Modification of acetazolamide synthesis: new derivatives and investigation of their biological properties

IF 2.2 4区 化学 Q2 Engineering
Maryam Falakshahi, Nosrat O. Mahmoodi, Behzad Khalili, Sarah Poormoradkhan Melal
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Abstract

Acetazolamide 1 is a carbonic anhydrase inhibitor used in the medical treatment of glaucoma, epileptic seizure, idiopathic intracranial hypertension, altitude sickness, etc. The synthesis of acetazolamide from the corresponding thiol derivative 4 requires oxidation and converting it to the sulfonyl chloride intermediate 5. This research aimed to enhance the safety, environmental conditions, and efficiency of the oxidation process by substituting chlorine gas for sodium hypochlorite (commercial bleach). The use of chlorine gas in place of conventional oxidation methods offered significant benefits, including the synthesis of several novel compounds with a high level of purity, specifically designated as 6a-6f. These novel compounds were produced through the reaction of synthesized key sulfonyl chloride 5 with various amines, hydrazones, and bis-amine precursors, leading to the creation of new sulfonamide derivatives. A thorough investigation was conducted to determine the antibacterial activity (ABA) and antioxidant activity (AOA) of the newly synthesized compounds. The results indicated that the ABA impact of the prefabricated bis-products (7a and 7b) was significantly higher than that of the standard mono-product (6a). This suggests that the bis-products possess enhanced antibacterial properties compared to their mono-product counterparts. Moreover, the hydrazine-based products synthesized (8a-8g) demonstrated remarkable efficacy against both Gram-positive and Gram-negative bacteria. These products, particularly compound 9g, showed superior antibacterial effects when compared to commonly used antibiotics such as ciprofloxacin and tetracycline. This highlights the potential of these new compounds as effective antibacterial agents. In terms of antioxidant activity, a comparison with ascorbic acid revealed that compounds 9c, 9a, 9b, 9e, and 8d exhibited superior AOA. This indicates that these compounds have a strong potential to act as antioxidants, which can be beneficial in various applications where oxidative stress is a concern. In summary, the substitution of chlorine gas for sodium hypochlorite in the oxidation process not only improved safety and environmental conditions but also led to the efficient synthesis of highly pure novel compounds. These compounds displayed significant ABA and AOA, suggesting their potential as valuable agents in medical and industrial applications. The enhanced properties of the bis-products and hydrazine-based compounds, in particular, underscore the importance of this research in developing new, effective chemical entities. Future research will focus on further optimizing these compounds for clinical use, evaluating their pharmacokinetics and toxicity profiles, and exploring their applications in other therapeutic areas such as anticancer and antiviral treatments.

Graphical abstract

Abstract Image

修改乙酰唑胺的合成:新衍生物及其生物特性研究
乙酰唑胺 1 是一种碳酸酐酶抑制剂,用于治疗青光眼、癫痫发作、特发性颅内高压、高原病等。从相应的硫醇衍生物 4 合成乙酰唑胺需要将其氧化并转化为磺酰氯中间体 5。这项研究旨在用氯气代替次氯酸钠(商用漂白剂),从而提高氧化过程的安全性、环境条件和效率。使用氯气代替传统氧化方法具有显著的优势,包括合成了几种高纯度的新型化合物,具体命名为 6a-6f。这些新型化合物是通过合成的关键磺酰氯 5 与各种胺、肼和双胺前体反应生成的,从而产生了新的磺酰胺衍生物。研究人员对新合成化合物的抗菌活性(ABA)和抗氧化活性(AOA)进行了深入研究。结果表明,预制双产品(7a 和 7b)的 ABA 影响明显高于标准单产品(6a)。这表明,与单体产品相比,双体产品具有更强的抗菌性能。此外,合成的肼基产品(8a-8g)对革兰氏阳性菌和革兰氏阴性菌都有显著疗效。与环丙沙星和四环素等常用抗生素相比,这些产品(尤其是化合物 9g)显示出更优越的抗菌效果。这凸显了这些新化合物作为有效抗菌剂的潜力。在抗氧化活性方面,与抗坏血酸进行比较后发现,化合物 9c、9a、9b、9e 和 8d 的抗氧化活性更强。这表明这些化合物具有作为抗氧化剂的强大潜力,可用于各种关注氧化应激的应用中。总之,在氧化过程中用氯气代替次氯酸钠,不仅改善了安全性和环境条件,还高效合成了高纯度的新型化合物。这些化合物显示出明显的 ABA 和 AOA,表明它们有可能成为医疗和工业应用中的重要药物。特别是双产品和肼基化合物的性能增强,凸显了这项研究在开发新的有效化学实体方面的重要性。今后的研究重点将是进一步优化这些化合物的临床应用,评估它们的药代动力学和毒性特征,并探索它们在抗癌和抗病毒治疗等其他治疗领域的应用。
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来源期刊
Chemical Papers
Chemical Papers Chemical Engineering-General Chemical Engineering
CiteScore
3.30
自引率
4.50%
发文量
590
期刊介绍: Chemical Papers is a peer-reviewed, international journal devoted to basic and applied chemical research. It has a broad scope covering the chemical sciences, but favors interdisciplinary research and studies that bring chemistry together with other disciplines.
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