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Catalog: | HY-P2036A |
Brand: | MCE |
CAS: | - |
MDL | - |
---|---|
Molecular Weight | 1780.18 |
Molecular Formula | C82H141F3N14O20S |
SMILES | - |
TLR2
|
TLR6
|
MMP-9
|
FSL-1 significantly reduces HSV-2 replication in human vaginal epithelial cells (EC)
[1]
.
FSL-1 induces significant resistance to experimental genital HSV-2 infection through elaboration of a specific cytokine response profile
[1]
.
FSL-1 (50 ng/mL, 24 hours) induces MMP-9 expression at both mRNA and protein levels in human monocytic THP-1 cells
[2]
.
FSL-1 activates the MAP kinase/NF-κB signaling pathway
[2]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Cell Viability Assay [1]
Cell Line: | V11I, V12I or V19I immortalized human vaginal EC |
Concentration: | 6 μg or 0.1 μg |
Incubation Time: | Added at 24, 6 or just prior to HSV-2 inoculation (10 4 pfu/well) |
Result: | The 6 μg does produced significant reductions when delivered at 24 or 6 h prior to HSV-2 inoculation. The 0.1 μg dose produced reduced HSV-2 replication at 24 or 6 h prior to viral challenge. |
FSL-1 application significantly protectes against genital HSV-2 challenge in mice [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Female Swiss-Webster mice (weighing 20-25 g) [1] |
Dosage: | 2 or 6 μg |
Administration: | Delivered vaginally using a positive displacement pipet, prior to or following viral challenge as specified for each experiment. |
Result: |
The 2 μg does delivered 6 h prior to HSV-2 challenge increased the ID50 (260 pfu) and LD50 (660 pfu) by 10-fold compared to DPBS vehicle control.
The single 6 μg dose produced significantly improved outcomes compared to DPBS vehicle application. |
Solid
Shipping with dry ice.
-80°C
H 2 O : 50 mg/mL ( 28.09 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 0.5617 mL | 2.8087 mL | 5.6174 mL |
5 mM | 0.1123 mL | 0.5617 mL | 1.1235 mL |
10 mM | 0.0562 mL | 0.2809 mL | 0.5617 mL |
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