Molecular structure of 5′-Deoxyuridine, CAS Number: 15958-99-3
5′-Deoxyuridine (CAS 15958-99-3)
Application:
5′-Deoxyuridine is A uridine derivative
CAS Number:
15958-99-3
Molecular Weight:
228.20
Molecular Formula:
C9H12N2O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
5'-Deoxyuridine is a derivative of Uridine (sc-296685) that is lacking the hydroxyl group on the hydroxymethyl moiety of the parent compound. 5'-Deoxyuridine has been described to be useful in the study of nucleoside transport proteins and serves as a probe compound for the specificity of nucleoside-handling mechanisms.
5′-Deoxyuridine (CAS 15958-99-3) References
- Functional production and reconstitution of the human equilibrative nucleoside transporter (hENT1) in Saccharomyces cerevisiae. Interaction of inhibitors of nucleoside transport with recombinant hENT1 and a glycosylation-defective derivative (hENT1/N48Q). | Vickers, MF., et al. 1999. Biochem J. 339 (Pt 1): 21-32. PMID: 10085223
- Developmental regulation of the concentrative nucleoside transporters CNT1 and CNT2 in rat liver. | del Santo, B., et al. 2001. J Hepatol. 34: 873-80. PMID: 11451171
- Phase I trial of capecitabine in combination with interferon alpha in patients with metastatic renal cancer: toxicity and pharmacokinetics. | Chang, DZ., et al. 2001. Cancer Chemother Pharmacol. 48: 493-8. PMID: 11800031
- Molecular requirements of the human nucleoside transporters hCNT1, hCNT2, and hENT1. | Chang, C., et al. 2004. Mol Pharmacol. 65: 558-70. PMID: 14978234
- Residue 33 of human equilibrative nucleoside transporter 2 is a functionally important component of both the dipyridamole and nucleoside binding sites. | Visser, F., et al. 2005. Mol Pharmacol. 67: 1291-8. PMID: 15644498
- Cyclic stretch induces proliferation and TGF-beta1-mediated apoptosis via p38 and ERK in ureteric bud cells. | Fujita, H., et al. 2010. Am J Physiol Renal Physiol. 299: F648-55. PMID: 20392803
- Stereoselective synthesis of uridine-derived nucleosyl amino acids. | Spork, AP., et al. 2011. J Org Chem. 76: 10083-98. PMID: 22059552
- [Identification and properties of insulin receptors in neuroblastoma C 1300 N 18 cells in various functional states]. | Gulaia, NM., et al. 1988. Ukr Biokhim Zh (1978). 60: 3-10. PMID: 3046084
- Pyrimidine salvage in Toxoplasma gondii as a target for new treatment. | Elati, HAA., et al. 2023. Front Cell Infect Microbiol. 13: 1320160. PMID: 38162577
- The binding site for the adenosyl group of coenzyme B12 in diol dehydrase. | Toraya, T. 1985. Arch Biochem Biophys. 242: 470-7. PMID: 3904627
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
5'-Deoxyuridine, 250 mg | sc-210409 | 250 mg | $406.00 |