Uridine (highly Pure)

<strong>Uridine (highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2014058_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 100 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 244.2 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> 1-β-D-Ribofuranosyluracil, Uracil-1-β-D-ribofuranoside_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: Arbour CA, Imperiali B. Uridine natural products: Challenging targets and inspiration for novel small molecule inhibitors Bioorg Med Chem. 2020 Sep 15;28(18):115661._x000D_ 2: Schaffrath R, Leidel SA. Wobble uridine modifications-a reason to live, a reason to die?! RNA Biol. 2017 Sep 2;14(9):1209-1222._x000D_ 3: Yamamoto T, Koyama H, Kurajoh M, Shoji T, Tsutsumi Z, Moriwaki Y. Biochemistry of uridine in plasma Clin Chim Acta. 2011 Sep 18;412(19-20):1712-24._x000D_ 4: Connolly GP, Duley JA. Uridine and its nucleotides: biological actions, therapeutic potentials Trends Pharmacol Sci. 1999 May;20(5):218-25._x000D_ 5: Zheng WV, Li Y, Cheng X, Xu Y, Zhou T, Li D, Xiong Y, Wang S, Chen Z. Uridine alleviates carbon tetrachloride-induced liver fibrosis by regulating the activity of liver-related cells J Cell Mol Med. 2022 Feb;26(3):840-854._x000D_ 6: Gupta R, Laxman S. tRNA wobble-uridine modifications as amino acid sensors and regulators of cellular metabolic state Curr Genet. 2020 Jun;66(3):475-480._x000D_ 7: Walker UA, Venhoff N. Uridine in the prevention and treatment of NRTI-related mitochondrial toxicity Antivir Ther. 2005;10 Suppl 2:M117-23._x000D_ 8: van Groeningen CJ, Peters GJ, Pinedo HM. Modulation of fluorouracil toxicity with uridine Semin Oncol. 1992 Apr;19(2 Suppl 3):148-54._x000D_ 9: Duan H, Hu K, Zheng D, Cheng Y, Zhang Z, Wang Y, Liang L, Hu J, Luo T. Recognition and release of uridine and hCNT3: From multivariate interactions to molecular design Int J Biol Macromol. 2022 Dec 31;223(Pt A):1562-1577._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/35621108">10: Maslova AA, Matyugina EC, Shustova EY, Volok VP, Kozlovskaya LI, Kochetkov SN, Khandazhinskaya AL. [New Analogues of Uridine as Possible Anti-Viral Agents Specific to SARS-CoV-2] Mol Biol (Mosk). 2022 May-Jun;56(3):510-515. </a>_x000D_ _x000D_ <strong>Products Related to Uridine (highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>