A novel isocoumarin with anti-influenza virus activity from Strobilanthes cusia

被引:31
作者
Gu, Wei [1 ,2 ]
Wang, Wei [4 ]
Li, Xiao-nian [3 ]
Zhang, Yu [3 ]
Wang, Li-ping [1 ,2 ]
Yuan, Chun-mao [1 ,2 ]
Huang, Lie-jun [1 ,2 ]
Hao, Xiao-jiang [1 ,2 ,3 ]
机构
[1] Key Lab Chem Nat Prod Guizhou Prov, Guiyang 550002, Guizhou, Peoples R China
[2] Chinese Acad Sci, Guiyang 550002, Guizhou, Peoples R China
[3] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China
[4] Ocean Univ China, Sch Med & Pharm, Qingdao 266100, Shandong, Peoples R China
关键词
Strobilanthes cusia; Novel isocoumarin; Unprecedented skeleton; Anti-influenza virus activity; GLYCOSIDES;
D O I
10.1016/j.fitote.2015.10.009
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Strobilanthes A (1), a novel isocoumarin with an unusual tetrahydro-4 H-pyran-4-one moiety fused isocoumarin core skeleton, together with a known compound (2) was isolated from Strobilanthes cusia. Its chemical structures were elucidated by 2D NMR spectroscopy, mass spectrometry and single-crystal X-ray diffraction analysis. The biosynthetic pathway of 1 could be supposed to be originally derived from 3-methylisocoumarin, a product of AA-MA pathway. Both of two compounds displayed anti-influenza virus activity in vitro. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 62
页数:3
相关论文
共 11 条
[1]   Indole-Diterpenoids with Anti-H1N1 Activity from the Aciduric Fungus Penicillium camemberti OUCMDZ-1492 [J].
Fan, Yaqin ;
Wang, Yi ;
Liu, Peipei ;
Fu, Peng ;
Zhu, Tonghan ;
Wang, Wei ;
Zhu, Weiming .
JOURNAL OF NATURAL PRODUCTS, 2013, 76 (07) :1328-1336
[2]   ON ENANTIOMORPH-POLARITY ESTIMATION [J].
FLACK, HD .
ACTA CRYSTALLOGRAPHICA SECTION A, 1983, 39 (NOV) :876-881
[3]   Iota-Carrageenan is a potent inhibitor of rhinovirus infection [J].
Grassauer, Andreas ;
Weinmuellner, Regina ;
Meier, Christiane ;
Pretsch, Alexander ;
Prieschl-Grassauer, Eva ;
Unger, Hermann .
VIROLOGY JOURNAL, 2008, 5 (1)
[4]   Indole Alkaloid Glycosides from the Aerial Parts of Strobilanthes cusia [J].
Gu, Wei ;
Zhang, Yu ;
Hao, Xiao-Jiang ;
Yang, Fu-Mei ;
Sun, Qian-Yun ;
Morris-Natschke, Susan L. ;
Lee, Kuo-Hsiung ;
Wang, Yue-Hu ;
Long, Chun-Lin .
JOURNAL OF NATURAL PRODUCTS, 2014, 77 (12) :2590-2594
[5]  
Hill R.A., 1986, FORT CHEM ORG NAT, V49, P1, DOI [10.1007/978-3-7091-8846-0_1, DOI 10.1007/978-3-7091-8846-0_1]
[6]   Determination of absolute structure using Bayesian statistics on Bijvoet differences [J].
Hooft, Rob W. W. ;
Straver, Leo H. ;
Spek, Anthony L. .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2008, 41 :96-103
[7]  
Kong LY., 2008, CHEM COUMARINS, P178
[8]  
Rubani Shahni Rubani Shahni, 2013, International Journal of PharmTech Research, V5, P1281
[9]   A new lignan glycoside and phenylethanoid glycosides from Strobilanthes cusia BREMEK [J].
Tanaka, T ;
Ikeda, T ;
Kaku, N ;
Zhu, XH ;
Okawa, M ;
Yokomizo, K ;
Uyeda, M ;
Nohara, T .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2004, 52 (10) :1242-1245
[10]   ACCUMULATION AND METABOLISM OF THE SPERMINE ALKALOID APHELANDRINE IN ROOTS OF APHELANDRA-TETRAGONA [J].
WERNER, C ;
HEDBERG, C ;
LORENZIRIATSCH, A ;
HESSE, M .
PHYTOCHEMISTRY, 1993, 33 (05) :1033-1036