作者: Jeffrey B. Arterburn , Colleen B. Jonsson , William B. Parker
DOI:
关键词: Stereochemistry 、 Alkyl 、 RNA 、 Polymerase 、 DNA 、 Azole 、 Aryl 、 Chemistry 、 DNA polymerase 、 Organic chemistry 、 Prodrug
摘要: Azole nucleosides represented by the formulae (I) and (II); wherein A = C or N B X H; C1-C6 alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclo, halogen such as F, C1, Br I; OH, NH2, NH-(C1-C6 heterocyclo); Z Cl, Br, heterocyclo; E= (CH2)HONHR1; n is an integer from 0-6 more typically 0-3; R1= aryl each of W, Y, R individually selected group consisting O, Oalkyl, Oaryl, provided that at least one other than H both W Y together can be =O; D Fl H;pharmaceutically acceptable salts thereof, prodrugs thereof mixtures are provided. Compounds this disclosure useful inhibitors viral RNA DNA polymerases as, but not limited to, Influenza, Hantaan Virus, Crimean Congo hemorrhagic fever virus, hepatitis B, C, Polio, Coxsackie Rhino, Echo, orthopoxvirus (small pox), HIV, Ebola, West Nile virus polymerases; especially orthopoxvirus, B.