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|Title:||12-Amino-andrographolide analogues: Synthesis and cytotoxic activity|
|Keywords:||Biochemistry, Genetics and Molecular Biology;Chemistry;Pharmacology, Toxicology and Pharmaceutics|
|Citation:||Archives of Pharmacal Research. Vol.36, No.12 (2013), 1454-1464|
|Abstract:||Andrographolide, a diterpenoid lactone of the plant Andrographis paniculata, has been shown to be cytotoxic against various cancer cells in vitro. In the present study, a series of β-amino-γ-butyrolactone analogues has been synthesized from naturally occurring andrographolide via one pot tandem aza-conjugate addition-elimination reaction. By using economic procedure without any base or catalyst at room temperature, the products obtained were in fair to excellent yields with high stereoselectivity. The cytotoxicity of all new amino analogues were evaluated against six cancer cell lines and revealed their potential for being developed as promising anti-cancer agents. © 2013 The Pharmaceutical Society of Korea.|
|Appears in Collections:||Scopus 2011-2015|
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