Abstract
Phytochemical investigation of the roots of Albizia chevalieri led to the isolation of two new 5-deoxyflavan-3,4-diol glucosides from roots of A. chevalieri, Chevalieriflavanosides A and B. Their structures were established by 2D NMR techniques, UV, IR, CD, and mass spectrometry. Cytotoxicity of the two compounds was evaluated against acute promyelocytic leukemia HL60 cells. The antibacterial activities of 1 and 2 also were evaluated against Pseudomonas aeruginosa and Staphylococcus aureus using the agar diffusion test.
Original language | English |
---|---|
Pages (from-to) | 893-896 |
Number of pages | 4 |
Journal | Magnetic Resonance in Chemistry |
Volume | 54 |
Issue number | 11 |
DOIs | |
Publication status | Published - 2016 Nov 1 |
Keywords
- C
- H
- Albizia chevalieri
- cytotoxicity
- flavan-3,4-diols
- Leguminosae
- NMR