Bisphenol A diglycidyl ether
Based on 1 Customer Validation
Bisphenol A diglycidyl ether is a synthesis product of Bisphenol A (HY-18260). Bisphenol A diglycidyl ether inhibits CYP19 activity in a dose-dependent manner and weakly induces ROS generation. Bisphenol A diglycidyl ether has antiestrogenic effects on vitellogenin production. Bisphenol A diglycidyl ether disrupts the lipidome by reducing diacylglycerols, triglycerides, and membrane lipids. Bisphenol A diglycidyl ether is widely used in protective coatings for food and beverage cans, as well as in various paints and adhesives.
For research use only. We do not sell to patients.
- Purity : 95.0%
- CAS No.: 1675-54-3
- Formula: C21H24O4
- Molecular Weight:340.42
-
Storage:
Store at room temperature 3 years.
In solvent -80°C, 2 years , -20°C, 1 year
Biological Activity
Description
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| JEG-3 | IC50 |
39 μM
|
Inhibition of CYP19 (aromatase) activity in human placental choriocarcinoma JEG-3 cells incubated for 24 hrs, measured by the conversion of 1β-3H-androst-4-ene-3,17-dione to 3H2O.
Inhibition of CYP19 (aromatase) activity in human placental choriocarcinoma JEG-3 cells incubated for 24 hrs, measured by the conversion of 1β-3H-androst-4-ene-3,17-dione to 3H2O.
|
30366299 |
| JEG-3 | EC50 |
43 μM
|
Cytotoxicity against human placental choriocarcinoma JEG-3 cells assessed as reduction in cell viability after 24 hrs exposure by Alamar Blue assay.
Cytotoxicity against human placental choriocarcinoma JEG-3 cells assessed as reduction in cell viability after 24 hrs exposure by Alamar Blue assay.
|
30366299 |
| JEG-3 | EC50 |
38 μM
|
Cytotoxicity against human placental choriocarcinoma JEG-3 cells assessed as reduction in cell viability after 24 hrs exposure by CFDA-AM assay.
Cytotoxicity against human placental choriocarcinoma JEG-3 cells assessed as reduction in cell viability after 24 hrs exposure by CFDA-AM assay.
|
30366299 |
In Vitro
Bisphenol A diglycidyl ether (5-200 μM; 24 h) exhibits significant cytotoxicity in JEG-3 cells after 24 h exposure with EC50 values of 43 μM (Alamar Blue) and 38 μM (CFDA-AM)[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:JEG-3
-
Concentration:5 to 200 μM
-
Incubation Time:24 h
-
Result:Showed significant cytotoxicity with EC50 values of 43 μM as measured by Alamar Blue and 38 μM as measured by CFDA-AM.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 1675-54-3
-
Appearance Viscous Liquid
-
Molecular Weight 340.42
-
Formula C21H24O4
-
Color Colorless to light yellow
-
SMILES
CC(C1=CC=C(OCC2OC2)C=C1)(C3=CC=C(OCC4OC4)C=C3)C
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Store at room temperature 3 years
In solvent -80°C 2 years -20°C 1 year
Solvent & Solubility
In Vitro:
DMSO : 100 mg/mL (293.75 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)
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Working solution concentration: 0.22 mg/mL
Purity & Documentation
-
Data Sheet (273 KB)
-
SDS (538 KB)
- English - EN (538 KB)
- Français - FR (538 KB)
- Deutsch - DE (538 KB)
- Norwegian - NO (538 KB)
- Español - ES (538 KB)
- Swedish - SV (538 KB)
- Italian - IT (538 KB)
- Korean - KR (538 KB)
- Portuguese - PT (538 KB)
-
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 | 2.9375 mL | 14.6877 mL | 29.3755 mL | 73.4387 mL |
| 5 mM | 0.5875 mL | 2.9375 mL | 5.8751 mL | 14.6877 mL | |
| 10 mM | 0.2938 mL | 1.4688 mL | 2.9375 mL | 7.3439 mL | |
| 15 mM | 0.1958 mL | 0.9792 mL | 1.9584 mL | 4.8959 mL | |
| 20 mM | 0.1469 mL | 0.7344 mL | 1.4688 mL | 3.6719 mL | |
| 25 mM | 0.1175 mL | 0.5875 mL | 1.1750 mL | 2.9375 mL | |
| 30 mM | 0.0979 mL | 0.4896 mL | 0.9792 mL | 2.4480 mL | |
| 40 mM | 0.0734 mL | 0.3672 mL | 0.7344 mL | 1.8360 mL | |
| 50 mM | 0.0588 mL | 0.2938 mL | 0.5875 mL | 1.4688 mL | |
| 60 mM | 0.0490 mL | 0.2448 mL | 0.4896 mL | 1.2240 mL | |
| 80 mM | 0.0367 mL | 0.1836 mL | 0.3672 mL | 0.9180 mL | |
| 100 mM | 0.0294 mL | 0.1469 mL | 0.2938 mL | 0.7344 mL |
Keywords
- Bisphenol A diglycidyl ether
- 1675-54-3
- Biochemical Assay Reagents
- Drug Derivative
- Cytochrome P450
- Reactive Oxygen Species (ROS)
- Estrogen Receptor/ERR
- Drug derivative
- CYPs
- vitellogenin production
- reactive oxygen species generation
- androgen receptor antagonist
- PPARγ antagonist
- adipogenic gene expression
- stromal stem cells
- aromatase inhibitor
- CYP19 activity
- obesity
- JEG-3 cells
- Inhibitor
- inhibitor
- inhibit