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Phytochemical investigation on the aerial parts of Veratrum versicolor f. viride Nakai and their biological activities.
Hong, Seong Su; Lee, Jae Yeon; Jeong, Yeon Woo; Lee, Ji Eun; Choi, Yun-Hyeok; Jeong, Wonsik; Ahn, Eun-Kyung; Choi, Chun Whan; Ahn, Il Ho; Oh, Joa Sub.
Afiliación
  • Hong SS; Bio-Center, Gyeonggido Business & Science Accelerator (GBSA), Suwon, Republic of Korea.
  • Lee JY; NewCellPharm Co., Ltd., Seongnam, Republic of Korea.
  • Jeong YW; College of Pharmacy, Dankook University, Cheonan, Republic of Korea.
  • Lee JE; Bio-Center, Gyeonggido Business & Science Accelerator (GBSA), Suwon, Republic of Korea.
  • Choi YH; Bio-Center, Gyeonggido Business & Science Accelerator (GBSA), Suwon, Republic of Korea.
  • Jeong W; Bio-Center, Gyeonggido Business & Science Accelerator (GBSA), Suwon, Republic of Korea.
  • Ahn EK; Bio-Center, Gyeonggido Business & Science Accelerator (GBSA), Suwon, Republic of Korea.
  • Choi CW; Bio-Center, Gyeonggido Business & Science Accelerator (GBSA), Suwon, Republic of Korea.
  • Ahn IH; Bio-Center, Gyeonggido Business & Science Accelerator (GBSA), Suwon, Republic of Korea.
  • Oh JS; Bio-Center, Gyeonggido Business & Science Accelerator (GBSA), Suwon, Republic of Korea.
Turk J Chem ; 47(6): 1346-1354, 2023.
Article en En | MEDLINE | ID: mdl-38544705
ABSTRACT
Veratrum spp. have traditionally been used in folk medicine to treat various pathologies. In this study, nine compounds, comprising one simple phenolic compound (1), three stilbenoids (2-4), and five flavonoids (5-9), were isolated from the aerial parts of Veratrum versicolor f. viride Nakai. The structures of these compounds were elucidated by spectroscopic analyses and comparison with reported data. Together, all reported compounds were isolated from V. versicolor f. viride for the first time in the study. Among them, two flavone aglycone tricetins (7 and 9) have never been isolated from the genus Veratrum or the family Melanthiaceae. The ethanol extract and isolated compounds were assessed for their inhibitory effects on elastase, tyrosinase, and melanin synthesis. Compounds 5 and 7 inhibited elastase (IC50 292.25 ± 14.39 and 800.41 ± 5.86 µM, respectively), whereas compounds 2-5 inhibited tyrosinase with IC50 values in the range of 6.42 ~ 51.19 µM, respectively. In addition, compounds 3-6 and 8 exhibited dose-dependent inhibition (70.4% ~ 91.0%) of melanogenesis at a concentration of 100 µM.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Turk J Chem Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Turk J Chem Año: 2023 Tipo del documento: Article