Structurally diverse diterpenoids from Isodon oresbius and their bioactivity

被引:8
作者
Qiu, Cai-Ling [1 ,2 ]
Ye, Zhen-Nan [3 ]
Yan, Bing-Chao [1 ,2 ]
Hu, Kun [1 ,2 ]
Yang, Jin [1 ,2 ]
Yang, Xing-Zhi [1 ,2 ]
Li, Hong-Mei [1 ,2 ]
Li, Xiao-Nian [1 ,2 ]
Sun, Han-Dong [1 ,2 ]
Puno, Pema-Tenzin [1 ,2 ]
机构
[1] Kunming Inst Bot, Chinese Acad Sci, State Key Lab Phytochemistry & Plant Resources Wes, Kunming 650201, Yunnan, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Affiliated Hosp Guangdong Med Univ, Inst Nephrol, Key Lab Prevent & Management Chron Kidney Dis Zhan, Zhanjiang 524001, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Isodon oresbius; Diterpenoids; Cytotoxicity; Apoptosis; Lysosomal activity; ENT-KAURANE DITERPENOIDS; KAURENE DITERPENOIDS; PATHWAY; PROTEIN; LEAVES; CELLS;
D O I
10.1016/j.bioorg.2022.105811
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Twelve new diterpenoids, isoresbins A-L (1-12), together with twenty-eight known ones, were isolated from the aerial parts of Isodon oresbius. Their diverse structures included 6,7-seco-ent-kaurane, 7,20-epoxy-ent-kaurane, 6,7:8,15-diseco-ent-kaurane, and abietanes skeletons, which were elucidated by spectroscopic data interpretation, single-crystal X-ray diffraction, and quantum chemical calculation. Isoresbins A (1) and B (2) possessed a new rearranged 15(8 -> 11)-abeo-6,7-seco-ent-kaurane skeleton. 1 and 5 promoted lysosomal function, which was evaluated by LysoTracker Red staining and DQ-ovalbumin dequenching assay. 1 showed cytotoxicity against six human tumor cell lines with IC50 values in 2.07-4.04 mu M range. Moreover, 1 induced damage of mitochondrial membrane potential, G2/M cell cycle arrest and apoptosis in SW480 cells.
引用
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页数:11
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