Cytotoxic activities of novel hexahydroindolizino[8,7-b]indole derivatives prepared by 1,3-dipolar cycloaddition reactions of 3,4-dihydro-β-carboline ylides-Reference-Cited by-同舟云学术

Cytotoxic activities of novel hexahydroindolizino[8,7-b]indole derivatives prepared by 1,3-dipolar cycloaddition reactions of 3,4-dihydro-β-carboline ylides

Published:2001-08 Issue:8 Volume:9 Page:2155-2164
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Bertrand Martial,Poissonnet Guillaume,Théret-Bettiol Marie-Hélène,Gaspard Christiane,Werner Georges H.,Pfeiffer Bruno,Renard Pierre,Léonce Stéphane,Dodd Robert H.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference25 articles.

1. Antitumor agents 201.1 Cytotoxicity of harmine and β-carboline analogs

2. Structures and Biogenesis of Manzamines and Related Alkaloids

3. Eudistomins From the New Zealand Ascidian Ritterella sigillinoides

4. Azatoxin derivatives with potent and selective action on topoisomerase II

5. Fascaplysin, an unusual antimicrobial pigment from the marine sponge Fascaplysinopsis sp

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