ABSTRACT
Objective: To study the chemical structure and bioactivity of the alkaloids from Zanthoxylum schinifolium. Methods The alkaloids were isolated and purified by silica gel, Sephadex LH-20 column chromatography, recrystallization, and semi-preparetive HPLC. Their structures were elucidated by physical and spectroscopic analysis. The cytotoxic activity of these compounds were tested by MTS. Results Nine alkaloids were obtained and identified as dictamnine (1), skimmianine (2), schinifoline (3), 6-methoxy-furanoquinolone (4), (+)-(S)-isoplatydesmine (5), (+)-(S)-araliopsine (6), (−)-(S)-ribalinine (7), (−)-(S)-edulinine (8), and (−)-(S)-6-acetonyldihydrochelerythrine (9). Conclusion Compound 4 is a new natural product and compounds 5—9 are isolated from this plant for the first time. Compound 9 has potential cytotoxicity towards HL-60, SMMC-7721, and A549.
ABSTRACT
Objective: To study the anti-inflammatory components from the root barks of Zanthoxylum schinifolium. Methods: The compounds were isolated and purified by silica gel, MCI, Sephadex LH-20 column chromatographies, and semi-preparative HPLC, and their structures were elucidated by physical and spectroscopic analysis. The anti-inf1ammatory activity was evaluated by the levels of NO in LPS-induced RAW264.7 tested by Griess reagent. Results: Four coumarins, namely zantholin A (1), 7-methoxycoumarin (2), isoscopoletin (3), and esculetin (4), were isolated from the root barks of Z. schinifolium. Compounds 1-4 exhibited anti-inflammatory activities on inhibition of lipopolysaccharide (LPS)-induced NO production in RAW 264.7 macrophages with IC50 values of (0.21 ± 0.03), (0.92 ± 0.16), (0.15 ± 0.02), and (0.26 ± 0.04) μmol/L, respectively. Conclusion: Compound 1 is a new compound, a rare terpenylated coumarin named zantholin A, and compounds 3 is obtained from this plant for the first time. All compounds exhibited anti-inflammatory activities.