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Argifin

Catalog No. TP2140 Copy Product Info
Purity: 99.86%
🥰Excellent
Argifin is a chitinase inhibitor produced by the metabolism of soil microorganisms, with inhibitory activity at the sub-nanomolar level; its IC50 values against Serratia marcescens chitinase A and B, Aspergillus fumigatus chitinase B1 and human chitotriosidase are 0.025 μM, 6.4 μM, 1.1 μM and 4.5 μM, respectively [1].

Argifin

Copy Product Info
🥰Excellent
Catalog No. TP2140

Argifin is a chitinase inhibitor produced by the metabolism of soil microorganisms, with inhibitory activity at the sub-nanomolar level; its IC50 values against Serratia marcescens chitinase A and B, Aspergillus fumigatus chitinase B1 and human chitotriosidase are 0.025 μM, 6.4 μM, 1.1 μM and 4.5 μM, respectively [1].

Argifin
Cas No. 243975-37-3
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$98-In Stock
5 mg$277-In Stock
10 mg$428-In Stock
25 mg$698-In Stock
50 mg$968-In Stock
100 mg$1,280-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.86%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Argifin is a chitinase inhibitor produced by the metabolism of soil microorganisms, with inhibitory activity at the sub-nanomolar level; its IC50 values against Serratia marcescens chitinase A and B, Aspergillus fumigatus chitinase B1 and human chitotriosidase are 0.025 μM, 6.4 μM, 1.1 μM and 4.5 μM, respectively [1].
Targets&IC50
SmChiB:6.4 μM , Chitotriosidase (human):4.5 μM , Chitinase B1 (aspergillus fumigatus):1.1 μM , SmChiA:0.025 μM , SmChiA:0.025 μM, SmChiB:6.4 μM, Chitinase B1 (aspergillus fumigatus):1.1 μM, Chitotriosidase (human):4.5 μM
In vitro
Methods: The inhibitory activity of Argifin against L. cuprina chitinase was determined at 37 °C and 20 °C.
Results: Argifin inhibited L. cuprina chitinase, with an IC₅₀ of 3.7 μM at 37 °C and 0.10 μM at 20 °C[1].
In vivo
Methods: L. cuprina was treated with Argifin.
Results: Argifin exhibited inhibitory effects on the ecdysis of L. cuprina[1].
Chemical Properties
Molecular Weight675.70
FormulaC29H41N9O10
Cas No.243975-37-3
SmilesC([C@@H]1N(C)C(=O)[C@H](CCCNC(NC(NC)=O)=N)NC(=O)[C@@H](C)NC(=O)C[C@@H](C(O)=O)NC(=O)C[C@@H](C(O)=O)NC1=O)C2=CC=CC=C2
Relative Density.1.49 g/cm3 (Predicted)
SequenceCyclo({d-Ala}-{N5-[imino[[(methylamino)carbonyl]amino]methyl]-L-ornithyl}-{Phe(Me)}-{Bas}-{Bas})
Sequence ShortCyclo({d-Ala}-{N5-[imino[[(methylamino)carbonyl]amino]methyl]-L-ornithyl}-{Phe(Me)}-{Bas}-{Bas})
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: 80.00 mg/mL (118.40 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.4799 mL7.3997 mL14.7995 mL73.9973 mL
5 mM0.2960 mL1.4799 mL2.9599 mL14.7995 mL
10 mM0.1480 mL0.7400 mL1.4799 mL7.3997 mL
20 mM0.0740 mL0.3700 mL0.7400 mL3.6999 mL
50 mM0.0296 mL0.1480 mL0.2960 mL1.4799 mL
100 mM0.0148 mL0.0740 mL0.1480 mL0.7400 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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
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μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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