28 Results for "

anti-HCV activity

" in MedChemExpress (MCE) Product Catalog:
Products (28)

28 Results for "anti-HCV activity" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-17470
CAS No.: 50924-49-7
Synonyms: NSC 289637; HE 69
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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5
5 Cited Publications
Cat. No.: HY-10443
CAS No.: 690270-29-2
Purity:  97.22%
Synonyms: Ro 4588161; R1626
Target:  

HCV DNA/RNA Synthesis

Research Areas:  

Infection

Balapiravir (Ro 4588161; R1626) is an orally active proagent of a nucleoside analogue inhibitor of the RNA-dependent RNA polymerase (RdRp) of HCV (R1479; 4'-Azidocytidine). Balapiravir has anti-HCV activity . Balapiravir is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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3
3 Cited Publications
Cat. No.: HY-N0588
CAS No.: 78763-58-3
Deapioplatycodin D is a triterpenoid saponin isolated from Platycodon grandiflorum, with anti-HCV activity .
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Cat. No.: HY-N7765
CAS No.: 104987-36-2
Oenothein B is a dimeric macrocyclic ellagitannin and has widely pharmacological activities, including antioxidant, anti-inflammatory, antifungal, anti-HCV, and antitumor properties. Oenothein B is a potent and specific inhibitor of poly(ADP-ribose) glycohydrolase .
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Cat. No.: HY-112712
CAS No.: 1509904-96-4
Purity:  99.55%
Target:  

Cyclophilin HCV

Research Areas:  

Infection

Cyclophilin inhibitor 1 is a potent and orally bioavailable cyclophilin A inhibitor, with a Kd of 5 nM, shows effective anti-HCV activity, with an EC50 of 98 nM for HCV 2a .
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Cat. No.: HY-173011
Target:  

PROTACs Cyclophilin HIV HCV

Research Areas:  

Infection

RJS308 is a selective Cyclophilin A (CypA) PROTAC degrader. RJS308 induces ubiquitin-dependent CypA degradation by recruiting the VHL E3 ligase complex, and forms a ternary complex with CypA and VHL/elongin C/elongin B. RJS308 exhibits anti-HIV-1 and anti-HCV activities. RJS308 can be used in studies related to viral infections .
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Cat. No.: HY-173011A
Target:  

PROTACs Cyclophilin HIV HCV

Research Areas:  

Infection

RJS308 TFA is a selective Cyclophilin A (CypA) PROTAC degrader. RJS308 TFA induces ubiquitin-dependent CypA degradation by recruiting the VHL E3 ligase complex, and forms a ternary complex with CypA and VHL/elongin C/elongin B. RJS308 TFA exhibits anti-HIV-1 and anti-HCV activities. RJS308 TFA can be used in studies related to viral infections .
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Cat. No.: HY-115988
CAS No.: 1001426-49-8
Target:  

HCV

Research Areas:  

Infection

IMB-26 is a HCV inhibitor with an EC50 of 2.1 μM. IMB-26 shows potent an anti-HCV activity .
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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-N3918
CAS No.: 524-15-2
γ-Fagarine is a furoquinoline alkaloid naturally occurring in Rutae Herba. γ-Fagarine has strong anti-HCV activities with IC50 of 20.4 μg/mL and is also a sister chromatid exchanges (SCEs) inducer .
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Cat. No.: HY-146648
CAS No.: 1676100-30-3
Target:  

Cyclophilin HCV

Research Areas:  

Infection

Cyclophilin inhibitor 3 (compound 7c) is a potent cyclophilin A (CypA) inhibitor with an potent anti-HCV activity (EC50 of 4.2 μM) .
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Cat. No.: HY-128924
CAS No.: 1589093-01-5
Target:  

Cyclophilin HCV

Research Areas:  

Infection

NIM258 is a potent nonimmunosuppressive cyclophilin inhibitor (cyclophilin A Kd = 1.2 nM) with anti-HCV activity (EC50 = 40 nM). NIM258 can be used for HCV infection research .
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Cat. No.: HY-173009
Target:  

PROTACs Cyclophilin HCV HIV

Research Areas:  

Infection

PROTAC CG167 is a selective bifunctional PROTAC degrader targeting CypA, with a DC50 of 123 nM. PROTAC CG167 drives ubiquitin-dependent and ubiquitin-like modification-dependent proteasomal degradation of CypA by recruiting the VHL E3 ligase complex. PROTAC CG167 exhibits anti-HIV‑1 and anti-HCV replication activities, and selectively reduces CypA levels in various cells. PROTAC CG167 can be used in studies related to viral infections .
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Cat. No.: HY-157291
CAS No.: 872201-68-8
Target:  

HCV

Research Areas:  

Infection

Antiviral agent 44 (compound 7b) is an antiviral agent that has anti-HCV activity in vitro .
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Cat. No.: HY-129057
CAS No.: 581772-30-7
Target:  

HCV

Research Areas:  

Infection

2',5-Difluoro-2'-deoxycytidine, compound 13, has potent anti-HCV activity and toxicity to ribosomal RNA (rRNA) .
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Cat. No.: HY-169746
CAS No.: 1613591-70-0
Target:  

DNA/RNA Synthesis HCV

Research Areas:  

Infection

Antiviral agent 63 is a nucleoside analog with anti-HCV activity. Antiviral agent 63 can inhibit viral replication by inhibiting the activity of HCV RNA-dependent RNA polymerase or other virus-related enzymes .
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Cat. No.: HY-115989
CAS No.: 3035807-39-4
Target:  

HCV

Research Areas:  

Infection

HCV-IN-38 is a potent, selective and orally active HCV inhibitor (EC50=15 nM, SI=431). HCV-IN-38 has high anti-HCV activity and low cytotoxicity. HCV-IN-38 has a good safety and oral pharmacokinetic profile .
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Cat. No.: HY-W555382S
Synonyms: 2-Nonylquinolin-4(1H)-one-d4
Pseudane IX-d4 (2-Nonylquinolin-4(1H)-one-d4) is deuterium labeled Pseudane IX. 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-177299
CAS No.: 1255860-45-7
Target:  

HCV

Research Areas:  

Infection

HCV NS5B polymerase-IN-3 (Compound 30a) is an inhibitor of the HCV NS5B polymerase. HCV NS5B polymerase-IN-3 exhibits anti-HCV activity in the Huh7 replicon cell line with an EC50 of 0.23 μM and shows no obvious cytotoxicity. HCV NS5B polymerase-IN-3 can be used in research related to the hepatitis C virus .
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