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J Med Chem ; 52(6): 1522-4, 2009 Mar 26.
Article in English | MEDLINE | ID: mdl-19256507

ABSTRACT

In this communication, we report the discovery of 1S (apremilast), a novel potent and orally active phosphodiesterase 4 (PDE4) and tumor necrosis factor-alpha inhibitor. The optimization of previously reported 3-(1,3-dioxo-1,3-dihydroisoindol-2-yl)-3-(3,4-dimethoxyphenyl)propionic acid PDE4 inhibitors led to this series of sulfone analogues. Evaluation of the structure-activity relationship of substitutions on the phthalimide group led to the discovery of an acetylamino analogue 1S, which is currently in clinical trials.


Subject(s)
Drug Discovery , Phosphodiesterase 4 Inhibitors , Phosphodiesterase Inhibitors/pharmacology , Thalidomide/analogs & derivatives , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Administration, Oral , Animals , Humans , Phosphodiesterase Inhibitors/administration & dosage , Phosphodiesterase Inhibitors/chemistry , Rats , Stereoisomerism , Structure-Activity Relationship , Thalidomide/administration & dosage , Thalidomide/chemistry , Thalidomide/pharmacology
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