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Phenyl glycosides from Bacopa monnieri with their antioxidant and anti-inflammatory activities.
Dinh, Thi Phuong Anh; Thuy, Le Thi; Thuy My, Nguyen Thi; Nguyen, Van Thong; Tram, Le Huyen; Nguyen, Tuan Anh; Toan, Dao Huy; Tran, Thu Huong; Tran, Thu Ha; Bui Van, Thanh; Van Bach, Nguyen.
Afiliación
  • Dinh TPA; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Thuy LT; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Thuy My NT; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Nguyen VT; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Tram LH; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Nguyen TA; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Toan DH; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Tran TH; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Tran TH; Intellectual Property Office of Vietnam, Hanoi, Vietnam.
  • Bui Van T; Institute of Ecology and Biological Resources (IEBR), Vietnam Academy of Science and Technology (VAST), Caugiay, Vietnam.
  • Van Bach N; Vietnam Military Medical University, Hanoi, Vietnam.
Nat Prod Res ; : 1-6, 2023 Sep 21.
Article en En | MEDLINE | ID: mdl-37732634
ABSTRACT
Bacopa monnieri (L.) Wettst (Plantaginaceae), is traditionally used in many countries as neural tonic and memory enhancer, or to relieve acute pain and inflammation. This study described the isolation and identification of one new, bacomoside D3 (1), and seven known phenyl glycosides (2 - 8). The structures of isolates were established by analysis of their spectroscopic data or hydrolysis followed by HPLC analysis together with a comparison to those reported in the literature. These compounds were evaluated for antioxidant and anti-inflammatory activities. Among them, compounds 4 and 5 exhibited strong DPPH radical scavenging activity with IC50 values of 9.77 ± 0.08 and 3.50 ± 0.04 µM, respectively. Compounds 2 and 5 significantly inhibited TNF-α production in LPS-stimulated RAW264.7 cells with IC50 values of 40.60 ± 3.05 and 38.19 ± 1.75 µM, respectively. Furthermore, the active compounds could be efficient inhibitors of oxidants by interfering with the DPPH activity in silico study.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Prod Res Año: 2023 Tipo del documento: Article País de afiliación: Vietnam

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Prod Res Año: 2023 Tipo del documento: Article País de afiliación: Vietnam
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