Cytotoxic benzopyranone and xanthone derivatives from a coral symbiotic fungus <i>Cladosporium halotolerans</i> GXIMD 02502
Chao‐Nan Wang, Humu Lu, Chenghai Gao, Lang Guo, Zhenyu Zhan, Junjian Wang, Junjian Wang, Yonghong Liu, Songtao Xiang, Jian Wang, Jian Wang, Xiaowei Luo
Abstract
Coral-derived microorganisms have been historically proven to be prolific sources of bioactive secondary metabolites. Twelve benzopyranone and/or xanthone derivatives, including a new benzopyranone with an uncommon carboxyl group at C-8, coniochaetone K (1), were obtained from the Beibu Gulf-derived coral symbiotic fungus Cladosporium halotolerans GXIMD 02502. Their structures were determined by extensive spectroscopic data interpretation and comparison with literature values. The absolute configuration of 1 was accomplished by comparison of specific optical rotation as well as quantum chemical ECD calculations. The in vitro cytotoxicity of compounds 1–12 against two human prostatic cancer cell lines, C4-2B and 22RV1, were evaluated. And compounds 1, 3, 6–8, and 10–11 demonstrated significant cytotoxicity with inhibitions ranging from 55.8% to 82.1% at the concentration of 10 μM.