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Cycloheximide

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Catalog No. T1225Cas No. 66-81-9
Alias Naramycin A, CHX, Actidione

Cycloheximide (Naramycin A) is a natural product . Cycloheximide‘s IC50 values for protein synthesis and RNA synthesis in vivo are 532.5 nM and 2880 nM, respectively. Cycloheximide inhibits ferroptosis and autophagy and is an antifungal antibiotic.

Cycloheximide

Cycloheximide

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Purity: 99.95%
Catalog No. T1225Alias Naramycin A, CHX, ActidioneCas No. 66-81-9
Cycloheximide (Naramycin A) is a natural product . Cycloheximide‘s IC50 values for protein synthesis and RNA synthesis in vivo are 532.5 nM and 2880 nM, respectively. Cycloheximide inhibits ferroptosis and autophagy and is an antifungal antibiotic.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
200 mg$71In StockIn Stock
500 mg$142-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.95%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Cycloheximide (Naramycin A) is a natural product . Cycloheximide‘s IC50 values for protein synthesis and RNA synthesis in vivo are 532.5 nM and 2880 nM, respectively. Cycloheximide inhibits ferroptosis and autophagy and is an antifungal antibiotic.
Targets&IC50
Plasmodium falciparum:150 nM, HeLa cells:532.5 nM (human), RNA synthesis:2880 nM, Vero cells (Kidney cells):530 nM, CEM (T-cell leukemia):120 nM, Protein biosynthesis:532.5 nM., Saccharomyces cerevisiae:7420 nM
In vitro
METHODS: Three different tumor cell lines, HeLa, MDA-MB231 and Jurkat T cells, were incubated with Cycloheximide (2.5 µM) for 24 hours. The inhibitory effects of the compounds on translation and transcription were detected by metabolic labeling.
RESULTS: The IC50 values of Cycloheximide for protein synthesis and RNA synthesis in vivo were 532.5 nM and 2880 nM, respectively. [1]
In vivo
METHODS: To investigate the effect of Cycloheximide on the latency of the memory test in mice, 30, 60 or 120 mg/kg of Cycloheximide was injected before training with 200 μA electric shock.
RESULTS: Cycloheximide has a significant effect on the latency of the memory test. In the control group, the delay time of the test was significantly higher than that of the training. The test of the lowest dose of Cycloheximide, namely 30 mg/kg, resulted in a significantly higher latency of the test than that of the control group. After receiving two higher doses of Cycloheximide, the performance of either mouse in the experiment was comparable to that of the control group, and the higher doses did not impair memory under these conditions, thus forming an inverted U-shaped dose-response curve. [2]
SynonymsNaramycin A, CHX, Actidione
Chemical Properties
Molecular Weight281.35
FormulaC15H23NO4
Cas No.66-81-9
Smiles[C@H](CC1CC(=O)NC(=O)C1)(O)[C@]2(C(=O)[C@@H](C)C[C@H](C)C2)[H]
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 260 mg/mL (924.12 mM), Sonication is recommended.
H2O: 20 mg/mL (71.09 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (17.77 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 mM3.5543 mL17.7715 mL35.5429 mL177.7146 mL
5 mM0.7109 mL3.5543 mL7.1086 mL35.5429 mL
10 mM0.3554 mL1.7771 mL3.5543 mL17.7715 mL
20 mM0.1777 mL0.8886 mL1.7771 mL8.8857 mL
50 mM0.0711 mL0.3554 mL0.7109 mL3.5543 mL
DMSO
1mg5mg10mg50mg
100 mM0.0355 mL0.1777 mL0.3554 mL1.7771 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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%
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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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