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SDH-IN-25

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Catalog No. T206959Cas No. 3052432-15-9

SDH-IN-25 is an SDH inhibitor with an IC50 of 4.82 mg/L, demonstrating broad-spectrum and potent antifungal activity. By binding to SDH amino acid residues (TRP173, TYR58, and ARG43), it mimics the action mode of the commercial fungicide flutolanil. SDH-IN-25 induces changes in hyphal morphology, disrupts respiratory metabolism by binding to complex II, generates reactive oxygen species (ROS), and affects mitochondrial membrane potential (MMP) in hyphae. This compound is utilized in agricultural disease control research.

SDH-IN-25

SDH-IN-25

😃Good
Catalog No. T206959Cas No. 3052432-15-9
SDH-IN-25 is an SDH inhibitor with an IC50 of 4.82 mg/L, demonstrating broad-spectrum and potent antifungal activity. By binding to SDH amino acid residues (TRP173, TYR58, and ARG43), it mimics the action mode of the commercial fungicide flutolanil. SDH-IN-25 induces changes in hyphal morphology, disrupts respiratory metabolism by binding to complex II, generates reactive oxygen species (ROS), and affects mitochondrial membrane potential (MMP) in hyphae. This compound is utilized in agricultural disease control research.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
SDH-IN-25 is an SDH inhibitor with an IC50 of 4.82 mg/L, demonstrating broad-spectrum and potent antifungal activity. By binding to SDH amino acid residues (TRP173, TYR58, and ARG43), it mimics the action mode of the commercial fungicide flutolanil. SDH-IN-25 induces changes in hyphal morphology, disrupts respiratory metabolism by binding to complex II, generates reactive oxygen species (ROS), and affects mitochondrial membrane potential (MMP) in hyphae. This compound is utilized in agricultural disease control research.
In vitro
SDH-IN-25 (Compound 7IIj) demonstrates exceptional broad-spectrum fungicidal activity against eight plant pathogenic strains, including R. solani (EC 50 = 0.179 mg/L), P. piricola (EC 50 = 0.301 mg/L), S. sclerotiorum (EC 50 = 3.47 mg/L), V. mali (EC 50 = 0.789 mg/L), F. graminearum (EC 50 = 6.29 mg/L), B. cinerea (EC 50 = 0.647 mg/L), P. capsici (EC 50 = 5.78 mg/L), and G. graminis (EC 50 = 0.549 mg/L). At concentrations of 5-20 mg/L for durations of 1-9 hours, SDH-IN-25 can inhibit the respiratory metabolism of R. solani. Additionally, at 0-20 mg/L for 2 days, SDH-IN-25 shows outstanding SDH inhibitory activity against R. solani, with an IC 50 value of 4.82 mg/L.
In vivo
SDH-IN-25 (Compound 7IIj) at a concentration of 200 mg/L for 24 hours exhibits significant protective effects on apple twigs infected with V. mali, achieving a 69.7% control rate. When applied at 100 mg/L for 10 minutes, SDH-IN-25 shows marked efficacy against rice leaves and plants infected with rice blast fungus, with control effects of 88.7% and 69.8%, respectively, and has confirmed safety for rice. At a concentration of 1 mg/L for 72 hours, SDH-IN-25 causes abnormal growth in R. solani mycelia, resulting in a dry, collapsed, and wrinkled surface. Additionally, at 0.179 mg/L, it increases ROS levels and disrupts MMP in the mycelia.
Chemical Properties
Molecular Weight486.143
FormulaC19H15BrCl2N2O4
Cas No.3052432-15-9
SmilesO=C1OC(C=2C=C(Cl)C=C(Cl)C2OCC(=O)NNC3=CC=C(Br)C=C3)CC1=C
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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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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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