Abstract
Five novel cytotoxic antibiotics, NF00659A1, A2, A3), B1 and B2 were discovered. They were isolated from a culture mycelium of Aspergillus sp. These compounds were proved to have 4,5-seco-tricyclic diterpene α-pyrone structure by spectroscopic analyses. They showed potent antitumor activities against human ovarian carcinoma A2780 and human colorectal adenocarcinoma SW480 cells, but did not show any antimicrobial activities at 1000 μg/ml against Gram-positive and Gram-negative bacteria, yeasts and fungi.
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CITATION STYLE
Suzuki, K., Kuwahara, A., Yoshida, H., Fujita, S., Nishikiori, T., & Nakagawa, T. (1997). NF00659A1, A2, A3, B1 and B2, novel antitumor antibiotics produced by Aspergillus sp. NF 00659. I. Taxonomy, fermentation, isolation and biological activities. Journal of Antibiotics, 50(4), 314–317. https://doi.org/10.7164/antibiotics.50.314
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