Product Name :
2′-Deoxy-5-hydroxyuridine (CAS 5168-36-5)
Synonym :
5-hydroxy-2′-deoxyuridine
Application :
CAS:
5168-36-5
Purity:
Molecular Weight:
244.20
Formula :
C9H12N2O6
Physical state:
Solid
solubility :
Shipping Condition :
Store at -20° C
Melting point:
245.Buy883-40-9 48° C (Predicted)
SMILES:
C1[C@@H]([C@H](O[C@H]1N2C=C(C(=O)NC2=O)O)CO)O
References:
:Reperfusion-triggered stress protein response in the myocardium is blocked by post-conditioning.4-Methylbenzenesulfonyl cyanide site Systems biology pathway analysis highlights the key role of the canonical aryl-hydrocarbon receptor pathway.PMID:33691552 | Vilahur, G., et al. 2013. Eur Heart J. 34: 2082-93. PMID: 22851653Synthesis and antiviral activity of various 3′-azido analogues of pyrimidine deoxyribonucleosides against human immunodeficiency virus (HIV-1, HTLV-III/LAV). | Lin, TS., et al. 1988. J Med Chem. 31: 336-40. PMID: 3339606Probing telomereric-like G4 structures with full or partial 2′-deoxy-5-hydroxyuridine substitutions. | Szeltner, Z., et al. 2023. Biochimie.. PMID: 36707016Nucleosides. LXI. Transformations of pyrimidine nucleosides in alkaline media. IV. The conversion of 5-hydroxyuridines into imidazoline nucleosides. | Otter, BA., et al. 1969. J Org Chem. 34: 2636-42. PMID: 5803812Synthesis and antiherpesviral activity of 5-C-substituted uracil nucleosides. | Sakata, S., et al. 1980. Nucleic Acids Symp Ser. s39-42. PMID: 6265881Major oxidative products of cytosine, 5-hydroxycytosine and 5-hydroxyuracil, exhibit sequence context-dependent mispairing in vitro. | Purmal, AA., et al. 1994. Nucleic Acids Res. 22: 72-8. PMID: 8127657