“…Chrysomycin analogs are one group of glycosides with a benzonaphthopyranone structure obtained from several Streptomyces strains [ 8 , 9 ], which display a broad spectrum of biological properties, including anti-phage, anti-bacterial, and cytotoxic activities [ 10 , 11 , 12 , 13 ]. Especially, chrysomycin A ( Figure 1 ) showed a potent inhibitory effect on multidrug-resistant (MDR) and extensively drug-resistant (XDR) Mycobacterium tuberculosis , methicillin-resistant Staphylococcus aureus (MRSA), and vancomycin-resistant Enterococcus (VRE) [ 13 , 14 , 15 , 16 ].…”