
Indoxyl sulfate potassium salt
CAS No. 2642-37-7
Indoxyl sulfate potassium salt ( Potassium 3-indoxyl sulfate )
产品货号. M19767 CAS No. 2642-37-7
Indoxyl硫酸盐(钾盐)是人类芳基烃受体(AHR)的激动剂。芳基烃受体 (AhR) 最近已成为免疫炎症条件的病理生理调节剂,硫酸吲哚酚已被证明是 AhR 的配体。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
10MG | ¥437 | 有现货 |
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25MG | ¥729 | 有现货 |
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50MG | ¥1126 | 有现货 |
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100MG | ¥1847 | 有现货 |
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200MG | ¥2778 | 有现货 |
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500MG | ¥4836 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Indoxyl sulfate potassium salt
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Indoxyl硫酸盐(钾盐)是人类芳基烃受体(AHR)的激动剂。芳基烃受体 (AhR) 最近已成为免疫炎症条件的病理生理调节剂,硫酸吲哚酚已被证明是 AhR 的配体。
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产品描述Indoxyl sulfate (potassium salt) is an agonist for the human aryl hydrocarbon receptor (AHR). The aryl hydrocarbon receptor (AhR) has recently emerged as a pathophysiological regulator of immune-inflammatory conditions and Indoxyl sulfate has been shown to be a ligand for AhR. Indoxyl sulfate is also a metabolite of tryptophan derived from dietary protein. Tryptophan is metabolized by intestinal bacteria into indole which is absorbed into the blood and then further metabolized to indoxyl sulfate in the liver which is normally excreted in urine. In chronic kidney disease patients where renal function is compromised indoxyl sulfate can accumulate in serum as a uremic toxin inducing oxidative stress and accelerating progression of the disease. Indoxyl sulfate at 250 μM can induce the activation of NF-κB promoting the expression of both TGF-β1 and Smad3 expression in proximal tubular cells of rats which is associated with profibrotic activity.
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体外实验——
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体内实验——
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同义词Potassium 3-indoxyl sulfate
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通路Endocrinology/Hormones
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靶点AhR
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受体AhR
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研究领域——
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适应症——
化学信息
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CAS Number2642-37-7
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分子量251.3
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分子式C8H6KNO4S
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纯度>98% (HPLC)
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溶解度DMSO:10 mM
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SMILES[K+].[O-]S(=O)(=O)Oc1c[nH]c2ccccc12
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Zgoda-Pols J R Chowdhury S Wirth M et al. Metabolomics analysis reveals elevation of 3-indoxyl sulfate in plasma and brain during chemically-induced acute kidney injury in mice: Investigation of nicotinic acid receptor agonists[J]. Toxicology & Applied Pharmacology 2011 255(1):48-56.