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GSK2879552

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Catalog No. T3677Cas No. 1401966-69-5
Alias GSK2879552 2HCl

GSK2879552 is a selective, orally bioavailable, irreversible, mechanism-based inactivator of lysine-specific demethylase 1 (LSD1)/corepressor, with potential antineoplastic activity.

GSK2879552

GSK2879552

🥰Excellent
Purity: 99.22%
Catalog No. T3677Alias GSK2879552 2HClCas No. 1401966-69-5
GSK2879552 is a selective, orally bioavailable, irreversible, mechanism-based inactivator of lysine-specific demethylase 1 (LSD1)/corepressor, with potential antineoplastic activity.
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2 mg$109In Stock
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Purity:99.22%
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Product Introduction

Bioactivity
Description
GSK2879552 is a selective, orally bioavailable, irreversible, mechanism-based inactivator of lysine-specific demethylase 1 (LSD1)/corepressor, with potential antineoplastic activity.
Targets&IC50
LSD1:1.7 μM(Ki)
In vitro
In 165 cell lines, GSK2879552 inhibits the growth of 9/28 small cell lung carcinoma (SCLC) lines and 20/29 AML lines ranged from 40% to 100%. The subset of SCLC lines and primary samples that undergo growth inhibition in response to GSK2879552 exhibit DNA hypomethylation of a signature set of probes. [1]
In vivo
In SCLC xenograft bearing mice, GSK2879552 (1.5 mg/kg, p.o.) demonstrates tumor growth inhibition by 17%-83%. [1]
Kinase Assay
LSD1 enzyme assay: LSD1 activity was measured using a horseradish peroxidase (HRP) coupled assay with amplex red as an electron donor. The formation of product over time is measured using fluorescence intensity, Ex 531 nm and Em 595 nm, in a PerkinElmer EnVision plate reader. Final assay conditions are: 5 nM LSD1, 2.5 μM H3K4me2 peptide, 50 mM HEPES pH 7, 1 U/ml of HRP, 1 mM CHAPS, 0.03% dBSA and 10 μM amplex red.
Cell Research
The optimal cell seeding is determined empirically for all cell lines by examining the growth of a wide range of seeding densities in a 384-well format to identify conditions that permitted proliferation for 6?days. Cells are then plated at the optimal seeding density 24?h before treatment (in duplicate) with a 20-point twofold dilution series of GSK2879552 or 0.15% DMSO. Plates are incubated for 6?days at 37°C in 5% CO2. Cells are then lysed with CellTiter-Glo (CTG) (Promega) and chemiluminescent signal is detected with a TECAN Safire2 microplate reader. In addition, an untreated plate of cells is harvested at the time of compound addition (T0) to quantify the starting number of cells. CTG values obtained after the 6?day treatment are expressed as a percent of the T0 value and plotted against compound concentration. Data are fit with a four-parameter equation to generate a concentration response curve and the concentration of GSK126 required to inhibit 50% of growth (growth IC50) is determined.(Only for Reference)
AliasGSK2879552 2HCl
Chemical Properties
Molecular Weight364.48
FormulaC23H28N2O2
Cas No.1401966-69-5
SmilesOC(=O)c1ccc(CN2CCC(CN[C@@H]3C[C@H]3c3ccccc3)CC2)cc1
Relative Density.1.20 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: <1 mg/mL
DMSO: 27 mg/mL (74.1 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7436 mL13.7182 mL27.4363 mL137.1817 mL
5 mM0.5487 mL2.7436 mL5.4873 mL27.4363 mL
10 mM0.2744 mL1.3718 mL2.7436 mL13.7182 mL
20 mM0.1372 mL0.6859 mL1.3718 mL6.8591 mL
50 mM0.0549 mL0.2744 mL0.5487 mL2.7436 mL

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