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Updated: Aug 22, 2026

Fluorescence-based Monitoring of PAD4 Activity via a Pro-fluorescence Substrate Analog
Published on: November 5, 2014
Discovery of new orally active phosphodiesterase (PDE4) inhibitors
Hiroshi Ochiai1, Akiharu Ishida, Tazumi Ohtani
1Minase Research Institute, Ono Pharmaceutical Co., Ltd., Mishima, Osaka 618-8585, Japan.
Abstract:
A series of 4-anilinopyrazolopyridine derivatives were synthesized and biologically evaluated as inhibitors of phosphodiesterase (PDE4). Chemical modification of 3, a structurally new chemical lead that was found in our in-house library, was focused on 1- and 3-substituents. Full details of the discovery of a new orally active chemical lead 5 are presented. Structure-activity relationship data, pharmacological evaluation, and the subtype selectivity study are also presented.
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