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N6022

Catalog No. T6901Cas No. 1208315-24-5

N6022(IC50 of 8 nM) is an effective, reversible, and selective S-Nitrosoglutathione reductase(GSNOR) inhibitor.

N6022

N6022

Purity: 98.32%
Catalog No. T6901Cas No. 1208315-24-5
N6022(IC50 of 8 nM) is an effective, reversible, and selective S-Nitrosoglutathione reductase(GSNOR) inhibitor.
Pack SizePriceAvailabilityQuantity
1 mg$40In Stock
2 mg$55In Stock
5 mg$96In Stock
10 mg$140In Stock
25 mg$273In Stock
50 mg$453In Stock
100 mg$667In Stock
500 mg$1,420In Stock
1 mL x 10 mM (in DMSO)$100In Stock
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Purity:98.32%
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Product Introduction

Bioactivity
Description
N6022(IC50 of 8 nM) is an effective, reversible, and selective S-Nitrosoglutathione reductase(GSNOR) inhibitor.
Targets&IC50
GSNOR:8 nM
In vitro
N6022 binds to rat plasma proteins in a concentration-dependent manner. At lower drug concentrations (20 μM), N6022 show more effect on ATP than on GSH. N6022 (IC50 of 8 nM and a Ki of 2.5 nM) binds in the GSNO substrate binding pocket like a competitive inhibitor. N6022 is uncompetitive with cofactors NAD+ and NADH.
In vivo
N6022 treats rats in 50 mg/kg leading to a slight increase in the incidence of granulomas. In serum, N6022 remained in solution is up to 5 mg/mL.
Cell Research
N6022 is dissolved in 5% DMSO. N6022 is tested using a rat hepatoma (H4IIE) cell line whereby cells are seeded into 96-well plates and cultured in medium containing 20% bovine serum. Following an equilibration period of 48 h, the cells are treated with N6022 (5% DMSO vehicle) at concentrations of 0, 1, 5, 10, 20, 50, 100, and 300 μM for 24 h at 37°C in 5% CO2. Camptothecin and rotenone are included as positive controls. The cell supernatant or the cells themselves are harvested for biochemical analysis.
Chemical Properties
Molecular Weight414.46
FormulaC24H22N4O3
Cas No.1208315-24-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 45 mg/mL (108.58 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4128 mL12.0639 mL24.1278 mL120.6389 mL
5 mM0.4826 mL2.4128 mL4.8256 mL24.1278 mL
10 mM0.2413 mL1.2064 mL2.4128 mL12.0639 mL
20 mM0.1206 mL0.6032 mL1.2064 mL6.0319 mL
50 mM0.0483 mL0.2413 mL0.4826 mL2.4128 mL
100 mM0.0241 mL0.1206 mL0.2413 mL1.2064 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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