Two new triterpenoid glycosides from Bacopa monnieri and their cytotoxic activity

  • Nat Prod Res. 2024 Apr;38(7):1120-1126. doi: 10.1080/14786419.2022.2132498.
Duong Thi Hai Yen  1 Nguyen Thi Cuc  1 Bui Huu Tai  1 Phan Van Kiem  1 Manh Hoang Duc  2 Nguyen Xuan Nhiem  1 Su-Hyeon Cho  3 Sung Baek Jeong  4 Yohan Seo  4 SeonJu Park  3
Affiliations
  • 1. Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi Vietnam.
  • 2. National Institute of Medicinal Materials, Hanoi, Vietnam.
  • 3. Chuncheon Center, Korea Basic Science Institute, Chuncheon, Republic of Korea.
  • 4. New Drug Development Center, Daegu Gyeongbuk Medical Innovation Foundation, Daegu, Republic of Korea.
Abstract

Using combined chromatographic methods, two new triterpenoid glycosides, bacopasaponin K (1) and bacopasaponin L (2), along with eight known compounds, bacopaside IV (3), bacopaside VII (4), bacopasaponin E (5), bacoside A3 (6), bacopasaponin F (7), bacopasaponin C (8), bacopaside I (9), and bacopaside II (10) were isolated from the methanol extract of the Bacopa monnieri. Their structures were elucidated by 1D-, 2D-NMR spectroscopic analysis, HR-ESI-MS and comparing with the NMR data reported in the literature. All these compounds were evaluated for their cytotoxic activity using the cell counting kit-8 (CCK-8) assay. Compounds 4, 6, 8, and 10 exhibited potential cytotoxic effects against human lung Cancer cells (PC9) and human colon Cancer cells (SW620).

Keywords
Bacopa monnieri; bacopasaponin; bacopasaponin K; bacopasaponin L; triterpenoid glycoside.
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