viral infection

Rho target

Antiviral compound

Virus type

Functional mechanism

Ref.

RhoA

Bafilomycin A(1)

RSV

Restriction of viral egress and excretion of pro-inflammatory cytokines (in vitro)

[178]

Cdc42

PIK-24

RSV

Inhibition of cell-to-cell fusion during syncytium formation (in vitro)

[179]

RhoA/ROCK

HA-1077

Ebola virus (EBOV)

Reversal of the vascular permeability defects (in vivo and in vitro)

[180]

RAC1

Statin

RSV

Combination of cholesterol- and isoprenoid-mediated effects on RAC1 activation (in vitro)

[5]

RhoA/CDC42

Ivermectin and atorvastatin

COVID-19

Interference of nuclear transport and vesicle transport (in vitro)

[181]

Cdc42

ZCL278

Junin virus (JUNV)

Prevention of cellular entry of enveloped viruses (in vivo and in vitro)

[182]

RhoA

Simvastatin

IAV

Suppression of RhoA activation and LC3 membrane localization (in vitro)

[183]

ROCK1

GSK269962A

Human enterovirus A71 (EV‐A71)

Inhibition of ROCK1 kinase activity (in vitro)

[184]

Rac1

NSC23766

HSV-1

Inhibition of Rac1 activity (in vitro)

[185]

Rac1

NSC23766

IAV

Effect on activity of viral polymerase complex (in vitro)

[186]

ROCK1

Thiazovivin

Buffalopox virus (BPXV)

Induction of viral mRNA attenuation in BPXV infected cells (in vitro)

[4]

ROCK1/2

Ki16425

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

Promotion of antiviral innate immunity (in vitro)

[187]

ROCK1

EV‐A71

Hepatitis C virus (HCV)

Occupancy of the activation potential involved on the surface of the ROCK1 active pocket; blocking the secretion of proinflammatory factors (in vitro)

[188]

RhoA, Cdc42, and Rac1

Atorvastatin

SARS-CoV-2

Inhibition of actin cytoskeleton-dependent trafficking (in vivo and in vitro)

[181]

ROCK

Y27632

Human cytomegalovirus (HCMV)

Inhibition of nuclear translocation and subsequent activation of ROCK

[75]

ROCK

HA-1077

Hepatitis C virus (HCV)

Inhibition of ROCK activity (in vivo and in vitro)

[189]