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LabAutomation 2006 - SLAS

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Where Laboratory Technologies Emerge and Merge<br />

11:00 am Monday, January 23, <strong>2006</strong> Track 3: High-Throughput Technologies Room: Learning Center<br />

Wyndham Palm Springs Hotel<br />

Stefan Werner<br />

University of Pittsburgh<br />

Pittsburgh, Pennsylvania<br />

stw15@pitt.edu<br />

From Chemical Methodologies to Library Development: Design, Synthesis and<br />

Biological Evaluation of Small Molecule Libraries in the UPCMLD<br />

The University of Pittsburgh Center for Chemical Methodologies and Library Development (UPCMLD) applies methodologies that were<br />

developed in our Department to library synthesis. Library compounds are screened in biological assays and all results are made accessible<br />

to the scientific community.<br />

This talk will focus on examples from several mid-size solution phase small molecule libraries. E-alkene and cyclopropyl dipeptide isosteres<br />

will be discussed as well as the synthesis of novel heterocycles via transition metal catalyzed carbon-carbon bond forming reactions.<br />

Skeletal diversity is introduced by the choice of the metal catalyst or by the order of reagents. Microwave assisted organic synthesis, polymer<br />

bound reagents, scavenging techniques and SPE play an important role in the automated synthesis of the presented compound libraries.<br />

11:30 am Monday, January 23, <strong>2006</strong> Track 3: High-Throughput Technologies Room: Learning Center<br />

Wyndham Palm Springs Hotel<br />

Jeffrey Noonan<br />

Neurogen Corporation<br />

Branford, Connecticutt<br />

jnoonan@nrgn.com<br />

Advancing Drug Discovery Through Integrated Parallel Solution Phase Library Synthesis<br />

Automated library synthesis has become an essential component in modern drug discovery efforts supporting a spectrum of activities<br />

from file enrichment through lead optimization. Common to each pursuit is the aspiration to advance the pace of drug discovery by offering<br />

an unprecedented combination of synthesis speed, value, and quantity. To meet these challenges, the Neurogen High Speed Synthesis<br />

(HSS) group strategy focuses on the continuing creation and characterization of chemical libraries using parallel solution phase techniques.<br />

Central to our effort is a collection of novel workstations that are tightly integrated into our informatics architecture supporting the efficient<br />

movement of library samples and data. Ultimately, our pragmatic approach facilitates synthesis throughput and the utilization of equipment,<br />

creating a cost effective library production environment.<br />

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