Charge transportation in nanostructured functional selenium-containing liquid crystalline materials
US-11814346-B1 · Nov 14, 2023 · US
US12377058B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-12377058-B1 |
| Application number | US-202418649785-A |
| Country | US |
| Kind code | B1 |
| Filing date | Apr 29, 2024 |
| Priority date | Apr 29, 2024 |
| Publication date | Aug 5, 2025 |
| Grant date | Aug 5, 2025 |
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A method for inhibiting proliferation of cancer cells includes contacting the cancer cells with a cytotoxic effective amount of an anticancer compound of Formula (I); where R1 to R8 are each independently selected from a group consisting of a hydrogen atom, a halogen atom, and an optionally substituted alkyl. The anticancer compound exhibits an IC 50 of from 2 micrograms per milliliters (μg/ml) to 10 μg/ml for inhibiting the proliferation and inducing the apoptosis of cancer cells.
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The invention claimed is: 1. A method for inhibiting proliferation of cancer cells, comprising: contacting the cancer cells with a cytotoxic effective amount of an anticancer compound of Formula (I); wherein R 1 to R 8 are each independently selected from a group consisting of a hydrogen atom, a halogen atom, and an optionally substituted alkyl; and wherein the anticancer compound exhibits an IC 50 of from 2 to 10 μg/ml for inhibiting the proliferation and inducing the apoptosis of cancer cells. 2. The method of claim 1 , wherein the anticancer compound has a Formula (II) 3. The method of claim 1 , wherein the cancer cells comprise one or more cancer stem cells selected from a group consisting of a breast cancer stem cell, a lung cancer stem cell, a prostate cancer stem cell, an osteosarcoma cancer stem cell, an ovarian cancer stem cell, a colon carcinoma stem cell, and a melanoma stem cell. 4. The method of claim 1 , wherein the cancer cells are A549 lung cancer stem cells, and wherein the method has an IC 50 of about 5-7.5 μg/ml. 5. The method of claim 1 , wherein the cancer cells are PC3 cancer stem cells, and wherein the method has an IC 50 of about 4-6.5 μg/ml. 6. The method of claim 1 , wherein the cancer cells are FaDu cancer stem cells, and wherein the method has an IC 50 of about 5-7 μg/ml. 7. The method of claim 1 , wherein the cancer cells are triple-MDA-MB-468 cancer stem cells, and wherein the method has an IC 50 of about 5-7 μg/ml. 8. The method of claim 1 , wherein the cancer cells are HeLa cancer stem cells, and wherein the method has an IC 50 of about 5.5-7 μg/ml. 9. The method of claim 2 , wherein the contacting the cancer cells with the anticancer compound of Formula (II) is in the presence of doxorubicin, and wherein the method exhibits an improved inhibition efficiency at a reduced cytotoxic effective amount as compared to the use of anticancer compound in the absence of doxorubicin. 10. The method of claim 1 , further comprising preparing the anticancer compound of Formula (I) by: mixing a phenol compound, a benzaldehyde compound, and an inorganic base in a solvent to form a mixture; and heating the mixture at a temperature of from 120 to 160° C.; wherein a molar ratio of the phenol compound to the benzaldehyde compound is in a range of 1:2 to 2:1. 11. The method of claim 10 , wherein the phenol compound is 4-pentoxyphenol. 12. The method of claim 10 , wherein the benzaldehyde compound is 4-fluorobenzaldehyde. 13. The method of claim 10 , wherein the inorganic base is at least one of potassium carbonate, and sodium carbonate. 14. The method of claim 10 , wherein the solvent is dimethyl sulfoxide (DMSO). 15. The method of claim 10 , wherein a molar ratio of the phenol compound to the inorganic base is in a range of 1:1 to 1:2, and wherein a molar ratio of the benzaldehyde compound to the inorganic base is in a range of 1:1 to 1:2.
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