Molecular structure of 1-β-D-Arabinofuranosyluracil-13C,15N2 5′-Monophosphate
1-β-D-Arabinofuranosyluracil-13C,15N2 5′-Monophosphate
Molecular Weight:
327.16
Molecular Formula:
(13C)C8H13(15N)2O9P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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A labeled metablite of 1--D-Arabinofuranosyluracil.
1-β-D-Arabinofuranosyluracil-13C,15N2 5′-Monophosphate References
- Preparation of a mixture of nucleoside triphosphates suitable for use in synthesis of nucleotide phosphate sugars from ribonucleic acid using nuclease P1, a mixture of nucleoside monophosphokinases and acetate kinase. | Haynie, SL. and Whitesides, GM. 1990. Appl Biochem Biotechnol. 23: 205-20. PMID: 1693485
- Acid-base properties of nucleosides and nucleotides as a function of concentration. Comparison of the proton affinity of the nucleic base residues in the monomeric and self-associated, oligomeric 5'-triphosphates of inosine (ITP), guanosine (GTP), and adenosine (ATP). | Corfù, NA. and Sigel, H. 1991. Eur J Biochem. 199: 659-69. PMID: 1868851
- Metabolism of 1-beta-D-arabinofuranosyluracil in mouse L5178Y cells. | Müller, WE. and Zahn, RK. 1979. Cancer Res. 39: 1102-7. PMID: 427752
- Ribonucleoside phosphates via phosphorimidazolidate intermediates. Synthesis of pseudoadenosine 5'-triphosphate. | Kozarich, JW., et al. 1973. Biochemistry. 12: 4458-63. PMID: 4584326
- Identification of potent, selective P2Y-purinoceptor agonists: structure-activity relationships for 2-thioether derivatives of adenosine 5'-triphosphate. | Fischer, B., et al. 1993. J Med Chem. 36: 3937-46. PMID: 8254622
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-β-D-Arabinofuranosyluracil-13C,15N2 5'-Monophosphate, 2.5 mg | sc-213304 | 2.5 mg | $1480.00 |