Novel alkenyl substituted aryl bicyclic furano pyrimidines have been prepared and evaluated in vitro against Varicella Zoster Virus (VZV). The para-substituted analogues retain the nanomolar potency we have reported for p-alkyl analogues, while the ortho- and meta-alkenyl systems lose 3–4 orders of potency
Bicyclic pyrimidine nucleoside analogues (BCNAs) represent highly potent and selective inhibitors of...
Background: Recently, the synthesis and antiviral activity of a series of 2′-fluoro derivatives of t...
Bicyclic furano pyrimidines have been previously reported by us to be highly potent and selective ...
In addition to our recent report on the potent anti-varicella-zoster virus (VZV) activity of some un...
Bicyclic furano pyrimidine nucleosides have been found to be highly potent and selective inhibitors ...
We have recently reported the discovery of an entirely new category of potent antivaricella-zoster v...
We herein report the discovery of an entirely new category of potent antiviral agents based on nove...
We have previously reported bicyclic furanopyrimidines as potent and selective inhibitors of varicel...
Several novel bicyclic furanopyrimidine deoxy nucleosides have been designed, prepared and evaluated...
We have discovered bicyclic alkyl furano pyrimidines as a new family of selective inhibitors of vari...
BACKGROUND: Recently, the synthesis and antiviral activity of a series of 2'-fluoro derivatives of t...
Abstract(E)-5-(2-bromovinyl)-2′-deoxyuridine (BVDU) is a potent inhibitor of herpes simplex virus ty...
Bicyclic pyrimidine nucleoside analogues (BCNAs) represent highly potent and selective inhibitors of...
Background: Recently, the synthesis and antiviral activity of a series of 2′-fluoro derivatives of t...
Bicyclic furano pyrimidines have been previously reported by us to be highly potent and selective ...
In addition to our recent report on the potent anti-varicella-zoster virus (VZV) activity of some un...
Bicyclic furano pyrimidine nucleosides have been found to be highly potent and selective inhibitors ...
We have recently reported the discovery of an entirely new category of potent antivaricella-zoster v...
We herein report the discovery of an entirely new category of potent antiviral agents based on nove...
We have previously reported bicyclic furanopyrimidines as potent and selective inhibitors of varicel...
Several novel bicyclic furanopyrimidine deoxy nucleosides have been designed, prepared and evaluated...
We have discovered bicyclic alkyl furano pyrimidines as a new family of selective inhibitors of vari...
BACKGROUND: Recently, the synthesis and antiviral activity of a series of 2'-fluoro derivatives of t...
Abstract(E)-5-(2-bromovinyl)-2′-deoxyuridine (BVDU) is a potent inhibitor of herpes simplex virus ty...
Bicyclic pyrimidine nucleoside analogues (BCNAs) represent highly potent and selective inhibitors of...
Background: Recently, the synthesis and antiviral activity of a series of 2′-fluoro derivatives of t...
Bicyclic furano pyrimidines have been previously reported by us to be highly potent and selective ...