EN460
Based on 15 publication(s) in Google Scholar
EN460 is a selective endoplasmic reticulum oxidation 1 (ERO1) inhibitor. EN460 (IC50 of 1.9 μM) interacts selectively with the reduced, active form of ERO1α and prevents its reoxidation.
For research use only. We do not sell to patients.
- Purity: 99.94%
- CAS No.: 496807-64-8
- Formula: C22H12ClF3N2O4
- Molecular Weight:460.79
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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) EN460
More- Nat Cell Biol. 2026 Jun 12. [Abstract]
- J Adv Res. 2026 Apr 6:S2090-1232(26)00298-5. [Abstract]
- J Exp Clin Cancer Res. 2019 Jan 31;38(1):44. [Abstract]
- J Exp Med. 2021 Sep 6;218(9):e20202637. [Abstract]
- Diabetes Metab J. 2026 Jan;50(1):62-76. [Abstract]
- Free Radic Biol Med. 2026 Feb 16:244:452-463.
- Ecotoxicol Environ Saf. 2023 Dec:268:115711. [Abstract]
- Biomed J. 2025 Aug;48(4):100875. [Abstract]
- Int J Mol Sci. 2022 Oct 1;23(19):11660. [Abstract]
- Prog Neurobiol. 2024 Nov:242:102674. [Abstract]
- Fish Shellfish Immunol. 2024 Dec:155:110020. [Abstract]
- Vet Res. 2024 Jun 14;55(1):78. [Abstract]
- Vet Res. 2023 Feb 3;54(1):9. [Abstract]
- Vet Microbiol. 2022 Oct:273:109548. [Abstract]
- bioRxiv. 2025 Oct 6.
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RT-PCR
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Cell Imaging/Staining
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Cell Proliferation/Viability Assay
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WB
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Flow Cytometry
Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| MM1.S | IC50 |
14.74 μM
Compound: EN460
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Cytotoxicity against human MM1S cells assessed as reduction in cell viability measured after 72 hrs by MTT assay
Cytotoxicity against human MM1S cells assessed as reduction in cell viability measured after 72 hrs by MTT assay
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[PMID: 30850265] |
| U-266 | IC50 |
10.1 μM
Compound: EN460
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Cytotoxicity against human U266 cells assessed as reduction in cell viability measured after 72 hrs by MTT assay
Cytotoxicity against human U266 cells assessed as reduction in cell viability measured after 72 hrs by MTT assay
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[PMID: 30850265] |
Exposure of cells to EN460 or QM295 resulted in the accumulation of an ERO1α form with lower mobility, indicative of the reduced state. EN460 and QM295 were also found to activate an unfolded protein response reporter in cultured 293T cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 496807-64-8
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Appearance Solid
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Molecular Weight 460.79
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Formula C22H12ClF3N2O4
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Color Pink to red
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SMILES
FC(F)(F)C1=NN(C2=CC(C(O)=O)=C(Cl)C=C2)C(/C1=C\C3=CC=C(C4=CC=CC=C4)O3)=O
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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 (15)
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Journal Impact Factor
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Most Recent
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Nat Cell Biol
ERO1a fosters glioblastoma aggressiveness and metabolic flexibility by regulating mitochondria-associated membrane dynamics. [Abstract]2026 Jun 12. PMID: 42286227 -
J Adv Res
LPCAT3 deficiency Drives phospholipid remodeling and mitochondrial oxidative dysfunction to accelerate MASH-HCC development. [Abstract]2026 Apr 6:S2090-1232(26)00298-5. PMID: 41951050 -
J Exp Clin Cancer Res
CYT997(Lexibulin) induces apoptosis and autophagy through the activation of mutually reinforced ER stress and ROS in osteosarcoma. [Abstract]2019 Jan 31;38(1):44. PMID: 30704503
EN460 purchased from MedChemExpress. Usage Cited in: J Exp Clin Cancer Res. 2019 Jan 31;38(1):44. [Abstract]
143B cells are treated with CYT997 (80 nM) and/or EN460 (8 μM) for 24 h, and apoptosis, autophagy and ER stress-related proteins including c-PARP, caspase-4, LC3B, Beclin-1, CHOP and ERO1 are analyzed by western blotting.
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J Exp Med
2021 Sep 6;218(9):e20202637. PMID: 34342641 -
Diabetes Metab J
Serpina3c Mitigates Adipose Tissue Inflammation by Inhibiting the HIF1α-Mediated Endoplasmic Reticulum Overoxidation in Adipocytes. [Abstract]2026 Jan;50(1):62-76. PMID: 40403760 -
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Ecotoxicol Environ Saf
Mitochondrial dysfunction and endoplasmic reticulum stress induced by activation of PPARα leaded testicular to apoptosis in SD rats explored to di-(2-ethylhexyl) phthalate (DEHP). [Abstract]2023 Dec:268:115711. PMID: 37979351 -
Biomed J
IRE1-Mediated Endoplasmic Reticulum Stress Response Regulates Oxidative Damage in CYP4V2 Deficient Human Retinal Pigment Epithelial Cells. [Abstract]2025 Aug;48(4):100875. PMID: 40466971
EN460 purchased from MedChemExpress. Usage Cited in: Biomed J. 2025 Aug;48(4):100875. [Abstract]
EN460 (5, 10, 15 μM), an ERO1-Lα inhibitor, regulated ERO1A mRNA.
EN460 purchased from MedChemExpress. Usage Cited in: Biomed J. 2025 Aug;48(4):100875. [Abstract]
H2DCFDA staining of intracellular ROS (EN460 15 μM, 48 h).
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Int J Mol Sci
Hepatocyte-Derived Prostaglandin E2-Modulated Macrophage M1-Type Polarization via mTOR-NPC1 Axis-Regulated Cholesterol Transport from Lysosomes to the Endoplasmic Reticulum in Hepatitis B Virus x Protein-Related Nonalcoholic Steatohepatitis. [Abstract]2022 Oct 1;23(19):11660. PMID: 36232960 -
Prog Neurobiol
ERO1A inhibition mitigates neuronal ER stress and ameliorates UBQLN2ALS phenotypes in Drosophila melanogaster. [Abstract]2024 Nov:242:102674. PMID: 39395630 -
Fish Shellfish Immunol
Grass Carp Reovirus (GCRV) infection activates the PERK-eIF2α pathway to promote the viral replication. [Abstract]2024 Dec:155:110020. PMID: 39528019 -
Vet Res
Regulatory effects of Trichinella spiralis serpin-type serine protease inhibitor on endoplasmic reticulum stress and oxidative stress in host intestinal epithelial cells. [Abstract]2024 Jun 14;55(1):78. PMID: 38877574
EN460 purchased from MedChemExpress. Usage Cited in: Vet Res. 2024 Jun 14;55(1):78. [Abstract]
EN460 at dosages of 0, 4, 8, 12, 16, and 20 mM were cocultured with IPEC for 1 h, respectively. Then, a CCK-8 cell activity detection kit was used to determine the optimal interaction concentration.
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Vet Res
Porcine epidemic diarrhea virus activates PERK-ROS axis to benefit its replication in Vero E6 cells. [Abstract]2023 Feb 3;54(1):9. PMID: 36737830
EN460 purchased from MedChemExpress. Usage Cited in: Vet Res. 2023 Feb 3;54(1):9. [Abstract]
Vero E6 cells were infected with PEDV with or without EN460 (5 μM). Dimethylsulfoxide (DMSO) was used as solvent control. A The effects of ERO1α inhibition on CHOP, ERO1α, and PEDV N expression were shown by Western blotting with β-actin used as loading control.
EN460 purchased from MedChemExpress. Usage Cited in: Vet Res. 2023 Feb 3;54(1):9. [Abstract]
Vero E6 cells were infected with PEDV with or without EN460 (5 μM). Dimethylsulfoxide (DMSO) was used as solvent control. Cells collected at 36 hpi were measured for changes in cytosolic ROS level by flow cytometry after incubation with 10 μM DCFH-DA for 30 min at 37 °C.
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Vet Microbiol
2022 Oct:273:109548. PMID: 36037618 -
Solvent & Solubility
DMSO : 12.5 mg/mL (27.13 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, 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.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 1.25 mg/mL (2.71 mM); Clear solution
This protocol yields a clear solution of ≥ 1.25 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (12.5 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: 1.25 mg/mL (2.71 mM); Suspended solution; Need ultrasonic
This protocol yields a suspended solution of 1.25 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (12.5 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.
Purity & Documentation
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Data Sheet (280 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)
- Korean - KR (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 | 2.1702 mL | 10.8509 mL | 21.7019 mL | 54.2546 mL |
| 5 mM | 0.4340 mL | 2.1702 mL | 4.3404 mL | 10.8509 mL | |
| 10 mM | 0.2170 mL | 1.0851 mL | 2.1702 mL | 5.4255 mL | |
| 15 mM | 0.1447 mL | 0.7234 mL | 1.4468 mL | 3.6170 mL | |
| 20 mM | 0.1085 mL | 0.5425 mL | 1.0851 mL | 2.7127 mL | |
| 25 mM | 0.0868 mL | 0.4340 mL | 0.8681 mL | 2.1702 mL |