TN-783
TN-783 is an orally active, brain-penetrant NLRP3 (IC50 = 19.3 nM) inhibitor. TN-783 enhances the effects of the GLP-1 receptor agonist semaglutide. TN-783 requires sustained targeted action, not permanent metabolic remodeling. TN-783 can be used for the study of obesity.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 分子式: C16H11F4IN4O2
- 分子量:494.18
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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生物活性
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化学情報
- 純度とドキュメンテーション
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Help & FAQs
生物活性
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NLRP3 19.3 nM (IC50) |
TN-783 (2 h) can effectively inhibit the secretion of IL-1β (IC50 = 45.9 nM) by THP-1 cells, under Lipopolysaccharides (HY-D1056) (LPS)/Nigericin (HY-127019) stimulation[1].
TN-783 (0.3 nM-6 μM, 1 h) can dose-dependently inhibit the secretion of IL-1β (IC50 = 5.17 nM) and IL-18 (IC50 = 12.3 nM) in THP-1 cells induced by Palmitic acid (HY-N0830)-BSA complex[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Diet-induced obese (DIO) and Normal chow (NC)-fed lean mice[1].
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Dosage:50 mg/kg
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Administration:P.o., twice daily for 15 days
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Result:Caused a decrease in body weight in DIO mice, but did not affect the body weight of lean mice.
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Animal Model:Diet-induced obese (DIO) and Normal chow (NC)-fed lean mice[1].
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Dosage:0.5 mg/kg, 2 mg/kg, 50 mg/kg
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Administration:P.o., twice daily for 28 days
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Result:50 mg/kg induced progressive and sustained weight loss in DIO mice; lower doses were ineffective.
The weight loss was due to a significant reduction in fat mass, while lean body mass was preserved. It did not affect lean mice.
The weight loss was driven by sustained inhibition of food intake, without altering weight-corrected energy expenditure or activity levels.
Improved glucose tolerance in DIO mice.
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Animal Model:Diet-induced obese (DIO) and Normal chow (NC)-fed lean mice[1].
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Dosage:50 mg/kg
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Administration:P.o., twice daily for 14-28 days
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Result:Reversed microglia activation and significantly alleviated the dysregulation of a large number of genes and protein expression.
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Animal Model:Diet-induced obese (DIO) and Normal chow (NC)-fed lean mice[1].
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Dosage:50 mg/kg; Smegglutide: 0.0041 mg/kg (1 nmol/kg)
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Administration:P.o., twice daily for 66 days; s.c., once daily for 66 days
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Result:Combination therapy produced more significant and sustained weight loss than either drug alone.
Effectively prevented weight rebound.
化学情報
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分子量 494.18
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分子式 C16H11F4IN4O2
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SMILES
O=C(NC1=NC=C(C=N1)F)CN2C[C@H](C3=C(C2=O)C=CC(I)=C3)C(F)(F)F
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
TN-783 関連分類
HY-179131 関連分類
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