CAS 14599-46-3
:5-carboxy-2'-deoxyuridine
Description:
5-Carboxy-2'-deoxyuridine is a nucleoside analog derived from uridine, characterized by the presence of a carboxylic acid group at the 5-position of the pyrimidine ring. This modification alters its biochemical properties and interactions within nucleic acid structures. The compound is typically white to off-white in appearance and is soluble in polar solvents, which facilitates its incorporation into nucleic acid synthesis. It plays a role in various biochemical pathways, particularly in studies related to nucleic acid metabolism and the synthesis of modified nucleotides. The presence of the carboxylic acid group can influence its reactivity and binding affinity to enzymes involved in nucleotide metabolism. Additionally, 5-carboxy-2'-deoxyuridine has been investigated for its potential applications in molecular biology and medicinal chemistry, particularly in the context of drug design and the development of therapeutic agents targeting nucleic acid processes. Its unique structural features make it a valuable compound for research in biochemistry and pharmacology.
Formula:C10H12N2O7
InChI:InChI=1S/C10H12N2O7/c13-3-6-5(14)1-7(19-6)12-2-4(9(16)17)8(15)11-10(12)18/h2,5-7,13-14H,1,3H2,(H,16,17)(H,11,15,18)/t5-,6+,7+/m0/s1
InChI key:InChIKey=GAGYTXTVUMXAOC-RRKCRQDMSA-N
SMILES:O=C1N([C@@H]2O[C@H](CO)[C@@H](O)C2)C=C(C(O)=O)C(=O)N1
Synonyms:- 1-(2-Deoxy-β-<span class="text-smallcaps">D</span>-erythro-pentofuranosyl)-1,2,3,4-tetrahydro-2,4-dioxo-5-pyrimidinecarboxylic acid
- 2'-Deoxy-5-carboxyuridine
- 5-Pyrimidinecarboxylic acid, 1-(2-deoxy-beta-D-erythro-pentofuranosyl)-1,2,3,4-tetrahydro-2,4-dioxo-
- 5-Pyrimidinecarboxylic acid, 1-(2-deoxy-β-<span class="text-smallcaps">D</span>-erythro-pentofuranosyl)-1,2,3,4-tetrahydro-2,4-dioxo-
- Uridine, 5-Carboxy-2'-Deoxy-
- 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-1,2,3,4-tetrahydro-2,4-dioxo-5-pyrimidinecarboxylic acid
- 5-Pyrimidinecarboxylic acid, 1-(2-deoxy-β-D-erythro-pentofuranosyl)-1,2,3,4-tetrahydro-2,4-dioxo-
- 5-Carboxy-2'-deoxyuridine
- 5-Carboxy-2′-deoxyuridine
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Found 9 products.
Trifluridine Related Compound A (5-Carboxy-2'-deoxyuridine)
CAS:Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoiFormula:C10H12N2O7Color and Shape:White Off-White PowderMolecular weight:272.064455-Pyrimidinecarboxylic acid, 1-(2-deoxy-β-D-erythro-pentofuranosyl)-1,2,3,4-tetrahydro-2,4-dioxo-
CAS:Formula:C10H12N2O7Purity:95%Color and Shape:SolidMolecular weight:272.2115Trifluridine Related Compound A
CAS:Formula:C10H12N2O7Color and Shape:Pale Yellow SolidMolecular weight:272.215-Carboxy-2'-deoxyuridine
CAS:<p>5-Carboxy-2'-deoxyuridine is a nucleoside analogue that inhibits herpes simplex virus type 1 (HSV-1) and 2 (HSV-2) replication. It is used to treat genital herpes infections caused by HSV-1 or HSV-2. 5-Carboxy-2'-deoxyuridine has been shown to inhibit the growth of human cancer cells in culture, and is currently being investigated as a potential anticancer drug. This drug binds with high affinity to the viral DNA polymerase, forming a covalent bond with the uracil base in the viral DNA chain. This prevents further elongation of the chain, inhibiting viral replication. 5-Carboxy-2'-deoxyuridine also inhibits cellular protein synthesis and cell division, which may be due to its ability to bind with aldehyde groups on surfactant proteins.END></p>Formula:C10H12N2O7Purity:Min. 95%Color and Shape:PowderMolecular weight:272.21 g/mol5-Carboxy-2'-deoxyuridine
CAS:Controlled Product<p>Applications 5-Carboxy-2'-deoxyuridine, is a derivative of Trifluridine, an anti-herpesvirus antiviral drug, used primarily on the eye.<br>References Kuster, P., et al.: CLAO J. 24(2), 122 (1998); O’Brien, W., Invest. Opthalmol. Vis. Sci., 32 (9), 2455 (1991);<br></p>Formula:C10H12N2O7Color and Shape:NeatMolecular weight:272.21









