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ChemicalBook--->CAS DataBase List--->6318-41-8

6318-41-8

6318-41-8 Structure

6318-41-8 Structure
IdentificationBack Directory
[Name]

2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)-
[CAS]

6318-41-8
[Synonyms]

PI 3-Kγ Inhibitor VII - CAS 6318-41-8 - Calbiochem
2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)-
Inhibitor,PI3Kγ,inhibit,Phosphoinositide 3-kinase,AS 041164,AS-041164,anti-inflammatory,neutrophil,recruitment,AS041164,RANTES,PI3K
[Molecular Formula]

C11H7NO4S
[MDL Number]

MFCD18382117
[MOL File]

6318-41-8.mol
[Molecular Weight]

249.24
Chemical PropertiesBack Directory
[density ]

1.595±0.06 g/cm3(Predicted)
[storage temp. ]

+2C to +8C
[solubility ]

Soluble in DMSO (up to 25 mg/ml).
[form ]

Yellow solid
[pka]

7.13±0.20(Predicted)
[color ]

Yellow
[Stability:]

Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
Hazard InformationBack Directory
[Description]

The phosphatidylinositol 3-kinases (PI3Ks) are lipid and protein kinases involved in diverse biological processes, including cell growth, migration, and metabolism. AS-041164 is a potent inhibitor of PI3K with selectivity for the class IB isoform PI3Kγ (IC50 = 70 nM), compared to PI3Kα (IC50 = 240 nM), PI3Kβ (IC50 = 1.45 μM), and PI3Kδ (IC50 =1.70 μM). When tested at 1.0 μM, it shows little or no activity against 38 other common kinases. When given orally to mice, AS-041164 shows a pharmacokinetic profile that is similar to the general PI3K inhibitor LY294002 but is three times more potent (ED50 = 27.4 mg/kg for AS-041164 versus 81.6 mg/kg for LY294002) in blocking neutrophil recruitment induced by RANTES.
[storage]

4°C, protect from light
[References]

1) Ferrandi et al. (2007) Phosphoinositide 3-kinase gamma inhibition plays a crucial role in early steps of inflammation by blocking neutrophil recruitment: J. Pharmacol. Exp. Ther. 322 923
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