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Studies on Chemical‐Structure Modification and StructureActivity Relationship of Gambogic Acid Derivatives at Carbon(34)
Author(s) -
Zhang XiaoJin,
Li Xiang,
Yang YingRui,
Sun HaoPeng,
Gao Yuan,
Zhang Lei,
Wang JinXin,
Guo QingLong,
You QiDong
Publication year - 2012
Publication title -
chemistry and biodiversity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 70
eISSN - 1612-1880
pISSN - 1612-1872
DOI - 10.1002/cbdv.201200081
Subject(s) - gambogic acid , chemistry , natural product , lead compound , a549 cell , cell culture , chemical structure , structure–activity relationship , cancer cell lines , stereochemistry , combinatorial chemistry , cell , cancer cell , biochemistry , cancer , organic chemistry , in vitro , biology , genetics
Gambogic acid (GA), a natural product, was identified as a promising antitumor agent. To further explore the structureactivity relationship of GA and discover novel GA derivatives as antitumor agents, 19 novel GA derivatives modified at C(34) were synthesized and evaluated against A549, BGC‐823, U251, HepG2, and MB‐231 cancer cell lines by cellular assays. Among them, 15 compounds were found to be more potent than GA against some cancer cell lines. Notably, compound 3 possessed potent inhibitory activities against five cell lines with IC 50 values ranging between 0.24 and 1.09 μ M . Compounds 9 and 18 were seven to eightfold more active than GA against A549 cell line. Chemical modification at C(34) of GA by introducing of hydrophilic aliphatic amines resulted in increased activity and improved drug‐like properties. These findings will enhance our understanding of the SAR of GA and can lead to the discovery of novel GA derivatives as potential antitumor agents.