LDN-214117 [1627503-67-6]

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Référence NB-64-09308-5mg

Conditionnement : 5mg

Marque : Neo Biotech

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LDN-214117

Catalog No. T1944 Copy Product Info
Purity: 99.83%
LDN-214117 is a potent and selective ALK2 inhibitor.

LDN-214117

Copy Product Info

LDN-214117 is a potent and selective ALK2 inhibitor.

LDN-214117
Cas No. 1627503-67-6
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Purity:99.83%
Color:White
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Product Introduction

Bioactivity
Description
LDN-214117 is a potent and selective ALK2 inhibitor.
Targets&IC50
ALK2:24 nM
In vivo
LDN-214117 exhibits selective inhibition towards BMP6 over BMP2 or BMP4. In cell-based assays, it preferentially inhibits BMP6 with an IC50 around 100 nM, being 164 times more selective for BMP6 than for TGF-β1. Among kinases, LDN-214117 most effectively inhibits ALK2 (IC50 = 24 nM), followed by TNIK, RIPK2, and ABL1. It specifically inhibits the kinase activity of ALK2 and ALK1 more than that of ALK3.
Kinase Assay
ALK2 kinase assay: Puri?ed recombinant ALK2 proteins, ATP, ATP[γ-32P], and dephosphorylated casein at ?nal concentrations of 2.5 nM, 6 μM, 0.05 μCi/μL , and 0.5 mg/mL, respectively, are aliquoted in kinase bu?er containing 0.2% BSA supplemented with 10 mM MnCl2 into 96-microwell plates, in combination with inhibitor compounds diluted at varying concentrations (0.01 nM to 100 μM). Positive control samples lacking inhibitor compounds, and negative controls lacking recombinant kinase, are also measured. The mixture is reacted at RT for 45 min, quenched with a ?nal concentration of 2% phosphoric acid. The reaction mixture is transferred to 96-well P81 phosphocellulose ?lter plates and bound for 5 min. The plates are washed 20 times with 150 μL of 1% phosphoric acid solution per well by vacuum manifold. Plates are dried at RT for 1 h, sealed, and assayed with Microscint 20 scintillation ?uid using a Spectramax L luminometer. Data is normalized to positive controls at 100% enzyme activity, with negative controls being subtracted as background.
Cell Research
Cells are seeded at 25000 cells per well in 96-well plates and incubated for 2 h at 37℃ and 5% CO2. Compounds of LDN-214117 or DMSO are diluted in DMEM and added at ?nal compound concentrations of 1, 10, and 100 μM. Cells are incubated for 4 and 24 h, after which the media is discarded. Cells are lysed by adding 30 μL of passive lysis bu?er and shaken at RT for 15 min. Cell viability is determined by quantifying the ATP present in each well by adding 10 μL of Cell Titer Glo per well and measuring the light output by Spectramax L luminometer. Data is normalized to 100% viability for cells receiving only DMSO.(Only for Reference)
Chemical Properties
Molecular Weight419.52
FormulaC25H29N3O3
Cas No.1627503-67-6
SmilesCOc1cc(cc(OC)c1OC)-c1cc(cnc1C)-c1ccc(cc1)N1CCNCC1
Relative Density.1.134 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
Ethanol: 42 mg/mL (100.11 mM), Sonication is recommended.
DMSO: 4.2 mg/mL (10.01 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (2.38 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO/Ethanol
1mg5mg10mg50mg
1 mM2.3837 mL11.9184 mL23.8368 mL119.1838 mL
5 mM0.4767 mL2.3837 mL4.7674 mL23.8368 mL
10 mM0.2384 mL1.1918 mL2.3837 mL11.9184 mL
Ethanol
1mg5mg10mg50mg
20 mM0.1192 mL0.5959 mL1.1918 mL5.9592 mL
50 mM0.0477 mL0.2384 mL0.4767 mL2.3837 mL
100 mM0.0238 mL0.1192 mL0.2384 mL1.1918 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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