Fungal metabolites. Part 12. Potent immunosuppressant, 14-deoxomyriocin, (2S, 3R, 4R)-(e)-2-amino-3,4-dihydroxy-2-hydroxymethyleicos-6-enoic acid and structure-activity relationships of myriocin derivatives

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Abstract

In order to investigate the structure-activity relationships, fourteen derivatives of myriocin ((2S, 3R, 4R)-(E)-2-amino-3, 4-dihydroxy-2-hydroxymethyl-14-oxoeicos-6-enoic acid) were prepared and examined for immunosuppressive activity on mouse allogeneic mixed lymphocyte reaction in vitro. Among them, 14-deoxomyriocin ((2S, 3R, 4R)-(E)-2-amino-3, 4-dihydroxy-2-hydroxymethyl-eicos-6-enoic acid) was the most potent. It also suppressed the generation of allo-reactive cytotoxic T lymphocytes in mice upon intraperitoneal administration, with a potency 10-fold greater than that of myriocin. © 1994, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.

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Fujita, T., Inoue, K., Yamamoto, S., Ikumoto, T., Sasaki, S., Toyama, R., … Okumoto, T. (1994). Fungal metabolites. Part 12. Potent immunosuppressant, 14-deoxomyriocin, (2S, 3R, 4R)-(e)-2-amino-3,4-dihydroxy-2-hydroxymethyleicos-6-enoic acid and structure-activity relationships of myriocin derivatives. The Journal of Antibiotics, 47(2), 216–224. https://doi.org/10.7164/antibiotics.47.216

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