The Constituents of Michelia compressa var. formosana and Their Bioactivities

被引:17
作者
Chan, Yu-Yi [1 ]
Juang, Shin-Hun [2 ]
Huang, Guan-Jhong [3 ]
Liao, Yu-Ren [4 ]
Chen, Yu-Fon [5 ]
Wu, Chia-Che [6 ]
Chang, Hui-Ting [6 ]
Wu, Tian-Shung [4 ]
机构
[1] Southern Taiwan Univ Sci & Technol, Dept Biotechnol, Tainan 71005, Taiwan
[2] China Med Univ, Grad Inst Pharmaceut Chem, Taichung 40402, Taiwan
[3] China Med Univ, Dept Pharm, Taichung 40402, Taiwan
[4] Natl Cheng Kung Univ, Dept Chem, Tainan 70101, Taiwan
[5] Natl Cheng Kung Univ, Dept Life Sci, Tainan 70101, Taiwan
[6] Natl Taiwan Univ, Sch Forestry & Resource Conservat, Taipei 10617, Taiwan
关键词
Michelia formosana; Magnoliaceae; NO inhibition; macrophage; cytotoxicity; CHEMICAL-CONSTITUENTS; CYTOTOXIC PRINCIPLES; ANNONA-CHERIMOLA; ALKALOIDS; STEMS; LIGNANS; LEAVES; PLANTS; ROOT;
D O I
10.3390/ijms150610926
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Phytochemical investigation of the heartwood of Michelia compressa afforded forty-four compounds, which were identified by comparison of experimental and literature analytical and spectroscopic data. Some compounds were evaluated for their anti-inflammatory and anticancer bioactivities. The result showed that soemerine (1) and cyathisterol (2) exhibited significant nitric oxide (NO) inhibition, with IC50 values of 8.5 +/- 0.3 and 9.6 +/- 0.5 mu g/mL, respectively. In addition, liriodenine (3) and oliveroline (4) exhibited cytotoxicity to human nasopharyngeal carcinoma (NPC-TW01), non-small cell lung carcinoma (NCI-H226), T cell leukemia (Jurkat), renal carcinoma (A498), lung carcinoma (A549) and fibrosarcoma (HT1080) cell lines with IC50 values in the range of 15.7-3.68 mu M.
引用
收藏
页码:10926 / 10935
页数:10
相关论文
共 45 条
[1]
STUDIES ON THE SYNTHESES OF LACTONES .15. SYNTHESES OF 4 POSSIBLE DIASTEREOISOMERS OF BOHLMANN STRUCTURE OF ISOEPOXYESTAFIATIN - THE STEREOCHEMICAL ASSIGNMENT OF ISOEPOXYESTAFIATIN [J].
ANDO, M ;
YOSHIMURA, H .
JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (15) :4127-4131
[2]
[Anonymous], 1999, J NAT PROD, V62, P22
[3]
Anti-inflammatory activities of tormentic acid from suspension cells of Eriobotrya Japonica ex vivo and in vivo [J].
Chang, Chwen-Tzuei ;
Huang, Shyh-Shyun ;
Lin, Shiang-Shiou ;
Amagaya, Sakae ;
Ho, Hui-Ya ;
Hou, Wen-Chi ;
Shie, Pei-Hsin ;
Wu, Jin-Bin ;
Huang, Guan-Jhong .
FOOD CHEMISTRY, 2011, 127 (03) :1131-1137
[4]
Chemical constituents from Annona glabra III [J].
Chang, FR ;
Chen, CY ;
Hsieh, TJ ;
Cho, CP ;
Wu, YC .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 2000, 47 (4B) :913-920
[5]
STRUCTURE ELUCIDATION AND TOTAL SYNTHESIS OF NEW TANSHINONES ISOLATED FROM SALVIA-MILTIORRHIZA BUNGE (DANSHEN) [J].
CHANG, HM ;
CHENG, KP ;
CHOANG, TF ;
CHOW, HF ;
CHUI, KY ;
HON, PM ;
TAN, FWL ;
YANG, Y ;
ZHONG, ZP ;
LEE, CM ;
SHAM, HL ;
CHAN, CF ;
CUI, YX ;
WONG, HNC .
JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (11) :3537-3543
[6]
Cheritamine, a new N-fatty acyl tryptamine and other constituents from the stems of Annona cherimola [J].
Chen, CY ;
Chang, FR ;
Teng, CM ;
Wu, YC .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 1999, 46 (01) :77-86
[7]
The constituents from the stems of Annona cherimola [J].
Chen, CY ;
Chang, FR ;
Wu, YC .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 1997, 44 (03) :313-319
[8]
Chemical constituents of Neolitsea parvigemma and Neolitsea konishii [J].
Chen, KS ;
Chang, FR ;
Chia, YC ;
Wu, TS ;
Wu, YC .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 1998, 45 (01) :103-110
[9]
Bioactive alkaloids from Illigera luzonensis [J].
Chen, KS ;
Wu, YC ;
Teng, CM ;
Ko, FN ;
Wu, TS .
JOURNAL OF NATURAL PRODUCTS, 1997, 60 (06) :645-647
[10]
Sodium aristolochates from the flowers and fruits of Aristolochia zollingeriana [J].
Chiang, CY ;
Leu, YL ;
Chan, YY ;
Wu, TS .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 1998, 45 (01) :93-97