14 Results for "

3C+protease

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "3C+protease" in MCE Product Catalog:

8
8 Cited Publications
Cat. No.: HY-106161
CAS No.: 223537-30-2
Purity:  99.36%
Synonyms: AG7088
Rupintrivirvr (AG7088), an antiviral agent, is a potent, selective and irreversible inhibitor of human rhinovirus (HRV) 3C protease. Rupintrivirvr inhibits replication of a panel of 48 different HRV serotypes in H1-HeLA and MRC-5 cell protection assays, with a mean EC50 of 0.023 μM. Rupintrivirvr shows immune-modulatory effect .
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Cat. No.: HY-E70370
Target:  

Virus Protease

Research Areas:  

Others

hrv 3c Protease is a protease originated from human rhinoviruses. hrv 3c Protease recognizes the sequence LEVLFQGP and cleaves precisely between the Q and GP residues. hrv 3c Protease can be used to remove additional tags from the target proteins .
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Cat. No.: HY-19476
CAS No.: 343565-99-1
Target:  

Virus Protease

Research Areas:  

Infection

AG-7404 is an orally active, irreversible inhibitor of the picornavirus 3C protease. AG-7404 blocks the processing of viral polyproteins, thereby inhibiting viral replication. AG-7404 has synergistic antiviral activity with capsid inhibitors such as V-073 (HY-104074) or BTA798 (HY-106254) and is effective against V-073-resistant variants. AG-7404 is used in the study of enterovirus infections such as poliovirus [3].
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Cat. No.: HY-N1341
CAS No.: 54835-70-0
Research Areas:  

Infection

Roseoside is an inhibitor of DNA gyrase and HAV 3C protease, and also inhibits HCV NS5A/B replicase in human systems with an IC50 of 20 μM. Roseoside binds to the active site of enzymes and stabilizes the interaction by forming hydrogen bonds with key amino acid residues. Roseoside inhibits the growth of Gram-positive bacteria, Gram-negative bacteria, and Candida albicans, and interferes with HCV RNA replication in vitro by inhibiting HCV NS5A/B replicase (IC50=20 μM). Roseoside shows no cytotoxicity and serves as a research tool for studies related to bacterial infections, candidiasis, HAV and HCV .
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Cat. No.: HY-E70528
CAS No.: 2178107-79-2
Research Areas:  

Others

HRV-3C protease fuses with GST is a recombinant protease fused with HRV-3C protease and GST, which recognizes the LEVLFQGP polypeptide sequence. HRV-3C protease fuses with GST precisely cleaves between glutamine and glycine-proline residues to remove fusion tags from target proteins. HRV-3C protease fuses with GST exhibits cleavage activity both in vitro in silkworm fat body lysates and in vivo in silkworm larval fat bodies, and achieves functional expression in E. coli and silkworm-baculovirus expression systems. HRV-3C protease fuses with GST can be applied to recombinant protein-related research .
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Cat. No.: HY-123517
CAS No.: 1158264-37-9
Purity:  99.12%
Target:  

Enterovirus

Research Areas:  

Infection

DC07090 dihydrochloride is a low toxicity, potent, reversible and competitive non-peptidyl human enterovirus 71 3C protease inhibitor with an IC50 and a Ki value for 21.72 μM and 23.29 μM. DC07090 dihydrochloride could also inhibit coxsackievirus A16 (CVA16) replication with an EC50 value of 27.76 μM .
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Cat. No.: HY-161352
CAS No.: 1429218-68-7
Target:  

Virus Protease

Research Areas:  

Infection

NPI52 (Compound E1) is a foot-and-mouth disease virus 3C protease (FMDV 3Cpro) inhibitor, with IC50 values of 0.05 and 0.11 µM in FRET and cell-based assay, respectively .
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Cat. No.: HY-P11081
Target:  

Enterovirus

Research Areas:  

Infection

P08 is a substrate for EV71 3C protease cleavage with a Kcat/Km of 11.8 mM −1 min −1 .
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Cat. No.: HY-123517A
CAS No.: 879070-72-1
Target:  

Enterovirus

Research Areas:  

Infection

DC07090 is a potent, reversible and competitive non-peptidyl human enterovirus 71 3C protease inhibitor with an IC50 and a Ki value for 21.72 μM and 23.29 μM. DC07090 could also inhibit coxsackievirus A16 (CVA16) replication with an EC50 value of 27.76 μM .
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Cat. No.: HY-170412
Target:  

Enterovirus

Research Areas:  

Infection Inflammation/Immunology

Cox B-IN-1 (7a) exhibits antiviral activity against Coxsackievirus B (Cox B). Cox B-IN-1 (7a) possesses dual activity that inhibits viral adsorption and replication. Cox B-IN-1 (7a) demonstrates substantial potential as an inhibitor of the 3C protease from coxsackievirus .
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Cat. No.: HY-106161S1
Synonyms: AG7088-d7
Rupintrivir-d7 is a deuterated labeled Rupintrivir . Rupintrivirvr (AG7088), an antiviral agent, is a potent, selective and irreversible inhibitor of human rhinovirus (HRV) 3C protease. Rupintrivirvr inhibits replication of a panel of 48 different HRV serotypes in H1-HeLA and MRC-5 cell protection assays, with a mean EC50 of 0.023 μM. Rupintrivirvr shows immune-modulatory effect [3].
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Cat. No.: HY-P701920
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Genome polyprotein
Species:  
Source:  
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Cat. No.: HY-P701921
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Genome polyprotein
Species:  
Source:  
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Cat. No.: HY-106161R
CAS No.: 223537-30-2
Synonyms: AG7088 (Standard)
Rupintrivir (Standard) is the analytical standard of Rupintrivir (HY-106161). This product is intended for research and analytical applications. Rupintrivirvr (AG7088), an antiviral agent, is a potent, selective and irreversible inhibitor of human rhinovirus (HRV) 3C protease. Rupintrivirvr inhibits replication of a panel of 48 different HRV serotypes in H1-HeLA and MRC-5 cell protection assays, with a mean EC50 of 0.023 μM. Rupintrivirvr shows immune-modulatory effect .
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