Аннотация:
A series of phosphorylated flavonoids has been synthesized and evaluated in vitro for inhibitory activity against carboxylesterase, acetylcholinesterase and butyrylcholinesterase as well as for their cytotoxicity towards human adenocarcinoma A549 and human glioblastoma U251 cell lines. Diethylphosphoryl derivatives of chrysin and 7-hydroxyflavone were found to be the most effective with bimolecular rate constants for carboxylesterase inhibition ki=2.0×106 and 5.7×106dm3mol−1min−1, respectively.
Образец цитирования:
V. V. Abzianidze, D. S. Prokofieva, P. P. Beltyukov, V. A. Kuznetsov, A. S. Bogachenkov, K. S. Rodygin, “Phosphorylated flavonoids as selective carboxylesterase inhibitors”, Mendeleev Commun., 29:1 (2019), 61–63
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1422
https://www.mathnet.ru/rus/mendc/v29/i1/p61
Эта публикация цитируется в следующих 2 статьяx:
P. A. Volkov, K. O. Khrapova, A. A. Telezhkin, A. I. Albanov, B. A. Trofimov, “Three-component reaction between phenanthridine, acetylenic ketones and bis(polyfluoroalkyl) H-phosphonates: synthesis of E-N-acylethenyl-6-bis(polyfluoroalkyl)phosphoryl-5,6-dihydrophenanthridines”, Russ Chem Bull, 73:1 (2024), 221
Yan Jia, Jiayue Wang, Peng Li, Xiaochi Ma, Keli Han, “Directionally Modified Fluorophores for Super-Resolution Imaging of Target Enzymes: A Case Study with Carboxylesterases”, J. Med. Chem., 64:21 (2021), 16177