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ChemMedChem ; 14(21): 1840-1848, 2019 11 06.
Artículo en Inglés | MEDLINE | ID: mdl-31444850

RESUMEN

Although the advantages of sp3 -rich, sterically complicated molecules in drug development have been pointed out, modern screening libraries are filled with planar, sp2 -rich components. Compounds that are sp3 -rich are difficult to synthesize, and thus we aimed to invent an efficient method to construct sp3 -rich libraries. By modifying sp3 -rich 7-azanorbornane scaffolds through click chemistry, we efficiently prepared a small set of compounds. These compounds were not only sp3 -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.


Asunto(s)
Compuestos Aza/química , Norbornanos/química , Bibliotecas de Moléculas Pequeñas/química , Compuestos Aza/farmacología , Células Cultivadas , Células HEK293 , Humanos , Estructura Molecular , Norbornanos/farmacología , Receptores de Ghrelina/agonistas , Bibliotecas de Moléculas Pequeñas/farmacología , Solubilidad , Termodinámica , Agua/química
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