Four triterpenes, including two new triterpenes recurvatanes A and B, were isolated from the aerial parts of Mussaenda recurvata. The chemical structures of the compounds were identified through spectroscopic data and literature comparison. Compounds 1 and 2 showed moderate inhibitory activity on NO production in LPS-stimulated RAW264.7 cells.
Bioactive-guided investigation of the aerial parts of Mussaenda recurvata Naiki, Tagane, and Yahara (Rubiaceae) led to the isolation of four triterpenes, including two new triterpenes recurvatanes A and B (1 and 2), along with two known compounds 3 beta,6 beta,23-trihydroxyolean-12-en-28-oic acid (3) and 3 beta,6 beta,19 alpha,23-tetrahydroxyolean-12-en-28-oic acid (4). The chemical structures of the compounds were identified from spectroscopic data and by comparison with the literature. A comprehensive review of NMR data of the oleanane-type triterpenes bearing 3-hydroxy and 4-hydroxymethylene groups indicated the characteristic spectroscopic features in this series. Compounds 1-4 were evaluated for the inhibitory NO production in LPS-stimulated RAW264.7 cells. Compounds 2 and 3 showed a moderate reduction of nitrite accumulation with IC50 values of 55.63 +/- 2.52 and 60.08 +/- 3.17 mu M, respectively. Molecular docking model dedicated to compound 3 or pose 420, which is the best candidate among docking poses of compounds 1-4 interacted well with the crystal structure of enzyme 4WCU: PDB. The best ligand molecule, pose 420 in terms of binding energy obtained from docking studies on molecular dynamics (MD) simulations for 100 ns exhibited non-bonding interactions with the protein and remained stable inside the active site.
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