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Prochloraz

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Catalog No. T20625Cas No. 67747-09-5
Alias Sporgon, Prelude

Prochloraz (Prelude) is a broad-spectrum contact imidazole fungicide. Prochloraz inhibits human placental microsomal aromatase in vitro (IC50 = 40 nM). Prochloraz also acts as an estrogen receptor (IC50s = 25 μM) and androgen receptor (IC50 = 4 μM) antagonist, and activates aryl hydrocarbon receptors (EC50 = 1 μM).

Prochloraz

Prochloraz

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🥰Excellent
Purity: 99.79%
Catalog No. T20625Alias Sporgon, PreludeCas No. 67747-09-5
Prochloraz (Prelude) is a broad-spectrum contact imidazole fungicide. Prochloraz inhibits human placental microsomal aromatase in vitro (IC50 = 40 nM). Prochloraz also acts as an estrogen receptor (IC50s = 25 μM) and androgen receptor (IC50 = 4 μM) antagonist, and activates aryl hydrocarbon receptors (EC50 = 1 μM).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
200 mg$34In StockIn Stock
1 mL x 10 mM (in DMSO)$45In 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:99.79%
Appearance:Solid
Color:Yellow
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Product Introduction

Prochloraz AI Summary
Prochloraz demonstrates broad-spectrum fungicidal activity against various fungi, including both tebuconazole-adapted and nonadapted wild type Colletotrichum graminicola strains, Fusarium culmorum, Fusarium oxysporum, Macrophomina phaseolina, Oculimacula yallundae, Phytophthora cactorum, Alternaria alternata, Diplodia mutila, Neofusicoccum luteum, Zymoseptoria tritici, and Monilinia laxa. It exhibits potent inhibitory effects on mycelial growth and disease incidence with varying EC50 and MIC values depending on the fungal species and environmental conditions. The compound also affects multiple signaling pathways, acting as an agonist or antagonist for androgen receptor, farnesoid X receptor, thyroid hormone receptor beta, peroxisome proliferator-activated receptor (delta and gamma), estrogen receptor alpha, aryl hydrocarbon receptor (AhR), p53 signaling pathway, antioxidant response element (ARE) signaling pathway, and pregnane X receptor (both rat and human). These bioactivities indicate its potential to interact with diverse biological targets, making it a versatile agent for controlling fungal infections and potentially other applications..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Prochloraz (Prelude) is a broad-spectrum contact imidazole fungicide. Prochloraz inhibits human placental microsomal aromatase in vitro (IC50 = 40 nM). Prochloraz also acts as an estrogen receptor (IC50s = 25 μM) and androgen receptor (IC50 = 4 μM) antagonist, and activates aryl hydrocarbon receptors (EC50 = 1 μM).
Targets&IC50
Antifungal:40 nM, ERR:25 μM, AhR:1 μM(EC50), Androgen receptor:4 μM
SynonymsSporgon, Prelude
Chemical Properties
Molecular Weight376.67
FormulaC15H16Cl3N3O2
Cas No.67747-09-5
SmilesC(N(CCOC1=C(Cl)C=C(Cl)C=C1Cl)CCC)(=O)N2C=CN=C2
Relative Density.1.405 g/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
DMSO: 250 mg/mL (663.71 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (2.65 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 mM2.6548 mL13.2742 mL26.5484 mL132.7422 mL
5 mM0.5310 mL2.6548 mL5.3097 mL26.5484 mL
10 mM0.2655 mL1.3274 mL2.6548 mL13.2742 mL
20 mM0.1327 mL0.6637 mL1.3274 mL6.6371 mL
50 mM0.0531 mL0.2655 mL0.5310 mL2.6548 mL
100 mM0.0265 mL0.1327 mL0.2655 mL1.3274 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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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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