Solution Phase Synthesis of Chemical Libraries for Lead Discovery
By integrating advanced computational design and synthesis, a series of structurally diverse reaction products based on three core scaffolds were prepared by a propietary high throughput synthesis method. Incorporation of auto-mated work stations and sample handling techniques allowed for the produc...
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Veröffentlicht in: | Journal of biomolecular screening 1996-06, Vol.1 (4), p.179-186 |
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container_issue | 4 |
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container_title | Journal of biomolecular screening |
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creator | Garr, Cheryl D. Peterson, John R. Schultz, Lauri Oliver, Amy R. Underiner, Ted L. Cramer, Richard D. Ferguson, Allan M. Lawless, Michael S. Patterson, David E. |
description | By integrating advanced computational design and synthesis, a series of structurally diverse reaction products based on three core scaffolds were prepared by a propietary high throughput synthesis method. Incorporation of auto-mated work stations and sample handling techniques allowed for the production of more than 20,000 compounds in a relatively short time. A method to efficiently obtain quantitative and qualitative analytical data on these compounds was developed. Structural comparison of the individual members of this library with a database of clinical drug candidates revealed a significant degree of similarity based on Tanimoto coefficients. |
doi_str_mv | 10.1177/108705719600100404 |
format | Article |
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source | Alma/SFX Local Collection |
title | Solution Phase Synthesis of Chemical Libraries for Lead Discovery |
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