Zaloglanstat (ISC-27864; GRC-27864) is a selective, orally active microsomal mPGES-1 inhibitor. Zaloglanstat has an IC 50 of 5 nM for human mPGES-1 without significant inhibitory effect on COX-1/2 ( IC 50 >10 μM). Zaloglanstat blocks the conversion of arachidonic acid metabolite prostaglandin PGH 2 to prostaglandin PGE 2 , thereby inhibiting inflammation-related PGE 2 overproduction and reducing inflammatory responses and pain. Zaloglanstat inhibits IL-1β-induced PGE 2 release in A549 cells and human synovial fibroblasts in vitro . Zaloglanstat inhibits PGE2 release in pig and dog whole blood with IC 50 s of 161 nM and 154 nM, respectively. Zaloglanstat can be used in the study of asthma, osteoarthritis, and neurodegenerative diseases.
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