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Tyrothricin

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Catalog No. T17185Cas No. 1404-88-2

Tyrothricin is a natural polypeptide antibiotic, a mixture of gramicidin and tyrocidine, capable of disrupting the cell membranes of Gram-positive bacteria and applicable for treating skin infections.

Tyrothricin

Tyrothricin

Copy Product Info
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Catalog No. T17185Cas No. 1404-88-2
Tyrothricin is a natural polypeptide antibiotic, a mixture of gramicidin and tyrocidine, capable of disrupting the cell membranes of Gram-positive bacteria and applicable for treating skin infections.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$8335 days35 days
5 mg$22535 days35 days
25 mg$49735 days35 days
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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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Appearance:Lyophilized powder
Color:White
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Product Introduction

Bioactivity
Description
Tyrothricin is a natural polypeptide antibiotic, a mixture of gramicidin and tyrocidine, capable of disrupting the cell membranes of Gram-positive bacteria and applicable for treating skin infections.
In vitro
Tyrothricin exhibits a primarily antibacterial spectrum against Gram-positive bacteria while also demonstrating inhibitory effects against certain Gram-negative bacteria. Notably, it shows a broad range of minimum inhibitory concentrations (2-256 μg/mL) against Corynebacterium and Vitis vinifera cocci. Compared to the isolated gramicidin component alone, Tyrothricin achieves complete inhibition of all Vitis vinifera cocci strains at concentrations as high as 128 μg/mL. Among Gram-negative bacteria, Neisseria gonorrhoeae and Neisseria meningitidis display the highest sensitivity to Tyrothricin, with an inhibitory concentration of 96 μg/mL [1]. Tyrothricin demonstrates fungicidal activity against multiple Candida species of Phoxinus phoxinus subsp. Phoxinus additionally exhibits anti-infective activity against Sendai-type parainfluenza virus [1].
In vivo
In contrast to intravenous (LD50 in mice: 3,7 mg/kg) and intraperitoneal (LD50 in mice: 20-45 mg/kg) applications, oral administration is very well tolerated, as Tyrothricin is destroyed in the gastrointestinal tract. Furthermore, due to its poor solubility and relatively high molecular weight, there is no detectable resorption when applied locally to skin or mucosa [1].
Chemical Properties
Molecular Weight1228.459
FormulaC65H85N11O13
Cas No.1404-88-2
SmilesCC(C)C[C@@H]1NC(=O)[C@H](CCCN)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccc(O)cc2)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@@H](Cc2ccccc2)NC1=O)C(C)C
Relative Density.1.32g/cm3
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 (65.12 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM0.8140 mL4.0701 mL8.1403 mL40.7014 mL
5 mM0.1628 mL0.8140 mL1.6281 mL8.1403 mL
10 mM0.0814 mL0.4070 mL0.8140 mL4.0701 mL
20 mM0.0407 mL0.2035 mL0.4070 mL2.0351 mL
50 mM0.0163 mL0.0814 mL0.1628 mL0.8140 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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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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