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  3. Tetradifon

Tetradifon is a broad-spectrum organochlorine insecticide and an inhibitor of the mitochondrial oligomycin sensitivity conferring protein (OSCP), which can be used to control a variety of mites. Tetradifon inhibits energy-related activities such as ADP-stimulated respiration, DNP and Mg2+-stimulated ATPase, with an IC50 of 4.5-27 nmoL/mg mitochondrial protein. Tetradifon exerts oligomycin-like activity by inhibiting the oxidative phosphorylation process, inducing oxidative stress and interfering with bone metabolism. Tetradifon is currently mainly used in the research of mitochondrial function regulation, bone remodeling mechanism and nephrotoxicity of environmental pollutants.

For research use only. We do not sell to patients.

Tetradifon

Tetradifon Chemical Structure

CAS No. : 116-29-0

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Description

Tetradifon is a broad-spectrum organochlorine insecticide and an inhibitor of the mitochondrial oligomycin sensitivity conferring protein (OSCP), which can be used to control a variety of mites. Tetradifon inhibits energy-related activities such as ADP-stimulated respiration, DNP and Mg2+-stimulated ATPase, with an IC50 of 4.5-27 nmoL/mg mitochondrial protein. Tetradifon exerts oligomycin-like activity by inhibiting the oxidative phosphorylation process, inducing oxidative stress and interfering with bone metabolism. Tetradifon is currently mainly used in the research of mitochondrial function regulation, bone remodeling mechanism and nephrotoxicity of environmental pollutants[1][2][3][4][5].

IC50 & Target

Mite

 

In Vitro

Tetradifon has a biological mechanism similar to Oligomycin (HY-N6782) and can be reversed by DNP[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Tetradifon (24.3 mg/kg; oral, 90 days) causes increased trabecular thickness and elevated serum alkaline phosphatase in female rats, and induces glomerular sclerosis and renal interstitial fibrosis in rats[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female Wistar rats (190 g, 8-9 weeks, n=12/group)[3]
Dosage: 2430 mg/kg cumulative (oral in drinking water, 90 days)
Administration: Daily oral gavage, 6 and 12 weeks
Result: At 12 weeks, increased creatinine/urea levels by 24%/43%, increased glomerular sclerosis rate to 22%, and increased interstitial fibrosis index by 200%.
Decreased renal SOD/GPx activities by 32%/17%, and decreased vitamin C content by 31%.
Molecular Weight

356.05

Formula

C12H6Cl4O2S

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=S(C1=C(C=C(C(Cl)=C1)Cl)Cl)(C2=CC=C(C=C2)Cl)=O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : 50 mg/mL (140.43 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.8086 mL 14.0430 mL 28.0859 mL
5 mM 0.5617 mL 2.8086 mL 5.6172 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

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g

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(per animal)

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Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
Purity & Documentation

Purity: 99.71%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.8086 mL 14.0430 mL 28.0859 mL 70.2149 mL
5 mM 0.5617 mL 2.8086 mL 5.6172 mL 14.0430 mL
10 mM 0.2809 mL 1.4043 mL 2.8086 mL 7.0215 mL
15 mM 0.1872 mL 0.9362 mL 1.8724 mL 4.6810 mL
20 mM 0.1404 mL 0.7021 mL 1.4043 mL 3.5107 mL
25 mM 0.1123 mL 0.5617 mL 1.1234 mL 2.8086 mL
30 mM 0.0936 mL 0.4681 mL 0.9362 mL 2.3405 mL
40 mM 0.0702 mL 0.3511 mL 0.7021 mL 1.7554 mL
50 mM 0.0562 mL 0.2809 mL 0.5617 mL 1.4043 mL
60 mM 0.0468 mL 0.2340 mL 0.4681 mL 1.1702 mL
80 mM 0.0351 mL 0.1755 mL 0.3511 mL 0.8777 mL
100 mM 0.0281 mL 0.1404 mL 0.2809 mL 0.7021 mL
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Tetradifon Related Classifications

Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Tetradifon
Cat. No.:
HY-119725
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