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Virus attachment / entry
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Viruses such as Sars-Cov2 must enter host cells for replication. Virus entry is initiated by attachment to receptors followed by penetration through or fusion with cellular membranes. The ACE2 host receptor is required for host cell entry of SARS-CoV-2. Researchers can save up to 50% on small molecules that affect virus attachment and entry, as they are up to half the price of other suppliers.
Camostat mesylate (HB3595)
Description:Serine protease inhibitor. Inhibits TMPRSS2 and partially blocks SARS-Cov2 entry in vitro.
Purity:>98%
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Cyclosporin A (HB0220)
Description:Potent calcineurin inhibitor. Inhibits MPTP opening.
Purity:>99%
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Disulfiram (HB1119)
Description:Reversibly stimulates SERCA Ca2+-ATPase. V-ATPase inhibitor.
Purity:>97%
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Imatinib mesylate (HB1943)
Description:Tyrosine kinase inhibitor that targets BCR‑ABL, c‑KIT, and PDGFR kinases
Purity:>98%
