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Secnidazole

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Catalog No. T0195Cas No. 3366-95-8
Alias RP-14539, PM-185184

Secnidazole (PM-185184) is a second-generation 5-nitroimidazole antimicrobial that is structurally related to other 5-nitroimidazoles including [DB00916] and [DB00911], but displays improved oral absorption and longer terminal elimination half-life than antimicrobial agents in this class [A27210]. Secnidazole is selective against many anaerobic Gram-positive and Gram-negative bacteria and protozoa.

Secnidazole

Secnidazole

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🥰Excellent
Purity: 98.86%
Catalog No. T0195Alias RP-14539, PM-185184Cas No. 3366-95-8
Secnidazole (PM-185184) is a second-generation 5-nitroimidazole antimicrobial that is structurally related to other 5-nitroimidazoles including [DB00916] and [DB00911], but displays improved oral absorption and longer terminal elimination half-life than antimicrobial agents in this class [A27210]. Secnidazole is selective against many anaerobic Gram-positive and Gram-negative bacteria and protozoa.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$34In StockIn Stock
10 mg$50In StockIn Stock
25 mg$58In StockIn Stock
50 mg$90In StockIn Stock
100 mg$108In StockIn Stock
200 mg$129In StockIn Stock
500 mg$156In StockIn Stock
1 mL x 10 mM (in DMSO)$42In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.86%
Appearance:Solid
Color:White
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Product Introduction

Secnidazole AI Summary
Secnidazole exhibits a broad range of biological activities with potential therapeutic applications. It shows antitrichomonas activity against Trichomonas vaginalis TVR87 with an IC50 of 810.0 nM and a high specificity index, indicating minimal cytotoxicity to human THP1 cells. It has no mutagenic effects in Salmonella Typhimurium YG1042 and TA100 strains. The compound acts as an inhibitor for various cellular targets and pathways, including ERK signaling, malarial parasite plastid delayed death, HCV replication, TDP-43, MBNL1-poly(CUG) RNA binding, and Ebola virus entry. It also inhibits N-terminal His-tagged Escherichia coli FabH with an IC50 of 28500.0 nM and shows low toxicity in erythrocytes. Secnidazole demonstrates potent inhibition of OATP1B3 and OATP1B1 transporters. Additionally, the compound exhibits cytotoxicity against several cell types and inhibits the proliferation of a range of pathogens, including Giardia intestinalis and Bacteroides fragilis with a MIC of 800.0 nM. It has antiparasitic activity against human African trypanosomiasis and shows antifungal and antibacterial properties against pathogens such as Candida albicans and Cryptococcus neoformans. The compound also demonstrates antiviral activity against SARS-CoV-2 by reducing cytotoxicity in various cell models, although its effectiveness varies depending on the assay conditions. Secnidazole inhibits human HDAC6 enzyme activity and shows antigiardial activity against Giardia intestinalis with an IC50 of 4410.0 nM. Collectively, these findings suggest that Secnidazole has diverse bioactivities with potential implications for treating multiple diseases, including infections caused by viruses, bacteria, fungi, parasites, and certain human cell pathologies..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Secnidazole (PM-185184) is a second-generation 5-nitroimidazole antimicrobial that is structurally related to other 5-nitroimidazoles including [DB00916] and [DB00911], but displays improved oral absorption and longer terminal elimination half-life than antimicrobial agents in this class [A27210]. Secnidazole is selective against many anaerobic Gram-positive and Gram-negative bacteria and protozoa.
SynonymsRP-14539, PM-185184
Chemical Properties
Molecular Weight185.18
FormulaC7H11N3O3
Cas No.3366-95-8
SmilesCC(O)CN1C(C)=NC=C1[N+]([O-])=O
Relative Density.1.39g/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
H2O: 34 mg/mL (183.61 mM), Sonication is recommended.
Ethanol: 35 mg/mL (189.01 mM), Sonication is recommended.
DMSO: 60 mg/mL (324.01 mM), Sonication is recommended.
Solution Preparation Table
H2O/Ethanol/DMSO
1mg5mg10mg50mg
1 mM5.4002 mL27.0008 mL54.0015 mL270.0076 mL
5 mM1.0800 mL5.4002 mL10.8003 mL54.0015 mL
10 mM0.5400 mL2.7001 mL5.4002 mL27.0008 mL
20 mM0.2700 mL1.3500 mL2.7001 mL13.5004 mL
50 mM0.1080 mL0.5400 mL1.0800 mL5.4002 mL
100 mM0.0540 mL0.2700 mL0.5400 mL2.7001 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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

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