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Tetra-aryl cyclobutane and stilbenes from the rhizomes of Rheum undulatum and their α-glucosidase inhibitory activity: Biological evaluation, kinetic analysis, and molecular docking simulation.
Ha, Manh Tuan; Kim, Minji; Kim, Chung Sub; Park, Se-Eun; Kim, Jeong Ah; Woo, Mi Hee; Choi, Jae Sue; Min, Byung Sun.
Afiliación
  • Ha MT; College of Pharmacy, Drug Research and Development Center, Daegu Catholic University, Gyeongbuk 38430, Republic of Korea; Laboratory of Research and Applied Biochemistry, Center for Research and Technology Transfer, Vietnam Academy of Science and Technology, Hanoi, Viet Nam.
  • Kim M; College of Pharmacy, Drug Research and Development Center, Daegu Catholic University, Gyeongbuk 38430, Republic of Korea.
  • Kim CS; Department of Chemistry, Yale University, New Haven, CT 06520, United States.
  • Park SE; Department of Food and Life Science, Pukyong National University, Busan 48513, Republic of Korea.
  • Kim JA; College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu 41566, Republic of Korea.
  • Woo MH; College of Pharmacy, Drug Research and Development Center, Daegu Catholic University, Gyeongbuk 38430, Republic of Korea.
  • Choi JS; Department of Food and Life Science, Pukyong National University, Busan 48513, Republic of Korea.
  • Min BS; College of Pharmacy, Drug Research and Development Center, Daegu Catholic University, Gyeongbuk 38430, Republic of Korea. Electronic address: bsmin@cu.ac.kr.
Bioorg Med Chem Lett ; 30(8): 127049, 2020 04 15.
Article en En | MEDLINE | ID: mdl-32111435
One achiral tetra-aryl cyclobutane [rheundulin A (1)] and three stilbene glycosides [rheundulins B-D (2-4)] were isolated from the methanol extract of Rheum undulatum L., along with eight known compounds (5-12). Structural determination of the new compounds (1-4) was accomplished using comprehensive spectroscopic methods. Compound 1 represents the first example of a dimeric stilbene linked via a cyclobutane ring from the Rheum genus. All isolates were screened for their inhibition against α-glucosidase. Among them, stilbene derivatives (5 and 6) showed strong inhibitory effects on α-glucosidase with IC50 values of 0.5 and 15.4 µM, respectively, which were significantly higher than that of the positive control, acarbose (IC50 = 126.8 µM). Rheundulin A (1) showed moderate α-glucosidase inhibition with an IC50 value of 80.1 µM. In addition, kinetic analysis and molecular docking simulation of the most active compound (5) with α-glucosidase were performed for the first time. Kinetic studies revealed that compound 5 competitively inhibited the active site of α-glucosidase (Ki = 0.40 µM), while 6 had a mixed-type inhibitory effect against α-glucosidase (Ki = 15.34 µM). Molecular docking simulations of 5 and 6 demonstrated negative-binding energies, indicating high proximity to the active site and tight binding to α-glucosidase enzyme.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rheum / Estilbenos / Extractos Vegetales / Ciclobutanos / Rizoma / Alfa-Glucosidasas / Inhibidores de Glicósido Hidrolasas Límite: Humans Idioma: En Revista: Bioorg Med Chem Lett Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2020 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rheum / Estilbenos / Extractos Vegetales / Ciclobutanos / Rizoma / Alfa-Glucosidasas / Inhibidores de Glicósido Hidrolasas Límite: Humans Idioma: En Revista: Bioorg Med Chem Lett Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2020 Tipo del documento: Article Pais de publicación: Reino Unido