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pNNP

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Catalog No. T34093Cas No. 330-13-2
Alias p-NNP, p-Nitrophenyl phosphate, p NNP, Nitrophenylphosphate

pNNP (Nitrophenylphosphate) can be used as a substrate for the PP2C assay. pNNP inhibits β-carbonic anhydrase and α-carbonate dehydrogenase, as well as H. pylori Helicobacter pylori. pNNP is a weakly active, tissue-nonspecific alkaline phosphatase modifier. pNNP has been shown to inhibit β-carbonic anhydrase and α-carbonate dehydrogenase.

pNNP

pNNP

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Purity: 99.82%
Catalog No. T34093Alias p-NNP, p-Nitrophenyl phosphate, p NNP, NitrophenylphosphateCas No. 330-13-2
pNNP (Nitrophenylphosphate) can be used as a substrate for the PP2C assay. pNNP inhibits β-carbonic anhydrase and α-carbonate dehydrogenase, as well as H. pylori Helicobacter pylori. pNNP is a weakly active, tissue-nonspecific alkaline phosphatase modifier. pNNP has been shown to inhibit β-carbonic anhydrase and α-carbonate dehydrogenase.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$33In StockIn Stock
25 mg$54In StockIn Stock
50 mg$81In StockIn Stock
100 mg$123In StockIn Stock
500 mg$297In 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:99.82%
Appearance:Solid
Color:White
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Product Introduction

pNNP AI Summary
pNNP exhibits multiple bioactivities across different enzymes and biological targets. It demonstrates inhibitory activity against human serum paraoxonase (PON1) with an IC50 value of 18,500,000 nM and against the Src protein tyrosine kinase SH2 domain with an IC50 value of 1,000,000 nM. Additionally, pNNP acts as an inhibitor of CD45 protein tyrosine phosphatase, with kinetic parameters including a k cat of 3.95 s^-1, a Km of 278,000 nM, and a kcat/Km ratio of 0.000142 M^-1 s^-1. For carbonic anhydrase enzymes, pNNP shows varying catalytic efficiencies. It exhibits a high kcat/Km ratio for mouse carbonic anhydrase 13, indicating strong catalytic efficiency, whereas for human carbonic anhydrase 1 and 2, it demonstrates moderate and lower ratios, respectively. It also inhibits esterase activities of these enzymes as measured by the CO2 hydration method. Moreover, pNNP has inhibitory effects on several phosphatases, including Yersinia pestis PTPase (Km of 600,000 nM), and human STEP (Km of 745,000 nM). It also shows inhibitory activity against PtpB (Km of 1,336,000 nM) and DLODP in human HepG2 microsomal membranes, with an IC50 value of 4,200,000 nM. In terms of drug metabolism, pNNP is metabolized in mouse liver homogenates with significant hydrolysis at different pH levels, showing higher metabolism rates at pH 5 compared to pH 9.6. This indicates efficient liver metabolism under acidic conditions..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
pNNP (Nitrophenylphosphate) can be used as a substrate for the PP2C assay. pNNP inhibits β-carbonic anhydrase and α-carbonate dehydrogenase, as well as H. pylori Helicobacter pylori. pNNP is a weakly active, tissue-nonspecific alkaline phosphatase modifier. pNNP has been shown to inhibit β-carbonic anhydrase and α-carbonate dehydrogenase.
Synonymsp-NNP, p-Nitrophenyl phosphate, p NNP, Nitrophenylphosphate
Chemical Properties
Molecular Weight219.09
FormulaC6H6NO6P
Cas No.330-13-2
SmilesO(P(=O)(O)O)C1=CC=C(N(=O)=O)C=C1
Relative Density.1.712 g/cm3 (Predicted)
Storage & Solubility Information
Storagekeep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 60 mg/mL (273.86 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.5643 mL22.8217 mL45.6433 mL228.2167 mL
5 mM0.9129 mL4.5643 mL9.1287 mL45.6433 mL
10 mM0.4564 mL2.2822 mL4.5643 mL22.8217 mL
20 mM0.2282 mL1.1411 mL2.2822 mL11.4108 mL
50 mM0.0913 mL0.4564 mL0.9129 mL4.5643 mL
100 mM0.0456 mL0.2282 mL0.4564 mL2.2822 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:
% DMSO
%
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Tech Support

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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