Adrian S. Ray, Gilead Sciences Inc., Foster City, CA, USA (Fig. 7). Adrian started his lecture with photos of William (Bill) Prusoff and reminisced of his days with Bill, Raymond Schinazi and Yung-Chi (Tommy) Cheng. Adrian presented examples to illustrate two models of how a prodrug strategy

can transform a potential drug into a much improved clinical candidate. In the first, the prodrug alters the distribution of the pharmacologically active nucleotide analog to tissues where viral infection is taking place (on-target) and away from tissues resulting in adverse events (off-target). In the second, the prodrug enables one to select a drug candidate based more directly on the intrinsic properties this website of the active nucleotide-triphosphate analog via by-passing an inefficient activation (phosphorylation) of the corresponding nucleoside analog. Sofosbuvir (Sovaldi®),

a prodrug of 2′-F-2′-C-MeUMP, was approved in the USA on 6th December, 2013 for treatment of patients with hepatitis C. This is a fine example of a prodrug enhancing the activity of the parent compound. The nucleoside analogue, 2′-F-2′-C-MeU, is poorly active due to restricted phosphorylation to the monophosphate. Sofosbuvir, a nucleotide analogue prodrug of 2′-F-2′-C-MeU, delivers the monophosphate into the cell and this is then further phosphorylated efficiently selleck inhibitor to give high levels of the triphosphate which inhibits HCV RNA polymerase. Adrian recalled being much impressed by a result reported at the meeting in 2007 of the American Association for the Study of Liver Diseases (AASLD). In a Phase II monotherapy trial in patients with HCV, at day 3, the viral loads were reduced by log103.2 and log101.1 for VX-950 (1250 mg bid, n=10) and RG-7128 (1500 mg bid, n=8), respectively. However, from day 4 to 13, the polymerase inhibitor (RG-7128) had continued to reduce the viral load,

reaching a reduction of log102.7. On the other hand, the protease inhibitor (VX-950) did not give a sustained reduction, with the viral load starting to increase from day 6. At day 13, the viral load was only log102.2 less than baseline. Nucleotide analogues have two advantages over other classes of inhibitors. There is a high genetic barrier to resistance selection, due to the HCV RNA polymerase being FER highly specific for its natural substrates and template. This specificity can be altered but only under extreme evolutionary pressure (see Section 3). Also, nucleotide analogs often have pan-genotype activity because the active site of the HCV NS5B polymerase is so highly conserved. As an example of how prodrugs can impact a discovery program, allowing for more targeted delivery and for the optimization of the intrinsic properties of the triphosphate, Adrian presented the history of the GS-6620 program. The C-adenine analogue (2′-C-Me-4-aza-7,9-dideazaA, C-Nuc1) was compared to the corresponding N-nucleoside, MK608.