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Uridine 5′-diphosphoglucuronic Acid Trisodium Salt

<strong>Uridine 5′-diphosphoglucuronic Acid Trisodium Salt</strong>_x000D_ <strong>Catalog number:</strong> B2017894_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 10 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 646.23 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> UDP-GlcA, UDPGA, Uridine-diphosphate-glucuronic acid trisodium salt, Uridine[5′]diphospho[1]-α-D-glucopyranosuronic acid trisodium salt_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Falck E, Begrow F, Verspohl E, Wünsch B. Metabolism studies of ifenprodil, a potent GluN2B receptor antagonist J Pharm Biomed Anal. 2014 Jan;88:96-105._x000D_ 2: Aprile S, Del Grosso E, Grosa G. In vitro and in vivo phase II metabolism of combretastatin A-4: evidence for the formation of a sulphate conjugate metabolite Xenobiotica. 2009 Feb;39(2):148-61._x000D_ 3: Shaffer CL, Gunduz M, O'Connell TN, Obach RS, Yee S. Biotransformation of a GABAA receptor partial agonist in sprague-dawley rats and cynomolgus monkeys: identification of two unique N-carbamoyl metabolites Drug Metab Dispos. 2005 Nov;33(11):1688-99._x000D_ 4: Hauser SC, Ransil BJ, Ziurys JC, Gollan JL. Interaction of uridine 5'-diphosphoglucuronic acid with microsomal UDP-glucuronosyltransferase in primate liver: the facilitating role of uridine 5'-diphospho-N-acetylglucosamine Biochim Biophys Acta. 1988 Nov 17;967(2):141-8._x000D_ 5: Simon ES, Toone EJ, Ostroff G, Bednarski MD, Whitesides GM. Preparation of cytidine 5'-monophospho-N-acetylneuraminic acid and uridine 5'-diphosphoglucuronic acid; syntheses of alpha-2, 6-sialyllactosamine, alpha-2, 6-sialyllactose, and hyaluronic acid Methods Enzymol. 1989;179:275-87._x000D_ 6: Cappiello M, Giuliani L, Rane A, Pacifici GM. Uridine 5'-diphosphoglucuronic acid (UDPGLcUA) in the human fetal liver, kidney and placenta Eur J Drug Metab Pharmacokinet. 2000 Jul-Dec;25(3-4):161-3._x000D_ 7: Watkins JB, Klaassen CD. Determination of hepatic uridine 5'-diphosphoglucuronic acid concentration by conjugation with diethylstilbestrol J Pharmacol Methods. 1982 Mar;7(2):145-51._x000D_ 8: Savenije-Chapel EM, Bast A, Noordhoek J. Interaction of uridine 5'-diphosphoglucuronic acid (UDPGA) with cytochrome P 450 J Pharm Pharmacol. 1983 Aug;35(8):522-3._x000D_ 9: Stachowiak K, Zabiszak M, Grajewski J, Teubert A, Bajek A, Jastrzab R. Thermodynamic Studies of Complexes in Cu(II)/Uridine-5'-Diphosphoglucuronic Acid System Molecules. 2024 Aug 4;29(15):3695._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/3142526">10: Hauser SC, Ziurys JC, Gollan JL. A membrane transporter mediates access of uridine 5'-diphosphoglucuronic acid from the cytosol into the endoplasmic reticulum of rat hepatocytes: implications for glucuronidation reactions Biochim Biophys Acta. 1988 Nov 17;967(2):149-57. </a>_x000D_ _x000D_ <strong>Products Related to Uridine 5′-diphosphoglucuronic Acid Trisodium Salt can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>

Product Specifications

Short Description

Catalog Number: B2017894 (10 mg)

Weight

0.15

Length

2

Width

0.5

Height

0.5

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