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L30 is a novel small molecule phosphodiesterase 4 (PDE4) inhibitor. It was developed through structure-based optimization of the natural product moracin M, demonstrating significantly improved potency with an IC50 of 8.6 nM and remarkable selectivity (over 201-fold) against other PDE families. L30 effectively inhibits the release of inflammatory cytokines and chemokines in Raw264.7 and HaCaT cell lines. It has shown significant therapeutic effects in an imiquimod-induced psoriasis mouse model, indicating its potential as a treatment for psoriasis.
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