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V-9302

Chemical Structure : V-9302

CAS No.: 1855871-76-9

V-9302 (V9302)

Catalog No.: PC-50008Not For Human Use, Lab Use Only.

V-9302 (V9302) is a competitive, selective antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter ASCT2 with IC50 of 9.6 uM.

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Biological Activity

V-9302 (V9302) is a competitive, selective antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter ASCT2 with IC50 of 9.6 uM.
V-9302  displays 100-fold improvement in potency over γ-L-glutamyl-p-nitroanilide (GPNA).
V-9302  attenuates cancer cell growth and proliferation (CRC cell lines EC50=9-15 uM), increases cell death, and increases oxidative stress, which collectively contribute to antitumor responses in vitro and in vivo.

Physicochemical Properties

M.Wt 538.688
Formula C34H38N2O4
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(S)-2-amino-4-(bis(2-((3-methylbenzyl)oxy)benzyl)amino)butanoic acid

References

1. Schulte ML, et al. Nat Med. 2018 Jan 15. doi: 10.1038/nm.4464.

2. Schulte ML, et al. Bioorg Med Chem Lett. 2016 Feb 1;26(3):1044-1047.

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