Sucres du squelette et nucléobases

Applications 6-​Phenyl-​2-​thiouracil is a reagent used in the synthesis of antifungal agents. References Gullapelli, K. et al.: Int. J. Pharm. Biol. Sci., 4, 59 (2014);

1,3-Dipropyl-7-methylxanthine is a xanthine compound that is structurally related to caffeine. It has been shown to have an inhibitory effect on the production of reactive oxygen species and cytosolic calcium levels in primary cells, as well as a nonselective adenosine receptor antagonist activity. It has also been shown to antagonize the effects of adenosine receptors, p2 receptors, and p2y receptors. This drug is used for the treatment of basophilic leukemia.

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Applications 5-Hydroxymethyluracil (cas# 4433-40-3) is a compound useful in organic synthesis.

3',5'-O-Dipalmitoyl-5-Fluoro-2'-Deoxyuridine is a liposome binding drug that has been shown to inhibit the growth of tumour cells in vitro. It can be used as a monoclonal antibody, monolayer, or fluidity enhancer. 3',5'-O-Dipalmitoyl-5-Fluoro-2'-Deoxyuridine binds to the surface of endothelial cells and prevents the attachment of platelets to the vessel wall. This activity may be due to its anticoagulant properties. 3',5'-O-Dipalmitoyl-5-Fluoro-2'-Deoxyuridine is not active against the major strains of bacteria that cause sepsis, such as methicillin resistant Staphylococcus aureus (MRSA). However, it has shown potential for use as an antibiotic because it inhibits bacterial cell division

Sulfo-Cyanine 3 is an alternative dye primarily used for labeling peptides and oligos in replacing Cy3 that was originally developed by GE Healthcare.

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8-Azahypoxanthine is a hydroxyl analog of hypoxanthine. It contains a nitrogen atom in place of the oxygen atom on the 2-position. 8-Azahypoxanthine has been shown to be an effective inhibitor of purine biosynthesis in yeast cells and can be used as a replacement for xanthine during the synthesis of adenosine triphosphate (ATP) from uracil. 8-Azahypoxanthine was found to have good detection sensitivity, with an estimated detection limit of 0.2 µM. The optimum pH for this compound is 7.8, which is similar to that of wild type strain and tissue culture media. Mutants resistant to 8-azahypoxanthine were generated by exposure to high concentrations (>100 mM) for long periods (>2 days). Mutant strains showed no detectable enzyme activity against orotic acid or glycosidic bond formation with erythromycin

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