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Spectral and HPLC Analyses of Synthesized Butin and Butein.
Kamei, Takashi; Miyazaki, Jun; Hori, Ryoga; Saito, Hiroaki; Takahashi, Tatsuo; Shinohara, Ken-Ichi; Miura, Masakazu; Suzuki, Hirokazu.
Afiliação
  • Kamei T; Faculty of Pharmaceutical Sciences, Hokuriku University.
  • Miyazaki J; Healthy Aging Research Group, Hokuriku University.
  • Hori R; Department of Natural Sciences, School of Engineering, Tokyo Denki University.
  • Saito H; School of Materials Science, Japan Advanced Institute of Science and Technology (JAIST).
  • Takahashi T; Faculty of Pharmaceutical Sciences, Hokuriku University.
  • Shinohara KI; Faculty of Pharmaceutical Sciences, Hokuriku University.
  • Miura M; Healthy Aging Research Group, Hokuriku University.
  • Suzuki H; School of Materials Science, Japan Advanced Institute of Science and Technology (JAIST).
Chem Pharm Bull (Tokyo) ; 72(7): 648-657, 2024.
Article em En | MEDLINE | ID: mdl-38972722
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Chalconas Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Chalconas Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2024 Tipo de documento: Article