Terpenoids isolated from Chinese liverworts Lepidozia reptans and their anti-inflammatory activity

被引:17
作者
Li, Siwen [1 ]
Niu, Huanmin [2 ]
Qiao, Yanan [1 ]
Zhu, Rongxiu [3 ]
Sun, Yong [1 ]
Ren, Zhaojie [4 ]
Yuan, Huiqing [2 ]
Gao, Yun [1 ]
Li, Yi [1 ]
Chen, Wang [5 ]
Zhou, Jinchuan [1 ]
Lou, Hongxiang [1 ]
机构
[1] Shandong Univ, Minist Educ, Key Lab Chem Biol, Dept Nat Prod Chem, 44 West Wenhua Rd, Jinan 250010, Shandong, Peoples R China
[2] Shandong Univ, Sch Med, Dept Biochem & Mol Biol, Jinan, Shandong, Peoples R China
[3] Shandong Univ, Sch Chem & Chem Engn, Jinan, Shandong, Peoples R China
[4] Shandong Museum, Nat Dept, 11899 Jingshi Rd, Jinan, Shandong, Peoples R China
[5] Shanxi Univ Technol, Vitamin Res Inst D, 1 Dongyi Rd, Hanzhong 723000, Shanxi, Peoples R China
关键词
Liverworts; Terpenoids; Anti-inflammatory; NF-KAPPA-B; EUDESMANE-TYPE SESQUITERPENOIDS; KAURANE-TYPE DITERPENOIDS; DOLABELLANE DITERPENOIDS; INFLAMMATORY RESPONSES; JUNGERMANNIA-SUBULATA; CHEMICAL-CONSTITUENTS; SALVIA-PLEBEIA; BRYOPHYTES; CELLS;
D O I
10.1016/j.bmc.2018.03.040
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
Five new terpenoids (1-5) including two dollabellane-type, one ent-kaurane-type diterpenoids and two sesquiterpenoids were isolated from the Chinese liverwort Lepidozia reptans (L.) Dumort., together with nine known terpenoids (6-14). Their structures were determined on the basis of analysis of MS and NMR spectroscopic data, single-crystal X-ray diffraction and electronic circular dichroism calculations. The selected compounds 1, 2, 6, 7, 9 and 14 were screened for anti-inflammatory activities by the model of LPS-induced nitric oxide (NO) production with macrophage cells, and the mechanism of the active compounds 1 and 2 were further explored. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2392 / 2400
页数:9
相关论文
共 45 条
[1]   Recent advances in phytochemistry of bryophytes-acetogenins, terpenoids and bis(bibenzyl)s from selected Japanese, Taiwanese, New Zealand, Argentinean and European liverworts [J].
Asakawa, Y .
PHYTOCHEMISTRY, 2001, 56 (03) :297-312
[2]  
ASAKAWA Y, 1982, PROG CH ORG NAT PROD, V42, P1
[3]  
Asakawa Y., 1995, Progress in the Chemistry of Organic Natural Products, V65, P1, DOI 10.1007/978-3-7091-6896-7_1
[4]  
Asakawa Y., 2013, Chemical constituents of bryophyta
[5]   Phytochemical and biological studies of bryophytes [J].
Asakawa, Yoshinori ;
Ludwiczuk, Agnieszka ;
Nagashima, Fumihiro .
PHYTOCHEMISTRY, 2013, 91 :52-80
[6]   Synthesis and biological activity of new phthalimides as potential anti-inflammatory agents [J].
Bach, Duc-Hiep ;
Liu, Jian-Yu ;
Kim, Won Kyung ;
Hong, Ji-Young ;
Park, So Hyun ;
Kim, Donghwa ;
Qin, Si-Ning ;
Luu, Thi-Thu-Trang ;
Park, Hyen Joo ;
Xu, Yong-Nan ;
Lee, Sang Kook .
BIOORGANIC & MEDICINAL CHEMISTRY, 2017, 25 (13) :3396-3405
[7]  
Braulio M, 1996, J NAT PRODUCTS, V59, P952
[8]   Dolabellane diterpenoids from Aglaia odorata [J].
Cai, Xiang-Hai ;
Wang, Yuan-Yuan ;
Zhao, Pei-Ji ;
Li, Yan ;
Luo, Xiao-Dong .
PHYTOCHEMISTRY, 2010, 71 (8-9) :1020-1024
[9]   Synthesis and anti-inflammatory activity of isoquebecol [J].
Cardinal, Sebastien ;
Paquet-Cote, Pierre-Alexandre ;
Azelmat, Jabrane ;
Bouchard, Corinne ;
Grenier, Daniel ;
Voyer, Normand .
BIOORGANIC & MEDICINAL CHEMISTRY, 2017, 25 (07) :2043-2056
[10]   New diterpenoids and cytotoxic and anti-inflammatory diterpenoids from Amentotaxus formosana [J].
Chen, Hui-Ling ;
Lin, Kai-Wei ;
Gan, Kim-Hong ;
Wang, Jih-Pyang ;
Won, Shen-Jeu ;
Lin, Chun-Nan .
FITOTERAPIA, 2011, 82 (02) :219-224