Rifampicin (1) was converted into two inactivated products RIP-Ma and RIP-Mb by Mycobacterium smegmatis DSM43756. MS, NMR and chromatographic analysis showed the compounds to be 3-formyl-23-[0-(α-D-ribofuranosyl)]rifamycin SV (6) and 23-[O-(α-D-ribofur-anosyl)]rifampicin (7), respectively. © 1995, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
CITATION STYLE
Dabbs, E. R., Mikami, Y., & Iwasaki, S. (1995). Structure Determination of Ribosylated Rifampicin and Its Derivative: New Inactivated Metabolites of Rifampicin by Mycobacterial Strains. The Journal of Antibiotics, 48(11), 1299–1303. https://doi.org/10.7164/antibiotics.48.1299
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