Discovery of AVI-6451, a Potent and Selective Inhibitor of the SARS-CoV-2 ADP-Ribosylhydrolase Mac1 with Oral Efficacy In Vivo

The COVID-19 pandemic emphasized the need for effective antivirals acting at new targets. We recently described AVI-4206, a 9<i>H</i>-pyrimido[4,5-<i>b</i>]indole-based inhibitor of the SARS-CoV-2 macrodomain Mac1, an ADP-ribosylhydrolase thought to blunt the host immune response to viral infection. While AVI-4206 represents the first Mac1 inhibitor to demonstrate in vivo efficacy in mouse infection models, its low oral bioavailability necessitated IP administration. Herein, we describe an extensive medicinal chemistry campaign to identify new leads with improved cellular permeability and high oral bioavailability. Various tactics were employed toward these ends, including an exploration of urea isosteres to reduce hydrogen bond donor count and total polar surface area. These efforts ultimately produced AVI-6451, a potent Mac1 inhibitor with low intrinsic clearance and high oral bioavailability that achieves superior antiviral efficacy with once-daily oral administration in a mouse model of SARS-CoV-2 infection.

Authors

Institutions

Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-12-17
DOI
https://doi.org/10.1021/acs.jmedchem.5c02933
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Discovery of AVI-6451, a Potent and Selective Inhibitor of the SARS-CoV-2 ADP-Ribosylhydrolase Mac1 with Oral Efficacy In Vivo

Brian K. Shoichet, Morgan E. Diolaiti, Nevan J. Krogan, Mauricio Montaño et al.
Journal of Medicinal Chemistry
PARP inhibition in cancer therapy
article

Discovery of AVI-6451, a Potent and Selective Inhibitor of the SARS-CoV-2 ADP-Ribosylhydrolase Mac1 with Oral Efficacy In Vivo

Brian K. Shoichet, Morgan E. Diolaiti, Nevan J. Krogan, Mauricio Montaño, Taha Y. Taha, G.J. Correy, Adam R. Renslo, James S. Fraser, Takaya Togo, Alan Ashworth, Yusuke Matsui, Moira M. Rachman, Eric R. Hantz, Jonathan Pampel, Jeffrey Zheng, Julia Rosecrans, Melanie Ott, Priyadarshini Jaishankar, Maisie GV Stevens
article en

Abstract

The COVID-19 pandemic emphasized the need for effective antivirals acting at new targets. We recently described AVI-4206, a 9<i>H</i>-pyrimido[4,5-<i>b</i>]indole-based inhibitor of the SARS-CoV-2 macrodomain Mac1, an ADP-ribosylhydrolase thought to blunt the host immune response to viral infection. While AVI-4206 represents the first Mac1 inhibitor to demonstrate in vivo efficacy in mouse infection models, its low oral bioavailability necessitated IP administration. Herein, we describe an extensive medicinal chemistry campaign to identify new leads with improved cellular permeability and high oral bioavailability. Various tactics were employed toward these ends, including an exploration of urea isosteres to reduce hydrogen bond donor count and total polar surface area. These efforts ultimately produced AVI-6451, a potent Mac1 inhibitor with low intrinsic clearance and high oral bioavailability that achieves superior antiviral efficacy with once-daily oral administration in a mouse model of SARS-CoV-2 infection.

Journal of Medicinal ChemistryVol. 69(1)
Gladstone Institutes (US), University of California, San Francisco (US), UCSF Helen Diller Family Comprehensive Cancer Center (US)
Openalex Percentile: Top 44%
PARP inhibition in cancer therapy
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.