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SARS-CoV-2-IN-55 (compound 65) is a SARS-CoV-2 inhibitor with low cytotoxicity, characterized by an IC50 of 0.3 μM, and acts through direct interaction with VSV-S pseudoparticles [1].
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| 5 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | SARS-CoV-2-IN-55 (compound 65) is a SARS-CoV-2 inhibitor with low cytotoxicity, characterized by an IC50 of 0.3 μM, and acts through direct interaction with VSV-S pseudoparticles [1]. |
| In vitro | ARS-CoV-2-IN-55, at a concentration of 10 μM for 24 hours, inhibits SARS-CoV-2 activity in Vero E6 and A549-ACE2-TMPRSS2 cells, with IC50 values of 0.3 μM and 15.8 μM, respectively. Furthermore, it suppresses the activity of the Wuhan-Hu-1 strain (IC50=0.28 μM) and the Omicron BA.1 variant (IC50=6.24 μM) in Vero E6-TMPRSS2 cells [1]. |
| Molecular Weight | 2807.07 |
| Formula | C138H136N22O32S6 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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