(-)-JNJ-A07
Based on 1 publication(s) in Google Scholar
(-)-JNJ-A07 is a potent and selective DENV inhibitor with an EC50 value of 31 nM.
For research use only. We do not sell to patients.
- Purity: 99.97%
- CAS No.: 2135640-92-3
- Formula: C28H26ClF3N2O6
- Molecular Weight:578.96
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Storage:Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
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Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
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Solvent & Solubility
- Purity & Documentation
- References
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Help & FAQs
Publications Citing Use of MedChemExpress (MCE) (-)-JNJ-A07
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Biological Activity
EC50: 31 nM (DENV)[1]
Chemical Information
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CAS No. 2135640-92-3
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Appearance Solid
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Molecular Weight 578.96
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Formula C28H26ClF3N2O6
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Color White to light yellow
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SMILES
OC(CCCOC1=CC(OC)=CC(NC(C2=CC=C(C=C2)Cl)C(N3C4=CC(OC(F)(F)F)=CC=C4CC3)=O)=C1)=O.[Rotation (-)]
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years In solvent -80°C 6 months -20°C 1 month
Publications (1)
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Journal Impact Factor
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Most Recent
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Emerg Microbes Infect
CpG oligodeoxynucleotides and pan-serotype inhibitors control neurotropic Dengue infection in novel immune competent neonatal mouse model. [Abstract]2025 Dec;14(1):2477668. PMID: 40059770
Solvent & Solubility
DMSO : 100 mg/mL (172.72 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 (4.32 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.
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.
Purity & Documentation
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Data Sheet (273 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
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 |
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| DMSO | 1 mM | 1.7272 mL | 8.6362 mL | 17.2723 mL | 43.1809 mL |
| 5 mM | 0.3454 mL | 1.7272 mL | 3.4545 mL | 8.6362 mL | |
| 10 mM | 0.1727 mL | 0.8636 mL | 1.7272 mL | 4.3181 mL | |
| 15 mM | 0.1151 mL | 0.5757 mL | 1.1515 mL | 2.8787 mL | |
| 20 mM | 0.0864 mL | 0.4318 mL | 0.8636 mL | 2.1590 mL | |
| 25 mM | 0.0691 mL | 0.3454 mL | 0.6909 mL | 1.7272 mL | |
| 30 mM | 0.0576 mL | 0.2879 mL | 0.5757 mL | 1.4394 mL | |
| 40 mM | 0.0432 mL | 0.2159 mL | 0.4318 mL | 1.0795 mL | |
| 50 mM | 0.0345 mL | 0.1727 mL | 0.3454 mL | 0.8636 mL | |
| 60 mM | 0.0288 mL | 0.1439 mL | 0.2879 mL | 0.7197 mL | |
| 80 mM | 0.0216 mL | 0.1080 mL | 0.2159 mL | 0.5398 mL | |
| 100 mM | 0.0173 mL | 0.0864 mL | 0.1727 mL | 0.4318 mL |
(-)-JNJ-A07 Related Classifications
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