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o-Phenanthroline

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Catalog No. T5983Cas No. 66-71-7
Alias 1,10-Phenanthroline

o-Phenanthroline (1,10-Phenanthroline) , a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells.o-Phenanthroline protects mammalian cells from hydrogen peroxide-induced gene mutation and morphological transformation.

o-Phenanthroline

o-Phenanthroline

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Purity: 98.85%
Catalog No. T5983Alias 1,10-PhenanthrolineCas No. 66-71-7
o-Phenanthroline (1,10-Phenanthroline) , a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells.o-Phenanthroline protects mammalian cells from hydrogen peroxide-induced gene mutation and morphological transformation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 mg$31In StockIn Stock
100 mg$44In StockIn Stock
500 mg$66-In Stock
1 g$86-In Stock
1 mL x 10 mM (in DMSO)$48In StockIn 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:98.85%
Appearance:Solid
Color:White
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Product Introduction

o-Phenanthroline AI Summary
o-Phenanthroline exhibits a wide spectrum of bioactivities, including inhibitory effects on human farnesyltransferase with an IC50 of 4,000,000 nM, indicating its potential role in interfering with the farnesylation process. It demonstrates cytotoxic activity against both cisplatin-sensitive and -resistant A2780 ovarian cancer cell lines, with IC50 values of 3660.0 nM and 2730.0 nM, respectively. The compound inhibits N8-Acetylspermidine deacetylase from rat liver cytosol (Ki = 1,300,000 nM) and shows antibacterial activity against E. coli, P. aeruginosa, and S. aureus (MIC = 32.0 µg/mL). Additionally, o-Phenanthroline inhibits Chryseobacterium indologenes metallo-beta-lactamase (Ki = 7300.0 nM) and Pseudomonas aeruginosa VIM-1 and VIM-13 beta-lactamases with IC50 values of 73000.0 nM and 69300.0 nM, respectively. The compound demonstrates antimycobacterial activity against Mycobacterium smegmatis and varied inhibition of fungal, viral, and bacterial enzymes, including anthrax lethal factor and multiple matrix metalloproteinases. It inhibits acrAB AcrAB-TolC-mediated Nile Red efflux in E. coli and shows allosteric modulation at CCR8, CCR5, and CCR1 receptors. Moreover, o-Phenanthroline inhibits beta-lactamases in various bacterial strains, including NDM1, VIM2, and IMP1, and shows chelating activity that inhibits Clostridium botulinum enzyme activity (>95%). It also exhibits anti-tachyzoite activity against Toxoplasma gondii, with ED50 values of 2.01 µM and 2.28 µM after 72 and 96 hours, respectively, and a CC50 value of 70200.0 nM against NHDF cells, resulting in a selectivity index of 31.0. o-Phenanthroline possesses inhibitory potential against a variety of biological targets, making it a promising candidate for further pharmacological exploration..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
o-Phenanthroline (1,10-Phenanthroline) , a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells.o-Phenanthroline protects mammalian cells from hydrogen peroxide-induced gene mutation and morphological transformation.
Synonyms1,10-Phenanthroline
Chemical Properties
Molecular Weight180.21
FormulaC12H8N2
Cas No.66-71-7
Smilesc1cnc2c(c1)ccc1cccnc21
Relative Density.1.25 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 250 mg/mL (1387.27 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween-80+45% Saline: 2 mg/mL (11.1 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
DMSO
1mg5mg10mg50mg
1 mM5.5491 mL27.7454 mL55.4908 mL277.4541 mL
5 mM1.1098 mL5.5491 mL11.0982 mL55.4908 mL
10 mM0.5549 mL2.7745 mL5.5491 mL27.7454 mL
20 mM0.2775 mL1.3873 mL2.7745 mL13.8727 mL
50 mM0.1110 mL0.5549 mL1.1098 mL5.5491 mL
100 mM0.0555 mL0.2775 mL0.5549 mL2.7745 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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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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