Drug Development Research · 1994 · 27 citations · 20 references
PharmacyChemistryMedicinal ChemistryCombinatorial ChemistryDrug DiscoveryOrganic ChemistryChemical Library DesignCombinatorial SynthesisDiversity-oriented SynthesisHigh-throughput SynthesisChemical Library SynthesisCombinatorial Library SynthesisHigh-throughput Screening LibrariesMedicinal Chemistry ApplicationsOrganic Molecule SynthesisSmall-molecule Library ConstructionSmall-molecule Library DesignSolid-phase Synthesis Automation
Abstract The drug discovery process depends upon the synthesis and testing of thousands of compounds to bring a new drug through discovery, clinical testing, development, and FDA approval. Recent advances in high throughput screening have created the need for the accelerated synthesis of small organic molecules. By combining solid phase chemistry, organic synthesis, and automation with a unique apparatus capable of performing techniques common to organic synthesis, “libraries” of organic compounds (DIVERSOMERS TM ) are efficiently generated. This was demonstrated by the multiple simultaneous synthesis of 40 hydantoins and 40 benzodiazepines, related to Dilantin® and Valium®, respectively. © 1994 Wiley‐Less, Inc.
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