Isolation, Structure Elucidation, and Antiproliferative Activity of Butanolides and Lignan Glycosides from the Fruit of Hernandia nymphaeifolia

被引:12
作者
Aimaiti, Simayijiang [1 ]
Saito, Yohei [1 ]
Fukuyoshi, Shuichi [1 ]
Goto, Masuo [2 ]
Miyake, Katsunori [3 ]
Newman, David J. [4 ]
O'Keefe, Barry R. [5 ,6 ]
Lee, Kuo-Hsiung [2 ,7 ]
Nakagawa-Goto, Kyoko [1 ,2 ]
机构
[1] Kanazawa Univ, Sch Pharmaceut Sci, Coll Med Pharmaceut & Hlth Sci, Kanazawa, Ishikawa 9201192, Japan
[2] Univ N Carolina, Nat Prod Res Labs, UNC Eshelman Sch Pharm, Chapel Hill, NC 27599 USA
[3] Tokyo Univ Pharm & Life Sci, Hachioji, Tokyo 1920392, Japan
[4] NIH, Special Volunteer, Wayne, PA 19087 USA
[5] NCI, Nat Prod Branch, Dev Therapeut Program, Div Canc Treatment & Diag,NCI Frederick, Frederick, MD 21702 USA
[6] NCI, Mol Targets Program, Ctr Canc Res, NCI Frederick, Frederick, MD 21702 USA
[7] China Med Univ & Hosp, Chinese Med Res & Dev Ctr, Taichung 40447, Taiwan
关键词
Hernandia nymphaeifolia; butanolides; lignan glycosides; antiproliferative activity; NON-ANTAGONISTIC INHIBITOR; NUCLEAR EXPORT; ALKALOIDS; CONSTITUENTS; PEUMUSOLIDE; GLUCOSIDES; NEOLIGNANS; FAMILY;
D O I
10.3390/molecules24214005
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
Seven new butanolides, peltanolides A-G (1-7), and two lignan glucosides, peltasides A (8) and B (9), along with eleven known compounds, 10-20, were isolated from a crude CH3OH/CH2Cl2 (1:1) extract of the fruit of Hernandia nymphaeifolia (Hernandiaceae). The structures of 1-9 were characterized by extensive 1D and 2D NMR spectroscopic and HRMS analysis. The absolute configurations of newly isolated compounds 1-9 were determined from data obtained by optical rotation and electronic circular dichroism (ECD) exciton chirality methods. Butanolides and lignan glucosides have not been isolated previously from this genus. Several isolated compounds were evaluated for antiproliferative activity against human tumor cell lines. Lignans 15 and 16 were slightly active against chemosensitive tumor cell lines A549 and MCF-7, respectively. Furthermore, both compounds displayed significant activity (IC50 = 5 mu M) against a P-glycoprotein overexpressing multidrug-resistant tumor cell line (KB-VIN) but were less active against its parent chemosensitive cell line (KB).
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