C-N Bond-Forming Methodologies for the Synthesis of Small Molecules and Peptides
C-N Bond-Forming Methodologies for the Synthesis of Small Molecules and Peptides
批准号:
8242048
负责人:
Jennifer Lynn Stockdill
金额:
$3.0万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-04-01 至 2012-07-31
关键词:
Acetylcholinesterase InhibitorsAlder plantAlkaloidsAmidesAmino AcidsArchitectureBiological FactorsBiological ProcessBiomedical ResearchCell physiologyChemistryCyclizationDevelopmentDiels Alder reactionDiseaseElectronicsFamilyFosteringGlycoproteinsGoalsHIVImprove AccessKB CellsLeadLigationLiteratureMedicalMentorsMethodologyMethodsMissionMulti-Drug ResistanceNitrogenOutcomePeptidesPharmacologic SubstancePhasePositioning AttributePrevalencePropertyPublic HealthReactionResearchResistanceRoleSchemeStructureSystemTestingTherapeuticVincristinealkyl groupbasecycloadditiondesigndieneepimerizationexperiencehuman diseaseimprovednovelnovel strategiespreventprogramspublic health relevanceskillssmall moleculetertiary aminethioester
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The focus of the proposed research is the development of efficient methods for the construction of C-N bonds in the context of biologically active natural products and peptidic structures such as glycoproteins. There is significant demand for efficient syntheses of heterocyclic and peptidic structures because of their prevalence as pharmaceutical lead targets. The mentored K99 phase research will focus on the development of a methodology to access angularly-substituted decahydroquinolines. This method will enable rapid access to the recently isolated acetylcholinesterase inhibitor lycojapodine A. The independent R00 phase research will be centered on the use of nitrogen-centered radicals for new reaction methods. First, efforts will be directed toward a method for the formation of polycyclic structures containing a tertiary amine at a ring junction. This method will be utilized in the synthesis of the leuconicine family of alkaloids, which reverse vincristine resistance in KB cells. Additionally, a novel approach to the long-standing challenge of peptide ligation will be pursued. Together, the proposed methods will enable more efficient access to challenging architectures that are prevalent in natural products and will streamline the synthesis of homogeneous glycoproteins. Thus, the proposed research will improve access to important lead targets for the treatment of illnesses and to homogeneous versions of glycoproteins, which will enable studies of their function in cellular processes and diseases.
PUBLIC HEALTH RELEVANCE: Stockdill, Jennifer L. The proposed research is relevant to public health because it will enable rapid access to fused and bridged polycyclic tertiary amine products, thereby expediting the synthesis of bioactive small molecules. Furthermore, it will allow for an epimerization-free peptide ligation, substantially simplifying the synthetic approach toward homogeneous glycoproteins. These projects are supported by the NIH's mission to foster fundamental creative discoveries directed toward improving the Nation's ability to cure human diseases.
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Strategies for N to C solid-phase peptide synthesis
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批准号:10405530
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项目类别:
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资助金额:$21.44万
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财政年份:2019
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负责人:Jennifer Lynn Stockdill
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依托单位:
Strategies for N to C solid-phase peptide synthesis
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批准号:10183269
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项目类别:
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资助金额:$30.05万
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财政年份:2019
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依托单位:
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批准号:8534978
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项目类别:
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资助金额:$24.9万
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项目类别:
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资助金额:$9.0万
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批准号:8545182
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项目类别:
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项目类别:
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依托单位: