Antimicrobial, Cytotoxic Lignans and Terpenoids from the Twigs of Pseudolarix kaempferi

被引:37
作者
He, Wen-Jun [1 ,2 ]
Chu, Hong-Biao [1 ]
Zhang, Yu-Mei [1 ]
Han, Hong-Jin [1 ]
Yan, He [1 ,2 ]
Zeng, Guang-Zhi [1 ]
Fu, Zhao-Hui [1 ]
Olubanke, Ogunlana [3 ]
Tan, Ning-Hua [1 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources W China, Kunming 650204, Yunnan, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
[3] Covenant Univ, Dept Biol Sci, Coll Sci & Technol, Ota, Ogun State, Nigeria
基金
中国国家自然科学基金;
关键词
Pseudolarix kaempferi; Pinaceae; lignans; terpenoids; antimicrobial; cytotoxic; TU-JIN-PI; ACID-B; SEQUOIA-SEMPERVIRENS; DITERPENOIDS; IDENTIFICATION; TRITERPENOIDS; CONSTITUENTS; GLYCOSIDES;
D O I
10.1055/s-0031-1280020
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Seven new compounds, including four lignans, (+)-(8S, 8'S)-9,9'-dibenzoylsecoisolariciresinol (1), (+)-(8S*, 8'R*)-4,4'-dimethyloxomatairesinol (2), (+)-(7S*, 8R*, 8'R*, 9'S*)-9'-n-butoxytsugacetal (3), and pseudolarkaemin A (4), a pyronane glycoside, pseudolarkaemin B (5), an ent-beyerene glycoside, pseudolarkaemin C (6), and a triterpene, 25-epi-pseudolarolide Q (7), along with 25 known compounds (8-32) were isolated from the twigs of Pseudolarix kaempferi. Their structures were elucidated mainly by the analysis of their NMR and MS data. Pseudolarolide C acid (24) was isolated for the first time as a natural product. All compounds were evaluated for antimicrobial activity against Candida albicans and Staphylococcus aureus, and cytotoxic activity against K562, HT29, B16, BGC-823, BEL-7402, SGC-7901, U251, and A549 cancer cell lines were assayed. Results indicated that the new compounds 3, 7, and some known compounds showed antimicrobial and cytotoxic activities.
引用
收藏
页码:1924 / 1931
页数:8
相关论文
共 31 条
[1]  
[Anonymous], 2010, PHARMACOPOEIA CHIN 1, P16
[2]   THE ISOLATION AND STRUCTURAL ELUCIDATION OF 4 NOVEL TRITERPENE LACTONES, PSEUDOLAROLIDE-A, PSEUDOLAROLIDE-B, PSEUDOLAROLIDE-C, AND PSEUDOLAROLIDE-D, FROM PSEUDOLARIX-KAEMPFERI [J].
CHEN, GF ;
LI, ZL ;
PAN, DJ ;
TANG, CM ;
HE, X ;
XU, GY ;
CHEN, K ;
LEE, KH .
JOURNAL OF NATURAL PRODUCTS, 1993, 56 (07) :1114-1122
[3]   Structures and stereochemistry of pseudolarolides K and L, novel triterpene dilactones from Pseudolarix kaempferi [J].
Chen, K ;
Shi, Q ;
Li, ZL ;
Poon, CD ;
Tang, RJ ;
Lee, KH .
JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 1999, 1 (03) :207-214
[4]   DITERPENOIDS FROM SPIROSTACHYS-AFRICANA [J].
DURI, ZJ ;
HUGHES, NA ;
MUNKOMBWE, NM .
PHYTOCHEMISTRY, 1992, 31 (02) :699-702
[5]   Oxidative transformation of the natural lignan hydroxymatairesinol with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone [J].
Eklund, PC ;
Sjöholm, RE .
TETRAHEDRON, 2003, 59 (25) :4515-4523
[6]   (+)-TSUGACETAL, A LIGNAN ACETAL FROM TAIWAN HEMLOCK [J].
FANG, JM ;
WEI, KM ;
CHENG, YS ;
CHENG, MC ;
WANG, Y .
PHYTOCHEMISTRY, 1985, 24 (06) :1363-1365
[7]   ISOLATION OF SECOISOLARICIRESINOL DIESTERS FROM STEMS OF SIMABA-CUNEATA [J].
FO, ER ;
FERNANDES, JB ;
VIEIRA, PC ;
DA SILVA, MFGF .
PHYTOCHEMISTRY, 1992, 31 (06) :2115-2116
[8]   Natural inhibitors of DNA topoisomerase I with cytotoxicities [J].
Han, Hong-Jin ;
Tan, Ning-Hua ;
Zeng, Guang-Zhi ;
Fan, Jun-Ting ;
Huang, Huo-Qiang ;
Ji, Chang-Jiu ;
Jia, Rui-Rui ;
Zhao, Qin-Shi ;
Zhang, Ying-Jun ;
Hao, Xiao-Jiang ;
Wang, Li-Qin .
CHEMISTRY & BIODIVERSITY, 2008, 5 (07) :1364-1368
[9]   Pseudolaric acid analogs as a new class of peroxisome proliferator-activated receptor agonists [J].
Jardat, MS ;
Noonan, DJ ;
Wu, BG ;
Avery, MA ;
Feller, DR .
PLANTA MEDICA, 2002, 68 (08) :667-671
[10]  
KIM YG, 1994, MOKUZAI GAKKAISHI, V40, P414