EMT inhibitor-1
Based on 2 publication(s) in Google Scholar
EMT inhibitor-1 is an inhibitor of of Hippo, TGF-β, and Wnt signaling pathways with antitumor activities.
For research use only. We do not sell to patients.
- Purity: 99.82%
- CAS No.: 1638526-21-2
- Formula: C12H12Cl2N2O2S
- Molecular Weight:319.21
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) EMT inhibitor-1
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Biological Activity
Hippo, TGF-β, Wnt[1].
EMT inhibitor-1 (C19) (0-10μM; 24 hours) is an inhibitor of of Hippo, TGF-β, and Wnt signaling pathways with antitumor activities, inhibiting cancer cell migration, proliferation, and resistance to doxorubicin in vitro[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
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CAS No. 1638526-21-2
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Appearance Solid
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Molecular Weight 319.21
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Formula C12H12Cl2N2O2S
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Color White to off-white
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SMILES
OCCCCOC1=NSN=C1C2=CC=C(Cl)C(Cl)=C2
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (2)
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Journal Impact Factor
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Most Recent
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Technol Cancer Res Treat
EMT Participates in the Regulation of Exosomes Secretion and Function in Esophageal Cancer Cells. [Abstract]2021 Jan-Dec:20:15330338211033077. PMID: 34278849 -
Int Arch Allergy Immunol
Six1 Promotes Epithelial-Mesenchymal Transition in Bronchial Epithelial Cells via the TGFβ1/Smad Signalling Pathway. [Abstract]2021;182(6):479-488. PMID: 33631753
Solvent & Solubility
DMSO : 100 mg/mL (313.27 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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.
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 (276 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Portuguese - PT (393 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 3.1327 mL | 15.6637 mL | 31.3273 mL | 78.3184 mL |
| 5 mM | 0.6265 mL | 3.1327 mL | 6.2655 mL | 15.6637 mL | |
| 10 mM | 0.3133 mL | 1.5664 mL | 3.1327 mL | 7.8318 mL | |
| 15 mM | 0.2088 mL | 1.0442 mL | 2.0885 mL | 5.2212 mL | |
| 20 mM | 0.1566 mL | 0.7832 mL | 1.5664 mL | 3.9159 mL | |
| 25 mM | 0.1253 mL | 0.6265 mL | 1.2531 mL | 3.1327 mL | |
| 30 mM | 0.1044 mL | 0.5221 mL | 1.0442 mL | 2.6106 mL | |
| 40 mM | 0.0783 mL | 0.3916 mL | 0.7832 mL | 1.9580 mL | |
| 50 mM | 0.0627 mL | 0.3133 mL | 0.6265 mL | 1.5664 mL | |
| 60 mM | 0.0522 mL | 0.2611 mL | 0.5221 mL | 1.3053 mL | |
| 80 mM | 0.0392 mL | 0.1958 mL | 0.3916 mL | 0.9790 mL | |
| 100 mM | 0.0313 mL | 0.1566 mL | 0.3133 mL | 0.7832 mL |