CW069

貨號 Cat. No.
S7336
規格 Size
2mg、5mg
品牌 Brand
Selleckchem

Description

 



CW069
Catalog No.S7336

CW069 is an allosteric, and selective inhibitor of microtubule motor protein HSET with IC50 of 75 μM, significant selectivity over KSP.


















Size Price Stock Quantity  
















2mg USD 122 In stock  
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5mg USD 235 In stock  
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Distributor Tel: +886-2-2827-1197jimmy@new.abscience.com.tw


Biological Activity







































Description CW069 is an allosteric, and selective inhibitor of microtubule motor protein HSET with IC50 of 75 μM, significant selectivity over KSP.
Targets HSET          
IC50 75 μM [1]          
In vitro CW069 increases multipolar spindles in N1E-115 cells with supernumerary centrosomes without altering bipolar spindle morphology in normal human dermal fibroblast cells. CW069 inhibits growth in cancer N1E-115 cells with IC50 of 10 μM, but not in NHDF or primary human bone marrow cells. [1]
In vivo  
Features  

Protocol(Only for Reference)


Kinase Assay: [1]









In Vitro Enzymatic ATPase Assay The protocol is optimized for use with full-length, N-terminal, 6His-tagged HSET and KSP, and measured the MT-stimulated activity of the proteins. Inhibition of the Gsp synthetase activity of HSET/KSP is observed spectrophotometrically by coupling the hydrolysis of ATP to oxidation of NADH via pyruvate kinase/lactate dehydrogenase reactions. The assay is initiated by adding purified Gsp synthetase/amidase (12.8 nM) to an assay mixture containing the following components (final concentration): 6 nM protein, 0.07 mg/ml MTs (University Biologicals), 1.56 mM glutathione, 10 mM spermidine, 2 mM ATP, 2.7 mM MgCl2, 1 mM phospho(enol)-pyruvate, 0.2 mM NADH, 50 μg/ml lactate dehydrogenase, 100 μg/ml pyruvate kinase, and various concentrations of inhibitor all in 50 mM Na PIPES (pH 6.8) at 37°C. The ADP-Glo detection assay (Promega) is performed as described in the manufacturer’s instructions. All compound additions were performed using a multidrop BioMek Nxp. Plates were read using a Pherastar microplate reader.

Cell Assay: [1]





















Cell lines N1E-115 cells, NHDF and primary human bone marrow cells.
Concentrations ~400 μM
Incubation Time 72 hours
Method Cells are cultured in DMEM supplemented with 10% fetal calf serum (FCS) at 37°C and 5% CO2. All compounds used in the Sulforhodamine B colorimetric (SRB) assay are dissolved in DMSO and diluted in culture medium to a final concentration of 0.2% DMSO. For the SRB assay and live-cell imaging, cells are seeded in 96-well plates at a density of 2,500 cells per well. After 24 hr, the cells are treated with compound for 72 hr, with triplicate wells for each concentration. For the SRB assay, the cells are then fixed with trichloroacetic acid (TCA) and stained with SRB. Fluorescence is quantified using an Infinite 200 PRO plate-reader at a wavelength of 545 nm. Compound-treated wells are compared with solvent control wells and the concentration of compound that results in 50% of the solvent-control cell growth is designated as the IC50 concentration, calculated using Graphpad PRISM 6. At least three biological replicates are performed for each assay.

1


References


Chemical Information


 

















Molecular Weight (MW) 500.33
Formula

C23H21IN2O3


CAS No.  















Storage 3 years -20℃Powder
6 months-80℃in DMSO
Syonnyms N/A

 





















Solubility (25°C) * In vitro DMSO 100 mg/mL (199 mM)
Water <1 mg/mL (<1 mM)
Ethanol 4 mg/mL (7 mM)
* <1 mg/ml means slightly soluble or insoluble.

* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.


 








Chemical Name (S)-2-(2-(benzylamino)-3-phenylpropanamido)-5-iodobenzoic acid

 


 


 

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