Limonoids from the Seeds of Swietenia macrophylla and Their Anti-Inflammatory Activities

被引:27
作者
Chen, Li-Chai [1 ,2 ]
Liao, Hsiang-Ruei [3 ]
Chen, Pei-Yu [2 ]
Kuo, Wen-Lung [4 ]
Chang, Tsung-Hsien [5 ]
Sung, Ping-Jyun [6 ]
Wen, Zhi-Hong [1 ]
Chen, Jih-Jung [7 ,8 ]
机构
[1] Natl Sun Yat Sen Univ, Dept Marine Biotechnol & Resources, Asia Pacific Ocean Res Ctr, Kaohsiung 80424, Taiwan
[2] Kaohsiung Armed Forces Gen Hosp, Dept Pharm, Zuoying Branch, Kaohsiung 81342, Taiwan
[3] Chang Gung Univ, Grad Inst Nat Prod, Sch Tradit Chinese Med, Coll Med, Taoyuan 33302, Taiwan
[4] Chung Jen Jr Coll Nursing Hlth Sci & Management, Chiayi 60077, Taiwan
[5] Kaohsiung Vet Gen Hosp, Dept Med Educ & Res, Kaohsiung 813, Taiwan
[6] Natl Museum Marine Biol & Aquarium, Pingtung 944, Taiwan
[7] Tajen Univ, Dept Pharm, Pingtung 90741, Taiwan
[8] Tajen Univ, Grad Inst Pharmaceut Technol, Pingtung 90741, Taiwan
关键词
Swietenia macrophylla; Meliaceae; structure elucidation; limonoid; anti-inflammatory activity; PHRAGMALIN-TYPE; MAHAGONI JACQ; CONSTITUENTS; NEUTROPHILS; SESQUITERPENE; DERIVATIVES; FRUITS;
D O I
10.3390/molecules201018551
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
A new limonoid, swietemacrophin (1), was isolated from the seeds of Swietenia macrophylla, together with five known compounds 2-6. The structure of 1 was determined through extensive 1D/2D-NMR and mass-spectrometric analyses. Swietemacrophin (1), humilinolide F (2), 3,6-O,O-diacetylswietenolide (3), 3-O-tigloylswietenolide (4), and swietemahonin E (5) exhibited inhibition (IC50 values 45.44 M) of superoxide anion generation by human neutrophils in response to formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLP). Compounds 1, 4, 5, and swietenine (6) showed potent inhibition with IC50 values 36.32 M, against lipopolysaccharide (LPS)-induced nitric oxide (NO) generation.
引用
收藏
页码:18551 / 18564
页数:14
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