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Ifenprodil Tartrate

Name: Ifenprodil Tartrate
Brand: TargetMol
SKU: T1186
Price: 50 USD
Availability: InStock
Rating: 5 (10 reviews)

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Catalog No. T1186Cas No. 23210-58-4

Ifenprodil is a selective NMDA receptor (glutamate) antagonist.

Ifenprodil Tartrate

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Purity: 99.55%

Catalog No. T1186Cas No. 23210-58-4

Ifenprodil is a selective NMDA receptor (glutamate) antagonist.

Pack Size	Price	USA Warehouse	Global Warehouse
25 mg	$50	In Stock	In Stock
50 mg	$65	In Stock	In Stock
100 mg	$108	In Stock	In Stock
200 mg	$154	In Stock	In Stock
1 mL x 10 mM (in DMSO)	$68	In Stock	In Stock

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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]

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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Batch Information

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Purity:99.55%

Appearance:Solid

Color:White

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COA HNMR LCMS

Product Introduction

Bioactivity

Description	Ifenprodil is a selective NMDA receptor (glutamate) antagonist.
Targets&IC50	NMDAR:0.3 μM
In vivo	Ifenprodil inhibits NMDA-induced currents at both 10 μM and 100 μM, with IC50 values of 0.88 μM and 0.17 μM, respectively. In rat cortical neurons, Ifenprodil (10 μM) suppresses the majority of currents elicited by NMDA receptors.
Kinase Assay	In vitro biochemical and pharmacological assaysinhibition studies with recombinant human COX-1 and COX-2: Microsomal preparations of recombinant human COX-1 and COX-2 are prepared from a vaccinia virus-COS-7 cell expression system. Recombinant human COX-1 and COX-2 are expressed in baculovirus-Sf9 cells, and enzymes are purified. Enzymatic activity is monitored continuously by either a fluorescence assay measuring the appearance of the oxidized form of the reducing agent cosubstrate homovanillic acid or by oxygen consumption. The HPLC assay for the assessment of inhibition of purified COX-1 by Rofecoxib with 0.1 μM arachidonic acid substrate concentration, the determination of the stoichiometry of the complex between COX-2 and Rofecoxib, the dissociation rate constant of the enzyme-inhibitor complex by recovery of enzymatic activity, and the recovery of intact Rofecoxib from that complex are all performed as described previously. The solvent system for the HPLC analysis of Rofecoxib is 15:85 MeOH/aqueous potassium phosphate (1 g/liter), with elution by a linear gradient of 15 to 75% MeOH over 25 minutes with detection at 275 nm on a Novapak C18 column.

Chemical Properties

Molecular Weight	400.49
Formula	C₂₁H₂₇NO₂·1/2C₄H₆O₆
Cas No.	23210-58-4
Smiles	O[C@H]([C@@H](O)C(O)=O)C(O)=O.CC(C(O)c1ccc(O)cc1)N1CCC(Cc2ccccc2)CC1.CC(C(O)c1ccc(O)cc1)N1CCC(Cc2ccccc2)CC1
Relative Density.	no data available

Storage & Solubility Information

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

Solubility Information

DMSO: 83.33 mg/mL (208.07 mM), Sonication is recommended.

Ethanol: 58 mg/mL (144.82 mM), Sonication is recommended.

H2O: 9 mg/mL (22.47 mM), Sonication is recommended.

In Vivo Formulation

10% DMSO+90% Saline: 2 mg/mL (4.99 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/Ethanol/DMSO

	1mg	5mg	10mg	50mg
1 mM	2.4969 mL	12.4847 mL	24.9694 mL	124.8471 mL
5 mM	0.4994 mL	2.4969 mL	4.9939 mL	24.9694 mL
10 mM	0.2497 mL	1.2485 mL	2.4969 mL	12.4847 mL
20 mM	0.1248 mL	0.6242 mL	1.2485 mL	6.2424 mL

Ethanol/DMSO

	1mg	5mg	10mg	50mg
50 mM	0.0499 mL	0.2497 mL	0.4994 mL	2.4969 mL
100 mM	0.0250 mL	0.1248 mL	0.2497 mL	1.2485 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:

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 DMSO TargetMol | 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 DMSO TargetMol | reagent stock solution to 400 μL PEG300 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 ddH₂O TargetMol | 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.

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