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A lead compound would then be profiled against receptor panels to look for selectivity.
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Before the introduction of high-throughput screening (HTS) and combinatorial screening libraries, most screening for new CNS drugs was performed using biochemical methods, followed quickly by descriptive animal studies that could indicate whether or not a compound penetrated the BBB. A lead compound would then be profiled against receptor panels to look for selectivity. For instance, a synthetic derivative ABT-594, a very potent nonopiate analgesic, derived from the Central American tree frog compound epibatidine,5was profiled against more than 70 receptors and ion channels before clinical investigation.
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A lead compound would then be profiled against receptor panels to look for selectivity
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