Biological activities of novel pyrazolyl hydroxamic acid derivatives against human lung cancer cell line A549

European Journal of Medicinal Chemistry
2014.0

Abstract

We synthesized a series of novel pyrazolyl hydroxamic acid derivatives (4a-4l) and investigated their biological activities against human lung cancer cell line A549 in vitro to determine their mechanism of action. The results showed that the majority of derivatives had inhibitory effects on the growth of A549 cancer cells in dose and time-dependent manners, in which the compounds 4b, 4f, 4h and 4j (10 μM) exerted more effective anti-proliferation activity. However, it should be noted that 4j may result in necrosis at 10 μM. Furthermore, the three compounds 4b, 4f and 4h induced cell cycle arrest at G1 phase and triggered autophagy, but could not obviously induce apoptosis and necrosis under the stimulatory condition. Therefore, the pyrazolyl hydroxamic acid derivatives 4b, 4f and 4h can be used to investigate the regulatory mechanism of autophagy and offer new approaches to the prevention of lung cancer.

Knowledge Graph

Similar Paper

Biological activities of novel pyrazolyl hydroxamic acid derivatives against human lung cancer cell line A549
European Journal of Medicinal Chemistry 2014.0
Synthesis of 6-cinnamoyl-2H-benzo[b][1,4]oxazin-3(4H)-ones and their effects on A549 lung cancer cell growth
European Journal of Medicinal Chemistry 2014.0
Synthesis of pyrazole peptidomimetics and their inhibition against A549 lung cancer cells
Bioorganic & Medicinal Chemistry Letters 2012.0
Synthesis and preliminary mechanistic evaluation of 5-(p-tolyl)-1-(quinolin-2-yl)pyrazole-3-carboxylic acid amides with potent antiproliferative activity on human cancer cell lines
European Journal of Medicinal Chemistry 2014.0
Discovery of a new autophagy inducer for A549 lung cancer cells
Bioorganic & Medicinal Chemistry 2019.0
Design, synthesis and biological evaluation of novel pyrazolo-oxothiazolidine derivatives as antiproliferative agents against human lung cancer cell line A549
Bioorganic & Medicinal Chemistry Letters 2018.0
Synthesis and in vitro antiproliferative activity of novel pyrazolo[3,4-d]pyrimidine derivatives
MedChemComm 2015.0
Design and synthesis of novel pyrazolo[1,5-a]pyrimidine derivatives bearing nitrogen mustard moiety and evaluation of their antitumor activity in vitro and in vivo
European Journal of Medicinal Chemistry 2016.0
Synthesis of ( Z )-1-(1,3-diphenyl-1 H -pyrazol-4-yl)-3-(phenylamino)prop-2-en-1-one derivatives as potential anticancer and apoptosis inducing agents
European Journal of Medicinal Chemistry 2016.0
Synthesis and biological evaluation of novel pyrazole derivatives with anticancer activity
European Journal of Medicinal Chemistry 2011.0