T26A is a highly selective prostaglandin transporter (PGT) inhibitor.T26A does not interact with the PGT homolog OATPc, blocks PGT-mediated PGE2 influx, and blocks PGE2 metabolism.T26A retains PGE2 in the extracellular compartment and reduces intracellular PGE2 metabolites.T26A elevates circulating endogenous PGE2 levels, reduces circulating endogenous PGE2 metabolite levels, and slows metabolism of exogenously injected PGE2 in Rattus norvegicus via intravenous injection.T26A does not affect PGE2 synthesis.T26A can be used for the research of PGT function in adult animals[1].
Molekulargewicht:
729.79
CAS Nummer:
[958860-12-3]
Formel:
C35H43N11O7
Target-Kategorie:
COX,PGE synthase,Prostaglandin Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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