Inhibition of microorganisms by pyrimidine nucleosides was written by Mehta, Bipin M.; Hutchison, Dorris J.. And the article was included in Annals of the New York Academy of Sciences in 1975.Electric Literature of C9H12FN3O4 The following contents are mentioned in the article:
A microorganism, Streptococcus faecium variety durans, was sensitive to 1-β-D-arabinofuranosylcytosine (I) [147-94-4] but not methotrexate [59-05-2], 6-mercaptopurine [50-44-2], or 6-thioguanine [154-42-7], and thus is useful in determining I in the presence of these and other pyrimidine nucleosides. The inhibition of this microorganism by 22 pyrimidine nucleosides is given. This study involved multiple reactions and reactants, such as 4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one (cas: 56632-83-8Electric Literature of C9H12FN3O4).
4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one (cas: 56632-83-8) belongs to pyrimidine derivatives. Pyrimidine also found in many synthetic compounds such as barbiturates and the HIV drug, zidovudine. Pyrimidine derivatives also play an important role in drug development, either in concert with other compounds or on their own.Electric Literature of C9H12FN3O4
56632-83-8;4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one;The future of 56632-83-8;New trend of C9H12FN3O4;function of 56632-83-8