Millipore Sigma Vibrant Logo
Attenzione: Ci siamo trasferiti. Non è più possibile acquistare i prodotti Merck Millipore nel sito MerckMillipore.comPer saperne di più

341305 Fasentin - CAS 392721-37-8 - Calbiochem

341305
Purchase on Sigma-Aldrich

Panoramica

Replacement Information

Products

Numero di catalogoConfezionamento Qtà/conf
341305-25MG Fiala di plastica 25 mg
Description
OverviewA cell-permeable oxobutananilide compound that is predicted to interact with Glut (Glucose Transporter) at an intracellular site based on a virtual docking study and shown to inhibit Glut-mediated cellular glucose uptake (50% and 80% inhibition of 2-deoxy-D-glucose uptake in Glut1- and Glut4-overexpressing L6 myoblasts, respectively, at 300 µM). Fas-resistant cell lines that are made Fas-responsive upon medium glucose deprivation are also shown to be sensitized by Fasentin to Fas-mediated cell death (ED50 = 35 µM in PPC-1 cultures), while cells that remain Fas-resistant upon glucose deprivation, e.g. DU145, are shown not to be sensitized by Fasentin to Fas-mediated death.
Catalogue Number341305
Brand Family Calbiochem®
SynonymsGlucose Transporter Inhibitor, 6094911, N-(4-Chloro-3-(trifluoromethyl)phenyl)-3-oxobutanamide
References
ReferencesWood, T.E., et al. 2008. Mol. Cancer Ther. 7, 3546
Schimmer, A.D., et al. 2006. Cancer Res. 66, 2367.
Product Information
CAS number392721-37-8
FormOff-white solid
Hill FormulaC₁₁H₉ClF₃NO₂
Chemical formulaC₁₁H₉ClF₃NO₂
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Purity≥95% by HPLC
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Standard Handling
Storage +2°C to +8°C
Protect from Light Protect from light
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -2°C.
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Numero di catalogo GTIN
341305-25MG 04055977215649

Documentation

Fasentin - CAS 392721-37-8 - Calbiochem MSDS

Titolo

Scheda di sicurezza (MSDS) 

Fasentin - CAS 392721-37-8 - Calbiochem Certificati d'Analisi

TitoloNumero di lotto
341305

Riferimenti bibliografici

Panoramica delle referenze
Wood, T.E., et al. 2008. Mol. Cancer Ther. 7, 3546
Schimmer, A.D., et al. 2006. Cancer Res. 66, 2367.
Scheda tecnica

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision08-April-2011 RFH
SynonymsGlucose Transporter Inhibitor, 6094911, N-(4-Chloro-3-(trifluoromethyl)phenyl)-3-oxobutanamide
DescriptionA cell-permeable oxobutananilide compound that is predicted to interact with Glut (Glucose Transporter) at an intracellular site based on a virtual docking study and shown to inhibit Glut-mediated cellular glucose uptake (50% and 80% inhibition of 2-deoxy-D-glucose uptake in Glut1- and Glut4-overexpressing L6 myoblasts, respectively, at 300 µM). Fas-resistant cell lines that are made Fas-responsive upon medium glucose deprivation are also shown to be sensitized by Fasentin to Fas-mediated cell death (ED50 = 35 µM in PPC-1 cultures), while cells that remain Fas-resistant upon glucose deprivation, e.g. DU145, are shown not to be sensitized by Fasentin to Fas-mediated death.
FormOff-white solid
Intert gas (Yes/No) Packaged under inert gas
CAS number392721-37-8
Chemical formulaC₁₁H₉ClF₃NO₂
Structure formulaStructure formula
Purity≥95% by HPLC
SolubilityDMSO (20 mg/ml)
Storage Protect from light
+2°C to +8°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -2°C.
Toxicity Standard Handling
ReferencesWood, T.E., et al. 2008. Mol. Cancer Ther. 7, 3546
Schimmer, A.D., et al. 2006. Cancer Res. 66, 2367.