A synthetic precursor
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6-Chloropurine riboside-5'-O-diphosphate (sodium salt)

Item No. 38552

Technical Information
Formal Name
6-chloro-9-[5-O-[hydroxy(phosphonooxy)phosphinyl]-β-D-ribofuranosyl]-9H-purine, trisodium salt
Synonyms
  • 6-chloro PuTP
Molecular Formula
C10H10ClN4O10P2 • 3Na
Formula Weight
Purity
≥95%
A solution in water
Water: Soluble
SMILES
[O-]P([O-])(OP([O-])(OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)N2C3=NC=NC(Cl)=C3N=C2)=O)=O.[Na+].[Na+].[Na+]
InChi Code
InChI=1S/C10H13ClN4O10P2.3Na/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20;;;/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,18,19,20);;;/q;3*+1/p-3/t4-,6-,7-,10-;;;/m1.../s1
InChi Key
OYZDIYJSPCPFFP-MSQVLRTGSA-K
Shipping & Storage Information
Storage
-80°C
Shipping
Dry ice in continental US; may vary elsewhere
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    Product Description

    6-Chloropurine riboside-5'-O-diphosphate is a synthetic precursor and phosphorylated form of 6-chloropurine riboside (Item No. 36002).1,2 It has been used in the synthesis of cytokinins with anticancer activity and spin-labeled derivatives of NAD+ (Item No. 16077).

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Voller, J., Zatloukal, M., Lenobel, R., et alAnticancer activity of natural cytokinins: A structure-activity relationship study. Phytochemistry 71(11-12), 1350-1359 (2010).

    2. Wenzel, H.R., Pfleiderer, G., Trommer, W.E., et alThe synthesis of spin-label derivatives of NAD+ and its structural components and their binding to lactate dehydrogenase. Biochim. Biophys. Acta 452(2), 292-301 (1976).