Aurachin D
Based on 1 Customer Validation
Aurachin D is an antibiotic and selective cytochrome bd oxidase inhibitor. Aurachin D exhibits inhibitory effects against Gram-positive bacteria and a small number of fungi, with an IC50 value of 0.1 μM against Escherichia coli and an IC50 value ranging from 0.13 to 33 μM against Mycobacterium tuberculosis. Aurachin D binds to and inhibits cytochrome bd oxidase, thereby blocking the electron transfer process, disrupting the respiratory chain and energy metabolism of pathogens. Aurachin D can be used in research related to leishmaniasis, malaria, Chagas disease, African trypanosomiasis, and tuberculosis[2].
Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.
- Pureté: 99.55%
- CAS No.: 108354-13-8
- Formule: C25H33NO
- Masse moléculaire:363.54
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Stockage:Powder -20°C, 3 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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Activité biologique
Description
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| L6 | IC50 |
130.7 μM
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Cytotoxicity against rat skeletal myoblast L6 cells assessed via resazurin dye fluorescence measurement following 3 days of exposure to serial dilutions.
Cytotoxicity against rat skeletal myoblast L6 cells assessed via resazurin dye fluorescence measurement following 3 days of exposure to serial dilutions.
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36770729 |
In Vitro
Aurachin D selectively inhibits Escherichia coli cytochrome bd-II oxidase by binding to the hydrophobic pocket in the AppC subunit, stabilizing the Q-loop, and blocking quinol oxidation at the enzyme active site[2].
Aurachin D (50 nM; 4 min) inhibits NADH oxidation in bovine heart submitochondrial particles, with an IC50 of 50 nM[1].
Aurachin D potently inhibits the sodium-translocating NADH:ubiquinone oxidoreductase (Na+-NQR) of Vibrio cholerae by binding to the cytoplasmic surface of its NqrB subunit, which partially overlaps with the ubiquinol-binding site[2].
Aurachin D (up to 512 μM, 48 h-7 days) potently inhibits bacterial growth in M. tuberculosis mc26230 (MIC = 8 μM), but shows no obvious antibacterial activity in M. smegmatis mc2155 Wt and the Δqcr mutant (MIC > 512 μM)[4].\n
Aurachin D potently inhibits cytochrome bd oxidase in inverted membrane vesicles (IMVs) containing M. tuberculosis cytochrome bd oxidase and reduces oxygen consumption (IC50 = 0.15 μM)[4].
Aurachin D (48-72 h) exhibits potent anti-parasitic activity against Plasmodium falciparum NF54 (erythrocytic stage), Trypanosoma brucei rhodesiense STIB 900 (bloodstream form), Trypanosoma cruzi Tulahuen C4 (intracellular amastigote) and Leishmania donovani MHOM-ET-67/L82 (axenic amastigote), with IC50 values of 0.012 μM, 4.5 μM, 1.3 μM and 0.044 μM, respectively. It shows low cytotoxicity against rat skeletal muscle myoblast L6 cells (IC50 = 130.7 μM)[5].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 108354-13-8
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Appearance Solid
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Masse moléculaire 363.54
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Formule C25H33NO
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Color White to light brown
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SMILES
O=C1C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)\C)=C(C)NC2=C1C=CC=C2
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Structure Classification
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Initial Source
myxobacteria
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Powder -20°C 3 years In solvent -80°C 6 months -20°C 1 month
Solvant et solubilité
In Vitro:
DMSO : 50 mg/mL (137.54 mM; ultrasonic and warming and heat to 60°C; 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)
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.
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.
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 (276 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 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 | 2.7507 mL | 13.7536 mL | 27.5073 mL | 68.7682 mL |
| 5 mM | 0.5501 mL | 2.7507 mL | 5.5015 mL | 13.7536 mL | |
| 10 mM | 0.2751 mL | 1.3754 mL | 2.7507 mL | 6.8768 mL | |
| 15 mM | 0.1834 mL | 0.9169 mL | 1.8338 mL | 4.5845 mL | |
| 20 mM | 0.1375 mL | 0.6877 mL | 1.3754 mL | 3.4384 mL | |
| 25 mM | 0.1100 mL | 0.5501 mL | 1.1003 mL | 2.7507 mL | |
| 30 mM | 0.0917 mL | 0.4585 mL | 0.9169 mL | 2.2923 mL | |
| 40 mM | 0.0688 mL | 0.3438 mL | 0.6877 mL | 1.7192 mL | |
| 50 mM | 0.0550 mL | 0.2751 mL | 0.5501 mL | 1.3754 mL | |
| 60 mM | 0.0458 mL | 0.2292 mL | 0.4585 mL | 1.1461 mL | |
| 80 mM | 0.0344 mL | 0.1719 mL | 0.3438 mL | 0.8596 mL | |
| 100 mM | 0.0275 mL | 0.1375 mL | 0.2751 mL | 0.6877 mL |
Aurachin D Related Classifications
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