Xanthosine 5'-monophosphate (sodium salt)

• CAT Number: R065713
• CAS Number: 25899-70-1
• Molecular Formula: C10H11N4O9P • 2Na
• Molecular Weight: 408.17
• Purity: ≥95%
• Synonyms: XMP
• Target: DNA/RNA Synthesis
• Storage: -20°C
• IUPAC Name: disodium;[(2R,3S,4R,5R)-5-(2,6-dioxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate
• InChI: InChI=1S/C10H13N4O9P.2Na/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17;;/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18);;/q;2*+1/p-2/t3-,5-,6-,9-;;/m1../s1
• InChIKey: QQPVYRBCIRHGSZ-LGVAUZIVSA-L
• SMILES: O[C@H]1[C@@H](O)[C@H](N2C=NC(C(N3)=O)=C2NC3=O)O[C@@H]1COP([O-])([O-])=O.[Na+].[Na+]

Xanthosine 5′-monophosphate (sodium salt)(CAT: R065713) is a nucleotide monophosphate that plays a critical role in the purine metabolism pathway. As an intermediate in the synthesis of guanine nucleotides, it is crucial for the production of nucleic acids and energy molecules like ATP and GTP. Xanthosine 5′-monophosphate (XMP) is also involved in various biochemical processes, including DNA and RNA synthesis, and cellular signaling. The sodium salt form enhances its solubility, making it more convenient for use in biochemical assays, research, and diagnostic applications. This compound is particularly valuable in studies focused on nucleotide metabolism, enzymology, and cellular biochemistry.

Reference

1.Watkins, W.J.,Chen, J.M.,Cho, A., et al. Phosphonic acid-containing analogues of mycophenolic acid as inhibitors of IMPDH. Bioorganic & Medicinal Chemistry Letters 16(13), 3479-3483 (2006).