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BAN ORL 24 dihydrochloride

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Catalog No. T10457Cas No. 1401463-54-4

BAN ORL 24 is a highly potent nociceptin/orphan FQ (N/OFQ) receptor (NOP) antagonist that can be used to study neurological diseases.

BAN ORL 24 dihydrochloride

BAN ORL 24 dihydrochloride

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Purity: 95.03%
Catalog No. T10457Cas No. 1401463-54-4
BAN ORL 24 is a highly potent nociceptin/orphan FQ (N/OFQ) receptor (NOP) antagonist that can be used to study neurological diseases.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$69-In 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.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:95.03%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
BAN ORL 24 is a highly potent nociceptin/orphan FQ (N/OFQ) receptor (NOP) antagonist that can be used to study neurological diseases.
Targets&IC50
NOP receptor:50 μM, μ opioid receptor:0.224 μM
In vitro
BAN ORL 24 has antagonist for NOR (IC50=50 μM) and MOR (opioid receptor subtype) (IC50=0.224 μM). [1]
In vivo
BAN ORL 24 (10 mg/kg; i.v.) attenuated the duration of the thermal nociceptive antisensitization effect of BPRIM97 and inhibited BPRIM97-induced antinociceptive sensitization at 90 min postinjection. In tail-clip testing, BAN ORL 24 did not attenuate BPR1M97-induced antinociceptive sensitization at 30 min postinjection. [2]
Chemical Properties
Molecular Weight506.51
FormulaC27H37Cl2N3O2
Cas No.1401463-54-4
SmilesO=C([C@@H]1N(CCC1)CC2=CC=CC=C2)NCCCN3CCC4(CC3)C5=CC=CC=C5CO4.Cl.Cl
Relative Density.no data available
Storage & Solubility Information
Storagekeep away from direct sunlight,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 80 mg/mL (157.94 mM), Sonication is recommended.
DMSO: 180 mg/mL (355.37 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (9.87 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
H2O/DMSO
1mg5mg10mg50mg
1 mM1.9743 mL9.8715 mL19.7429 mL98.7147 mL
5 mM0.3949 mL1.9743 mL3.9486 mL19.7429 mL
10 mM0.1974 mL0.9871 mL1.9743 mL9.8715 mL
20 mM0.0987 mL0.4936 mL0.9871 mL4.9357 mL
50 mM0.0395 mL0.1974 mL0.3949 mL1.9743 mL
100 mM0.0197 mL0.0987 mL0.1974 mL0.9871 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

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

Keywords

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