CAS 496-76-4
:Acido isobarbiturico
- 1,3-Diazinane-2,4,5-trione
- 2,4,5(3H)-Pyrimidinetrione, dihydro-
- 5-Hydroxyuracil
- 5-hydroxypyrimidine-2,4(1H,3H)-dione
- Dihydro-2,4,5(3H)-pyrimidinetrione
- Isobarbituric acid
- NSC 95958
- dihydropyrimidine-2,4,5(3H)-trione
Isobarbituric Acid
CAS:Formula:C4H4N2O3Purezza:>97.0%(GC)Colore e forma:White to Yellow to Orange powder to crystalPeso molecolare:128.092,4,5-Trihydroxypyrimidine, 98%
CAS:2,4,5-Trihydroxypyrimidine studies show that it can form stable base pairs with all four bases in a DNA duplex. It has been used as oxidative DNA damage biomarker in tissue engineered skin. It acts as an antagonist of uracil in the growth of Lactobacillus casei. This Thermo Scientific Chemicals branFormula:C4H4N2O3Purezza:98%Colore e forma:Powder, White to pale creamPeso molecolare:128.09Fluorouracil Related Compound B (Dihydropyrimidine-2,4,5(3H)-trione)
CAS:Compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure, nesoiFormula:C4H4N2O3Colore e forma:White PowderPeso molecolare:128.02219Ref: 4Z-F-539
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaIsobarbituric Acid
CAS:Impurity Fluorouracil EP Impurity B; Fluorouracil USP Related Compound B
Applications A 5-hydroxy derivative of the nucleobase Uracil (U801000) and an isomer of Barbituric Acid (B118650). Studies show that it can form stable base pairs with all four bases in a DNA duplex. It has been used as oxidative DNA damage biomarker in tissue engineered skin. Fluorouracil EP Impurity B. Fluorouracil USP Related Compound B
References Varatharasa T. et al.: Chem. Comm., 3, 400 (2005); Jaruga, P. et al.: Nucleic Acid Res., 24, 1389 (1996); Rodriguez, H. et al.: Adv. Exp. Med. Biol., 534, 129 (2003);Formula:C4H4N2O3Colore e forma:NeatPeso molecolare:128.09Isobarbituric acid
CAS:Isobarbituric acid is a glycosylase that cleaves the bond between the amino group and the hydroxyl group of uridine in DNA. It has been shown to react with nucleophilic groups at neutral pH, such as an amine or hydroxyl group. Isobarbituric acid can be used to measure oxidative damage to DNA. This compound is reactive and sensitive to UV light, which makes it useful for detecting damaged DNA. Isobarbituric acid has been shown to induce neuronal death in rodents by interfering with dendritic spine formation.
Formula:C4H4N2O3Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:128.09 g/molRef: ST-EA-CP-F32002
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