Utilization of 6-methylamino-9-(3′-deoxy-β-D-ribofuranosyl) purine by KB cells was written by Shigeura, Harold T.; Sampson, Susan D.. And the article was included in Biochimica et Biophysica Acta, Nucleic Acids and Protein Synthesis in 1967.HPLC of Formula: 13146-72-0 The following contents are mentioned in the article:
The metabolism of 6-methylamino-9-(3′-deoxy-β-D-ribofuranosyl) purine by KB cells was investigated. The nucleoside was not directly cleaved to the methylated base but instead was slowly demethylated to 3′-deoxyadenosine which metabolized further via 2 sep. pathways: (1) it was converted to 3′-deoxyadenosine 5′-triphosphate and incorporated into RNA, and (2) alternatively, it was catabolized to 3′-deoxyinosine and to hypoxanthine. 16 references. This study involved multiple reactions and reactants, such as 9-((2R,3R,5S)-3-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-9H-purin-6-ol (cas: 13146-72-0HPLC of Formula: 13146-72-0).
9-((2R,3R,5S)-3-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-9H-purin-6-ol (cas: 13146-72-0) belongs to tetrahydrofuran derivatives. Tetrahydrofuran (THF), or oxolane, is mainly used as a precursor to polymers. Being polar and having a wide liquid range, THF is a versatile solvent. It is more basic than diethyl ether and forms stronger complexes with Li+, Mg2+, and boranes. It is a popular solvent for hydroboration reactions and for organometallic compounds such as organolithium and Grignard reagents.HPLC of Formula: 13146-72-0
13146-72-0;9-((2R,3R,5S)-3-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-9H-purin-6-ol;The future of 13146-72-0;New trend of C10H12N4O4 ;function of 13146-72-0