Synthesis of new heterocyclic derivatives (benzodioxane-2-yl)methanol and their effect on rat intraocular pressure

Alexander A. Ozerov, Lyudmila V. Naumenko, Alyona S. Taran, Dmitry S. Yakovlev, Alina M. Chebanko, Maria S. Pshenichnikova, Nadezhda M. Shcherbakova, G. N. Solodunova, D. Merezhkina, Александр A. Spasov
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Abstract

Objective: Synthesis of new compounds, melatonin isosters, and study of their ability to reduce intraocular pressure. Materials and methods: Based on the previously made forecast and on the similarity with the selected compounds, the synthesis of new compounds was carried out – melatonin isosters having a 2,3-dihydro-1,4-benzodioxin cycle connected by a linker of various chemical structure with a nitrogen-containing heterocyclic core. The structure of the synthesized compounds was proved by 1H- and 13C- NMR spectroscopy, purity and individuality – by chromatographic methods. Intraocular pressure in laboratory animals was measured using a contact veterinary tonometer Tonovet (Finland). Cytotoxicity was assessed using MTT test on normal rat skin fibroblasts. Results: Derivatives (benzodioxane-2-yl)methanol reduced the level of IOP in varying degrees of severity. The VMA-22-37 compound showed the greatest activity. With topical application of a 0.4% solution, the compound reduced the intraocular pressure of intact rats by 26.6%, while not affecting the control eye. This compound also has low cytotoxicity. Conclusion: Derivatives (benzodioxane-2-yl)methanol is promising for the search for compounds capable of reducing increased intraocular pressure.
新杂环衍生物(苯并二恶烷-2-基)甲醇的合成及其对大鼠眼压的影响
目的:合成新化合物--褪黑素异构体,并研究其降低眼压的能力。材料和方法:根据之前的预测以及与所选化合物的相似性,合成了新的化合物--褪黑素异构体,该异构体具有 2,3-二氢-1,4-苯并二恶英循环,通过不同化学结构的连接体与含氮杂环核心相连。合成化合物的结构由 1H 和 13C NMR 光谱法证明,纯度和独特性由色谱法证明。实验动物的眼内压是用接触式兽医眼压计 Tonovet(芬兰)测量的。对正常大鼠皮肤成纤维细胞的细胞毒性采用 MTT 试验进行评估。结果苯并二恶烷-2-基)甲醇衍生物在不同程度上降低了眼压水平。VMA-22-37 化合物的活性最强。通过局部使用 0.4% 的溶液,该化合物可将完整大鼠的眼压降低 26.6%,而对对照眼没有影响。这种化合物的细胞毒性也很低。结论(苯并二恶烷-2-基)甲醇衍生物有望用于寻找能够降低眼内压升高的化合物。
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