1. Signaling Pathways
  2. Anti-infection
  3. Enterovirus

Enterovirus

Rhinovirus; HRV; HRVs; HEV; HEVs

The genus Enterovirus (EV) belonging to the Picornaviridae family comprises 13 species, of which seven are human viruses. Four of the species are: (1) EV-A such as coxsackievirus (CV)-A6, CV-A10, CV-A16 and EV-A71, (2) EV-B such as the CV-B viruses, echoviruses (ECHO) and CV-A9, (3) EV-C such as polioviruses (PV) and CV-A21, (4) EV-D such as EV-D68 and EV-D70. The other three species are rhinoviruses RV-A, RV-B and RV-C which comprised over 100 different numbered RVs. Infection with enteroviruses can cause numerous clinical conditions including poliomyelitis, meningitis and encephalitis, hand-foot-and-mouth disease, acute flaccid paralysis, diarrhea, myocarditis and respiratory illness.

Enteroviruses are small, nonenveloped, positive-sense, single-stranded RNA viruses with an icosahedral capsid. The genome of ∼7.5 kb encodes a single polyprotein that is autoprocessed into structural proteins (VP1, VP2, VP3, and VP4), nonstructural proteins (2A, 2B, 2C, 3A, 3B, 3C, and 3D), and several functional processing intermediates. The viral nonstructural proteins, particularly the protease 3Cpro and the RNA-dependent RNA polymerase 3Dpol, are attractive targets for antiviral drug development.

Enterovirus Related Products (93):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-10578
    PD 169316
    Inhibitor 98.29%
    PD 169316 is a potent, cell-permeable and selective p38 MAP kinase inhibitor, with IC50 of 89 nM. PD169316 selectively inhibits the kinase activity of the phosphorylated p38 without hindering upstream kinases to phosphorylate p38. PD169316 shows antiviral activity against Enterovirus71. PD169316 shows antiviral activity against Enterovirus71.
    PD 169316
  • HY-125033
    EIDD-1931
    Inhibitor 99.96%
    EIDD-1931 (Beta-d-N4-hydroxycytidine; NHC) is a novel nucleoside analog and behaves as a potent anti-virus agent.
    EIDD-1931
  • HY-106161
    Rupintrivir
    Inhibitor 99.91%
    Rupintrivirvr (AG7088), an antiviral drug, is a potent, selective and irreversible inhibitor of human rhinovirus (HRV) 3C protease.
    Rupintrivir
  • HY-100540
    Golgicide A
    Inhibitor 99.85%
    Golgicide A (GCA) is a potent, highly specific, and reversible inhibitor of the cis-Golgi ADP-ribosylation factor guanine nucleotide exchange factors (ArfGEF) GBF1.
    Golgicide A
  • HY-B1030
    Lanatoside C
    Inhibitor 99.83%
    Lanatoside C is a cardiac glycoside, can be used in the treatment of congestive heart failure and cardiac arrhythmia.Lanatoside C has an IC50 of 0.19 μM for dengue virus infection in HuH-7 cells. Lanatoside C can effectively inhibit all four serotypes of dengue virus, flavivirus Kunjin, alphavirus Chikungunya, Sindbis virus and the human enterovirus 71.
    Lanatoside C
  • HY-10578R
    PD 169316 (Standard)
    Inhibitor
    PD 169316 (Standard) is the analytical standard of PD 169316 (HY-10578).
    PD 169316 (Standard)
  • HY-W344044
    Levomepromazine maleate
    Inhibitor
    Levomepromazine maleate (Methotrimeprazine maleate) is an orally active antipsychotic compound and Ca2+ release inducer.
    Levomepromazine maleate
  • HY-168923
    HR-568
    Inhibitor
    HR-568 exhibits broad-spectrum anti-enterovirus activity.
    HR-568
  • HY-B0154
    Fluticasone (propionate)
    Inhibitor 99.82%
    Fluticasone propionate, a potent topical anti-inflammatory corticosteroid, is a selective glucocorticoid receptor agonist, with an absolute affinity (KD) of 0.5 nM. Fluticasone propionate shows little or no activity at other steroid receptors. Anti-viral activity.
    Fluticasone (propionate)
  • HY-19952
    Pleconaril
    Inhibitor 99.48%
    Pleconaril is a picornavirus capsid binding inhibitor that prevents attachment and/or virus uncoating. Pleconaril has potential for use in rhinoviruses and enteroviruses research.
    Pleconaril
  • HY-W019670
    N4-Acetylcytidine
    Inhibitor 99.75%
    N4-Acetylcytidine is a chemical modification substance present on various RNAs.
    N4-Acetylcytidine
  • HY-106254A
    Vapendavir diphosphate
    Inhibitor 98.75%
    Vapendavir diphosphate (BTA798 diphosphate) is a potent enteroviral capsid binder (CB).
    Vapendavir diphosphate
  • HY-N7108
    7-Hydroxyflavone
    Inhibitor 99.84%
    7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity.
    7-Hydroxyflavone
  • HY-135867E
    NHC-triphosphate tetraammonium
    Inhibitor
    NHC-triphosphate tetraammonium is an active phosphorylated intracellular metabolite of β-d-N4-Hydroxycytidine (NHC) (HY-125033) as a triphosphate form.
    NHC-triphosphate tetraammonium
  • HY-N6715
    Tenuazonic acid
    Inhibitor 99.58%
    Tenuazonic acid is a nonhost-selective mycotoxin belonging to the tetramic acids family.
    Tenuazonic acid
  • HY-N0923
    Corydaline
    Inhibitor 99.70%
    Corydaline ((+)-Corydaline), an isoquinoline alkaloid isolated from Corydalis yanhusuo, is an AChE inhibitor with an IC50 of 226 μM. Corydaline is a μ-opioid receptor (Ki of 1.23 μM) agonist and inhibits enterovirus 71 (EV71) replication (IC50 of 25.23 μM). Corydaline has anti-angiogenic, anti-allergic and gastric-emptying and antinociceptive activities.
    Corydaline
  • HY-B1693
    Levomepromazine
    Inhibitor 99.98%
    Levomepromazine (Methotrimeprazine) is an orally active antipsychotic compound and Ca2+ release inducer.
    Levomepromazine
  • HY-16561A
    cis-Resveratrol
    Inhibitor 98.79%
    cis-Resveratrol exhibits signifcant antiviral activity.
    cis-Resveratrol
  • HY-N1549
    Prunin
    Inhibitor 99.92%
    Prunin is a potent inhibitor of human enterovirus A71 (HEVA71).
    Prunin
  • HY-104074
    Pocapavir
    Inhibitor 98.55%
    Pocapavir (SCH-48973) is an orally active capsid inhibitor.
    Pocapavir