Chen Weihao, Pang Xiaoyan, Song Yingying, Hu Yiwei, Wang Xueni, Wang Lishu, Wang Junfeng
Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, P. R. China.
CAS Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, P. R. China.
Nat Prod Res. 2024 Jun 9:1-8. doi: 10.1080/14786419.2024.2364930.
Chemical investigation of the EtOAc extract of a deep-sea derived fungus sp. SCSIO41032 resulted in the isolation of ten known compounds, including eight aspochalasins. Their structures were elucidated by using extensive NMR spectroscopic, mass spectrometric and single crystal X-ray diffraction analysis. The detailed crystallographic data for structures , , and , along with the relative configurations of aspochalasin E () determined by its acetonide derivative were reported for the first time. The results of antitumor and antiviral activities showed that displayed moderate antitumor activities against 22Rv1, PC-3, A549, and HCT-15 cell lines with IC values ranged from 5.9 ± 0.8 to 19.0 ± 7.7 μM, and exhibited moderate antiviral activities against HSV-1/2 with EC values of 9.5 ± 0.5 and 5.4 ± 0.6 μM, respectively. Plate clone formation assays results indicated that inhibited the 22Rv1, PC-3 cells growth in a dose-dependent manner.
对一株源自深海的真菌菌株SCSIO41032的乙酸乙酯提取物进行化学研究,从中分离出10种已知化合物,其中包括8种曲霉毒素。通过广泛的核磁共振光谱、质谱和单晶X射线衍射分析确定了它们的结构。首次报道了结构、和的详细晶体学数据,以及通过其丙酮化物衍生物确定的曲霉毒素E()的相对构型。抗肿瘤和抗病毒活性结果表明,对22Rv1、PC-3、A549和HCT-15细胞系表现出中等抗肿瘤活性,IC值范围为5.9±0.8至19.0±7.7μM,并且对HSV-1/2分别表现出中等抗病毒活性,EC值分别为9.5±0.5和5.4±0.6μM。平板克隆形成试验结果表明,以剂量依赖性方式抑制22Rv1、PC-3细胞的生长。