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pubmed-article:17335190pubmed:abstractTextA series of novel, potent orthopoxvirus egress inhibitors was identified during high-throughput screening of the ViroPharma small molecule collection. Using structure--activity relationship information inferred from early hits, several compounds were synthesized, and compound 14 was identified as a potent, orally bioavailable first-in-class inhibitor of orthopoxvirus egress from infected cells. Compound 14 has shown comparable efficaciousness in three murine orthopoxvirus models and has entered Phase I clinical trials.lld:pubmed
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pubmed-article:17335190pubmed:articleTitleN-(3,3a,4,4a,5,5a,6,6a-Octahydro-1,3-dioxo-4,6- ethenocycloprop[f]isoindol-2-(1H)-yl)carboxamides: Identification of novel orthopoxvirus egress inhibitors.lld:pubmed
pubmed-article:17335190pubmed:affiliationViroPharma Incorporated, 397 Eagleview Boulevard, Exton, Pennsylvania 19341, USA. tbailey@cephalon.comlld:pubmed
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