RKH
Based on 1 publication(s) in Google Scholar
RKH is an orally active tripeptide derived from Akkermansia muciniphila and a TLR4 inhibitor that binds to TLR4 with a Kd of 3.34 nM. RKH blocks LPS-induced TLR4/MD2 dimerization, inhibits LPS-induced proinflammatory cytokine expression and systemic inflammation, and exhibits stronger inhibition of TLR4-mediated cytokine expression than other TLR pathways in macrophages. RKH inhibits sepsis-induced systemic proinflammatory cytokine production as well as macrophage recruitment and proinflammatory activation. RKH prevents lethal sepsis and attenuates organ injury in mouse and piglet sepsis models. RKH can be used for research on sepsis.
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: C18H33N9O4
- 分子量:439.51
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
MedChemExpress(MCE)の使用を引用している文献 RKH
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生物活性
製品説明
IC50 & Target
[1]|
TLR4 3.34 nM (Kd) |
体外実験
RKH (125 μM) protects TLR4 protein from pronase hydrolysis in vitro; and exerts a thermal stabilizing effect on TLR4 in macrophages across the 37-67 °C CETSA gradient range[1].
RKH (125 μM; 15 min) inhibits LPS-induced TLR4 downstream P38, P65, JNK, and ERK signaling transduction in THP-1-dMs cells, thereby reducing LPS-induced pro-inflammatory factor expression in macrophages, with weak inhibitory effects on other TLRs[1].
RKH (125 μM; 15 min) reduces the binding of FITC-LPS to BMDMs and THP-1-dMs without altering TLR4/MD2 expression or internalization[1].
RKH inhibits LPS-induced TLR4-TLR4 and TLR4-MD2 dimerization in BMDMs and THP-1-dMs[1].
RKH-mediated inhibition of TLR4 dimerization in THP-1-dMs requires ARG264, LEU293, ASP294, and LYS362 on TLR4[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:THP-1-dMs cells
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Concentration:125 μM
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Incubation Time:15 min
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Result:Inhibited LPS-induced TLR4 downstream P38, P65, JNK, and ERK signaling transduction in THP-1-dMs cells, thereby reducing LPS-induced pro-inflammatory factor expression in macrophages, with weak inhibitory effects on other TLRs.
体内実験
RKH (50 mg/kg; intragastric administration; 2 h before LPS injection) pretreatment protects mice from LPS-induced lethal sepsis and organ injury[1].
RKH (1 mg/kg; intragastric administration; 2 h before LPS injection) pretreatment prolongs the survival time of LPS-induced septic piglets and alleviates excessive inflammation and organ injury[1].
RKH pretreatment exerts a protective effect in septic mice by prolonging survival time and alleviating acute tissue injury and inflammation, and it also exerts a protective effect against sepsis in a septic piglet model[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:C57BL/6 mice (mlae, 6-8 weeks, induced by CLP operation), TLR4 knockout (TLR4-/-) mice[1]
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Dosage:50 mg/kg
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Administration:intragastric administration; 2 h before LPS injection
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Result:Protected mice against CLP-induced lethal sepsis, organ injury, and systemic inflammation; and exerted no protective effect against CLP-induced lethal sepsis in TLR4 knockout mice.
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Animal Model:C57BL/6 mice (mlae, 6-8 weeks, induced by LPS administration)[1]
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Dosage:50 mg/kg
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Administration:intragastric administration; 2 h before LPS injection
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Result:Protected mice from LPS-induced lethal sepsis and organ injury.
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Animal Model:piglet (induced by LPS administration, LPS (300 μg/kg) was injected intravenously for 30 min)[1]
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Dosage:1 mg/kg
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Administration:intragastric administration; 2 h before LPS injection
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Result:Prolonged the survival time of LPS-induced septic piglets and alleviates excessive inflammation and organ injury.
化学情報
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分子量 439.51
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分子式 C18H33N9O4
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配列
Arg-Lys-His
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シーケンスの短縮
RKH
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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.
Publications (1)
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Journal Impact Factor
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Most Recent
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JCI Insight
CD4+ T helper 2 cell-macrophage crosstalk induces IL-24-mediated breast cancer suppression. [Abstract]2025 Jan 9;10(1):e180962. PMID: 39782693
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)