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壳聚糖磺酸催化绿色合成萘基吖嗪作为潜在抗癌剂

Chitosan-sulfonic acid-catalyzed green synthesis of naphthalene-based azines as potential anticancer agents.

作者信息

Alzahrani Abdullah Ya, Gomha Sobhi M, Zaki Magdi Ea, Farag Basant, Abdelgawad Fathy E, Mohamed Mahmoud A

机构信息

Department of Chemistry, Faculty of Science & Arts, King Khalid University, Mohail Assir, Saudi Arabia.

Department of Chemistry, Faculty of Science, Islamic University of Madinah, Madinah, 42351, Saudi Arabia.

出版信息

Future Med Chem. 2024 Apr;16(7):647-663. doi: 10.4155/fmc-2023-0351. Epub 2024 Feb 22.

DOI:10.4155/fmc-2023-0351
PMID:38385167
Abstract

This study focuses on advancing green chemistry in anticancer drug discovery, particularly through the synthesis of azine derivatives with a naphthalene core using CS-SOH as a catalyst. Novel benzaldazine and ketazine derivatives were synthesized using ()-(naphthalen-1-ylmethylene)hydrazine and various carbonyl compounds. The methods employed included thermal and grinding techniques, utilizing CS-SOH as an eco-friendly and cost-effective catalyst. The approach resulted in high yields, short reaction times and demonstrated catalyst reusability. Cytotoxicity tests highlighted compounds and as potent against the HEPG2-1. This study successfully aligns with the objectives of eco-conscious drug development in organic chemistry. Molecular docking and studies further indicate the potential of these ligands as antitumor medicines, with favorable oral bioavailability properties.

摘要

本研究致力于推进抗癌药物发现中的绿色化学,特别是通过使用CS-SOH作为催化剂合成具有萘核心的嗪衍生物。使用()-(萘-1-基亚甲基)肼和各种羰基化合物合成了新型苯甲醛嗪和酮嗪衍生物。所采用的方法包括热法和研磨技术,利用CS-SOH作为一种环保且经济高效的催化剂。该方法产率高、反应时间短,并证明了催化剂的可重复使用性。细胞毒性测试突出显示化合物 和 对HEPG2-1具有强效作用。本研究成功符合有机化学中注重生态的药物开发目标。分子对接和 研究进一步表明这些配体作为抗肿瘤药物的潜力,具有良好的口服生物利用度特性。

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