Latanoprost acid, an analog of prostaglandin (PG) F2alpha, is an selective prostanoid receptor (FP) agonist that specifically activates the FP-PG receptor[1]. Latanoprost acid inhibits RANKL-induced osteoclastgenesis and function by inhibiting ERK, AKT, JNK, and p38 cascade, following by the c-fos/NFATc1 pathway. Latanoprost acid is a medication which works to lower pressure inside the eyes[1][2].
Molekulargewicht:
390.51
Reinheit:
99.62
CAS Nummer:
[41639-83-2]
Formel:
C23H34O5
Target-Kategorie:
Akt,ERK,JNK,p38 MAPK,Prostaglandin Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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