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The Vanderbilt Specialized Chemistry Center for Accelerated Probe Development

The Vanderbilt Specialized Chemistry Center for Accelerated Probe Development
范德比尔特专业化学中心加速探针开发
批准号:
8517185
负责人:
CRAIG LINDSLEY
金额:
$264.46万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-01 至 2015-05-31

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中文摘要
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英文摘要
We are proposing the establishment of a specialized chemistry center, the Vanderbilt Specialized Chemistry Center for Accelerated Probe Development, to expedite the discovery and development of high quality probe compounds which will significantly impact the goals of the MLPCN Research Network. Building on the infrastructure, resources and broad drug discovery (hit-to-lead-to-proof of concept-to-clinic) experience within the Lindsley Technology Enabled Synthesis (TES) Lab and the Conn Lab, we are poised to support probe development projects in collaboration with external Specialty Screening and Comprehensive Centers in the MLPCN Network. Due to our state-of-the-art technology platform for high-throughput medicinal chemistry and our M.S. and Ph.D. level staff chemists, our proposed center will be capable of supporting five (5) probe development projects, with internal or external centers, in parallel (~20 probe development programs/year) and require less than three months to develop probes and advanced molecular tools for in vitro and/or in vivo proof of concept experiments. The proposed Vanderbilt Specialized Chemistry Center for Accelerated Probe Development is unique from other centers in that the PI has eight years hit-to-lead-to-proof of concept experience in the pharmaceutical industry and has built a fully equipped high-throughput synthesis and purification lab, at the industry standard, within Vanderbilt which allows minimal human resources to develop probe compounds with expedited timelines. Our initial goal will be to deliver probe compounds that meet or exceed MPLCN guidelines and/or meet specific requirements for a probe of the investigator that initiated the screen. When aligned with NIH/NIMH and MLPCN goals, we will use a portion of our MLPCN and internal resources in the Lindsley and Conn Labs (synthesis/medicinal chemistry, pharmacology, DMPK and adiochemistry) in Center-Driven Research Projects to further refine and develop probes for therapeutically relevant targets to ensure in vivo proof of concept experiments can be performed to provide 'quick kills' or validate targets as potential therapeutic agents for unmet medical needs. Finally, we will offer training sabbaticals to other chemists within the MLPCN to learn parallel synthesis techniques and library design strategies.
期刊论文(53)
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会议论文
DOI: 10.1016/j.tetlet.2015.01.140
发表时间: 2015-03-04
期刊: Tetrahedron letters
影响因子: 1.8
作者: [Senter TJ, O'Reilly MC, Chong KM, Sulikowski GA, Lindsley CW]
通讯作者: Lindsley CW
Discovery of potent and selective GIRK1/2 modulators via 'molecular switches' within a series of 1-(3-cyclopropyl-1-phenyl-1H-pyrazol-5-yl)ureas.
通过一系列 1-(3-环丙基-1-苯基-1H-吡唑-5-基)脲中的“分子开关”发现有效且选择性的 GIRK1/2 调节剂。
DOI: 10.1016/j.bmcl.2014.08.061
发表时间: 2014
期刊: Bioorganic & medicinal chemistry letters
影响因子: 2.7
作者: [Wen,Wandong, Wu,Wenjun, Weaver,CDavid, Lindsley,CraigW]
通讯作者: Lindsley,CraigW
Roles of the M1 muscarinic acetylcholine receptor subtype in the regulation of basal ganglia function and implications for the treatment of Parkinson's disease.
M1 毒蕈碱乙酰胆碱受体亚型在基底神经节功能调节中的作用及其对帕金森病治疗的影响。
DOI: 10.1124/jpet.111.187856
发表时间: 2012
期刊: The Journal of pharmacology and experimental therapeutics
影响因子: --
作者: [Xiang,Zixiu, Thompson,AnalisaD, Jones,CarrieK, Lindsley,CraigW, Conn,PJeffrey]
通讯作者: Conn,PJeffrey
Total synthesis of stemaphylline N-oxide and related C9a-epimeric analogues.
茎茶碱 N-氧化物和相关 C9a-差向异构类似物的全合成。
DOI: 10.1002/chem.201302669
发表时间: 2013
期刊: Chemistry (Weinheim an der Bergstrasse, Germany)
影响因子: --
作者: [Schulte,MichaelL, Turlington,MarkL, Phatak,SharangdharS, Harp,JoelM, Stauffer,ShaunR, Lindsley,CraigW]
通讯作者: Lindsley,CraigW
27
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