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NKL 22

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Catalog No. T3206Cas No. 537034-15-4
Alias PAOA, Histone Deacetylase Inhibitor IV

NKL 22 (Histone Deacetylase Inhibitor IV) is an effective Histone Deacetylase Inhibitor.

NKL 22

NKL 22

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Purity: 96.24%
Catalog No. T3206Alias PAOA, Histone Deacetylase Inhibitor IVCas No. 537034-15-4
NKL 22 (Histone Deacetylase Inhibitor IV) is an effective Histone Deacetylase Inhibitor.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$29In StockIn Stock
25 mg$58In StockIn Stock
50 mg$94In StockIn Stock
100 mg$148In StockIn Stock
200 mg$219-In Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:96.24%
Color:White
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Product Introduction

NKL 22 AI Summary
NKL 22 exhibits significant bioactivity as a histone deacetylase (HDAC) inhibitor, particularly potent against HDAC1 and HDAC3/NCOR2 with IC50 values of 199.0 nM and 69.0 nM, respectively. It also shows moderate activity against HDAC2 (IC50 = 1590.0 nM) and HDAC8 (IC50 = 5000.0 nM), but negligible activity against HDAC4, HDAC5, HDAC7, and HDAC8 (IC50 > 180,000.0 nM). In U937 cells, NKL 22 inhibits HDAC1 by 28.9% at 5 µM without affecting HDAC4 and induces granulocytic differentiation as evidenced by an 18.3% increase in CD11c expression after 30 hours at the same concentration. Additionally, the compound enhances FXN mRNA expression and frataxin protein levels in lymphocytes from Friedreich's ataxia patients and exhibits inhibition of HDACs in HeLa cell extracts. For its antiviral properties, NKL 22 inhibits SARS-CoV-2 3CL-Pro protease by 9.33% at 20 µM and demonstrates modest antiviral activity by reducing SARS-CoV-2 induced cytotoxicity in VERO-6 cells at 10 µM with an inhibition rate of 0.26%. Furthermore, NKL 22 shows cytotoxic activity against human HepG2 cells with an IC50 of 11700.0 nM, indicating its potential as a cytotoxic agent..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
NKL 22 (Histone Deacetylase Inhibitor IV) is an effective Histone Deacetylase Inhibitor.
Targets&IC50
HDAC8:5 μM (IC50), HDAC1:0.199 μM (IC50), HDAC3:0.069 μM (IC50), HDAC2:1.59 μM (IC50)
SynonymsPAOA, Histone Deacetylase Inhibitor IV
Chemical Properties
Molecular Weight325.4
FormulaC19H23N3O2
Cas No.537034-15-4
SmilesNc1ccccc1NC(=O)CCCCCC(=O)Nc1ccccc1
Relative Density.1.213g/cm3
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
DMSO: 50 mg/mL (153.66 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0731 mL15.3657 mL30.7314 mL153.6570 mL
5 mM0.6146 mL3.0731 mL6.1463 mL30.7314 mL
10 mM0.3073 mL1.5366 mL3.0731 mL15.3657 mL
20 mM0.1537 mL0.7683 mL1.5366 mL7.6829 mL
50 mM0.0615 mL0.3073 mL0.6146 mL3.0731 mL
100 mM0.0307 mL0.1537 mL0.3073 mL1.5366 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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Dose Conversion

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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