[CAS NO. 1855871-76-9]  V-9302

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PRODUCTS SPECIFICATIONS [1855871-76-9]

Catalog
SLK-S8818
Brand
Selleck
CAS
1855871-76-9

DESCRIPTION [1855871-76-9]

Overview

MDLMFCD32062750
Molecular Weight538.68
Molecular FormulaC34H38N2O4
SMILESO=C(O)[C@@H](N)CCN(CC1=CC=CC=C1OCC2=CC=CC(C)=C2)CC3=CC=CC=C3OCC4=CC=CC(C)=C4

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM1.8564 mL9.2819 mL18.5639 mL
5 mM0.3713 mL1.8564 mL3.7128 mL
10 mM0.1856 mL0.9282 mL1.8564 mL
50 mM0.0371 mL0.1856 mL0.3713 mL

Description

V-9302 is a competitive small molecule antagonist of transmembrane glutamine flux, that selectively and potently targets the amino acid transporter (SLC1A5) with an IC50 value of 9.6 μM for inhibition of glutamine uptake in HEK-293 cells. V-9302 blocks and the as observed in 143B osteosarcoma cells, HCC1806 breast cancer cells and Xenopus laevis oocytes.

Targets

ASCT2 [1]
(HEK293 cells)
9.6 μM

In vitro

V-9302 inhibits ASCT2-mediated glutamine uptake in human cells in a concentration-dependent fashion and exhibits a 100-fold improvement in potency (IC50 V-9302 = 9.6 µM) over gamma-L-glutamyl-p-nitroanilide (GPNA; IC50 = 1000 µM).