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FGI-106 tetrahydrochloride

FGI-106 tetrahydrochloride
FGI-106 tetrahydrochloride demonstrates potent inhibitory activity across a broad spectrum of viruses, including those causing hemorrhagic fevers such as Ebola, Rift Valley, and Dengue Fever, with half-maximal effective concentrations (EC50s) of 100 nM, 800 nM, and 400-900 nM, respectively. Additionally, it effectively inhibits non-hemorrhagic fever viruses, notably HCV and HIV-1, with EC50s of 200 nM and 150 nM, respectively, indicating its broad-spectrum antiviral potential.
Catalog No. T11281LCas No. 1149348-10-6
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Purity:98.98%
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FGI-106 tetrahydrochloride

Catalog No. T11281LCas No. 1149348-10-6

FGI-106 tetrahydrochloride demonstrates potent inhibitory activity across a broad spectrum of viruses, including those causing hemorrhagic fevers such as Ebola, Rift Valley, and Dengue Fever, with half-maximal effective concentrations (EC50s) of 100 nM, 800 nM, and 400-900 nM, respectively. Additionally, it effectively inhibits non-hemorrhagic fever viruses, notably HCV and HIV-1, with EC50s of 200 nM and 150 nM, respectively, indicating its broad-spectrum antiviral potential.
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Pack SizePriceAvailabilityQuantity
1 mg$79In Stock
5 mg$173In Stock
10 mg$273In Stock
25 mg$452In Stock
50 mg$636In Stock
100 mg$858In Stock
200 mg$1,150In Stock
1 mL x 10 mM (in DMSO)$230In Stock
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Product Introduction

Bioactivity
Description
FGI-106 tetrahydrochloride demonstrates potent inhibitory activity across a broad spectrum of viruses, including those causing hemorrhagic fevers such as Ebola, Rift Valley, and Dengue Fever, with half-maximal effective concentrations (EC50s) of 100 nM, 800 nM, and 400-900 nM, respectively. Additionally, it effectively inhibits non-hemorrhagic fever viruses, notably HCV and HIV-1, with EC50s of 200 nM and 150 nM, respectively, indicating its broad-spectrum antiviral potential.
Targets&IC50
EBOV:(EC50)100 nM , DENV: 400-900 nM , HCV: 200 nM , HIV-1:150 nM , Rift Valley virus: 800 nM
In vitro
In cell-based assays, treatment with FGI-106 inhibits viral replication by divergent virus families, including positive and negative-strand RNA viruses.Treatment with 2 μM FGI-106 mediated a 4 log reduction in infectious viral titers relative to matched controls, with an EC90 for inhibition of viral killing of host cells (Vero E6 cells) estimated to be 0.6 μM.
In vivo
FGI-106??treatment decreases mortality from Zaire EBOV in a dose-dependent manner.
Chemical Properties
Molecular Weight604.48
FormulaC28H42Cl4N6
Cas No.1149348-10-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 7.5 mg/ml (12.41 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6543 mL8.2716 mL16.5431 mL82.7157 mL
5 mM0.3309 mL1.6543 mL3.3086 mL16.5431 mL
10 mM0.1654 mL0.8272 mL1.6543 mL8.2716 mL

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