Discovery and Synthesis
of a Phosphoramidate Prodrug
of a Pyrrolo[2,1‑f][triazin-4-amino] Adenine C‑Nucleoside (GS-5734) for the Treatment of Ebola
and Emerging Viruses
Version 2 2020-05-07, 20:43Version 2 2020-05-07, 20:43
Version 1 2017-02-14, 19:04Version 1 2017-02-14, 19:04
journal contribution
posted on 2020-05-07, 20:43authored byDustin Siegel, Hon C. Hui, Edward Doerffler, Michael O. Clarke, Kwon Chun, Lijun Zhang, Sean Neville, Ernest Carra, Willard Lew, Bruce Ross, Queenie Wang, Lydia Wolfe, Robert Jordan, Veronica Soloveva, John Knox, Jason Perry, Michel Perron, Kirsten M. Stray, Ona Barauskas, Joy Y. Feng, Yili Xu, Gary Lee, Arnold L. Rheingold, Adrian S. Ray, Roy Bannister, Robert Strickley, Swami Swaminathan, William A. Lee, Sina Bavari, Tomas Cihlar, Michael K. Lo, Travis K. Warren, Richard L. Mackman
The
recent Ebola virus (EBOV) outbreak in West Africa was the largest
recorded in history with over 28,000 cases, resulting in >11,000
deaths
including >500 healthcare workers. A focused screening and lead
optimization
effort identified 4b (GS-5734) with anti-EBOV EC50 = 86 nM in macrophages as the clinical candidate. Structure
activity relationships established that the 1′-CN group and C-linked nucleobase were critical for optimal anti-EBOV
potency and selectivity against host polymerases. A robust diastereoselective
synthesis provided sufficient quantities of 4b to enable
preclinical efficacy in a non-human-primate EBOV challenge model.
Once-daily 10 mg/kg iv treatment on days 3–14 postinfection
had a significant effect on viremia and mortality, resulting in 100%
survival of infected treated animals [Nature 2016, 531, 381−385]. A phase 2 study
(PREVAIL IV) is currently enrolling and will evaluate the effect of 4b on viral shedding from sanctuary sites in EBOV survivors.