Abstract
The structure of ficellomycin, an antibiotic previously discovered by ARGOUDELIS et al., is elucidated as valyl-2-[4-guanidyl-1-azabicyclo[3.1.0]hexan-2-yl]glycine (1) by NMR, MS, and derivatization studies. The l-azabicyclo[3.1.0]hexane moiety in 1 represents an unusual ring system making ficellomycin a unique natural product compound. © 1989, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
Cite
CITATION STYLE
APA
Kuo, M. s., Yurek, D. A., & Mizsak, S. A. (1989). Structure elucidation of ficellomycin. The Journal of Antibiotics, 42(3), 357–360. https://doi.org/10.7164/antibiotics.42.357
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free