| Literature DB >> 33729773 |
G Stuart Cockerill1, Richard M Angell2, Alexandre Bedernjak1, Irina Chuckowree2, Ian Fraser1, Jose Gascon-Simorte2, Morgan S A Gilman3, James A D Good1, Rachel Harland1, Sara M Johnson4, John H Ludes-Meyers3, Edward Littler1, James Lumley1, Graham Lunn2, Neil Mathews1, Jason S McLellan3, Michael Paradowski5, Mark E Peeples4, Claire Scott1, Dereck Tait1, Geraldine Taylor6, Michelle Thom6, Elaine Thomas1, Carol Villalonga Barber2, Simon E Ward5, Daniel Watterson7, Gareth Williams2, Paul Young7, Kenneth Powell1.
Abstract
RV521 is an orally bioavailable inhibitor of respiratory syncytial virus (RSV) fusion that was identified after a lead optimization process based upon hits that originated from a physical property directed hit profiling exercise at Reviral. This exercise encompassed collaborations with a number of contract organizations with collaborative medicinal chemistry and virology during the optimization phase in addition to those utilized as the compound proceeded through preclinical and clinical evaluation. RV521 exhibited a mean IC50 of 1.2 nM against a panel of RSV A and B laboratory strains and clinical isolates with antiviral efficacy in the Balb/C mouse model of RSV infection. Oral bioavailability in preclinical species ranged from 42 to >100% with evidence of highly efficient penetration into lung tissue. In healthy adult human volunteers experimentally infected with RSV, a potent antiviral effect was observed with a significant reduction in viral load and symptoms compared to placebo.Entities:
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Year: 2021 PMID: 33729773 DOI: 10.1021/acs.jmedchem.0c01882
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446