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Indoxyl Sulfate-d5 (potassium salt)

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    Indoxyl Sulfate-d<sub>5</sub> (potassium salt)
  • Indoxyl Sulfate-d<sub>5</sub> (potassium salt)
Cat No: 34511
Cayman

Indoxyl sulfate-d5 is intended for use as an internal standard for the quantification of indoxyl sulfate (Item No. 16926) by GC- or LC-MS. Indoxyl sulfate is a uremic toxin and a metabolite of tryptophan (Item No. 29600).{27740} It is formed via sulfa...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 1H-indol-3-yl-2,4,5,6,7-d5 sulfate, potassium salt
Correlated keywords:
  • 1644527-73-0 deuterated deuterium GCMS LCMS SULT 1A1*2 Hep G2 OAT 1 3
Product Overview:
Indoxyl sulfate-d5 is intended for use as an internal standard for the quantification of indoxyl sulfate (Item No. 16926) by GC- or LC-MS. Indoxyl sulfate is a uremic toxin and a metabolite of tryptophan (Item No. 29600).{27740} It is formed via sulfation of indole, an intermediate generated from tryptophan by intestinal bacteria, by the sulfotransferase (SULT) isoform 1A1 variant 2 (SULT1A1*2) in the liver.{58559,27740} Indoxyl sulfate activates the aryl hydrocarbon receptor (AhR) in HepG2 40/6 hepatoma cells (EC50 = 12.1 nM in a reporter assay).{58560} It also inhibits the organic anion transporter (OAT) isoforms OAT1 and OAT3 (Kis = 34.2 and 74.4 µM, respectively for the rat transporters) in S2 proximal tubule cells.{58561} Indoxyl sulfate (0.2 and 1 mM) increases superoxide anion and nitric oxide levels in isolated human mononuclear blood cells.{58562} It increases serum creatinine and blood urea nitrogen (BUN) levels in the 5/6 nephrectomized rat model of chronic renal failure when administered at a dose of 50 mg/kg.{58561}
Size 1 mg
Shipping dry ice
CAS Number 1644451-34-2
Molecular Formula C8HD5NO4S • K
SMILES [O-]S(OC1=C([2H])NC2=C([2H])C([2H])=C([2H])C([2H])=C21)(=O)=O.[K+]
Molecular Weight 256,3
Formulation A solid
Purity ≥99% deuterated forms (d1-d5)
Custom Code 3822.19
UNSPSC code 12352100

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Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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ISO Guide 34:2009

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