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Xanthosine 3′,5′-cyclic Monophosphate

<strong>Xanthosine 3′,5′-cyclic Monophosphate</strong>_x000D_ <strong>Catalog number:</strong> B2014356_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 vial_x000D_ <strong>Molecular Weight or Concentration:</strong> 367.2 g/mol_x000D_ <strong>Supplied as:</strong> Solid_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> cXMP_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: Sigel H, Operschall BP, Griesser R. Xanthosine 5'-monophosphate (XMP). Acid-base and metal ion-binding properties of a chameleon-like nucleotide Chem Soc Rev. 2009 Aug;38(8):2465-94._x000D_ 2: Kulikowska E, Kierdaszuk B, Shugar D. Xanthine, xanthosine and its nucleotides: solution structures of neutral and ionic forms, and relevance to substrate properties in various enzyme systems and metabolic pathways Acta Biochim Pol. 2004;51(2):493-531._x000D_ 3: Oka N, Hirabayashi H, Kumada K, Ando K. Synthesis of xanthosine 2-phosphate diesters via phosphitylation of the carbonyl group Bioorg Med Chem Lett. 2021 Dec 15;54:128439._x000D_ 4: Ahmed SA, Sarma P, Barge SR, Swargiary D, Devi GS, Borah JC. Xanthosine, a purine glycoside mediates hepatic glucose homeostasis through inhibition of gluconeogenesis and activation of glycogenesis via regulating the AMPK/ FoxO1/AKT/GSK3_ signaling cascade Chem Biol Interact. 2023 Feb 1;371:110347._x000D_ 5: Rauner G, Barash I. Xanthosine administration does not affect the proportion of epithelial stem cells in bovine mammary tissue, but has a latent negative effect on cell proliferation Exp Cell Res. 2014 Oct 15;328(1):186-196._x000D_ 6: Mair S, Erharter K, Renard E, Brillet K, Brunner M, Lusser A, Kreutz C, Ennifar E, Micura R. Towards a comprehensive understanding of RNA deamination: synthesis and properties of xanthosine-modified RNA Nucleic Acids Res. 2022 Jun 24;50(11):6038-6051._x000D_ 7: Rttger K, Stellmacher R, Stuhldreier MC, Temps F. Ultrafast Electronic Deactivation Dynamics of Xanthosine Monophosphate Molecules. 2017 Jan 18;22(1):160._x000D_ 8: Choudhary RK, Choudhary S, Verma R. In vivo response of xanthosine on mammary gene expression of lactating Beetal goat Mol Biol Rep. 2018 Aug;45(4):581-590._x000D_ 9: Choudhary S, Li W, Bickhart D, Verma R, Sethi RS, Mukhopadhyay CS, Choudhary RK. Examination of the xanthosine response on gene expression of mammary epithelial cells using RNA-seq technology J Anim Sci Technol. 2018 Jul 13;60:18._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/30787180">10: Baccolini C, Witte CP. AMP and GMP Catabolism in Arabidopsis Converge on Xanthosine, Which Is Degraded by a Nucleoside Hydrolase Heterocomplex Plant Cell. 2019 Mar;31(3):734-751. </a>_x000D_ _x000D_ <strong>Products Related to Xanthosine 3′,5′-cyclic Monophosphate can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>

Product Specifications

Short Description

Catalog Number: B2014356 (1 vial)

Weight

0.15

Length

2

Width

0.5

Height

0.5

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