114 Results for "

HCV replication

" in MedChemExpress (MCE) Product Catalog:
Products (114)

114 Results for "HCV replication" in MCE Product Catalog:

Cat. No.: HY-W128400
CAS No.: 123402-21-1
Target:  

DNA/RNA Synthesis HCV

Research Areas:  

Infection

3′-Deoxy-3′-fluoroguanosine exhibits antiviral activity against tick-borne encephalitis virus (TBEV), through interaction with NS5B RdRp of HCV, resulting in suppression of viral RNA synthesis by disruption of further extension of the replicating viral RNA .
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Cat. No.: HY-19558
CAS No.: 1036915-08-8
Target:  

HCV HCV Protease

Research Areas:  

Infection

IDX184 is a potent and orally bioavailable inhibitor of HCV replication. IDX184 potently inhibits HCV polymerase (IC50=0.31 μM, Ki=52.3 nM) .
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Cat. No.: HY-W011834S
CAS No.: 2653209-08-4
2'-O-Methylcytidine-d3 is deuterium labeled 2'-O-Methylcytidine (HY-W011834). 2'-O-Methylcytidine is a 2'-substituted nucleoside as a inhibitor of HCV replication. 2'-O-Methylcytidine inhibits RNA-dependent RNA polymerase (NS5B)-catalyzed RNA synthesis in vitro, in a manner that is competitive with substrate nucleoside triphosphate.
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Cat. No.: HY-W555382
CAS No.: 55396-45-7
Synonyms: 2-Nonylquinolin-4(1H)-one
Pseudane IX, a compound isolated from the leaves of Ruta angustifolia, has strong anti-HCV activity with an IC50 value of 1.4 μg/mL. Pseudane IX reduces HCV RNA replication and viral protein synthesis levels .
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Cat. No.: HY-17470R
CAS No.: 50924-49-7
Synonyms: NSC 289637 (Standard); HE 69 (Standard)
Mizoribine (Standard) is the analytical standard of Mizoribine. This product is intended for research and analytical applications. Mizoribine (NSC 289637), an imidazole nucleoside, inhibits HCV RNA replication with IC50 of approximately 100 μM for anti-HCV activity. Immunosuppressant . Mizoribine, an IMPDH inhibitor, inhibits replication of SARS-CoV with IC50s of 3.5 μg/mL and 16 μg/mL for SARS-CoV Frankfurt-1 and SARS-CoV HKU39849, respectively .
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Cat. No.: HY-132600A
Purity:  95.38%
Synonyms: Temavirsen sodium
Target:  

MicroRNA HCV

Research Areas:  

Infection

RG-101 sodium is a hepatocyte targeted N-acetylgalactosamine conjugated oligonucleotide that antagonises miR-122. miR-122 is an important host factor for hepatitis C virus (HCV) replication .
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Cat. No.: HY-100603A
CAS No.: 1384097-27-1
Target:  

PI3K PI4K

Research Areas:  

Infection

(S)-GSK-F1 (Compound 28) is an inhibitor for type III phosphatidylinositol 4-kinase α (PI4KIIIα). (S)-GSK-F1 inhibits PI4Kα, PI4Kβ, PI4Kγ, PI3Kα, PI3Kβ and PI3Kδ with pIC50 of 8.3, 6.0, 5.6, 5.6, 5.1 and 5.6, respectively. (S)-GSK-F1 exhibits anti-hepatitis C virus (HCV) activity through inhibition of HCV replication. (S)-GSK-F1 exhibits moderate pharmacokinetic characters in rat model .
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Cat. No.: HY-15005A
CAS No.: 1190308-01-0
Purity:  98.24%
Target:  

HCV

Research Areas:  

Infection

PSI-7976 is the isomer of PSI-7977. PSI-7977 is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity.
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Cat. No.: HY-N8188
CAS No.: 117824-04-1
Dehydrojuncusol, a potent HCV inhibitor, targets HCV NS5A and is able to inhibit RNA replication of replicons harboring resistance mutations to anti-NS5A direct-acting antivirals. Dehydrojuncusol significantly inhibits HCV infection when added after virus inoculation of HCV genotype 2a (EC50=1.35?μM) .
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Cat. No.: HY-I0515
CAS No.: 1496552-51-2
Target:  

HCV

Research Areas:  

Infection

Sofosbuvir impurity K, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir (PSI-7977) is an inhibitor of HCV RNA replication, demonstrates potent anti-hepatitis C virus activity.
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Cat. No.: HY-132600
CAS No.: 1929655-04-8
Synonyms: Temavirsen
Target:  

MicroRNA HCV

Research Areas:  

Infection

RG-101 is a hepatocyte targeted N-acetylgalactosamine conjugated oligonucleotide that antagonises miR-122. miR-122 is an important host factor for hepatitis C virus (HCV) replication .
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Cat. No.: HY-15591
CAS No.: 1204416-97-6
Target:  

HCV

Research Areas:  

Infection

TMC647055 is a potent nonnucleoside NS5B polymerase inhibitor of HCV replication. TMC647055 has potent HCV combine activity with an IC50 value of 82 nM. TMC647055 can be used for the research of Hepatitis C virus (HCV) .
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Cat. No.: HY-15005B
CAS No.: 1496552-28-3
Purity:  97.43%
Target:  

Drug Metabolite

Research Areas:  

Others

Sofosbuvir impurity C is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity.
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Cat. No.: HY-15005S
CAS No.: 2070009-25-3
Synonyms: PSI-7977-13C,d3; GS-7977-13C,d3
Sofosbuvir- 13C,d3 is the deuterium labeled Sofosbuvir. Sofosbuvir (PSI-7977) is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity.
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Cat. No.: HY-19512
CAS No.: 870142-71-5
Synonyms: GS9132
Target:  

HCV Protease HCV

Research Areas:  

Infection

ACH-806 is an NS4A antagonist which can inhibit Hepatitis C Virus (HCV) replication with an EC50 of 14 nM.
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Cat. No.: HY-12633
CAS No.: 1350735-70-4
Purity:  98.93%
Target:  

HCV

Research Areas:  

Inflammation/Immunology

GS-6620 is potent and selective HCV inhibitor. GS-6620 inhibits HCV replication in genotype 1-6 subgenomic replicons and genotype 2a infectious virus, with EC50 values of 0.048-0.68 μM. GS-6620 can be used for the researches of infection and inflammation, such as Hepatitis C Virus (HCV) .
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Cat. No.: HY-118525
CAS No.: 869218-90-6
Purity:  99.68%
Target:  

HCV PI4K

Research Areas:  

Infection

AL-9 is a inhibitor of PI4KIIIα, with the IC50 of 0.57 μM, that can inhibit HCV replication .
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Cat. No.: HY-173013
Target:  

Cyclophilin HIV HCV

Research Areas:  

Infection

TWH106 is an inhibitor for Cyclophilin (Cyp) that exhibits good affinity to CypA and CypB with KD of 53 nM and 139 nM. TWH106 inhibits the replication of HIV and HCV, exhibiting antiviral activity .
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Cat. No.: HY-10241A
CAS No.: 1241946-89-3
Synonyms: TMC435 sodium; TMC435350 sodium
Research Areas:  

Infection

Simeprevir (TMC435; TMC435350) sodium is an oral, potent and highly specific hepatitis C virus (HCV) NS3/4A protease inhibitor with a Ki of 0.36 nM. Simeprevir sodium inhibits HCV replication with an EC50 of 7.8 nM. Simeprevir sodium also potently suppresses SARS-CoV-2 replication and synergizes with Remdesivir. Simeprevir sodium inhibits the main protease (M pro) and the RNA-dependent RNA polymerase (RdRp) of SARS-CoV-2, and also modulates host immune responses .
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Cat. No.: HY-15005C
CAS No.: 1496552-16-9
Target:  

HCV

Research Areas:  

Infection

Sofosbuvir impurity A, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir (PSI-7977) is an inhibitor of HCV RNA replication, demonstrates potent anti-hepatitis C virus activity.
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