McGuigan, Christopher  ORCID: https://orcid.org/0000-0001-8409-710X, Perrone, P., Luoni, G., Kelleher, M. R., Daverio, F., Angell, A., Mulready, S., Congiatu, C., Rajyaguru, S., Martin, J., Leveque, V., Le Pogam, S., Najera, I., Klumpp, K. and Smith, D.
2007.
Sub micromolar inhibitors of HCV generated from inactive nucleosides by application of ProTide technology [Abstract].
Antiviral Research
74
(3)
, A36-A37.
10.1016/j.antiviral.2007.01.032
|
Abstract
We report the application of our phosphoramidate ProTide technology to various 4′-substituted ribonucleoside analogues, designed as potential inhibitors of hepatitis C virus (HCV) (Fig. 1). Thus, ProTides were prepared from 4′-azidouridine (AZU), -cytidine (AZC), -adenosine (AZA) and -5-methyluridine (AZMeU), besides other 4′-substituted uridines and cytidines. In each case, ProTide families included variations in the aryl, ester, and amino acid regions. A number of compounds showed potent inhibitory properties in cell culture without detectable cytotoxicity. These results confirm that phosphoramidate ProTides can deliver monophosphates of ribonucleoside analogues and suggest a potential path to the generation of novel antiviral agents against HCV infection. Of particular note was the sub-μM potency displayed by certain ProTides of AZU; a nucleoside analogue, which was itself inactive in the assay. In some cases, we were able to separate, and separately evaluate the phosphate stereoisomers generated in the synthesis; in a few cases the absolute phosphate stereochemistry was solved (Fig. 2). The generic message is that ProTide synthesis from inactive parent nucleosides may be a warranted drug discovery strategy.
| Item Type: | Article |
|---|---|
| Date Type: | Publication |
| Status: | Published |
| Schools: | Schools > Pharmacy Research Institutes & Centres > Systems Immunity Research Institute (SIURI) |
| Additional Information: | Abstract no. 24 |
| Publisher: | Elsevier |
| ISSN: | 0166-3542 |
| Last Modified: | 17 Oct 2022 10:03 |
| URI: | https://orca.cardiff.ac.uk/id/eprint/6644 |
Actions (repository staff only)
 |
Edit Item |
Altmetric
Altmetric