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

2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)- Structure
  • ₹15469.99
  • Product name: 2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)-
  • CAS: 6318-41-8
  • MF: C11H7NO4S
  • MW: 249.24
  • EINECS:
  • MDL Number:MFCD18382117
  • Synonyms:2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)-;PI 3-Kγ Inhibitor VII - CAS 6318-41-8 - Calbiochem;Inhibitor,PI3Kγ,inhibit,Phosphoinositide 3-kinase,AS 041164,AS-041164,anti-inflammatory,neutrophil,recruitment,AS041164,RANTES,PI3K;5-(Benzo[d][1,3]dioxol-5-ylmethylene)thiazolidine-2,4-dione
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Brand

  • Sigma-Aldrich(India)

Package

  • 5MG
  • ManufacturerSigma-Aldrich(India)
  • Product number528114
  • Product descriptionPI 3-Kγ Inhibitor VII - CAS 6318-41-8 - Calbiochem The PI 3-Kγ Inhibitor VII, also referenced under CAS 6318-41-8, controls the biological activity of PI 3-Kγ. This small molecule/inhibitor is primaril
  • Packaging5MG
  • Price₹15469.99
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 528114 PI 3-Kγ Inhibitor VII - CAS 6318-41-8 - Calbiochem The PI 3-Kγ Inhibitor VII, also referenced under CAS 6318-41-8, controls the biological activity of PI 3-Kγ. This small molecule/inhibitor is primaril 5MG ₹15469.99 2022-06-14 Buy

Properties

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.

Safety Information

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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.

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