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Antitumor agents, 107. New cytotoxic 4-alkylamino analogues of 4'-demethyl-epipodophyllotoxin as inhibitors of human DNA topoisomerase II.
Lee, K H; Imakura, Y; Haruna, M; Beers, S A; Thurston, L S; Dai, H J; Chen, C H; Liu, S Y; Cheng, Y C.
Afiliação
  • Lee KH; Division of Medicinal Chemistry and Natural Products, School of Pharmacy, University of North Carolina, Chapel Hill 27599.
J Nat Prod ; 52(3): 606-13, 1989.
Article em En | MEDLINE | ID: mdl-2550587
A series of analogues of etoposide, the C-4 amino- and alkylamino-substituted 4'-demethyl-epipodophyllotoxins, have been synthesized and studied for their activity to inhibit type II human DNA topoisomerase as well as their activity in causing cellular protein-linked DNA breakage. Substitution of the glycosidic moiety of 1 by a 2"-hydroxyethylamino or 2"-methoxyethylamino chain at the C-4 beta position resulted in potent inhibitors of the human DNA topoisomerase II. This inhibitory activity correlates reasonably well with their activity in causing protein-linked DNA breakage in KB cells. The in vitro cytotoxicity (KB) appears to have no correlation with the inhibitory activity of the human DNA topoisomerase II.
Assuntos
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Base de dados: MEDLINE Assunto principal: Podofilotoxina / Inibidores da Topoisomerase II / Antineoplásicos Limite: Humans Idioma: En Revista: J Nat Prod Ano de publicação: 1989 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Podofilotoxina / Inibidores da Topoisomerase II / Antineoplásicos Limite: Humans Idioma: En Revista: J Nat Prod Ano de publicação: 1989 Tipo de documento: Article