CCX662 is a selective CXCR7 inhibitor with human IC50 values of 9 nM (buffer) and 18 nM (100% human serum), and rat IC50 of 14 nM (100% rat serum). CCX662 blocks CXCL12 binding to CXCR7, inhibits CXCR4-directed trans-endothelial migration of CXCR4+/CXCR7+ cells. CCX662 can be used for the research of glioblastoma multiforme[1][2].
Molekulargewicht:
539.69
Reinheit:
98.62
CAS Nummer:
[1226686-54-9]
Formel:
C28H37N5O4S
Target-Kategorie:
CXCR
Anwendungsbeschreibung:
MCE Product type: Reference compound
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