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AS041164 PI3Kg Inhibitor VII

Catalog # CD0240

Price:  1 mg - $15; 5 mg - $25; 10 mg - $50; 25 mg - $90; 50 mg - $180; 100 mg - $250

Availability:  In stock

 

 

 5-(Benzo[1,3]dioxol-5-ylmethylene)-thiazolidine-2,4-dione

 

Yellow solid. PROTECT FROM LIGHT. PACKAGED UNDER INERT GAS. Purity: 99% by HPLC. CAS# 6318-41-8. Solubility: DMSO (40 mg/mL). Molecular Formula: C11H7NO4S. Molecular Weight: 249.2.

 

 

A cell-permeable thiazolidinedione compound that acts as a potent, ATP-competitive, and isoform-selctive PI3-K inhibitor (g isoform IC50 = 0.07 M, (a isoform IC50 = 0.24 M, (b isoform IC50 = 1.45 M, and (d isoform IC50 = 1.70 M) with little or no activity against a panel of 38 other commonly studied kinases (<20% inhibition at 1.0 M). Exhibits similar pharmacokinetics as LY 294002 via oral administration, but is 3-times as potent (ED50 = 27.35 mg/kg, p.o.) in blocking rhRNATES-induced neutrophil peritoneal recruitment in mice in vivo. Also reported to exhibit significant in vivo prophylactic efficacy against carrageenan-induced tissue swelling in a rat paw edema model (100 mg/kg, p.o)

 

Reference: Ferrandi, C., et al.  J. Pharmacol. Exp. Ther. 2007, 322, 923.

 

 

SAME PRODUCT AS:

Axxora 

Cat. No. BML-E390

 

Cayman Chemical  

Cat. No. 13622

Enzo Life Sciences   

Cat. No. BML-E390

EMD

Cat. No. 528114

Tocris   

Cat. No. N/A

Sigma

Cat. No. N/A

 

 

 

 

Caution Not fully tested. For research use only. Not for human use.

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