Norcolocynthenins A and B, two cucurbitane 3-nor-Triterpenoids from Citrullus colocynthis and their cytotoxicity

被引:7
|
作者
Liu, Yushuang [1 ,2 ,4 ]
Zhang, Lu [1 ]
Xue, Jingjing [3 ]
Wang, Kaibo [4 ]
Hua, Huiming [3 ]
Yuan, Tao [1 ,2 ]
机构
[1] Jiangxi Normal Univ, Coll Life Sci, Lab Effect Subst Jiangxi Genuine Med Mat, Nanchang 330022, Peoples R China
[2] Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, Key Lab Plant Resources & Chem Arid Zone, State Key Lab Xinjiang Indigenous Med Plants Reso, Urumqi 830011, Peoples R China
[3] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang 110016, Peoples R China
[4] Purdue Univ, Coll Pharm, Dept Med Chem & Mol Pharmacol, W Lafayette, IN 47907 USA
基金
中国国家自然科学基金;
关键词
Citrullus colocynthis; Cucurbitane nortriterpenoid; Theoretical calculations; Cytotoxicity; L; ALKALOIDS; FRUIT; SEEDS;
D O I
10.1016/j.bioorg.2020.104045
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
Two novel cucurbitane 3-nor-triterpenoids, named norcolocynthenins A (1) and B (2), were isolated from the fruits of Citrullus colocynthis. The structures including their absolute configurations were determined by extensive spectroscopic analyses and theoretical calculations. Compound 1 features an unprecedented 5/6/6/5-fused ring system while compound 2 possesses a rare lactone moiety at modified ring A. Compounds 1 and 2 showed significant cytotoxic activity against human cancer cell lines of HL-60 (IC50 = 8.32, 6.49 mu M) and PC-3 (IC50 = 31.26, 13.42 mu M). The plausible biosynthetic pathway of compounds 1 and 2 via a key enzymatic Baeyer-Villiger reaction is proposed.
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页数:5
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