6-[(E)-4-Hydroxy-3-methylbut-2-enylamino]-9-ß-D-ribofuranosylpurine D5

6-[(E)-4-Hydroxy-3-methylbut-2-enylamino]-9-ß-D-ribofuranosylpurine D5 is a purine nucleoside analog that is used as an analytical standard in biochemical research. It is a deuterated form of the non-natural nucleoside analogue 6-[(E)-4-Hydroxy-3-methylbut-2-enylamino]-9-ß-D-ribofuranosylpurine, which has demonstrated antiviral, anticancer, and antiparasitic activity in various studies. The chemical formula of 6-[(E)-4-Hydroxy-3-methylbut-2-enylamino]-9-ß-D-ribofuranosylpurine D5 is C13H9D5N5O4, and its molecular weight is 313.3 g/mol. The compound is soluble in water and methanol, and it has a melting point range of 215-220°C. In terms of its mechanism of action, 6-[(E)-4-Hydroxy-3-methylbut-2-enylamino]-9-ß-D-ribofuranosylpurine D5 is believed to inhibit the activity of enzymes involved in nucleic acid synthesis, leading to the disruption of cellular replication and proliferation. This makes it a valuable tool in the study of DNA and RNA metabolism, as well as in the development of new drugs targeting these processes. Overall, 6-[(E)-4-Hydroxy-3-methylbut-2-enylamino]-9-ß-D-ribofuranosylpurine D5 is a versatile compound that has numerous applications in biochemical research. Its deuterated form offers unique advantages in terms of isotopic labeling and mass spectrometry analysis, making it an important tool for understanding the molecular mechanisms underlying cellular processes and disease pathology.