Faculty of Pharmaceutical Sciences, Hokuriku University.
Healthy Aging Research Group, Hokuriku University.
Chem Pharm Bull (Tokyo). 2024;72(7):648-657. doi: 10.1248/cpb.c24-00239.
Butin and butein are significant bioactive flavanones derived from plants, existing as tautomers of each other. However, their physicochemical attributes, such as their spectral profiles under varying experimental conditions in aqueous solutions and established chromatographic methods for distinguishing between them, remain undetermined. In this study, we determined the basic properties of butin and butein using conventional spectroscopic, reversed-phase, and chiral HPLC analyses. The spectra of the synthesized butin and butein were analyzed using a UV-Vis spectrophotometer in several solvents with different polarities as well as in aqueous solutions at various pH values. Furthermore, the behavior of the measured spectra was reproduced by calculations to reveal the effects of the solvent and pH on the spectra of butin and butein in organic and aqueous solutions. Subsequently, we assessed the structural stability of butin and butein using reversed-phase HPLC, which revealed that butein is unstable compared with butin in a general culture medium. The synthesized butin was effectively separated into R- and S-isomers with positive and negative Cotton effects, respectively, via HPLC using a chiral column. These findings will aid in uncovering the individual properties of both butin and butein that may have been concealed by their tautomerism and enable the synthesis of S-butin, which is typically challenging and time-consuming to isolate.
布替啡烷和布替啡因是来源于植物的重要生物活性黄酮类化合物,彼此互为互变异构体。然而,它们的物理化学性质,如在不同实验条件下水溶液中的光谱特征以及已建立的用于区分它们的色谱方法,仍未确定。在这项研究中,我们使用常规光谱、反相和手性 HPLC 分析来确定布替啡烷和布替啡因的基本性质。使用具有不同极性的几种溶剂以及在不同 pH 值的水溶液中,通过紫外可见分光光度计分析了合成的布替啡烷和布替啡因的光谱。此外,通过计算再现了测量光谱的行为,以揭示溶剂和 pH 值对有机和水溶液中布替啡烷和布替啡因光谱的影响。随后,我们使用反相 HPLC 评估了布替啡烷和布替啡因的结构稳定性,结果表明,与布替啡烷相比,布替啡因在一般培养基中不稳定。通过使用手性柱的 HPLC,成功地将合成的布替啡烷分离为 R-和 S-异构体,它们分别具有正和负的 Cotton 效应。这些发现将有助于揭示布替啡烷和布替啡因各自的特性,这些特性可能因互变异构而被掩盖,并能够合成通常难以分离和耗时的 S-布替啡烷。