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CAS 42155-08-8

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5′-Uridylic acid, 2′-deoxy-, sodium salt (1:2)

Description:
5′-Uridylic acid, 2′-deoxy-, sodium salt (1:2), commonly referred to as deoxyuridine monophosphate (dUMP) sodium salt, is a nucleotide derivative characterized by its role in nucleic acid metabolism. It is a pyrimidine nucleotide that consists of a uracil base, a deoxyribose sugar, and a phosphate group. The sodium salt form indicates that sodium ions are associated with the phosphate group, enhancing its solubility in aqueous solutions. This compound is crucial in DNA synthesis and repair, serving as a substrate for thymidylate synthase, which catalyzes the conversion of dUMP to deoxythymidine monophosphate (dTMP). Its structure allows for hydrogen bonding and base pairing, essential for the stability of nucleic acids. In laboratory settings, dUMP is often utilized in biochemical assays and research related to DNA synthesis and cellular metabolism. Additionally, its sodium salt form is typically more stable and easier to handle in various experimental conditions. Overall, 5′-Uridylic acid, 2′-deoxy-, sodium salt plays a significant role in molecular biology and biochemistry.
Formula:C9H13N2O8P·2Na
InChI:InChI=1S/C9H13N2O8P.2Na/c12-5-3-8(11-2-1-7(13)10-9(11)14)19-6(5)4-18-20(15,16)17;;/h1-2,5-6,8,12H,3-4H2,(H,10,13,14)(H2,15,16,17);;/t5-,6+,8+;;/m0../s1
InChI key:InChIKey=CWTUMDATELIIAI-CDNBRZBRSA-N
SMILES:O=C1N(C=CC(=O)N1)[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)C2.[Na]
Synonyms:
  • 2'-Deoxy-5'-Uridylic Acid
  • 2'-Deoxyuridine-5'-monophosphate,disodium salt
  • 2,4(1H,3H)-pyrimidinedione, 1-(2-deoxy-5-O-phosphonopentofuranosyl)-, monosodium salt
  • 2-Deoxyuridine-5-triphosphoric acid disodium salt
  • 2′-Deoxyuridine 5′-phosphate disodium salt
  • 5′-Uridylic acid, 2′-deoxy-, disodium salt
  • 5′-Uridylic acid, 2′-deoxy-, sodium salt (1:2)
  • Deoxyuridine 5′-monophosphate disodium salt
  • Disodium deoxyuridylate
  • dUMP.Na2
  • dUTP-Na2
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