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

CAS No.
6318-41-8
Chemical Name:
2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)-
Synonyms
PI 3-Kγ Inhibitor VII;PI 3-Kγ Inhibitor VII;AS-041164, 10 mM in DMSO;AS-041164, PI3K gamma inhibitor;PI 3-Kγ Inhibitor VII - CAS 6318-41-8 - Calbiochem;2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)-;5-(Benzo[d][1,3]dioxol-5-ylmethylene)thiazolidine-2,4-dione;Inhibitor,PI3Kγ,inhibit,Phosphoinositide 3-kinase,AS 041164,AS-041164,anti-inflammatory,neutrophil,recruitment,AS041164,RANTES,PI3K
CBNumber:
CB13232856
Molecular Formula:
C11H7NO4S
Molecular Weight:
249.24
MDL Number:
MFCD18382117
MOL File:
6318-41-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-31 08:06:23
Product description Number Pack Size Price
PI 3-Kγ Inhibitor VII - CAS 6318-41-8 - Calbiochem 528114 5mg $238
AS-041164 ≥98% 13622 5mg $80
AS-041164 ≥98% 13622 10mg $102
AS-041164 ≥98% 13622 25mg $228
AS-041164 ≥98% 13622 50mg $381

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

Melting point 256-258 °C(Solvent: Ethanol)
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.
InChI 1S/C11H7NO4S/c13-10-9(17-11(14)12-10)4-6-1-2-7-8(3-6)16-5-15-7/h1-4H,5H2,(H,12,13,14)/b9-4+
InChIKey SDGWAUUPHUBJNQ-RUDMXATFSA-N
UNSPSC Code 12352200

SAFETY

Risk and Safety Statements

WGK Germany  WGK 1
Storage Class 11 - Combustible Solids

2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)- price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 528114 PI 3-Kγ Inhibitor VII - CAS 6318-41-8 - Calbiochem 6318-41-8 5mg $238 2023-01-07 Buy
Cayman Chemical 13622 AS-041164 ≥98% 6318-41-8 5mg $80 2026-04-30 Buy
Cayman Chemical 13622 AS-041164 ≥98% 6318-41-8 10mg $102 2026-04-30 Buy
Cayman Chemical 13622 AS-041164 ≥98% 6318-41-8 25mg $228 2026-04-30 Buy
Cayman Chemical 13622 AS-041164 ≥98% 6318-41-8 50mg $381 2026-04-30 Buy
Product number Packaging Price Buy
528114 5mg $238 Buy
13622 5mg $80 Buy
13622 10mg $102 Buy
13622 25mg $228 Buy
13622 50mg $381 Buy

2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)- Chemical Properties,Uses,Production

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.

Uses

AS-041164 is a potent, selective and orally active PI3Kγ isoform inhibitor with an IC50 of 70 nM. AS-041164 shows less activity against PI3Kα, PI3Kβ, and PI3Kδ (IC50s of 240 nM, 1.45 μM, and 1.70 μM, respectively). AS-041164 has anti-inflammatory effects[1].

in vivo

AS-041164 (10-100 mg/kg; oral administration; once) treatment results in the reduction of inflammatory swelling in the model of carrageenan-induced paw edema[1].
AS-041164 (3-100 mg/kg p.o.) treatment dose-dependently decreases r-h regulated on activation normal T cell expressed and secreted (RANTES)-induced neutrophil recruitment in mice. The ED50 value for AS-041164 is 27.35 mg/kg. AS-041164 blocks RANTES-induced chemotaxis and reduces the level of AKT phosphorylation[1].

Animal Model:Male Wistar rats (100-150 g) injected with carrageenan[1]
Dosage:10 mg/kg, 30 mg/kg, 100 mg/kg
Administration:Oral administration; once
Result:Induced a significant reduction of paw thickness.

IC 50

PI3Kγ: 70 nM (IC50); PI3Kα: 240 nM (IC50); PI3Kβ: 1.4 μM (IC50); PI3Kδ: 1.7 μM (IC50)

References

[1] CHIARA FERRANDI. Phosphoinositide 3-kinase gamma inhibition plays a crucial role in early steps of inflammation by blocking neutrophil recruitment.[J]. Journal of Pharmacology and Experimental Therapeutics, 2007, 322 3: 923-930. DOI:10.1124/jpet.107.123026

2295-31-0
120-57-0
6318-41-8
Synthesis of 2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)- from 2,4-Thiazolidinedione and Piperonyl aldehyde

2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)- Preparation Products And Raw materials

Raw materials

Preparation Products

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

Global( 36)Suppliers
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TargetMol Chemicals Inc.
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MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8137 58

View Lastest Price from 2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)- manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
AS-041164 pictures 2026-08-08 AS-041164
6318-41-8
$31.00-92.00 99.59% 10g TargetMol Chemicals Inc.
  • AS-041164 pictures
  • AS-041164
    6318-41-8
  • $31.00-92.00
  • 99.59%
  • TargetMol Chemicals Inc.

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

6318-41-8(2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)-)Related Search:

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 AS-041164, PI3K gamma inhibitor AS-041164, 10 mM in DMSO PI 3-Kγ Inhibitor VII PI 3-Kγ Inhibitor VII 6318-41-8