6 Results for "

viral genomic RNA

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "viral genomic RNA" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-19743
CAS No.: 928659-17-0
Triazavirin is a nucleoside analogue of nucleic acid and an antiviral agent. Triazavirin works by inhibiting the synthesis of viral RNA and DNA and replication of genomic fragments. Triazavirin is also an effective protective agent on the transmission stage of influenza .
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Cat. No.: HY-12928
CAS No.: 1613465-33-0
Purity:  99.09%
Research Areas:  

Infection

ML336 is a Venezuelan equine encephalitis virus (VEEV) inhibitor with moderate passive blood-brain barrier permeability. ML336 inhibits viral RNA synthesis, virus-induced cytopathic effects and viral replication, reduces viral titers, and blocks the synthesis of VEEV genomic, subgenomic and template RNAs. ML336 can be used in studies related to VEEV infection .
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Cat. No.: HY-156892
CAS No.: 342884-62-2
Target:  

Dengue Virus

Research Areas:  

Infection

SDM25N is a Dengue virus (DENV) inhibitor with an EC50 of 1.9 µM. SDM25N inhibits DENV in a cell type-specific manner. SDM25N restricts genomic RNA replication by targeting the viral NS4B protein. SDM25N can be used for DENV infection research .
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Cat. No.: HY-107745
CAS No.: 342884-71-3
Research Areas:  

Infection Neurological Disease

SDM25N hydrochloride, a δ-opioid receptor antagonist, is a potent DENV inhibitor. SDM25N hydrochloride targets the viral NS4B protein and restricts genomic RNA replication .
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Cat. No.: HY-P10836
CAS No.: 869011-94-9
Target:  

Dengue Virus

Research Areas:  

Infection

DN59 is a 33 amino acid peptide that mimics the dengue virus type 2 E stem region. DN59 inhibits all four serotypes of dengue virus (IC50: 2-5 μM) as well as other flaviviruses. N59 causes the release of genomic RNA by interacting directly with viral particles. DN59 has antiviral activity .
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Cat. No.: HY-N16775
CAS No.: 206876-12-2
Gylongiposide I is a selective inhibitor against the enterovirus EV71 with an EC50 of 1.53 μM. Gylongiposide I exerts antiviral activity by reducing viral protein VP1 expression and viral genomic RNA levels. Gylongiposide I can be used in the development of anti-EV71 drugs related to hand, foot and mouth disease .
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