Bioactive sesquiterpene lactones and other compounds isolated from Vernonia cinerea

被引:44
作者
Youn, Ui Joung [1 ]
Miklossy, Gabriella [2 ,3 ]
Chai, Xingyun [1 ]
Wongwiwatthananukit, Supakit [4 ]
Toyama, Onoomar [5 ]
Songsak, Thanapat [6 ]
Turkson, James [2 ,3 ]
Chang, Leng Chee [1 ]
机构
[1] Univ Hawaii, Dept Pharmaceut Sci, Daniel K Inouye Coll Pharm, Hilo, HI 96720 USA
[2] Univ Hawaii, Nat Prod Program, Ctr Canc, Honolulu, HI 96813 USA
[3] Univ Hawaii, Expt Therapeut Program, Ctr Canc, Honolulu, HI 96813 USA
[4] Univ Hawaii, Dept Pharm Practice, Daniel K Inouye Coll Pharm, Hilo, HI 96720 USA
[5] Silpakorn Univ, Dept Pharmaceut Chem, Fac Pharm, Nakhon Pathom 73000, Thailand
[6] Rangsit Univ, Dept Pharmacognosy, Fac Pharm, Pathum Thani 12000, Thailand
基金
新加坡国家研究基金会;
关键词
Vernonia cinerea; Asteraceae; Sesquiterpene lactone; STAT3; NF-KAPPA-B; CANCER DEVELOPMENT; SIGNAL TRANSDUCER; STAT3; ACTIVATION; INFLAMMATION; INHIBITION; PLANTS; P65/NF-KAPPA-B; MECHANISMS; IMMUNITY;
D O I
10.1016/j.fitote.2013.12.013
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Four new sesquiterpene lactones, 8 alpha-(2'Z-tigloyloxy)-hirsutinolide (1), 8 alpha-(2'Z-tigloyloxy)-hirsutinolide-13-O-acetate (2), 8 alpha-(4-hydroxytigloyloxy)-hirsutinolide (3), and 8 alpha-hydroxy-13-O-tigloyl-hirsutinolide (4), along with seven known derivatives (5-11), three norisoprenoids (12-14), a flavonoid (15), and a linoleic acid derivative (16), were isolated from the chloroform partition of a methanol extract from the combined leaves and stems of Vernonia cinerea. Their structures were established by 1D and 2D NMR, UV, and MS analyses. Compounds 1-16 were evaluated for their inhibitory effects against the viability of U251MG glioblastoma and MDA-MB-231 breast cancer cells that harbour aberrantly-active STAT3, compared to normal NIH3T3 mouse fibroblasts that show no evidence of activated STAT3. Among the isolates, compounds 2 and 7 inhibited the aberrant STAT3 activity in glioblastoma or breast cancer cells. Further, compounds 7 and 8 inhibited viability of all three cell lines, compounds 2,4, and 9 predominantly inhibited the viability of the U251MG glioblastoma cell line. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:194 / 200
页数:7
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