96464-11-8Relevant academic research and scientific papers
Synthesis, Biochemistry, and Computational Studies of Brominated Thienyl Chalcones: A New Class of Reversible MAO-B Inhibitors
Mathew, Bijo,Haridas, Abitha,U?ar, Gülberk,Baysal, Ipek,Joy, Monu,Mathew, Githa E.,Lakshmanan, Baskar,Jayaprakash, Venkatesan
, p. 1161 - 1171 (2016)
A series of (2E)-1-(5-bromothiophen-2-yl)-3-(para-substituted phenyl)prop-2-en-1-ones (TB1–TB11) was synthesized and tested for inhibitory activity toward human monoamine oxidase (hMAO). All compounds were found to be competitive, selective, and reversibl
Novel pyrazolines: Synthesis and evaluation of their derivatives with anticancer and anti-inflammatory activities
Reddy, L. Siva Sanker,Raju, M. Bhagavan,Sridhar
, p. 247 - 254 (2016/01/09)
Objective: Synthesis of novel pyrazolines (P2-P4 & P7-P9) from the chalcones (C2-C10) obtained by condensing different aldehydes with 2-acetyl- 5-bromothiophene and evaluates them for in vitro anticancer and anti-inflammatory activities. Methods: The synt
Fly-ash:H2SO4 catalyzed solvent free efficient synthesis of some aryl chalcones under microwave irradiation
Thirunarayanan,Mayavel,Thirumurthy
experimental part, p. 18 - 22 (2012/05/05)
Some 2E aryl chalcones have been synthesized using greener catalyst Fly-ash:H2SO4 assisted solvent free environmentally benign Crossed-Aldol reaction. The yields of chalcones are more than 90%. The synthesized chalcones are characterized by their physical constants and spectral data.
