Discovery of inhibitors of BK polyomavirus
Discovery of inhibitors of BK polyomavirus
批准号:
9308839
负责人:
Glen Andrew Coburn
金额:
$34.35万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-07-02 至 2018-06-30
关键词:
AdultAllograftingAlpha CellAntiviral AgentsAutomobile DrivingBK VirusBiological AssayCell LineCollaborationsCystitisDevelopmentDoseDrug KineticsEvaluationFailureFeasibility StudiesFundingGenomeGoalsGrowthHemorrhageImmuneImmune systemImmunocompetentImmunosuppressionImmunosuppressive AgentsIndividualInfectionInflammationKidneyKidney DiseasesKidney TransplantationKineticsLeadLibrariesLuciferasesLytic PhaseMichiganOralPatientsPharmaceutical ChemistryPharmaceutical PreparationsPhasePolyomavirusPolyomavirus InfectionsPopulationPropertyRefractoryReporterReporter GenesRiskSeriesSmall Business Innovation Research GrantStenosisStructure-Activity RelationshipT-LymphocyteTechnologyTestingTherapeutic immunosuppressionTimeTransplant RecipientsTransplantationUniversitiesUrineVaccinesViremiaVirusVirus ReplicationVirus Sheddingcandidate selectioncell mediated immune responsecounterscreencytotoxiccytotoxicityhigh riskhigh throughput screeningimmune functionimmunosuppressedimprovedindexinginhibitor/antagonistinnovationkidney epithelial celllatent infectionlead seriesnovelnovel therapeuticspreventprogramsreconstitutionresponserestorationscreeningsmall molecule librariessuccessurinary
中文摘要
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英文摘要
PROJECT SUMMARY
Novel inhibitors of BK polyomavirus (BKPyV) are urgently needed to prevent the occurrence of virus-induced
nephropathy, allograft failure and hemorrhagic cystitis following transplantation. The objective of this Phase I SBIR
feasibility study is to identify drug-like compounds that specifically inhibit BKPyV replication. During the course of this
Phase I funding period, we will execute a hit finding campaign with a library of 100,000 compounds with optimal drug-like
properties. Quality hits that emerge from the assay will be subjected to follow-on testing that will investigate the potency,
selectivity, and mechanism of action. The most interesting of these compounds will be subjected to medicinal chemistry
driven hit-to-lead efforts to explore structure-activity relationships (SAR). The overall goal of this project is to discover one
or more novel lead series, which is defined as a chemotype inhibitor that demonstrates tractable SAR, potent antiviral
activity against the available BKPyV strains and minimal cytotoxicity. Success in these endeavors will trigger the
submission of a Phase II application that will advance the program from Early Lead Optimization through to Candidate
Selection.
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海外基金