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Z-LVG-CHN2

Cat. No. M14309

All AbMole products are for research use only, cannot be used for human consumption.

Z-LVG-CHN2 Structure
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Biological Activity

Z-LVG-CHN2 is a cell-permeable and irreversible inhibitor of cysteine proteinase. Z-LVG-CHN2 is a tripeptide derivative and mimics part of the human cysteine proteinase-binding center. Z-LVG-CHN2 displays an inhibition on HSV whereas no significant effect on poliovirus replication. Z-LVG-CHN2 effectively blocks SARS-COV-2 replication (EC50=190 nM) via inhibition of SARS-COV-2 3CL pro protease.

Chemical Information
Molecular Weight 445.51
CAS Number 119670-30-3
Solubility (25°C) DMSO 90 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Laura Riva, et al. Discovery of SARS-CoV-2 antiviral drugs through large-scale compound repurposing

[2] Laura Riva, et al. A Large-scale Drug Repositioning Survey for SARS-CoV-2 Antivirals

[3] L Bjrck, et al. Bacterial growth blocked by a synthetic peptide based on the structure of a human proteinase inhibitor

[4] L Bjrck, et al. Cystatin C, a human proteinase inhibitor, blocks replication of herpes simplex virus

[5] L Bjrck. Proteinase inhibition, immunoglobulin-binding proteins and a novel antimicrobial principle

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Keywords: Z-LVG-CHN2 supplier, Cathepsin, inhibitors, activators

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