Although the advantages of sp -rich, sterically complicated molecules in drug development have been pointed out, modern screening libraries are filled with planar, sp -rich components. Compounds that are sp -rich are difficult to synthesize, and thus we aimed to invent an efficient method to construct sp -rich libraries. By modifying sp -rich 7-azanorbornane scaffolds through click chemistry, we efficiently prepared a small set of compounds. These compounds were not only sp -rich, but also had sufficient "lead-like" properties in view of molecular weights and hydrophobicity. Screening assays of this library provided weak κ opioid receptor agonists and growth hormone secretagogue receptor agonists with high hit rates. These results indicate that the 7-azanorbornane scaffold may be a "privileged structure" for lead identification in drug discovery.
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http://dx.doi.org/10.1002/cmdc.201900398 | DOI Listing |
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