Sesquiterpenoids from Inula racemosa Hook. f. Inhibit Nitric Oxide Production

被引:29
作者
Zhang, Shou-De [2 ]
Qin, Jiang-Jiang [2 ]
Jin, Hui-Zi [2 ]
Yin, Yin-Hua [1 ]
Li, Hong-Lin [3 ]
Yang, Xian-Wen [4 ]
Li, Xia [1 ]
Shan, Lei [1 ]
Zhang, Wei-Dong [1 ,2 ]
机构
[1] Second Mil Med Univ, Dept Nat Product Chem, Sch Pharm, Shanghai 200433, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200030, Peoples R China
[3] E China Univ Sci & Technol, Shanghai Key Lab Chem Biol, Sch Pharm, Shanghai 200237, Peoples R China
[4] Chinese Acad Sci, Key Lab Marine Bioresources Sustainable Utilizat, S China Sea Inst Oceanol, Guangzhou, Guangdong, Peoples R China
关键词
Inula racemosa Hook. f; Compositae; sesquiterpenes; density functional theory; nitric oxide; ELECTRONIC CIRCULAR-DICHROISM; LACTONES; BRITANNICA; EUDESMANOLIDE; CONSTITUENTS; GROWTH;
D O I
10.1055/s-0031-1280294
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A novel trinorsesquiterpene (1), three new (2-4), and 10 known sesquiterpenes were isolated from the roots of Inula racemosa Hook. f. The structures and absolute configurations of the new sesquiterpenes were elucidated by extensive spectroscopic and computational methods. All compounds were evaluated for their inhibition of LPS-induced nitric oxide production in RAW264.7 macrophages, and the results indicated that compounds 9, 12, and 13 moderately inhibited nitric oxide production with IC50 values of 7.39 +/- 0.36, 6.35 +/- 0.26, and 5.39 +/- 0.18 mu M, respectively.
引用
收藏
页码:166 / 171
页数:6
相关论文
共 34 条
[1]  
[Anonymous], 1977, DICT TRADITIONAL CHI, V2, P2216
[2]  
[Anonymous], 1996, Methods in nitric oxide research
[3]   Sesquiterpene lactones from Inula britannica and their cytotoxic and apoptotic effects on human cancer cell lines [J].
Bai, NS ;
Lai, CS ;
He, K ;
Zhou, Z ;
Zhang, L ;
Quan, Z ;
Zhu, NQ ;
Zheng, QY ;
Pan, MH ;
Ho, CT .
JOURNAL OF NATURAL PRODUCTS, 2006, 69 (04) :531-535
[4]   Application of electronic circular dichroism in configurational and conformational analysis of organic compounds [J].
Berova, Nina ;
Di Bari, Lorenzo ;
Pescitelli, Gennaro .
CHEMICAL SOCIETY REVIEWS, 2007, 36 (06) :914-931
[5]   NATURALLY OCCURRING TERPENE DERIVATIVES .142. NEW SESQUITERPENE LACTONES FROM INULA SPECIES [J].
BOHLMANN, F ;
MAHANTA, PK ;
JAKUPOVIC, J ;
RASTOGI, RC ;
NATU, AA .
PHYTOCHEMISTRY, 1978, 17 (07) :1165-1172
[6]  
Cho S, 2001, JP Patent, Patent No. 2001039882
[7]   The current state of ab initio calculations of optical rotation and electronic circular dichroism spectra [J].
Crawford, T. Daniel ;
Tam, Mary C. ;
Abrams, Micah L. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2007, 111 (48) :12057-12068
[8]   RAPID COLORIMETRIC ASSAY FOR CELL-GROWTH AND SURVIVAL - MODIFICATIONS TO THE TETRAZOLIUM DYE PROCEDURE GIVING IMPROVED SENSITIVITY AND RELIABILITY [J].
DENIZOT, F ;
LANG, R .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 89 (02) :271-277
[9]   Systematic investigation of modern quantum chemical methods to predict electronic circular dichroism spectra [J].
Diedrich, C ;
Grimme, S .
JOURNAL OF PHYSICAL CHEMISTRY A, 2003, 107 (14) :2524-2539
[10]   Theoretical calculation of electronic circular dichroism of the rotationally restricted 3,8"-biflavonoid morelloflavone [J].
Ding, Yuanqing ;
Li, Xing-Cong ;
Ferreira, Daneel .
JOURNAL OF ORGANIC CHEMISTRY, 2007, 72 (24) :9010-9017