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揭示合成的杂环希夫碱配体衍生的过渡金属配合物的抗疟、抗菌、抗氧化效率及分子对接研究。

Unveiling Anti-Malarial, Antimicrobial, Antioxidant Efficiency and Molecular Docking Study of Synthesized Transition Metal Complexes Derived From Heterocyclic Schiff Base Ligands.

机构信息

Department of Chemistry, Guru Jambheshwar University of Science and Technology, Hisar, 125001, Haryana, India.

出版信息

Chem Asian J. 2024 Oct 1;19(19):e202400676. doi: 10.1002/asia.202400676. Epub 2024 Sep 9.

DOI:10.1002/asia.202400676
PMID:39039918
Abstract

Malaria, a persistent and ancient adversary, continues to impact vast regions worldwide, afflicting millions and severely affecting human health and well-being. Recently, despite significant progress in combating this parasitic disease, malaria remains a major global health concern, especially in areas with limited resources and vulnerable populations. Consequently, identifying and developing effective agents to combat malaria and its associated dysfunctions is essential therefore the two new Schiff base ligands incorporated Co(II), Ni(II), Cu(II) and Zn(II) ions were synthesized and thoroughly characterized. The synthesized compounds were assessed for in vitro anti-malarial and antimicrobial efficacy, compounds (9, 10) demonstrated highest potential with IC=1.08±0.09 to 1.18±0.04 μM against P. falciparum and MIC=0.0058 μmol/mL against C. albicans and E. coli, respectively. The complexes (5, 6) were effectively reduce mitigate oxidative stress with lowest IC value of 2.69±0.12 to 2.87±0.09 μM. Moreover, the biological findings were reinforced by a molecular docking investigation involving the potential compounds (2, 7-10) against dihydroorotate dehydrogenase and sterol 14-alpha demethylase proteins which exposed complex's excellent biological response than their parent ligands. ADMET profiling was used to confirm the compounds' oral drug-like features. This research offers promising prospects for future multi-functional drug innovations targeting malaria, pathogenic infections, and oxidative stress.

摘要

疟疾是一种持久而古老的对手,继续影响着世界上的大片地区,使数百万人患病,并严重影响人类的健康和福祉。尽管最近在对抗这种寄生虫病方面取得了重大进展,但疟疾仍然是一个主要的全球健康关注点,特别是在资源有限和人口脆弱的地区。因此,寻找和开发有效的药物来对抗疟疾及其相关功能障碍是至关重要的。因此,合成了两种新的席夫碱配体,其中包含 Co(II)、Ni(II)、Cu(II)和 Zn(II)离子,并对其进行了深入的表征。评估了合成化合物的体外抗疟和抗菌功效,化合物(9,10)表现出最高的潜力,对 P. falciparum 的 IC=1.08±0.09 至 1.18±0.04 μM,对 C. albicans 和 E. coli 的 MIC=0.0058 μmol/mL。配合物(5,6)能够有效减轻氧化应激,IC 值最低为 2.69±0.12 至 2.87±0.09 μM。此外,通过涉及潜在化合物(2,7-10)对二氢乳清酸脱氢酶和甾醇 14-α 脱甲基酶蛋白的分子对接研究,进一步证实了这些生物发现,这些化合物表现出比其母体配体更好的生物反应。ADMET 分析用于确认化合物的口服药物样特征。这项研究为未来针对疟疾、致病性感染和氧化应激的多功能药物创新提供了有希望的前景。

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