4-Methoxychalcone-1
Based on 1 Customer Validation
4-Methoxychalcone is a naturally occurring chalcone compound. 4-Methoxychalcone has antioxidant activity, anti-inflammatory activity, antitumor activity and antibacterial activity. 4-Methoxychalcone can be used to study inflammation and tumor models.
For research use only. We do not sell to patients.
- Purity: 99.20%
- CAS No.: 959-33-1
- Formula: C16H14O2
- Molecular Weight:238.28
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Storage:
Store at room temperature 3 years.
In solvent -80°C, 2 years , -20°C, 1 year
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A2780 | GI50 |
14.4 μM
Compound: 9
|
Antiproliferative activity against human A2780 cells assessed as cell growth inhibition measured after 72 hrs by trypan blue assay
Antiproliferative activity against human A2780 cells assessed as cell growth inhibition measured after 72 hrs by trypan blue assay
|
[PMID: 34262643] |
| A549 | IC50 |
5.2 μM
Compound: 5
|
Antiproliferative activity against human A549 cells assessed as cell growth inhibition measured after 48 hrs by CellTiter Aqueous One Solution MTS assay
Antiproliferative activity against human A549 cells assessed as cell growth inhibition measured after 48 hrs by CellTiter Aqueous One Solution MTS assay
|
[PMID: 37666364] |
| CAL-51 | GI50 |
2.69 μM
Compound: SSE14106
|
Antiproliferative activity against human CAL51 cells assessed as growth inhibition after 3 days by SRB assay
Antiproliferative activity against human CAL51 cells assessed as growth inhibition after 3 days by SRB assay
|
[PMID: 28743509] |
| CCRF-CEM | IC50 |
33.5 μM
Compound: 4c
|
Inhibitory concentration against CEM T-lymphocytes
Inhibitory concentration against CEM T-lymphocytes
|
[PMID: 12086496] |
| DLD-1 | EC50 |
52 μM
Compound: 9
|
Cytotoxicity against human DLD-1 cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
Cytotoxicity against human DLD-1 cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
|
[PMID: 36356534] |
| FHC | CC50 |
99 μM
Compound: 9
|
Cytotoxicity against human FHC cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
Cytotoxicity against human FHC cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
|
[PMID: 36356534] |
| HCT-116 | EC50 |
22 μM
Compound: 9
|
Cytotoxicity against human HCT-116 cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
Cytotoxicity against human HCT-116 cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
|
[PMID: 36356534] |
| HCT-116 | EC50 |
30 μM
Compound: 9
|
Cytotoxicity against p53-/- human HCT-116 cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
Cytotoxicity against p53-/- human HCT-116 cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
|
[PMID: 36356534] |
| HCT-116 | GI50 |
3.86 μM
Compound: SSE14106
|
Antiproliferative activity against human HCT116 cells assessed as growth inhibition after 3 days by SRB assay
Antiproliferative activity against human HCT116 cells assessed as growth inhibition after 3 days by SRB assay
|
[PMID: 28743509] |
| HepG2 | IC50 |
>100 μM
Compound: 4
|
Cytotoxicity against human HepG2 cells after 48 hrs by MTT assay
Cytotoxicity against human HepG2 cells after 48 hrs by MTT assay
|
[PMID: 22658085] |
| HK-2 | IC50 |
23.2 μM
Compound: 5
|
Growth inhibition of HK2 cells by sulforhodamine assay
Growth inhibition of HK2 cells by sulforhodamine assay
|
[PMID: 17383189] |
| HT-29 | EC50 |
32 μM
Compound: 9
|
Cytotoxicity against human HT-29 cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
Cytotoxicity against human HT-29 cells assessed as reduction in cell viability incubated for 48 hrs by AlamarBlue-based assay
|
[PMID: 36356534] |
| HT-29 | GI50 |
16.7 μM
Compound: 9
|
Antiproliferative activity against human HT-29 cells assessed as cell growth inhibition measured after 72 hrs by trypan blue assay
Antiproliferative activity against human HT-29 cells assessed as cell growth inhibition measured after 72 hrs by trypan blue assay
|
[PMID: 34262643] |
| HT-29 | IC50 |
54 μM
Compound: 5
|
Growth inhibition of HT29 cells by sulforhodamine assay
Growth inhibition of HT29 cells by sulforhodamine assay
|
[PMID: 17383189] |
| K562 | IC50 |
29 μM
Compound: 4-Methoxychalcone
|
Inhibition of NF-kappaB transactivation in TNF-alpha-stimulated human K562 cells preincubated for 2 hrs followed by TNF-alpha challenge measured after 6 hrs by dual luciferase reporter gene assay
Inhibition of NF-kappaB transactivation in TNF-alpha-stimulated human K562 cells preincubated for 2 hrs followed by TNF-alpha challenge measured after 6 hrs by dual luciferase reporter gene assay
|
[PMID: 24775915] |
| L1210 | IC50 |
50.4 μM
Compound: 4c
|
Inhibitory activity against L1210 leukemia cells
Inhibitory activity against L1210 leukemia cells
|
[PMID: 12086496] |
| MCF7 | IC50 |
90 μM
Compound: 5
|
Growth inhibition of MCF7 cells by sulforhodamine assay
Growth inhibition of MCF7 cells by sulforhodamine assay
|
[PMID: 17383189] |
| MSTO-211H | GI50 |
10.4 μM
Compound: 9
|
Antiproliferative activity against human MSTO-211H cells assessed as cell growth inhibition measured after 72 hrs by trypan blue assay
Antiproliferative activity against human MSTO-211H cells assessed as cell growth inhibition measured after 72 hrs by trypan blue assay
|
[PMID: 34262643] |
| P388 | IC50 |
10.63 μM
Compound: 4c
|
Inhibitory activity against Murine P388 cells
Inhibitory activity against Murine P388 cells
|
[PMID: 12086496] |
| RBL-1 | IC50 |
20 μM
Compound: 27
|
Inhibition of 5-lipoxygenase in rat RBL1 cells
Inhibition of 5-lipoxygenase in rat RBL1 cells
|
10.1007/s00044-013-0745-7 |
| RBL-1 | IC50 |
20 μM
Compound: 27
|
Inhibition of cyclooxygenase in rat RBL1 cells
Inhibition of cyclooxygenase in rat RBL1 cells
|
10.1007/s00044-013-0745-7 |
| TK-10 | IC50 |
53 μM
Compound: 5
|
Growth inhibition of TK10 cells by sulforhodamine assay
Growth inhibition of TK10 cells by sulforhodamine assay
|
[PMID: 17383189] |
Chemical Information
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CAS No. 959-33-1
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Appearance Solid
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Molecular Weight 238.28
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Formula C16H14O2
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Color Off-white to light yellow
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SMILES
O=C(C1=CC=CC=C1)/C=C/C2=CC=C(OC)C=C2
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Store at room temperature 3 years
In solvent -80°C 2 years -20°C 1 year
Solvent & Solubility
DMSO : 100 mg/mL (419.67 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:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
-
%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 (269 KB)
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SDS (392 KB)
- English - EN (392 KB)
- Français - FR (392 KB)
- Deutsch - DE (392 KB)
- Norwegian - NO (392 KB)
- Español - ES (392 KB)
- Swedish - SV (392 KB)
- Italian - IT (392 KB)
- Korean - KR (392 KB)
- Portuguese - PT (392 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 | 4.1967 mL | 20.9837 mL | 41.9674 mL | 104.9186 mL |
| 5 mM | 0.8393 mL | 4.1967 mL | 8.3935 mL | 20.9837 mL | |
| 10 mM | 0.4197 mL | 2.0984 mL | 4.1967 mL | 10.4919 mL | |
| 15 mM | 0.2798 mL | 1.3989 mL | 2.7978 mL | 6.9946 mL | |
| 20 mM | 0.2098 mL | 1.0492 mL | 2.0984 mL | 5.2459 mL | |
| 25 mM | 0.1679 mL | 0.8393 mL | 1.6787 mL | 4.1967 mL | |
| 30 mM | 0.1399 mL | 0.6995 mL | 1.3989 mL | 3.4973 mL | |
| 40 mM | 0.1049 mL | 0.5246 mL | 1.0492 mL | 2.6230 mL | |
| 50 mM | 0.0839 mL | 0.4197 mL | 0.8393 mL | 2.0984 mL | |
| 60 mM | 0.0699 mL | 0.3497 mL | 0.6995 mL | 1.7486 mL | |
| 80 mM | 0.0525 mL | 0.2623 mL | 0.5246 mL | 1.3115 mL | |
| 100 mM | 0.0420 mL | 0.2098 mL | 0.4197 mL | 1.0492 mL |