Key Laboratory for Forest Resources Conservation and Utilization in the Southwest Mountains of China, Ministry of Education, School of Forestry, Southwest Forestry University, Kunming 650224, PR China.
Key Laboratory of Forest Disaster Warning and Control of Yunnan Province, Southwest Forestry University, Kunming 650224, PR China.
Bioorg Med Chem. 2021 Dec 1;51:116495. doi: 10.1016/j.bmc.2021.116495. Epub 2021 Nov 10.
Four new 19-nor-clerodane diterpenoids (1-4), one new 15,16-dinor-ent-pimarane diterpenoid (5) together with four known diterpenoids (6-9) were isolated from whole plants of Croton yunnanensis. The structures of these compounds were determined by extensive spectroscopic methods including 1D, 2D NMR, HR-ESI-MS, and by comparing their NMR data with those of previously reported compounds. The experimental and calculated electronic circular dichroism data were used to define their absolute configurations. The H and C NMR spectra of 6 were completely assigned for the first time. All isolated compounds (1-9) were evaluated for their cytotoxic activities against five human cancer cell lines (including SMMC-7721, HL-60, A-549, MCF-7, and SW-480), and anti-inflammatory activities in LPS-induced RAW264.7 macrophages. Crotonyunnan E (5) exhibited selective cytotoxicities against three tumor cell lines, SMMC-7721 (human hepatoma cells, IC 4.47 ± 0.39 μM), HL-60 (human premyelocytic leukemia, IC 14.38 ± 1.19 μM), and A-549 (human lung cancer cells, IC 27.42 ± 0.48 μM), while none of the compounds showed obviously anti-inflammatory activities at 50 μM level.
从云南余甘子全株植物中分离得到四个新的 19-降 clerodane 二萜类化合物(1-4)、一个新的 15,16-二降-ent-pimarane 二萜类化合物(5)以及四个已知的二萜类化合物(6-9)。通过广泛的光谱方法,包括 1D、2D NMR、HR-ESI-MS,并通过比较它们的 NMR 数据与以前报道的化合物,确定了这些化合物的结构。实验和计算的电子圆二色谱数据用于确定它们的绝对构型。6 的 1H 和 13C NMR 谱首次被完全归属。所有分离得到的化合物(1-9)都被评估了对五种人类癌细胞系(包括 SMMC-7721、HL-60、A-549、MCF-7 和 SW-480)的细胞毒性活性,以及对 LPS 诱导的 RAW264.7 巨噬细胞的抗炎活性。云南余甘子 E(5)对三种肿瘤细胞系(人肝癌细胞 SMMC-7721,IC 4.47±0.39 μM;人早幼粒细胞白血病 HL-60,IC 14.38±1.19 μM;人肺癌细胞 A-549,IC 27.42±0.48 μM)表现出选择性细胞毒性,而在 50 μM 水平时,没有一种化合物表现出明显的抗炎活性。