Synthesis and cytotoxic activity of psorospermin and acronycine analogues in the 3-propyloxy-acridin-9(10 H )-one and -benzo[ b ]acridin-12(5 H )-one series-Reference-Cited by-同舟云学术

Synthesis and cytotoxic activity of psorospermin and acronycine analogues in the 3-propyloxy-acridin-9(10 H )-one and -benzo[ b ]acridin-12(5 H )-one series

Published:2010-02 Issue:2 Volume:45 Page:581-587
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Boutefnouchet Sabrina,Minh Nguyen Tuan,Putrus Rana,Pfeiffer Bruno,Léonce Stéphane,Pierré Alain,Michel Sylvie,Tillequin François,Lallemand Marie-Christine

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference31 articles.

1. Psorospermin, A New Antileukemic Xanthone From Psorospermum febrifugum

2. O5-Methyl-(.+-.)-(2'R,3'S)-psorospermin

3. Structure and stereochemistry of psorospermin and related cytotoxic dihydrofuranoxanthones from Psorospermum febrifugum

4. On the Mechanism of Asymmetric Nucleophilic Ring-Opening of Epoxides Catalyzed by (Salen)CrIII Complexes

5. Topoisomerase II Site-directed Alkylation of DNA by Psorospermin and Its Effect on Topoisomerase II-mediated DNA Cleavage

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