

HY-13988 · Free Sample (0.1 - 0.2 mg)
MedChemExpress · Cat: HY-13988
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medchemexpress.com/at-56.html
Description
AT-56 is a potent, selective and orally active inhibitor of lipocalin-type prostaglandin D synthase L-PGDS , with an IC50 of 95 ?M and Ki of 75 ?M. AT-56 could selectively suppress the drowsiness or pain reaction mediated by L-PGDS-catalyzed PGD2.







