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- W2977558082 endingPage "126720" @default.
- W2977558082 startingPage "126720" @default.
- W2977558082 abstract "Currently, it is in urgent need to develop novel selective PDE4 inhibitors with novel structural scaffolds to overcome the adverse effects and improve the efficacy. Novel 1-phenyl-3,4-dihydroisoquinoline amide derivatives were developed as potential PDE4 inhibitors based on the structure-based drug design and fragment identification strategy. A SARs analysis was performed in substituents attached in the C-3 side chain phenyl ring, indicating that the attachment of methoxy group or halogen atom substitution at the ortho-position of the phenyl ring was helpful to enhance both inhibitory activity toward PDE4B and selectivity. Compound 15 with excellent selectivity, exhibited the most potent inhibition in vitro and in vivo, which is a promising lead for development of a new class of selective PDE4 inhibitors." @default.
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- W2977558082 date "2019-11-01" @default.
- W2977558082 modified "2023-10-18" @default.
- W2977558082 title "Discovery of novel inhibitors of phosphodiesterase 4 with 1-phenyl-3,4-dihydroisoquinoline scaffold: Structure-based drug design and fragment identification" @default.
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- W2977558082 doi "https://doi.org/10.1016/j.bmcl.2019.126720" @default.
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