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Larsucosterol trimethylamine

🥰Excellent
Catalog No. T74147
Alias DV-928 trimethylamine, DUR-928 trimethylamine

Larsucosterol trimethylamine (DUR-928 trimethylamine) is a potent liver X receptor (LXR) antagonist that modulates endogenous epigenetics, reduces lipid accumulation in hepatocytes, attenuates lipopolysaccharide (LPS) and TNFα-induced inflammatory responses in macrophages, and alleviates LPS- and acetaminophen (ATMP)-induced multi-organ damage.

Larsucosterol trimethylamine

Larsucosterol trimethylamine

🥰Excellent
Purity: 97.0%
Catalog No. T74147Alias DV-928 trimethylamine, DUR-928 trimethylamine
Larsucosterol trimethylamine (DUR-928 trimethylamine) is a potent liver X receptor (LXR) antagonist that modulates endogenous epigenetics, reduces lipid accumulation in hepatocytes, attenuates lipopolysaccharide (LPS) and TNFα-induced inflammatory responses in macrophages, and alleviates LPS- and acetaminophen (ATMP)-induced multi-organ damage.
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1 mg$192In Stock
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Purity:97.0%
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Product Introduction

Bioactivity
Description
Larsucosterol trimethylamine (DUR-928 trimethylamine) is a potent liver X receptor (LXR) antagonist that modulates endogenous epigenetics, reduces lipid accumulation in hepatocytes, attenuates lipopolysaccharide (LPS) and TNFα-induced inflammatory responses in macrophages, and alleviates LPS- and acetaminophen (ATMP)-induced multi-organ damage.
In vitro
In a model of HG-induced MASLD in humanhepatocytes, Larsucosterol exhibits a specific inhibition of DNMTs. This results in the conversion of 5mCpG to CpG in the promoter regions of 1,074 genes within hepatocytes, leading to the upregulation of genes associated with key sig-naling pathways such as MAPK-ERK, calcium-AMPK, andtype II diabetes mellitus pathways. [1]
In vivo
In a mouse hepatectomy model, larsucosterol upregulates the expression of genes associated with cell replication, including Wt1 (Wilms’ tumor 1),PCNA (proliferating cell nuclear antigen), cMyc (myelocyto-matosis oncogene), cyclin A, FoxM1b (Forkhead Box M1b),and CDC25b (M-phase inducer phosphatase 2), whereas con-currently downregulating the expression of cell cycle arrestgene Chek2 (checkpoint kinase 2) and the apoptotic geneApaf1 (apoptotic peptidase activating factor 1). [1]
AliasDV-928 trimethylamine, DUR-928 trimethylamine
Chemical Properties
Molecular Weight541.83
FormulaC30H55NO5S
SmilesC[C@@H]([C@H]1CC[C@@H]2[C@]1(C)CC[C@H]3[C@H]2CC=C4[C@]3(C)CC[C@H](OS(=O)(O)=O)C4)CCCC(C)(O)C.CN(C)C
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 20 mg/mL (39.27 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8456 mL9.2280 mL18.4560 mL92.2799 mL
5 mM0.3691 mL1.8456 mL3.6912 mL18.4560 mL
10 mM0.1846 mL0.9228 mL1.8456 mL9.2280 mL
20 mM0.0923 mL0.4614 mL0.9228 mL4.6140 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:
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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
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