96755-00-9Relevant academic research and scientific papers
Design, synthesis, and evaluation of 1, 4-benzodioxan-substituted chalcones as selective and reversible inhibitors of human monoamine oxidase B
Kong, Zhuo,Sun, Demeng,Jiang, Yanmei,Hu, Yun
, p. 1513 - 1523 (2020/07/30)
The inhibition of monoamine oxidase B (MAO-B) could be an effective approach for the treatment of various neurological disorders. In this study, a series of 1, 4-benzodioxan-substituted chalcone derivatives were designed, synthesised and evaluated for the
SYNTHETIC ANALOGS OF NATURAL FLAVOLIGNANS. I. A NEW SYNTHESIS OF ANALOGUES OF SILANDRIN AND HYDNOCARPIN.
Aitmambetov, A.,Khilya, V.P.
, p. 320 - 323 (2007/10/02)
The synthesis of analogues of silandrin and hydnocarpin from 2'-hydroxy-3,4-ethylenedioxychalcones has been achieved.
CHEMISTRY OF ISOFLAVONE HETEROANALOGS. 11. BENZODIOXANE ANALOGS OF CHALCONE, FLAVONE, AND ISOFLAVONE
Khilya, V. P.,Aitmambetov, A.,Turov, A. V.,Kornilov, A. M.,Litkei, D.,at al.
, p. 149 - 154 (2007/10/02)
Benzodioxane analogs of chalcones and their epoxides have been prepared.Different types of analogs of natural flavonolignan - silibin have been synthesized from these compounds.The PMR spectra of the new compounds and the results of the preliminary biological testings are reported and discussed.
