Innovative Piperidine-Catalyzation in Protecting Carbonyl Compounds with Implications for Angiogenesis and Inflammation

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Abstract

Introduction: This study explores the application of piperidine-catalyzed protection, an innovative technique, for safeguarding various carbonyl compounds functioning as acetals in a generic reaction. Specifically, we investigate the catalysis of 2-amino-1,3-propanediol-2-methyl with various aromatic aldehydes, leading to the production of cis and trans-5-methyl-2-(mono or di-substitutions-phenyl)-1,3-dioxane-5-amine. Methods: Identification of all newly formed products is achieved through the utilization of spectroscopic techniques, including IR, 1H-NMR, and 13C-NMR spectroscopy. Molecular interactions and potential therapeutic applications of compounds E1 and E2 are demonstrated with cAMP-specific phosphodiesterase (1zkl) and oxidized purine nucleoside triphosphate hydrolase (5ws7). Detailed structural analyses highlight specific hydrogen bonds, pi-pi stacked interactions, and alkyl contacts formed by these compounds with target proteins. A comprehensive bioinformatics approach involves GO enrichment, STRING protein-protein association networks, KEGG pathway analysis, and Reactome pathways to elucidate biological processes, molecular functions, and cellular components associated with the compounds. Results: Compounds E1 and E2 exhibit diverse enrichment profiles, suggesting their involvement in various signaling cascades, neurotransmission, immune responses, and cancer pathways. Comparative analysis of five compound pairs (A1/A2, B1/B2, C1/C2, D1/D2, E1/E2) reveals subtle distinctions in enrichment patterns, implying unique pharmacological advantages for each pair. Conclusion: This study introduces a separate investigation on piperidine-catalyzed protection of carbonyl groups in aldehydes, presenting a practical approach. Emphasizing the significance of understanding distinct biological signatures, our findings guide therapeutic applications and compound optimization, particularly in the context of anti-cancer therapeutics. The compounds show potential in modulating neuronal function, neurotransmission, cancer mechanisms, and immune responses, suggesting promising avenues for future research and development.
哌啶催化保护羰基化合物的创新方法对血管生成和炎症的影响
简介:本研究探索了哌啶催化保护这一创新技术在一般反应中的应用,以保护作为乙醛的各种羰基化合物。具体来说,我们研究了 2-氨基-1,3-丙二醇-2-甲基与各种芳香醛的催化反应,从而生成顺式和反式-5-甲基-2-(单或双取代苯基)-1,3-二恶烷-5-胺。方法:利用红外光谱、1H-NMR 和 13C-NMR 光谱等光谱技术对所有新生成的产物进行鉴定。化合物 E1 和 E2 与 cAMP 特异性磷酸二酯酶(1zkl)和氧化嘌呤核苷三磷酸水解酶(5ws7)的分子相互作用和潜在治疗应用得到了证实。详细的结构分析强调了这些化合物与靶蛋白之间形成的特定氢键、pi-pi 叠加相互作用和烷基接触。综合生物信息学方法包括 GO 富集、STRING 蛋白质-蛋白质关联网络、KEGG 通路分析和 Reactome 通路,以阐明与化合物相关的生物过程、分子功能和细胞成分。研究结果化合物 E1 和 E2 表现出不同的富集特征,表明它们参与了各种信号级联、神经传递、免疫反应和癌症通路。对五对化合物(A1/A2、B1/B2、C1/C2、D1/D2、E1/E2)的比较分析显示了富集模式的细微差别,这意味着每对化合物都具有独特的药理优势。结论本研究对哌啶催化保护醛中的羰基进行了单独研究,提出了一种实用的方法。我们的研究结果强调了了解不同生物特征的重要性,为治疗应用和化合物优化提供了指导,尤其是在抗癌治疗方面。这些化合物在调节神经元功能、神经传递、癌症机制和免疫反应方面显示出潜力,为未来的研究和开发提供了广阔的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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