Four New Cassane Diterpenoids From the Seeds of Caesalpinia Mimosoides

被引:0
|
作者
Ma, Yu-Xin [1 ]
Pu, Xiao-Chen [1 ]
Xi, Rong-Gang [2 ]
Zhang, Yun-Qi [1 ,3 ,4 ]
Ma, Jun-Yi [1 ,3 ,4 ]
Wu, Zhao-Hua [5 ]
Gao, Hui-Yuan [1 ,3 ,4 ]
Wang, Miao [1 ,3 ,4 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Shenyang, Peoples R China
[2] 967th Hosp Joint Logist Support Force PLA, Dalian, Peoples R China
[3] Shenyang Pharmaceut Univ, Key Lab Pharmacodynam Subst Res & Translat Med Imm, Shenyang, Peoples R China
[4] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang, Peoples R China
[5] Mudanjiang Med Univ, Dept Pharmacol, Mudanjiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Caesalpinia mimosoides; cassane diterpenoids; norcassane-type; anti-inflammatory activity; FRUITS;
D O I
10.1002/cbdv.202403214
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
Four new cassane derivatives (1-4), along with five known compounds (5-9) were isolated from the seeds of Caesalpinia mimosoides. Their gross structures were elucidated by means of comprehensive spectroscopic analysis (ultraviolet, nuclear magnetic resonance, and high-resolution electrospray ionization mass spectrometry) as well as electronic circular dichroism calculations. Compounds 1-3 possessing norcassane-type skeleton were observed, which was a rare structural type in the Caesalpinia genus. The results of biological activity evaluation showed that compounds tested could inhibit the production of nitric oxide in lipopolysaccharide-induced RAW 264.7 cells, especially compound 8 exhibited excellent inhibitory activity, implying that these compounds may be potential anti-inflammatory candidates.
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页数:9
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