36854-32-7Relevant academic research and scientific papers
Synthesis and biological evaluation of cytotoxic properties of stilbene-based resveratrol analogs
de Lima, Denis Pires,Rotta, Rodrigo,Beatriz, Adilson,Marques, Maria Rita,Montenegro, Raquel C.,Vasconcellos, Marne C.,Pessoa, Claudia,de Moraes, Manoel O.,Costa-Lotufo, Leticia V.,Frankland Sawaya, Alexandra Christine Helena,Eberlin, Marcos Nogueira
, p. 701 - 707 (2009)
This work deals with the preparation of stilbene-based resveratrol analogs by employing the Perkin reaction, aiming at synthesizing potential antitumor lead compounds and evaluating their pharmacological activities. The proliferation inhibitor test against tumor cell lines identified analogs 9 and 11 as the most active among all synthesized derivatives, presenting IC50 in micromolar range for certain cell lines. For study on the embryonic development, compounds 8 and 9 at the lowest tested concentration (41.7 μM) that inhibited sea urchin egg development, but only after third cleavage were used. Both the compounds inhibited 100% of normal development since first cleavage. These data partially corroborated the results obtained with MTT assay using tumor cell lines. None of the tested compounds revealed hemolytic action in assay with mouse erythrocytes.
The first synthesis of phenylpropanoid derivative bromophenols including natural products: Formation of an indene derivative compound
Bayrak, Cetin,Menzek, Abdullah
, (2020/02/27)
Synthesis of the natural bromophenols 3,4-dibromo-5-(butoxymethyl)benzene-1,2-diol, (E)-3-(2,3-dibromo-4,5-dihydroxyphenyl)-2-methylacrylaldehyde (7), 3,4-dibromo-5-(3-hydroxy-2-methylpropyl)benzene-1,2-diol and 3-(2,3-dibromo-4,5-dihydroxyphenyl)-2-pheny
Antioxidant, anti-tyrosinase and anti-melanogenic effects of (E)-2,3-diphenylacrylic acid derivatives
Ullah, Sultan,Park, Yujin,Park, Chaeun,Lee, Sanggwon,Kang, Dongwan,Yang, Jungho,Akter, Jinia,Chun, Pusoon,Moon, Hyung Ryong
, p. 2192 - 2200 (2019/04/30)
During our continued search for strong skin whitening agents over the past ten years, we have investigated the efficacies of many tyrosinase inhibitors containing a common (E)-β-phenyl-α,β-unsaturated carbonyl scaffold, which we found to be essential for
