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SC75741

🥰Excellent
Catalog No. T6661Cas No. 913822-46-5

SC75741 is a potent P65 inhibitor with IC50 of 200 nM

SC75741

SC75741

🥰Excellent
Purity: 99.82%
Catalog No. T6661Cas No. 913822-46-5
SC75741 is a potent P65 inhibitor with IC50 of 200 nM
Pack SizePriceAvailabilityQuantity
1 mg$36In Stock
5 mg$71In Stock
10 mg$123In Stock
25 mg$247In Stock
50 mg$396In Stock
100 mg$596In Stock
1 mL x 10 mM (in DMSO)$97In Stock
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Purity:99.82%
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Product Introduction

Bioactivity
Description
SC75741 is a potent P65 inhibitor with IC50 of 200 nM
Targets&IC50
NF-κB:200 nM(EC50)
In vitro
SC75741 shows immunosuppressive activity by inhibiting human PBMC proliferation with IC50 of 2.2 μM. [1] SC75741 inhibits replication of influenza A and B viruses by inhibiting NF-κB-mediated signalling on a transcriptional level. Moreover, SC75741 shows a high barrier for development of resistant virus variants. [2]
In vivo
SC75741 (15 mg/kg i.p.) reduces virus replication and cytokine expression in mice lungs after H5N1 influenza virus infection. [2]
Kinase Assay
NF-κB reporter gene assay: The NF-κB reporter gene assay is prepared with A549-NF-κB-SEAP cell line according to manufacturer's instructions. In short, A549 cells stably transfected with pNF-κB-SEAP reporter gene plasmid are plated and allowed to attach overnight. The cells are subsequently incubated for 5 h with described compounds at 100, 30, 10, 3, 1, 0.3, 0.1, and 0 μM and then stimulated with 10 ng/ml TNF-α for 22 h. The supernatant of the cell is analyzed for SEAP activity using a chemiluminescent SEAP reporter gene assay.
Cell Research
Cell viability assay is prepared using a CellTiter-BluTM Cell Viability Assay. For each concentration of the compound four replicates are measured.(Only for Reference)
Chemical Properties
Molecular Weight565.67
FormulaC29H23N7O2S2
Cas No.913822-46-5
SmilesO=C(Nc1nc2ccc(cc2[nH]1)C(=O)c1ccccc1)c1csc(n1)C1CCN(CC1)c1ncnc2ccsc12
Relative Density.1.483 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 50 mg/mL (88.39 mM)
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.7678 mL8.8391 mL17.6782 mL88.3908 mL
5 mM0.3536 mL1.7678 mL3.5356 mL17.6782 mL
10 mM0.1768 mL0.8839 mL1.7678 mL8.8391 mL
20 mM0.0884 mL0.4420 mL0.8839 mL4.4195 mL
50 mM0.0354 mL0.1768 mL0.3536 mL1.7678 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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