Volume 64, Issue 5 pp. 825-829
Research Article

Synthesis of sparsomycin analogs as potential antitumor agents

R. J. Dubois

Corresponding Author

R. J. Dubois

Cancer Chemotherapy Department, Microbiological Associates, Bethesda, MD 20016

Cancer Chemotherapy Department, Microbiological Associates, Bethesda, MD 20016Search for more papers by this author
C.-C. L. Lin

C.-C. L. Lin

Cancer Chemotherapy Department, Microbiological Associates, Bethesda, MD 20016

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B. L. Michel

B. L. Michel

Cancer Chemotherapy Department, Microbiological Associates, Bethesda, MD 20016

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First published: May 1975
Citations: 5

Abstract

No information is available on the structural requirements for the antitumor activity of sparsomycin, an antibiotic obtained from the fermentation broth of Streptomyces sparsogenes. Its high in vivo and in vitro activity, novel structure, and uncommon mode of action have, therefore, suggested the synthesis of analogs. This report describes the preparation and screening of a series of N-substituted 3-aryl acrylamides which are closely related to sparsomycin. Three compounds exhibited some tumor inhibition but insufficient to warrant further testing.

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