Synthesis and Antiproliferative Activity of New Acylcatechins
- Autores: Pozdeev A.O.1, Rasadkina E.N.1, Burym A.A.1, Knyazev V.V.2, Koroteev M.P.1, Matyushin A.I.2, Koroteev A.M.1, Semeikin A.V.2, Shimanovskii N.L.2
- 
							Afiliações: 
							- Institute of Biology and Chemistry, Department of Organic Chemistry, Moscow State Pedagogical University
- Medical-Biology Department, Pirogov Russian National Research Medical University
 
- Edição: Volume 50, Nº 8 (2016)
- Páginas: 523-525
- Seção: Article
- URL: https://ogarev-online.ru/0091-150X/article/view/244428
- DOI: https://doi.org/10.1007/s11094-016-1481-3
- ID: 244428
Citar
Resumo
New peracyl derivatives of the natural flavonoid (±)-catechin were synthesized. It was shown that carboxylic-acid acyl residues enhanced to various degrees the cytotoxicity of peracyl catechins against HeLa cell line. The structures of the synthesized compounds were confirmed by PMR and 13C NMR spectroscopy and elemental analysis. The catechins were compared with previously studied analogous dihydroquercetin derivatives.
Palavras-chave
Sobre autores
A. Pozdeev
Institute of Biology and Chemistry, Department of Organic Chemistry, Moscow State Pedagogical University
							Autor responsável pela correspondência
							Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							3 Nesvizhskii Per., Moscow, 119021						
E. Rasadkina
Institute of Biology and Chemistry, Department of Organic Chemistry, Moscow State Pedagogical University
														Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							3 Nesvizhskii Per., Moscow, 119021						
A. Burym
Institute of Biology and Chemistry, Department of Organic Chemistry, Moscow State Pedagogical University
														Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							3 Nesvizhskii Per., Moscow, 119021						
V. Knyazev
Medical-Biology Department, Pirogov Russian National Research Medical University
														Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							9A/1 Bol’shaya Pirogovskaya St., Moscow, 119435						
M. Koroteev
Institute of Biology and Chemistry, Department of Organic Chemistry, Moscow State Pedagogical University
														Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							3 Nesvizhskii Per., Moscow, 119021						
A. Matyushin
Medical-Biology Department, Pirogov Russian National Research Medical University
														Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							9A/1 Bol’shaya Pirogovskaya St., Moscow, 119435						
A. Koroteev
Institute of Biology and Chemistry, Department of Organic Chemistry, Moscow State Pedagogical University
														Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							3 Nesvizhskii Per., Moscow, 119021						
A. Semeikin
Medical-Biology Department, Pirogov Russian National Research Medical University
														Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							9A/1 Bol’shaya Pirogovskaya St., Moscow, 119435						
N. Shimanovskii
Medical-Biology Department, Pirogov Russian National Research Medical University
														Email: Chemdept@mail.ru
				                					                																			                												                	Rússia, 							9A/1 Bol’shaya Pirogovskaya St., Moscow, 119435						
Arquivos suplementares
 
				
			 
						 
						 
						 
						 
					 
				 
  
  
  
  
  Enviar artigo por via de e-mail
			Enviar artigo por via de e-mail  Acesso aberto
		                                Acesso aberto Acesso está concedido
						Acesso está concedido Somente assinantes
		                                		                                        Somente assinantes
		                                					