Trisodium cytidine 5'-diphosphate

• CAT Number: L000091
• CAS Number: 34393-59-4
• Molecular Formula: C9H12N3Na3O11P2
• Molecular Weight: 469.12
• Purity: ≥95%
• IUPAC Name: trisodium;[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate
• InChI: InChI=1S/C9H15N3O11P2.3Na/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(22-8)3-21-25(19,20)23-24(16,17)18;;;/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H2,10,11,15)(H2,16,17,18);;;/q;3*+1/p-3/t4-,6-,7-,8-;;;/m1.../s1
• InChIKey: JENUKVZGXGULDX-LLWADOMFSA-K
• SMILES: C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])[O-])O)O.[Na+].[Na+].[Na+]

Trisodium cytidine 5′-diphosphate(Cat No.:L000091), a trisodium salt of cytidine 5′-diphosphate, plays a pivotal role in cellular biochemistry. Functioning as a nucleotide derivative, it participates in enzymatic reactions as a cofactor, particularly in metabolic pathways involving nucleic acids and energy transfer. In the pharmaceutical field, it can be utilized in drug development targeting nucleotide-based signaling cascades, potentially affecting gene expression or cellular processes. Furthermore, its involvement in nucleic acid synthesis makes it valuable in organic chemistry, enabling the creation of modified nucleotides for genetic research and molecular biology applications. Its multi-disciplinary significance underscores its importance in pharmaceuticals, molecular biology, and material chemistry.