Studies on mycotrienin antibiotics, a novel class of ansamycins: II. structure elucidation and biosynthesis of mycotrienins I and II

64Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

The structures of mycotrienins I and II have been determined mainly by their NMR spectral analysis. Mycotrienins are unique ansamycin antibiotics containing a 21-membered macrocyclic lactam ring and a cyclohexylcarbonyl moiety. The labeling experiments with sodium [1-13C]acetate and sodium [l-13C]propionate revealed that six acetate units and two propionate units were incorporated into the molecule of mycotrienin I. © 1982, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.

Cite

CITATION STYLE

APA

Sugita, M., Furihata, K., Seto, H., Ōtake, N., & Sasaki, T. (1982). Studies on mycotrienin antibiotics, a novel class of ansamycins: II. structure elucidation and biosynthesis of mycotrienins I and II. The Journal of Antibiotics, 35(11), 1467–1473. https://doi.org/10.7164/antibiotics.35.1467

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free