新化合物4-甲氧基-2-(4-甲氧基苯基)苯并[1,3,2]二恶波罗罗体外抗氧化、抗胆碱酯酶、抗脲酶、抗酪氨酸酶和细胞毒性的研究。

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacology Research & Perspectives Pub Date : 2025-02-01 DOI:10.1002/prp2.70044
Hamdi Temel, Emine Baydan
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引用次数: 0

摘要

本文采用1H、13C NMR、LC-MS-IT-TOF、UV-Vis和FTIR光谱对3-甲氧基儿茶酚和4-甲氧基苯基硼酸合成的新型硼化合物进行了结构表征。采用DPPH自由基清除能力、ABTS自由基清除能力和CUPRAC铜还原能力等方法对新合成化合物的抗氧化活性进行了评价。采用乙酰胆碱酯酶和丁基胆碱酯酶抑制剂测定抗胆碱酯酶活性。还检测了抗脲酶和抗甲状腺酶的抑制活性。采用MTT法对健康细胞系和乳腺癌、结肠癌细胞系进行细胞毒作用评价。结果表明,所合成的化合物具有较高的抗氧化活性。特别是在10 μg/mL浓度下获得的平均抗氧化活性值与α-TOC和BHT的参考值分别进行比较,发现新化合物更有效。在乙酰胆碱酯酶抑制方面,发现平均活性值有统计学意义(p
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Investigation of the In Vitro Antioxidant, Anticholinesterase, Antiurease, Antityrosinase, and Cytotoxic Properties of a Novel Compound: 4-Methoxy-2-(4-Methoxyphenyl)Benzo[d][1,3,2]Dioxaborole.

In this study, the structure of a new boron compound obtained using 3-methoxy catechol and 4-methoxy phenyl boronic acid was characterized by 1H, 13C NMR, LC-MS-IT-TOF, UV-Vis and FTIR spectroscopy. The antioxidant activities of the newly synthesized compound were evaluated by DPPH free radical scavenging, ABTS quation radical scavenging and CUPRAC copper reducing capacity methods. Anticholinesterase activities were determined by acetylcholinesterase and butyrylcholinesterase enzyme inhibitor assays. Antiurease and antithyrosinase enzyme inhibition activities were also examined. Cytotoxic effects were evaluated on healthy cell lines and breast and colon cancer cell lines using MTT method. The results showed that the synthesized compound has high antioxidant activity. Especially the average antioxidant activity values obtained at 10 μg/mL concentration were found to be statistically significantly (p < 0.05) higher than the reference values of α-TOC and BHT. When the antioxidant activity data (IC50) were compared separately with α-TOC and BHT reference values, the new compound was found to be more effective. In acetylcholinesterase enzyme inhibition, the average activity values were found to be statistically significantly (p < 0.05) higher than the galantamine reference value. However, no statistically significant difference was observed at BChE (% inhibition) level with galantamine reference value. In terms of urease and tyrosinase enzyme inhibition activities, the urease activity of the synthesized compound was statistically significantly (p < 0.05) lower than the thiurea reference value. Tyrosinase activity was statistically significantly (p < 0.05) lower than kojic acid reference values. The synthesized and characterized compound was found to have no toxic effect on healthy cell lines and did not show any cytotoxic effect on breast cancer (MCF-7) and colon cancer (HT-29) cell lines.

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来源期刊
Pharmacology Research & Perspectives
Pharmacology Research & Perspectives Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
5.30
自引率
3.80%
发文量
120
审稿时长
20 weeks
期刊介绍: PR&P is jointly published by the American Society for Pharmacology and Experimental Therapeutics (ASPET), the British Pharmacological Society (BPS), and Wiley. PR&P is a bi-monthly open access journal that publishes a range of article types, including: target validation (preclinical papers that show a hypothesis is incorrect or papers on drugs that have failed in early clinical development); drug discovery reviews (strategy, hypotheses, and data resulting in a successful therapeutic drug); frontiers in translational medicine (drug and target validation for an unmet therapeutic need); pharmacological hypotheses (reviews that are oriented to inform a novel hypothesis); and replication studies (work that refutes key findings [failed replication] and work that validates key findings). PR&P publishes papers submitted directly to the journal and those referred from the journals of ASPET and the BPS
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