Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 804, Taiwan.
Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Mar Drugs. 2020 Nov 19;18(11):573. doi: 10.3390/md18110573.
The present investigation on chemical constituents of the soft coral resulted in the isolation of seven new cembranoids, cherbonolides F-L (-). The chemical structures of - were determined by spectroscopic methods, including infrared, one- and two-dimensional (1D and 2D) NMR (COSY, HSQC, HMBC, and NOESY), MS experiments, and a chemical reduction of hydroperoxide by triphenylphosphine. The anti-inflammatory activities of - against neutrophil proinflammatory responses were evaluated by measuring their inhibitory ability toward -formyl-methionyl-leucyl-phenylalanine/cytochalasin B (fMLF/CB)-induced superoxide anion generation and elastase release in primary human neutrophils. The results showed that all isolates exhibited moderate activities, while cherbonolide G () and cherbonolide H () displayed a more active effect than others on the inhibition of elastase release (48.2% ± 6.2%) and superoxide anion generation (44.5% ± 4.6%) at 30 µM, respectively.
本研究对软珊瑚的化学成分进行了研究,分离得到了 7 个新的海鞘烷类化合物,分别为 cherbonolides F-L(-)。通过光谱方法,包括红外、一维和二维(1D 和 2D)NMR(COSY、HSQC、HMBC 和 NOESY)、MS 实验以及三苯基膦对过氧化物的化学还原,确定了-的化学结构。通过测量它们对甲酰基-甲硫氨酸-亮氨酸-苯丙氨酸/细胞松弛素 B(fMLF/CB)诱导的人原代中性粒细胞中超氧阴离子生成和弹性蛋白酶释放的抑制能力,评估了-对中性粒细胞前炎症反应的抗炎活性。结果表明,所有分离物均表现出中等活性,而 cherbonolide G()和 cherbonolide H()在抑制弹性蛋白酶释放(48.2%±6.2%)和超氧阴离子生成(44.5%±4.6%)方面的活性均强于其他化合物,在 30 µM 时的抑制作用最强。