Medicinal Chemistry Optimization of Anti-Alphaviral Leads and Elucidation of Target and Off Target Engagement
Medicinal Chemistry Optimization of Anti-Alphaviral Leads and Elucidation of Target and Off Target Engagement
批准号:
10116265
负责人:
Jennifer E. Golden
金额:
$186.58万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-03-06 至 2024-02-29
关键词:
ADME StudyAddressAlphavirusAlphavirus InfectionsAmericasAmidinesAntiviral AgentsBindingCell Culture TechniquesCellsCellular AssayCertificationCharacteristicsChemicalsCollaborationsDNA-Directed RNA PolymeraseDevelopmentDiseaseDoseDrug KineticsEastern Equine Encephalitis VirusEncephalitisEquus caballusFormulationGenerationsHumanIn VitroInfectionLeadMetabolicModelingMusNonstructural ProteinOralPharmaceutical ChemistryPharmaceutical PreparationsPlasmaRNA chemical synthesisRNA-Directed RNA PolymeraseRattusResearchResearch Project GrantsRisk AssessmentRouteSafetySeriesStructureSurveysSynthesis ChemistryTherapeuticToxic effectToxicologyVaccinesValidationVenezuelanWestern Equine Encephalitis Virusanalogbasebioweaponcandidate selectionclinical candidatedesignefficacy studyemerging pathogenhealth economicsimprovedin vivolead optimizationmanufacturing processnonhuman primatenovelpreventproduct developmentprogramsprophylacticprototypesafety studyscaffoldscreeningsmall moleculesmall molecule therapeuticstherapeutic candidatevaccine accessviral RNA
中文摘要
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英文摘要
Venezuelan (VEEV), Western (WEEV), and Eastern Equine Encephalitis viruses (WEEV), are
emerging pathogens that cause human encephalitis, yet there are no approved human vaccines
or antiviral agents for treating or preventing any alphaviruses infection. Our research objectives
include the development of a broad spectrum antiviral clinical candidate against these
encephalitic alphavirus infections in humans. The aims of Research Project 1 within the U19
Center of Excellence for Encephalitic Alphavirus Therapeutics (CEEAT) program focus on the
lead optimization activities of two distinct small molecule scaffolds with prophylactic and
therapeutic in vivo efficacy. Specifically, the project will improve lead prototypes through iterative
multi-parameter medicinal chemistry optimization, guided by ADME/PK assessment, cell culture
and mechanistic studies (Research Project 3) and in vivo assessments (Research Project 2) for
exposure, optimum dosing and safety in higher order species (i.e., rats and non-human primates).
The project will manage all synthetic chemistry needs including medicinal chemistry, non-GMP
scaling and validation of analogs, point of compound distribution to CEEAT labs, and
implementation of process manufacturing improvements prior to CRO engagement for API
synthesis to advanced GLP toxicological studies. Additionally, formulation and stability analyses
will be conducted, in collaboration with the UW-Madison Zeeh Formulation Station. Several
activities pertaining to API and formulation generation and characterization will be accompanied
by appropriate certification and analyses in accord with pre-IND requirements, coordinated and
overseen by product development and regulatory consultants within the CEEAT structure.
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会议论文
Accelerated discovery of cell-active SARS-CoV-2 polymerase inhibitors via molecular dynamic guided screening and optimization
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批准号:10238322
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项目类别:
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资助金额:$44.25万
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财政年份:2021
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负责人:Jennifer E. Golden
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依托单位:
Medicinal Chemistry Optimization of Anti-Alphaviral Leads and Elucidation of Target and Off Target Engagement
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批准号:10359714
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项目类别:
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资助金额:$58.36万
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财政年份:2019
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负责人:Jennifer E. Golden
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依托单位:
Medicinal Chemistry Optimization of Anti-Alphaviral Leads and Elucidation of Target and Off Target Engagement
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批准号:10563176
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项目类别:
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资助金额:$197.11万
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财政年份:2019
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负责人:Jennifer E. Golden
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依托单位:
Medicinal Chemistry Optimization of Anti-Alphaviral Leads and Elucidation of Target and Off Target Engagement
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批准号:9886197
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项目类别:
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资助金额:$104.3万
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财政年份:--
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负责人:Jennifer E. Golden
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依托单位:
海外基金