V-9302 is a competitive antagonist of transmembrane glutamine flux. V-9302 selectively and potently targets the amino acid transporter ASCT2 (SLC1A5) not ASCT1. V-9302 inhibits ASCT2-mediated glutamine uptake (IC50=9.6 µM) in HEK-293 cells[1].
Molecular Weight:
538.68
Purity:
99.46
CAS Number:
[1855871-76-9]
Formula:
C34H38N2O4
Target:
ASCT
Application Notes:
MCE Product type: Reference compound
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