Indoxacarb
Based on 1 publication(s) in Google Scholar
Indoxacarb ((S)-DPX-JW062) is an orally active Insecticide, Voltage-dependent sodium channel blocker, and Nicotinic acetylcholine receptor modulator. Indoxacarb induces HSP70, modulates hepatic IGF-I/IGF-II, induces oxidative stress/ROS, inhibits oxidative phosphorylation, and triggers Autophagy/Apoptosis. Indoxacarb impairs neurological function and impedes nerve excitation. Indoxacarb has been widely used for the control of agricultural and forestry pests, showing significant control efficacy against Homoptera, Coleoptera, and especially Lepidoptera insects.
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- Pureté : 98.08%
- CAS No.: 173584-44-6
- Formule: C22H17ClF3N3O7
- Masse moléculaire:527.83
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Stockage:
-20°C, stored under nitrogen, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen, away from moisture)
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Activité biologique
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Chemical Information
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Solvant et solubilité
- Protocole
- Pureté et documentation
- Références
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Help & FAQs
Publications Citing Use of MedChemExpress (MCE) Indoxacarb
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Activité biologique
Description
In Vivo
Indoxacarb (2-4 mg/kg; oral; once daily; 90 days) combined with LPS potentiates endotoxin-induced immunotoxicity and DNA damage in Swiss albino mice with endotoxemia, as shown by lymphocytopenia and increased comet tail parameters[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Swiss albino (male, 8-10 weeks old)[1]
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Dosage:4 mg/kg/day; 2 mg/kg/day
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Administration:p.o.; once daily; 90 days
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Result:TLC was 2.34 ×10^3 with indoxacarb 4 mg/kg and 2.85 ×10^3 with indoxacarb 2 mg/kg.
Neutrophils were 46.8% with indoxacarb 4 mg/kg and 32.6% with indoxacarb 2 mg/kg.
Lymphocytes were 47.2% with indoxacarb 4 mg/kg and 56.2% with indoxacarb 2 mg/kg.
Tail length was 28.80 µm with indoxacarb 4 mg/kg and 19.36 µm with indoxacarb 2 mg/kg.
Tail moment was 10.23 with indoxacarb 4 mg/kg and 8.43 with indoxacarb 2 mg/kg.
Olive moment was 7.38 with indoxacarb 4 mg/kg and 5.93 with indoxacarb 2 mg/kg.
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Animal Model:Swiss albino (male, 8-10 weeks old)[1]
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Dosage:4 mg/kg/day; 2 mg/kg/day
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Administration:p.o.; once daily; 90 days
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Result:TLC was 4.96 ×10^3 with indoxacarb 4 mg/kg plus LPS, 4.20 ×10^3 with indoxacarb 2 mg/kg plus LPS, 6.94 ×10^3 with LPS alone, 2.34 ×10^3 with indoxacarb 4 mg/kg alone, and 2.85 ×10^3 with indoxacarb 2 mg/kg alone.
Neutrophils were 61.8% with indoxacarb 4 mg/kg plus LPS and 52.8% with indoxacarb 2 mg/kg plus LPS.
Lymphocytes were 33.2% with indoxacarb 4 mg/kg plus LPS and 44.4% with indoxacarb 2 mg/kg plus LPS.
Tail length was 43.29 µm with indoxacarb 4 mg/kg plus LPS and 38.36 µm with indoxacarb 2 mg/kg plus LPS.
Tail moment was 28.48 with indoxacarb 4 mg/kg plus LPS and 22.83 with indoxacarb 2 mg/kg plus LPS.
Olive moment was 14.95 with indoxacarb 4 mg/kg plus LPS and 13.97 with indoxacarb 2 mg/kg plus LPS.
- Kinase activity and phosphorylation assays
- Western Blot
- Detection of Apoptosis
- TUNEL staining for apoptotic DNA fragmentation
- Annexin V plus membrane-impermeant dye apoptosis staining
- ROS/oxidative-stress fluorescent staining
- Autophagy
- Apoptosis Solutions
- Protocol for Kinase activity and phosphorylation assays
- Lysosome and acidic-vesicle live-cell staining
- Macroautophagy Solutions
Chemical Information
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CAS No. 173584-44-6
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Appearance Powder
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Masse moléculaire 527.83
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Formule C22H17ClF3N3O7
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Color White to off-white
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SMILES
COC([C@@]12C(C3=CC=C(Cl)C=C3C1)=NN(CO2)C(N(C4=CC=C(C=C4)OC(F)(F)F)C(OC)=O)=O)=O
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Synonyms
(S)-DPX-JW062
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
-20°C, stored under nitrogen, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen, away from moisture)
Publications (1)
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Journal Impact Factor
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Most Recent
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Insect Sci
Genetic and pharmacological inhibition of the Kir2A channel in diamondback moth exhibits ovicidal activity. [Abstract]2026 May 11. PMID: 42116718
Solvant et solubilité
In Vitro:
DMSO : 100 mg/mL (189.45 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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 (stored under nitrogen, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
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 (stored under nitrogen, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
In Vivo:
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (4.74 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL. * In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen, away from moisture)
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Pureté et documentation
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Fiche technique (299 KB)
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SDS (789 KB)
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Instruction de manipulation (2659 KB)
Références
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 (stored under nitrogen, away from moisture). 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 | 1.8945 mL | 9.4727 mL | 18.9455 mL | 47.3637 mL |
| 5 mM | 0.3789 mL | 1.8945 mL | 3.7891 mL | 9.4727 mL | |
| 10 mM | 0.1895 mL | 0.9473 mL | 1.8945 mL | 4.7364 mL | |
| 15 mM | 0.1263 mL | 0.6315 mL | 1.2630 mL | 3.1576 mL | |
| 20 mM | 0.0947 mL | 0.4736 mL | 0.9473 mL | 2.3682 mL | |
| 25 mM | 0.0758 mL | 0.3789 mL | 0.7578 mL | 1.8945 mL | |
| 30 mM | 0.0632 mL | 0.3158 mL | 0.6315 mL | 1.5788 mL | |
| 40 mM | 0.0474 mL | 0.2368 mL | 0.4736 mL | 1.1841 mL | |
| 50 mM | 0.0379 mL | 0.1895 mL | 0.3789 mL | 0.9473 mL | |
| 60 mM | 0.0316 mL | 0.1579 mL | 0.3158 mL | 0.7894 mL | |
| 80 mM | 0.0237 mL | 0.1184 mL | 0.2368 mL | 0.5920 mL | |
| 100 mM | 0.0189 mL | 0.0947 mL | 0.1895 mL | 0.4736 mL |
Indoxacarb Related Classifications
HY-117146 Related Classifications
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Keywords
- Indoxacarb
- 173584-44-6
- (S)-DPX-JW062
- Insecticide
- Sodium Channel
- nAChR
- HSP
- IGF-1R
- Reactive Oxygen Species (ROS)
- Autophagy
- Apoptosis
- Oxidative Phosphorylation
- DCJW
- amidase
- esterase
- nerve excitation
- nerve function
- nicotinic acetylcholine receptor modulator
- sodium channels
- sodium ion flow
- sodium-channel blocker
- voltage-dependent sodium channel blocker
- Inhibitor
- inhibitor
- inhibit