Podophyllotoxin: distribution, sources, applications and new cytotoxic derivatives

Author:

Gordaliza M,Garcı́a P.A,Miguel del Corral J.M,Castro M.A,Gómez-Zurita M.A

Publisher

Elsevier BV

Subject

Toxicology

Reference197 articles.

1. Synthesis of podophyllotoxin and related analogues: part X—tetralone esters as intermediates for synthesis of analogues of β-apopicropodophyllin;Anjanamurthy;Ind. J. Chem.,1999

2. Design of two etoposide–amsacrine conjugates: topoisomerase II and tubuline polymerization inhibition and relation to cytotoxicity;Arimondo;Anticancer Drug Des.,2000

3. Lignans. Chemical, Biological and Clinical Properties;Ayres,1990

4. F 11782, a novel catalytic inhibitor of topoisomerases I and II, induces atypical, yet cytotoxic DNA double-strand breaks in CHO-K1 cells;Barret;Anticancer Res.,2002

5. Synthesis of analogues of podophyllotoxin: tetralones as intermediates for the synthesis of analogues of apopicropodophyllin;Basavaraju;Ind. J. Heterocyclic Chem.,2002

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