Comparison

AS-605240 European Partner

Item no. S1410-5
Manufacturer Selleckchem
CASRN 648450-29-7
Amount 5 mg
Quantity options 10 mg 100 mg 1 g 10 g 5 mg 50 mg 5 g
Category
Type Inhibitors
Specific against other
Smiles C1=CC2=NC=CN=C2C=C1C=C3C(=O)NC(=O)S3
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias 648450-29-7'
Similar products AS-605240
Available
Manufacturer - Targets
PI3K
Storage Conditions
2 years -80 in solvent
Molecular Weight
257, 27
Administration
Orally
Animal Models
RANTES-induced mouse model of peritonitis (female Balb/C or C3H), alphaCII-induced mouse model of arthritis, and collagen-induced mouse model of arthritis (CIA) (male DBA/1)
Cell lines
RAW264 macrophages
Concentrations
1 nM - 10 uM, dissolved in DMSO
Dosages
50 mg/kg
Formulation
Dissolved in 0.5% carboxymethylcellulose/0.25% Tween-20
IC50
8 nM, 8 nM, 8 nM, 8 nM, 8 nM, 8 nM
In vitro
AS-605240 is an ATP-competitive PI3Kgamma inhibitor, with Ki values of 7.8 nM. AS-605240 is isoform-selective, for AS-605240 also inhibits PI3Kalpha, beta, and delta, with IC50 of 60, 270, and 300 nM, respectively. AS-605240 inhibits C5a-mediated PKB phosphorylation with IC50 of 90 nM. In bone marrow-derived monocytes (BMDMs), AS-605240 (1 uM) blocks MCP-1- or CSF-1-induced PKB phosphorylation. [] At SC-CA1 synapses in mice, AS-605240 (100 nM) eliminates NMDAR LTD, without affecting mGluR LTD, depotentiation, and LTP. [2]
In vivo
In RANTES-induced mouse model of peritonitis, AS-605240 reduces neutrophil chemotaxis with ED50 of 9.1 mg/kg. In a alphaCII-induced arthritis, AS-605240 (50 mg/kg) protects against alphaCII-IA symptom. In a mouse model of collagen-induced arthritis, AS-605240 (50 mg/kg) also suppresses joint inflammation and damage. [1] In an obesity-induced diabetes model (ob/ob mice), AS-605240 (10 mg/kg) lowers blood glucose levels, significantly improves both insulin sensitivity and glucose tolerance without affecting body weight. AS-605240 (30 mg/kg) displays more profound effects with slightly less weight gain. Moreover, AS-605240 reduces the abundance of ATMs and the circulating levels of MCP-1. [3]
Incubation Time
30 min
Kinase Assay
In vitro PI3K lipid kinase assay, (1) For PI3Kgamma: human PI3Kgamma (100 ng) is incubated at RT with kinase buffer (10 mM MgCl2, 1 mM beta-glycerophosphate, 1 mM DTT, 0.1 mM Na3VO4, 0.1% Na Cholate and 15 uM ATP/100 nCi gamma[33P]ATP, final concentrations) and lipid vesicles containing 18 uM PtdIns and 250 uM of PtdSer (final concentrations), in the presence of AS-605240 or DMSO. Kinase reaction is stopped by adding 250 ug of Neomycin-coated Scintillation Proximity Assay (SPA) beads. (2) For PI3Kalpha, beta, and delta: varying amounts of ATP are incubated with the different purified PI3K isoforms and saturating concentrations of PtdIns. Consequently, IC50 determinations with PI3Kalpha, beta, and delta, to evaluate inhibitor selectivity are performed as follows: 60 ng of PI3Kalpha are incubated at RT with kinase buffer, as described for PI3Kgamma (but containing 89 uM ATP/300 nCi gamma[33P]ATP and no Na Cholate, instead) and lipid vesicles containing 212 uM PtdIns and 58 uM of PtdSer. 100 ng of PI3Kbeta are incubated at RT with kinase buffer (containing 70 uM ATP/300 nCi gamma[33P]ATP, 4 mM MgCl2 and no Na Cholate) and lipid vesicles containing 225 uM PtdIns and 45 uM of PtdSer. 90 ng of PI3Kdelta are incubated with kinase buffer (containing 65 uM ATP/300 nCi gamma[33P]ATP, 1 mM MgCl2, and no Na Cholate) and lipid vesicles containing 100 uM PtdIns and 170 uM of PtdSer. The reactions are stopped after 2 hours.
Method
After a 3-hour starvation in serum-free medium, Cells are pretreated with AS-605240 or DMSO for 30 min and stimulated for 5 min with 50 nM of C5a. PKB phosphorylation is monitored using phosphorylated Ser473 Akt–specific antibody and standard ELISA protocols.
Solubility (25C)
DMSO 0.4 mg/mL, Water <1 mg/mL, Ethanol <1 mg/mL
Information
AS-605240 selectively inhibits PI3Kγ with IC50 of 8 nM, over 30-fold and 7.5-fold more selective for PI3Kγ than PI3Kδ/β and PI3Kα in cell-free assays, respectively.
Chemical Name
(Z)-5-(quinoxalin-6-ylmethylene)thiazolidine-2, 4-dione
Features
AS-605240 is the most potent member of a new class of PI3Kgamma-selective inhibitors.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 5 mg
Available: In stock
available

Delivery expected until 9/11/2025 

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