A nucleotide diphosphate
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2'-Deoxycytidine 5'-diphosphate (sodium salt hydrate)

Item No. 22982

Technical Information
Formal Name
2’-deoxy-cytidine 5'-(trihydrogen diphosphate), trisodium salt, hydrate
CAS Number
151151-32-5
Synonyms
  • dCDP
Molecular Formula
C9H12N3O10P2 • 3Na [XH2O]
Formula Weight
Purity
≥95%
A crystalline solid
PBS (pH 7.2): 10 mg/ml
λmax
271 nm
SMILES
O=P(OP([O-])([O-])=O)([O-])OC[C@H]1O[C@@H](N2C(N=C(N)C=C2)=O)C[C@@H]1O.[Na+].[Na+].[Na+].O
InChi Code
InChI=1S/C9H15N3O10P2.3Na.H2O/c10-7-1-2-12(9(14)11-7)8-3-5(13)6(21-8)4-20-24(18,19)22-23(15,16)17;;;;/h1-2,5-6,8,13H,3-4H2,(H,18,19)(H2,10,11,14)(H2,15,16,17);;;;1H2/q;3*+1;/p-3/t5-,6+,8+;;;;/m0..../s1
InChi Key
DNKSTBDUNOLCRJ-OIXZBRQUSA-K
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    2’-Deoxycytidine 5’-diphosphate (dCDP) is a nucleotide diphosphate used in various biochemical research applications including studies of DNA synthesis.1,2,3 It is a substrate for various nucleoside diphosphate kinases to synthesize dCTP.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Sun, Q., Gong, S., Sun, J., et alA P(V)-N activation strategy for the synthesis of nucleoside polyphosphates. The Journal of Organic Chemistry 78(17), 8417-8426 (2013).

    2. Weiss, B. The deoxycytidine pathway for thymidylate synthesis in Escherichia coli. J. Bacteriol. 189(21), 7922-7926 (2007).

    3. Wallace, T.L., and Johnson, E.M., Jr. Cytosine arabinoside kills postmitotic neurons: Evidence that deoxycytidine may have a role in neuronal survival that is independent of DNA synthesis. J. Neurosci. 9(1), 115-124 (1989).

    4. Wishart, D.S., Jewison, T., Guo, A.C., et alHMDB 3.0--The Human Metabolome Database in 2013. Nucleic Acids Res. 41(Database issue), D801-D807 (2013).