抗真菌
烟草
植物
生物
立体化学
化学
传统医学
微生物学
医学
生物化学
基因
作者
Run‐Cheng Yan,Luyi Jiang,Ming Hu,Mingyue Shen,Mingzhu Liu,Yulan Shi,Ruirui Wang,Xing‐De Wu,Ganpeng Li
标识
DOI:10.1021/acs.jafc.5c00994
摘要
Sixteen previously undescribed cembrane-type diterpenoids, named nicotabacins A-P (1-16), were isolated from Nicotiana tabacum L., together with 12 known analogs (17-28). The structures of 1-16 were determined by extensive spectral analysis, single-crystal X-ray diffraction analysis, and ECD calculations. Compound 1 was a rare 4,5-seco-cembrane-type diterpene with 4,6-diketone and 8,11-oxygen-bridge moieties. Compounds 1-2, 4-11, 13-15, and 17-28 were evaluated for antifungal activities against Candida albicans (C. albicans), both alone and in combination with fluconazole (FLC). These compounds alone indicated no inhibitory activity against either the sensitive strain SC 5314 or the resistant strain ATCC 14053 of C. albicans. In contrast, compounds 10, 13, and 14, when combined with FLC, demonstrated a strong inhibitory effect on C. albicans resistant strain, with fractional inhibitory concentration index (FICI) values of 0.02 ± 0.01, 0.03 ± 0.01, and 0.03 ± 0.02, respectively, indicating a strong synergistic effect.
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