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HMGB1-IN-2

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Catalog No. T82189

HMGB1-IN-2 (compound 15) is a selective inhibitor of the highly conserved nuclear protein HMGB1, showing no inhibitory effect at an IC50 of 20.2 μM in RAW264.7 cells. At 30 μM, it reduces IL-1β, TNF-α, and caspase-1 p20 levels, inhibits NF-κB p65 phosphorylation, and provides anti-apoptotic effects. In vivo, 15 mg/kg of HMGB1-IN-2 administered intraperitoneally alleviates kidney injury in a mouse model of septic acute kidney injury. Additionally, it inhibits Huh7 and A549 cells with IC50 values of 77.0 μM and 82.0 μM, respectively [1].

HMGB1-IN-2

HMGB1-IN-2

😃Good
Catalog No. T82189
HMGB1-IN-2 (compound 15) is a selective inhibitor of the highly conserved nuclear protein HMGB1, showing no inhibitory effect at an IC50 of 20.2 μM in RAW264.7 cells. At 30 μM, it reduces IL-1β, TNF-α, and caspase-1 p20 levels, inhibits NF-κB p65 phosphorylation, and provides anti-apoptotic effects. In vivo, 15 mg/kg of HMGB1-IN-2 administered intraperitoneally alleviates kidney injury in a mouse model of septic acute kidney injury. Additionally, it inhibits Huh7 and A549 cells with IC50 values of 77.0 μM and 82.0 μM, respectively [1].
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Product Introduction

Bioactivity
Description
HMGB1-IN-2 (compound 15) is a selective inhibitor of the highly conserved nuclear protein HMGB1, showing no inhibitory effect at an IC50 of 20.2 μM in RAW264.7 cells. At 30 μM, it reduces IL-1β, TNF-α, and caspase-1 p20 levels, inhibits NF-κB p65 phosphorylation, and provides anti-apoptotic effects. In vivo, 15 mg/kg of HMGB1-IN-2 administered intraperitoneally alleviates kidney injury in a mouse model of septic acute kidney injury. Additionally, it inhibits Huh7 and A549 cells with IC50 values of 77.0 μM and 82.0 μM, respectively [1].
In vivo
HMGB1-IN-2 (compound 15) is dissolved in a 10% polyoxyethylene castor oil aqueous solution [1].
Chemical Properties
Molecular Weight926.14
FormulaC53H71N3O11
Relative Density.no data available
Storage & Solubility Information
StorageShipping with blue ice.

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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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