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Fasentin

SIGMA/F5557 - ≥98% (HPLC)

Synonym: N-[4-Chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide

CAS Number: 392721-37-8
Empirical Formula (Hill Notation): C11H9ClF3NO2
Molecular Weight: 279.64
MDL Number: MFCD01001285
Linear Formula: C11H9ClF3NO2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-F5557-5MG 5 mg
$121.00
1/EA
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45-F5557-25MG 25 mg
$462.00
1/EA
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assay ≥98% (HPLC)
color white to off-white
form powder
InChI 1S/C11H9ClF3NO2/c1-6(17)4-10(18)16-7-2-3-9(12)8(5-7)11(13,14)15/h2-3,5H,4H2,1H3,(H,16,18)
InChI key GNYIJZMBLZXJEJ-UHFFFAOYSA-N
Quality Level 100 
SMILES string CC(=O)CC(=O)Nc1ccc(Cl)c(c1)C(F)(F)F
solubility DMSO: >10 mg/mL
storage temp. room temp
Application: Fasentin has been used as a glucose transporter (GLUT1) inhibitor to assess its effects on the vulnerability of a wide range of triple-negative breast cancer (TNBC) cell lines and to study its effects on cytotoxic drugs induced by hydrocortisone (HC).
Biochem/physiol Actions: Fasentin is a novel inhibitor of glucose uptake, GluT1 inhibitor. Fasentin is a novel inhibitor of glucose uptake that sensitizes cells to FAS-induced cell death. Fasentin selectively sensitized to death ligands, but did not decrease FLIP expression. It alters expression of genes associated with nutrient and glucose deprivation. Fasentin interacted with a unique site in the intracellular channel of the glucose transport protein GLUT1.
Biochem/physiol Actions: Fastentin is a novel inhibitor of glucose uptake, GluT1 inhibitor.
Packaging: 5, 25 mg in glass bottle
Hazard Codes Xn
Risk Statements 22
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. room temp
UNSPSC 12352200

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