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para-Nitroblebbistatin

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Catalog No. T12360Cas No. 1621326-32-6
Alias p-Nitroblebbistatin

para-Nitroblebbistatin is a non-cytotoxic, non-fluorescent, photostable, and specific inhibitor of myosin II. para-Nitroblebbistatin can be used to study the specific roles of myosin II in physiology, development, and cell biology.

para-Nitroblebbistatin

para-Nitroblebbistatin

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Purity: 99.84%
Catalog No. T12360Alias p-NitroblebbistatinCas No. 1621326-32-6
para-Nitroblebbistatin is a non-cytotoxic, non-fluorescent, photostable, and specific inhibitor of myosin II. para-Nitroblebbistatin can be used to study the specific roles of myosin II in physiology, development, and cell biology.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$89In StockIn Stock
5 mg$223In StockIn Stock
10 mg$333In StockIn Stock
25 mg$538In StockIn Stock
50 mg$732-In Stock
100 mg$990-In Stock
200 mg$1,330-In Stock
1 mL x 10 mM (in DMSO)$227In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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Purity:99.84%
Appearance:Solid
Color:Orange
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Product Introduction

para-Nitroblebbistatin AI Summary
para-Nitroblebbistatin exhibits moderate apparent permeability in human Caco2 cells, with Papp values of 32.5 x 10^-6 cm/s from the apical to basolateral side and 2.23 x 10^-6 cm/s from the basolateral to apical side. It demonstrates good drug recovery, achieving 34.0% recovery from the apical to basolateral side and 72.0% recovery from the basolateral to apical side in Caco2 cells. The compound shows relatively high aqueous solubility in pH 7.4 PBS, with a concentration of 31700.0 nM after 24 hours. Additionally, para-Nitroblebbistatin is photostable, with a half-life greater than 1.5 hours under irradiation at 390 to 470 nm in a DMSO/H2O solvent. Regarding bioactivity, para-Nitroblebbistatin inhibits rabbit skeletal muscle myosin 2 with an IC50 of 400.0 nM, and Dictyostelium discoideum myosin 2 ATPase activity with an IC50 of 2300.0 nM in NADH-coupled assays. It also acts as an inhibitor of actin-activated rabbit skeletal muscle myosin 2 with an IC50 of 500.0 nM and of actin-activated bovine heart muscle myosin 2 with an IC50 of 2100.0 nM. The selectivity ratio of IC50 for bovine heart muscle myosin 2 to rabbit skeletal muscle myosin 2 is 4.2, indicating some level of target selectivity..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
para-Nitroblebbistatin is a non-cytotoxic, non-fluorescent, photostable, and specific inhibitor of myosin II. para-Nitroblebbistatin can be used to study the specific roles of myosin II in physiology, development, and cell biology.
In vitro
METHODS: HeLa cells were treated with para-Nitroblebbistatin (p-Nitroblebbistatin) (20 μM, 3 days) and the changes in cell number and death rate were tracked.
RESULTS para-Nitroblebbistatin effectively inhibited cytokinesis and had no effect on cell number and death rate. [1]
Synonymsp-Nitroblebbistatin
Chemical Properties
Molecular Weight337.33
FormulaC18H15N3O4
Cas No.1621326-32-6
SmilesCc1ccc2N=C3N(CC[C@@]3(O)C(=O)c2c1)c1ccc(cc1)[N+]([O-])=O
Relative Density.1.47 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
DMSO: 25 mg/mL (74.11 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.9645 mL14.8223 mL29.6446 mL148.2228 mL
5 mM0.5929 mL2.9645 mL5.9289 mL29.6446 mL
10 mM0.2964 mL1.4822 mL2.9645 mL14.8223 mL
20 mM0.1482 mL0.7411 mL1.4822 mL7.4111 mL
50 mM0.0593 mL0.2964 mL0.5929 mL2.9645 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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