Journal of Medicinal Chemistry p. 484 - 486 (1988)
Update date:2022-08-05
Topics:
Lin, Tai-Shun
Zhang, Xiao-Hui
Wang, Zi-Hou
Prusoff, W.H.
Carbocyclic analogues of 2'-azido- and 2'-amino-2'-deoxycytidine, compounds 8 and 9, were synthesized by an eight-step synthesis from (+/-)-(1α,2α,3β,5β)-3-amino-5-(hydroxymethyl)-1,2-cyclopentanediol (1), which was prepared from cyclopentadiene via an eight-step route.These compounds were tested in vitro against herpes simplex virus type 1 (HSV-1).The 2'-amino analogue was found to show moderate antiviral activity, with an ED50 of 50 μM.However, the 2'-azido analogue was not active at a concentration up to 400 μM.
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