5-Methoxyindole
Based on 1 Customer Validation
5-Methoxyindole is an L-tryptophan metabolite with antifungal activity, and also serves as a pharmaceutical intermediate. Metabolites of 5-Methoxyindole exhibit COX-2 inhibitory, anti-inflammatory and anti-tumor activities. 5-Methoxyindole induces morphological distortion of hyphae and conidia, ROS accumulation, apoptosis and cell death in Gaeumannomyces graminis. 5-Methoxyindole can be used in studies related to fungal infections and organic synthesis.
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- Pureté: 99.92%
- CAS No.: 1006-94-6
- Formule: C9H9NO
- Masse moléculaire:147.18
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Stockage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Activité biologique
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Chemical Information
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Solvant et solubilité
- Pureté et documentation
- Références
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Help & FAQs
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HY-W001160
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3,3'-Diindolylmethane
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HY-W015229
3-Indolepropionic acid
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3-Indoleacetic acid,suitable for plant cell culture
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HY-18569R
3-Indoleacetic acid (standard)
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HY-W001160R
5-Hydroxyindole (Standard)
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HY-Y0136
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HY-W015229R
3-Indolepropionic acid (Standard)
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3-Indoleacetonitrile (Standard)
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Activité biologique
5-Methoxyindole is a metabolite of L-tryptophan that regulates the expression of COX-2 at the transcriptional level, and its derivatives exhibit COX-2 inhibitory, anti-inflammatory and anti-tumor activities[1].
5-Methoxyindole (0.1-4 mM; 1-3 days) potently inhibits colony growth of Fusarium graminearum PH-1 on PDA, CM and MM media; suppresses its sporulation on CMC medium; potently inhibits conidial germination; modulates the activity of antifungal compounds on CM medium, abolishes the inhibitory effect mediated by H2O2, and enhances the inhibitory effects mediated by Congo Red (HY-D0236) and CFW[2].
5-Methoxyindole (0.1-1 mM; 3 days) induces morphological malformation (swelling) of hyphae (1 mM) and conidia (0.1 mM) in Fusarium graminearum PH-1[2].
5-Methoxyindole (0.1 mM; 2-5 h) induces significant reactive oxygen species accumulation in hyphae and conidia of Fusarium graminearum PH-1, and downregulates the expression of extracellular ROS-scavenging enzyme genes[2].
5-Methoxyindole (0.1 mM; 3 days) induces apoptosis and death in hyphae and conidia of Fusarium graminearum PH-1[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 1006-94-6
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Appearance Solid
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Masse moléculaire 147.18
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Formule C9H9NO
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Color White to yellow
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SMILES
COC1=CC2=C(NC=C2)C=C1
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Solvant et solubilité
DMSO : 100 mg/mL (679.44 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. 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. 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)
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 (16.99 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.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (16.99 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 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
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.
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 (286 KB)
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SDS (394 KB)
- English - EN (394 KB)
- Français - FR (394 KB)
- Deutsch - DE (394 KB)
- Norwegian - NO (394 KB)
- Español - ES (394 KB)
- Swedish - SV (394 KB)
- Italian - IT (394 KB)
- Korean - KR (394 KB)
- Portuguese - PT (394 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. 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 | 6.7944 mL | 33.9720 mL | 67.9440 mL | 169.8600 mL |
| 5 mM | 1.3589 mL | 6.7944 mL | 13.5888 mL | 33.9720 mL | |
| 10 mM | 0.6794 mL | 3.3972 mL | 6.7944 mL | 16.9860 mL | |
| 15 mM | 0.4530 mL | 2.2648 mL | 4.5296 mL | 11.3240 mL | |
| 20 mM | 0.3397 mL | 1.6986 mL | 3.3972 mL | 8.4930 mL | |
| 25 mM | 0.2718 mL | 1.3589 mL | 2.7178 mL | 6.7944 mL | |
| 30 mM | 0.2265 mL | 1.1324 mL | 2.2648 mL | 5.6620 mL | |
| 40 mM | 0.1699 mL | 0.8493 mL | 1.6986 mL | 4.2465 mL | |
| 50 mM | 0.1359 mL | 0.6794 mL | 1.3589 mL | 3.3972 mL | |
| 60 mM | 0.1132 mL | 0.5662 mL | 1.1324 mL | 2.8310 mL | |
| 80 mM | 0.0849 mL | 0.4247 mL | 0.8493 mL | 2.1233 mL | |
| 100 mM | 0.0679 mL | 0.3397 mL | 0.6794 mL | 1.6986 mL |
5-Methoxyindole Related Classifications
HY-W007328 Related Classifications
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