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Aditoprime

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Catalog No. T60699Cas No. 56066-63-8
Alias Aditoprime, Aditoprim

Aditoprime (Aditoprim) is a selective inhibitor of bacterial dihydrofolate reductase (DHFR) that exhibits potent enzymatic inhibition with IC50 values of 47 nM for Escherichia coli DHFR and 520 nM for Lactobacillus casei DHFR, Aditoprime functions by blocking the conversion of dihydrofolic acid to tetrahydrofolic acid.Aditoprime also demonstrate broad-spectrum antibacterial activity combined with favorable pharmacokinetic properties that support its use in antimicrobial research and drug development studies.

Aditoprime

Aditoprime

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Purity: 99.89%
Catalog No. T60699Alias Aditoprime, AditoprimCas No. 56066-63-8
Aditoprime (Aditoprim) is a selective inhibitor of bacterial dihydrofolate reductase (DHFR) that exhibits potent enzymatic inhibition with IC50 values of 47 nM for Escherichia coli DHFR and 520 nM for Lactobacillus casei DHFR, Aditoprime functions by blocking the conversion of dihydrofolic acid to tetrahydrofolic acid.Aditoprime also demonstrate broad-spectrum antibacterial activity combined with favorable pharmacokinetic properties that support its use in antimicrobial research and drug development studies.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$107-In Stock
5 mg$263-In Stock
10 mg$428-In Stock
25 mg$818-In Stock
50 mg$1,280-In Stock
100 mg$1,760-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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Purity:99.89%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Aditoprime (Aditoprim) is a selective inhibitor of bacterial dihydrofolate reductase (DHFR) that exhibits potent enzymatic inhibition with IC50 values of 47 nM for Escherichia coli DHFR and 520 nM for Lactobacillus casei DHFR, Aditoprime functions by blocking the conversion of dihydrofolic acid to tetrahydrofolic acid.Aditoprime also demonstrate broad-spectrum antibacterial activity combined with favorable pharmacokinetic properties that support its use in antimicrobial research and drug development studies.
Targets&IC50
DHFR (L.casei):520 nM, DHFR (E.coli):47 nM
In vitro
Method: Antibacterial susceptibility testing was performed against bacterial isolates from swine, poultry, calves, sheep, and fish.
Result: Aditoprime demonstrated broad antibacterial activity comparable to trimethoprim, with MIC or MIC₅₀ values ≤ 4 μg/mL against multiple Gram-negative and Gram-positive pathogens[1].
In vivo
Method: Aditoprime was administered intramuscularly at doses of 10–40 mg/kg body weight in swine infected with Streptococcus, and pharmacokinetic parameters were evaluated across pigs, calves, monkeys, and sheep.
Result: Aditoprime showed longer elimination half-lives (3.3–14.8 h), larger distribution volumes (4.6–10.4 L/kg), and effectively treated swine streptococcosis at 10–40 mg/kg.[1]
SynonymsAditoprime, Aditoprim
Chemical Properties
Molecular Weight303.36
FormulaC15H21N5O2
Cas No.56066-63-8
SmilesN=1C=C(C(=NC1N)N)CC2=CC(OC)=C(C(OC)=C2)N(C)C
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (263.71 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.2964 mL16.4821 mL32.9641 mL164.8207 mL
5 mM0.6593 mL3.2964 mL6.5928 mL32.9641 mL
10 mM0.3296 mL1.6482 mL3.2964 mL16.4821 mL
20 mM0.1648 mL0.8241 mL1.6482 mL8.2410 mL
50 mM0.0659 mL0.3296 mL0.6593 mL3.2964 mL
100 mM0.0330 mL0.1648 mL0.3296 mL1.6482 mL

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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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%
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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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