Phenamil methanesulfonate, an analog of Amiloride (HY-B0285), is a more potent and less reversible epithelial sodium channel (ENaC) blocker with an IC50 of 400 nM[2]. Phenamil methanesulfonate is also a competive inhibitor of TRPP3 and inhibits TRPP3-mediated Ca2+ transport with an IC50 of 140 nM in a Ca2+ uptake assay[1]. Phenamil methanesulfonate is an intriguing small molecule to promote bone repair by strongly activating BMP signaling pathway[4]. Phenamil methanesulfonate is used for the research of cystic fibrosis lung disease[5].
Molekulargewicht:
401.83
Reinheit:
98.1
CAS Nummer:
[1161-94-0]
Formel:
C13H16ClN7O4S
Target-Kategorie:
Sodium Channel,TRP Channel
Anwendungsbeschreibung:
MCE Product type: Reference compound
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