Quantitative structure -: Activity relationship of sesquiterpene lactones as inhibitors of the transcription factor NF-κB

被引:222
作者
Siedle, B
García-Piñeres, AJ
Murillo, R
Schulte-Mönting, J
Castro, V
Rüngeler, P
Klaas, CA
Da Costa, FB
Kisiel, W
Merfort, I [1 ]
机构
[1] Univ Freiburg, Lehrstuhl Pharmaczeut Biol, Inst Pharmazeut Wissensch, D-79104 Freiburg, Germany
[2] Univ Costa Rica, Escuela Quim & CIPRONA, San Jose, Costa Rica
[3] Univ Sao Paulo, Fac Ciencias Farmaceut, Sao Paulo, Brazil
[4] Univ Freiburg, Inst Med Biometrie & Med Informat, D-79104 Freiburg, Germany
[5] Polish Acad Sci, Inst Pharmacol, Dept Phytochem, PL-31343 Krakow, Poland
关键词
D O I
10.1021/jm049937r
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Sesquiterpene lactones (SLs) are the active compounds of a variety of tradionally used medicinal plants from the Asteraceae family. They are known to possess a considerable antiinflammatory activity in different inflammation models. They inhibit the transcription factor NF-kappaB probably by alkylating cysteine38 in the DNA binding domain of the p65 subunit. Here we investigate a set of 103 different sesquiterpene lactones representing 6 structural groups (44 germacranolides, 16 heliangolides, 22 guaianolides, 9 pseudoguaianolides, 2 hypocretenolides, 10 eudesmanolides) for their NF-kappaB inhibiting properties and the resulting IC100-values were submitted to a QSAR study. Properties important for the inhibition potency are discussed for the whole data set and for subsets of the different structural classes.
引用
收藏
页码:6042 / 6054
页数:13
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