Abstract
In the course of the chemical screening study on the metabolites from actinomycetes, two unusual amino acids were isolated: l-β-(5-Hydroxy-2-pyridyl)-alanine (1) and l-β-(3-hydroxyureido)-alanine (9). The structures of 1 and 9 were elucidated from the physico-chemical properties of these amino acids and derivatives, and supported by synthesis. Antibacterial activities of 1 and its methylester (2) were antagonized by L-tyrosine, and those of 9 and its derivative (17) by l-glutamine. © 1975, The Pharmaceutical Society of Japan. All rights reserved.
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CITATION STYLE
Inouye, S., Shomura, T., Tsuruoka, T., Ogawa, Y., Watanabe, H., Yoshida, J., & Niida, T. (1975). l-β-(5-Hydroxy-2-pyridyl)-alamne and L-β-(3-Hydroxyureido)-alanine from Streptomyces. Chemical and Pharmaceutical Bulletin, 23(11), 2669–2677. https://doi.org/10.1248/cpb.23.2669
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