6952-68-7Relevant academic research and scientific papers
Identification and in-vitro ADME assessment of a series of novel anti-malarial agents suitable for hit-to-lead chemistry
Edlin, Chris D.,Morgans, Garreth,Winks, Susan,Duffy, Sandra,Avery, Vicky M.,Wittlin, Sergio,Waterson, David,Burrows, Jeremy,Bryans, Justin
, p. 570 - 573 (2012)
Triage of a set of antimalaria hit compounds, identified through high throughput screening against the Chloroquine sensitive (3D7) and resistant (Dd2) parasite Plasmodium falciparum strains identified several novel chemotypes suitable for hit-to-lead chemistry investigation. The set was further refined through investigation of their in vitro ADME properties, which identified templates with good potential to be developed further as antimalarial agents. One example was profiled in an in vivo murine Plasmodium berghei model of malaria infection.
X-ray crystal structure guided discovery of new selective, substrate-mimicking sirtuin 2 inhibitors that exhibit activities against non-small cell lung cancer cells
Yang, Ling-Ling,Wang, Hua-Li,Zhong, Lei,Yuan, Chen,Liu, Si-Yu,Yu, Zhu-Jun,Liu, Sha,Yan, Yu-Hang,Wu, Chengyong,Wang, Yuxi,Wang, Zhouyu,Yu, Yamei,Chen, Qiang,Li, Guo-Bo
supporting information, p. 806 - 823 (2018/06/27)
Human sirtuin 2 (SIRT2) is a nicotinamide adenine dinucleotide (NAD+)-dependent deacylase, and is implicated in human diseases including cancer. Selective small-molecule inhibitors for SIRT2 are sought as chemical tools and potential therapeuti
Antiviral imidazo- and triazolo-pyridines
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, (2008/06/13)
Thioacetonitrile of imidazo- and triazolo pyridines and their use as antiviral agents are disclosed.
