Abstract
A new alkylamine derivative and a common fatty acid were isolated from Streptomyces sp. YIM 66142. On the basis of spectral data, including HRMS, NMR and 2D NMR, their structures were determined as medelamine C (1) and isomyristic acid (2). The ω-hydroxyl group in structure 1 is rare in a natural alkylamine. The possible biosynthetic pathway in the genus Streptomyces from isomyristic acid (2) to medelamines is proposed. Compound 1 showed no obvious cytotoxicity against HL-60, SMMC-7721, A-549, MCF-7, SW480 cell lines. The ω-hydroxyl and the acetyl at NH in compound 1 decreased its cytotoxicity in comparison with that of medelamine.
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Zhang, J. C., Yang, Y. B., Zhou, H., Peng, T. F., Yang, F. F., Xu, L. H., & Ding, Z. T. (2014). Medelamine C, a new ω-hydroxy alkylamine derivative from endophytic Streptomyces sp. YIM 66142. Natural Product Communications, 9(1), 99–100. https://doi.org/10.1177/1934578x1400900129
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