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2-Thenoyltrifluoroacetone (Synonyms: TTFA, TTA, HTTA)

Catalog No. Fr13361 Copy Product Info
Purity: 97.96%
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2-Thenoyltrifluoroacetone (TTFA) is a specific inhibitor of mitochondrial respiratory chain complex II (SQR/SDH) with an IC₅₀ value of 51.5 μM. 2-Thenoyltrifluoroacetone can complex with various metal ions and exhibits cytotoxic and antitumor activity. It possesses anti-Mycobacterium tuberculosis activity and can inhibit the growth of Mycobacterium tuberculosis. 2-Thenoyltrifluoroacetone can be used in mechanistic studies of diseases associated with mitochondrial dysfunction.

2-Thenoyltrifluoroacetone

Copy Product Info
🥰Excellent
Catalog No. Fr13361
Synonyms TTFA, TTA, HTTA

2-Thenoyltrifluoroacetone (TTFA) is a specific inhibitor of mitochondrial respiratory chain complex II (SQR/SDH) with an IC₅₀ value of 51.5 μM. 2-Thenoyltrifluoroacetone can complex with various metal ions and exhibits cytotoxic and antitumor activity. It possesses anti-Mycobacterium tuberculosis activity and can inhibit the growth of Mycobacterium tuberculosis. 2-Thenoyltrifluoroacetone can be used in mechanistic studies of diseases associated with mitochondrial dysfunction.

2-Thenoyltrifluoroacetone
Cas No. 326-91-0
Pack SizePriceUSA StockGlobal StockQuantity
10 mg$29-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:97.96%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
2-Thenoyltrifluoroacetone (TTFA) is a specific inhibitor of mitochondrial respiratory chain complex II (SQR/SDH) with an IC₅₀ value of 51.5 μM. 2-Thenoyltrifluoroacetone can complex with various metal ions and exhibits cytotoxic and antitumor activity. It possesses anti-Mycobacterium tuberculosis activity and can inhibit the growth of Mycobacterium tuberculosis. 2-Thenoyltrifluoroacetone can be used in mechanistic studies of diseases associated with mitochondrial dysfunction.
Targets&IC50
Mitochondrial respiratory chain complex II/SDH/SQR:51.5 μM
In vitro
Methods: RTH-149 rainbow trout liver cell lines stably transfected with KFERQ-PA-mCherry1 were treated with 10 μM 2-Thenoyltrifluoroacetone and 25 mM high glucose for 16 hours, and CMA puncta were counted using fluorescence microscopy.
Results: Treatment with 2-thenoil-trifluoroacetone blocked the activity of complex II of the mitochondrial electron transport chain and prevented high-glucose-induced CMA puncta formation. [1]
Methods: TET21N, SK-N-BE(2), SH-SY5Y neuroblastoma cells, and U1810 lung cancer cells were treated with 100 μM 2-thienoyltrifluoroacetone and 5 μg/mL cisplatin for 24 hours, and Western blot analysis was performed to detect the levels of cleaved caspase-3 and cleaved PARP.
Results: Under normoxic conditions, 2-Thenoyltrifluoroacetone significantly enhanced cisplatin-induced apoptosis, with a significant increase in the expression of caspase-3 and cleaved PARP. [2]
Methods: PC12 rat pheochromocytoma cells were treated with 10 μM 2-Thenoyltrifluoroacetone and 1 μM rotenone for 24 hours, and intracellular H₂O₂ levels were detected using H₂DCFDA fluorescence staining.
Results: 2-Thienoyltrifluoroacetone significantly reduced the H₂O₂ production induced by rotenone. [3]
SynonymsTTFA, TTA, HTTA
Chemical Properties
Molecular Weight222.18
FormulaC8H5F3O2S
Cas No.326-91-0
SmilesO=C(C=1SC=CC1)CC(=O)C(F)(F)F
Relative Density.1.4373 g/cm3 (Estimated)
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 mg/mL (360.07 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.5009 mL22.5043 mL45.0086 mL225.0428 mL
5 mM0.9002 mL4.5009 mL9.0017 mL45.0086 mL
10 mM0.4501 mL2.2504 mL4.5009 mL22.5043 mL
20 mM0.2250 mL1.1252 mL2.2504 mL11.2521 mL
50 mM0.0900 mL0.4501 mL0.9002 mL4.5009 mL
100 mM0.0450 mL0.2250 mL0.4501 mL2.2504 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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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.
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