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Synthesis and membrane-protective activity of novel derivatives of α-mangostin at the C-4 position.
Buravlev, Evgeny V; Shevchenko, Oksana G; Kutchin, Aleksandr V.
Afiliação
  • Buravlev EV; Institute of Chemistry, Komi Scientific Center, Ural Branch of the Russian Academy of Sciences, 48, Pervomayskaya St., 167982 Syktyvkar, Komi Republic, Russian Federation. Electronic address: eugeneburavlev@gmail.com.
  • Shevchenko OG; Institute of Biology, Komi Scientific Center, Ural Branch of the Russian Academy of Sciences, 28, Kommunisticheskaya St., 167982 Syktyvkar, Komi Republic, Russian Federation.
  • Kutchin AV; Institute of Chemistry, Komi Scientific Center, Ural Branch of the Russian Academy of Sciences, 48, Pervomayskaya St., 167982 Syktyvkar, Komi Republic, Russian Federation.
Bioorg Med Chem Lett ; 25(4): 826-9, 2015 Feb 15.
Article em En | MEDLINE | ID: mdl-25592715
ABSTRACT
A series of new C-4-derivatives of α-mangostin has been synthesized with the use of Mannich reaction and alkylation with 4-bromomethyl-2,6-dialkylphenols. It has been shown on a model of H2O2-induced erythrocyte hemolysis that the Mannich bases containing morpholinomethyl and piperidinomethyl fragments differ from parent α-mangostin by their high antioxidant and membrane-protective activity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Xantonas Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Xantonas Idioma: En Ano de publicação: 2015 Tipo de documento: Article